Table of Contents
Advances in Vascular Medicine
Volume 2014, Article ID 689815, 11 pages
http://dx.doi.org/10.1155/2014/689815
Review Article

Diverse Functions of Secretory Phospholipases A2

1Department of Internal Medicine, Division of Endocrinology and Cardiovascular Research Center, University of Kentucky, 900 S. Limestone, 567 Wethington Building, Lexington, KY 40536-0200, USA
2Molecular and Biomedical Pharmacology, University of Kentucky, Lexington, KY 40536-0200, USA

Received 7 May 2014; Accepted 21 June 2014; Published 15 July 2014

Academic Editor: David Tanne

Copyright © 2014 Preetha Shridas and Nancy R. Webb. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Phospholipase A2 enzymes (PLA2s) catalyze the hydrolysis of glycerophospholipids at their sn-2 position releasing free fatty acids and lysophospholipids. Mammalian PLA2s are classified into several categories of which important groups include secreted PLA2s (sPLA2s) and cytosolic PLA2s (cPLA2s) that are calcium-dependent for their catalytic activity and calcium-independent cytosolic PLA2s (iPLA2s). Platelet-activating factor acetylhydrolases (PAF-AHs), lysosomal PLA2s, and adipose-specific PLA2 also belong to the class of PLA2s. Generally, cPLA2 enzymes are believed to play a major role in the metabolism of arachidonic acid, the iPLA2 family to membrane homeostasis and energy metabolism, and the sPLA2 family to various biological processes. The focus of this review is on recent research developments in the sPLA2 field. sPLA2s are secreted enzymes with low molecular weight (with the exception of GIII sPLA2), Ca2+-requiring enzymes with a His-Asp catalytic dyad. Ten enzymatically active sPLA2s and one devoid of enzymatic activity have been identified in mammals. Some of these sPLA2s are potent in arachidonic acid release from cellular phospholipids for the biosynthesis of eicosanoids, especially during inflammation. Individual sPLA2 enzymes exhibit unique tissue and cellular localizations and specific enzymatic properties, suggesting their distinct biological roles. Recent studies indicate that sPLA2s are involved in diverse pathophysiological functions and for most part act nonredundantly.

1. Introduction

Secreted phospholipases A2 (sPLA2s) are secreted from a variety of cells and act in autocrine or paracrine manners on cell membranes and other extracellular phospholipids, including lipoprotein particles, surfactant and dietary lipids, microbial membranes, and microvesicles  [1]. Even though sPLA2s are considered to act as extracellularly requiring millimolar concentrations of Ca2+, few in vitro reports also indicate possible intracellular activity prior to or during secretion  [2]. To date, eleven sPLA2 enzymes, group IB (GIB), group IIA (GIIA), group IIC (GIIC), group IID (GIID), group IIE (GIIE), group IIF (GIIF), group III (GIII), group V (GV), group X (GX), group XIIA (GXIIA), and group XIIB (GXIIB), have been identified in mammals [35]. GIII sPLA2 is an atypical sPLA2 that contains unique N-terminal and C-terminal domains and a central sPLA2 domain, the S domain, which has higher homology with bee venom sPLA2 (a prototypic group III enzyme) than with other known mammalian sPLA2s [6]. Another unique member is GXIIB protein which has structural features similar to those of the GXIIA sPLA2 subgroup. However, GXIIB sPLA2 has a mutation in the active site, which replaces the canonical histidine by a leucine thus making the enzyme catalytically inactive [7].

Recently some unexpected novel roles for individual sPLA2s have been described, which form the basis of this review. The review does not provide details of several in vitro studies regarding substrate specificities, biochemical properties, and structure and sequence homology of different sPLA2s as they have been covered by a number of earlier reviews [4, 811] but focuses on several recently described physiological functions of selected sPLA2s.

2. Functions of sPLA2s in Asthma and Inflammation

Eicosanoids, including leukotrienes and prostaglandins, play complex roles in the pathogenesis of airway inflammation [1214]. Prostaglandin D2 (PGD2) triggers asthmatic responses [12], while prostaglandin I2 (PGI2) and prostaglandin E2 (PGE2) serve as inhibitors of allergic response [15, 16]. Leukotrienes (LTs) generally promote the development of asthma; 5-lipoxygenase products are found to be necessary for ovalbumin-induced airway responsiveness in mice [17]. In contrast, 12/15-lipoxygenase products are generally considered protective [18, 19]. PGD2; thromboxane A2 (TXA2) and cysteinyl leukotrienes (cys-LTs) are reported to function as bronchoconstrictors while PGE2 is considered to act as bronchodilator [20].

The rate-limiting step in eicosanoid biosynthesis is the release of unesterified arachidonic acid (AA) from the sn-2 position of membrane phospholipids by PLA2s [21]. Some sPLA2s find importance in the development of asthma through the generation of arachidonic acid (AA). However the role of individual sPLA2s in the disease depends on the metabolic fate of AA released. It is interesting to observe that AA released from the same cell type by different classes of PLA2s is metabolized differently. The reason for this difference could be the difference in cellular localization and mode and rate of release. Using specific inhibitors, it has been demonstrated that sPLA2 and cPLA2 play opposing roles in asthma pathophysiology with sPLA2s linked to the production of the bronchoconstrictor Cys-LT whereas cPLA2 promotes the production of the bronchodilator PGE2. In cells that play a key role in asthma, namely, human eosinophils and basophils, PGE2 is produced from a cPLA2-linked pool [20, 2224].

sPLA2s are found at high levels in bronchoalveolar lavage (BAL) fluid and bronchotracheal smooth muscle cells [25, 26]. Studies have identified an increase in sPLA2 activity in BAL fluid from subjects with asthma [27] and also an increase in sPLA2 activity after allergen challenge [2830]. Four sPLA2s (GIB, GIIA, GV, and GX) are reported to be expressed in human lungs, the highest being GX sPLA2 followed by GV- and GIIA-sPLA2s in the BAL fluid of patients with asthma [31]. GX sPLA2 displays the greatest potency among mammalian sPLA2s in hydrolyzing the phosphatidylcholine- (PC-) rich extracellular leaflet of mammalian plasma membranes [1, 32] and has the strongest ability to initiate eicosanoid synthesis in mammalian cells [32]. Immunohistochemical studies indicate that GX sPLA2 is expressed in airway epithelial cells and macrophages in BAL fluid [33]. GX sPLA2 has the highest expression in the airways of patients with asthma [31, 34] and is strongly expressed in the airway epithelium relative to the other sPLA2 genes [31]. Human GX sPLA2 is also found in induced sputum samples in patients with exercise-induced asthma and its levels in BAL fluid correlated with asthma severity [31]. The activity of GX sPLA2 appears to correlate with lung functions, neutrophil recruitment, and prostaglandin levels [31]. GX sPLA2 is known to specifically initiate Cys-LT synthesis by eosinophils [35]. It is also believed that GX sPLA2 is released from airway epithelial cells and may act on eosinophils in a paracrine manner to produce lysophosphatidylcholine (LPC), which in turn triggers Ca2+ influx leading to activation of cPLA2α and thereby production of Cys-LT [35]. The expression of GX sPLA2 is upregulated by cytokines implicated in asthma, including TNF/IL-1β, IL-17, and to a lesser extent IL-13 but is suppressed by IL-4 [36]. Deficiency of GX sPLA2 in mice dampens the development of asthma. Ovalbumin- (OVA-) induced Cys-LT and PGD2 production were near fully blocked in GX sPLA2-deficient mice (GX KO mice), indicating this as a possible mechanism [33]. Insertion of the human GX sPLA2 gene in GX KO mice restored the capacity for the development of airway inflammation, which could further be abolished by an active site-directed inhibitor of human GX sPLA2 [37]. These results indicate inhibition of GX sPLA2 as a novel therapeutic target in asthma.

The action of GV sPLA2 in asthma and other respiratory diseases appears to be complex. GV sPLA2 expressed by both myeloid cells and lung-resident nonmyeloid cells and participates in the innate immune response to pulmonary infection [38]. GV sPLA2 is also induced in bronchial epithelial cells in antigen-challenged mice and intratracheal application of an antibody against GV sPLA2 ameliorates airway inflammation, suggesting a proinflammatory action of this enzyme in the airway [39]. GV sPLA2-deficient mice (GV KO) exposed to an extract of house dust mite Dermatophagoides farinae had markedly reduced pulmonary inflammation and goblet cell metaplasia compared with wild-type (WT) mice [40]. GV KO mice had also impaired Th2-type adaptive immune responses to D. farinae compared with WT mice. Processing of antigen-presenting cells is significantly dampened in GV KO mice and the mice also display a reduction of Th2 polarization, thus preventing further propagation of inflammation [40]. Thus, GV sPLA2 appears to function in a dual manner in airway-resident cells, one to facilitate airway inflammation possibly via surfactant degradation and secondly in antigen-presenting cells to regulate antigen processing and thereby the Th2 immune response. In another study, Degousee et al. [38] demonstrated that GV sPLA2 is important for leukocyte recruitment to the lung and for efficient pulmonary clearance of bacteria in a mouse model of E. coli pneumonia. GV KO mice cleared bacteria from lung parenchyma and the alveolar space less efficiently than the wild type (WT) mice after pulmonary infection with E. coli. Similarly, in severe systemic candidiasis, reduced clearance of Candida albicans was observed in GV KO mice compared to similarly treated WT mice. However, cytokine production and eicosanoid generation were not impaired by the lack of GV sPLA2 [41]. Injection of lipopolysaccharide (LPS) into the air pouches of mice results in the attraction of leukocytes and deficiency of GV sPLA2 is found to reduce leukocyte recruitment in this model [42]. GV sPLA2 likely plays a role in hydrolyzing pulmonary surfactants. Transgenic mice that overexpress mouse GV sPLA2 (GV-Tg) die of respiratory failure during the neonatal period [43]. In these mice, excessive hydrolysis of the pulmonary surfactant has been observed, which interrupts respiratory function [43]. The lungs of these mice exhibit atelectasis with thickened alveolar walls and narrow air spaces and pronounced infiltration of macrophages, but with modest changes in eicosanoid levels. This severe pulmonary defect in GV-Tg mice is attributable to marked reduction of the lung surfactant phospholipids, dipalmitoyl-PC, and phosphatidylglycerol. Asthma and airway inflammation is thus one example where the two closely related GV and GX sPLA2s exhibit different modes of action in disease pathophysiology. In contrast with GV-Tg mice, mice overexpressing human GX sPLA2 (GX-Tg) do not have an overt defect in the lung. The reason for the lack of phenotype is attributed to the existence of GX sPLA2 as an inactive proenzyme in the transgenic mice, which becomes activated upon inflammatory challenge [43].

sPLA2s are also involved in other inflammatory diseases. A recent report indicates that GX sPLA2 protein and mRNA expression are increased in the lungs of mice following H1N1 pandemic influenza infection [44]. Both epithelial cells and leukocytes were found to be sources of GX sPLA2 during infection and GX sPLA2 expression was detected in epithelial cells 3 days prior to the infiltration of leukocytes. The targeted deletion of GX sPLA2 led to increased survival in mice challenged with H1N1. Lack of GX sPLA2 resulted in decreased levels of PGD2, LTB4, cys-LT, PGE2, and Lipoxin A4 and increased adaptive immune responses at 3 days following H1N1 infection indicating the role of GX sPLA2 in the generation of these lipid mediators following infection [44]. Thus it appears that deficiency of GX sPLA2 in mice was beneficial to the host during influenza infection.

GX sPLA2 is not the only isoform associated with inflammation. Several sPLA2 isoforms are expressed by inflammatory cells such as neutrophils, eosinophils, basophils, T cells, monocytes, macrophages, and mast cells [45, 46]. The expression of some of the sPLA2s is known to be upregulated with inflammation, while the expression of some other sPLA2s appears to be constitutive [4, 47, 48]. The level of GIIA sPLA2 in serum correlates with the severity of inflammatory diseases such as rheumatoid arthritis and sepsis. Its expression is markedly induced by proinflammatory stimuli in a wide variety of cells and tissues of various animal species [5]. Expression of GIIA sPLA2 is induced by inflammatory stimuli such as IL-6, TNFα, IFN-, LPS, cAMP-elevating agents, and phorbol esters [4, 48]. GIIA sPLA2 is thought to play an important role in innate immunity. Transgenic mice expressing human GIIA sPLA2 are protected against group B streptococcal (GBS) infection. Consistent with this finding, serum isolated from humans with acute invasive GBS infection has increased levels of GIIA sPLA2 [49]. Similarly, transgenic mice expressing human GIIA sPLA2 are found to be resistant to experimental Bacillus anthracis infection [50, 51]. GV sPLA2 is present in the phagosomes of macrophages and regulates phagocytosis [52]. Mammalian sPLA2s are also known to participate in host defense against viruses. In vitro studies performed in mammalian cell lines indicate that GX and GV sPLA2s prevent adenoviral infections in mammalian cell lines by preventing the entry of viruses into the cells, an effect that is mimicked by LPC [53].

3. Role of sPLA2s in Atherosclerosis

Atherosclerosis is a chronic inflammatory disease of the vessel wall characterized by the accumulation of macrophages filled with lipids and fibrotic material. According to the “response-to-retention” hypothesis, the disease is initiated by the accumulation of modified lipoproteins in the vessel wall, such as oxidized LDL. It has been shown by several investigators that several sPLA2 isoforms are expressed in atherosclerotic lesions [54, 55], some of which are capable of hydrolyzing phospholipids (PLs) present in low density lipoprotein (LDL). There is now accumulating evidence that several sPLA2 isoforms, namely GIIA-, GIII-, GV-, and GX-sPLA2s, play significant, distinct, or overlapping roles in one or several steps of atherogenesis [5663].

In human aortic tissues, GIIA sPLA2 ismore strongly expressed in the arterial intima of atherosclerotic than of nonatherosclerotic tissue. The majority of GIIA PLA2 is localized along the extracellular matrix, associated with collagen fibers and other extracellular matrix structures [64]. GIIA sPLA2 binds to cell-surface proteoglycans with high affinity and this binding to proteoglycans increases their potency to hydrolyze phosphatidylcholine (PC) present in LDL [65]. Circulating levels of GIIA sPLA2 are an independent risk factor for cardiovascular events in humans [66]. Studying the in vivo function of GIIA sPLA2 in host defense and inflammatory conditions has been limited by the fact that inbred C57BL/6 mouse strain is naturally deficient for this sPLA2 [67]. Most of the studies relating to the in vivo effects of the enzyme have been carried out in transgenic mouse models or mice in which the recombinant enzyme has been injected. Transgenic mice that constitutively express GIIA sPLA2 exhibit spontaneous atherosclerosis in the absence of hyperlipidemia indicating that this enzyme may take part in atherogenesis and not just serum marker for the disease [68]. These mice also had elevated VLDL/LDL cholesterol levels and lower HDL levels with decreased paraoxonase activity, suggesting that changes in lipoproteins may play a role in GIIA sPLA2’s atherogenic effect [68]. The decreased HDL is thought to be due to an increase in hepatic selective uptake of HDL-cholesterol ester and plasma clearance of HDL [69, 70]. Low density lipoprotein receptor-deficient mice overexpressing GIIA sPLA2 in bone marrow-derived cells demonstrated larger atherosclerotic lesion formation compared to WT mice in both aortic sinus and aortic arch when fed a high fat diet [71]. The transgenic mice had increased collagen deposition in lesions independent of lesion size without any effect on systemic cholesterol levels indicating a proatherosclerotic role for GIIA sPLA2 [56].

GV sPLA2 is detected in human and mouse artherosclerotic lesions and hyperlipidemic high fat diet upregulates expression of GV sPLA2 in mice [72]. In vitro studies using recombinant proteins indicate that GV sPLA2 is much more potent in hydrolyzing lipoprotein PC than GIIA sPLA2 [73]. Hydrolysis of LDL by GV sPLA2 decreases the particle size, induces spontaneous aggregation and enhances foam cell formation in cultured mouse peritoneal macrophages indicating a potential proatherosclerotic role for the enzyme [74]. Enhanced uptake of GV sPLA2-modified LDL was independent of scavenger receptors SR-A and CD36 but dependent on cell-surface proteoglycans [63]. In vitro studies performed in macrophages indicated that syndecan-4 is involved in the uptake of GV sPLA2-modified LDL particles [75]. Fatty acids released by GV sPLA2 hydrolysis of LDL stimulate nuclear factor-kappaB (NF-kB) activation in macrophages resulting in the production of proinflammatory cytokines [63]. The proatherogenic role of GV sPLA2 was demonstrated later by gain-of-function and loss-of-function studies in mice; whereas retroviral vector-mediated overexpression of GV sPLA2 in bone marrow-derived cells increased lesion size, deletion of GV sPLA2 in bone marrow-cells reduced atherosclerosis [61]. Subsequent studies demonstrated that lack of GV sPLA2 in bone marrow-derived cells does not alter lesion development in apolipoprotein E-deficient mice, possibly due to marked differences in lipoprotein particles that circulates in mice compared to mice [76].

GIII sPLA2-modified LDL, like GV sPLA2- or GX sPLA2-treated LDL, facilitated the formation of foam cells from macrophages ex vivo. Accumulation of GIII sPLA2 was detected in atherosclerotic lesions of humans and mice. Furthermore, following an atherogenic diet, aortic atherosclerotic lesions were more severe in GIII sPLA2 transgenic mice than in control mice on the background, in combination with elevated plasma lysophosphatidylcholine and TXB2 levels. These results collectively suggest a potential functional link between GIII sPLA2 and atherosclerosis [60].

GX sPLA2 is present in human atherosclerotic lesions. In vitro studies indicate a proatherogenic role for GX sPLA2 [55, 57]. Consistent with this belief, our lab has observed that upon angiotensin II infusion, deficiency of GX sPLA2 in a background reduces the development of atherosclerosis as indicated by reduction of lesion size in the aortic arch area [77]. However, a later study performed in mice indicated deficiency of GX sPLA2 in the bone marrow-derived cells to accelerate the development of atherosclerotic lesions in the aortic sinus through an exacerbated Th1 immunoinflammatory response [78], indicating a protective role for GX sPLA2 in the development of atherosclerosis. The reasons for the discrepancy between the studies are not very clear, maybe due to differences between the mouse strains vs or the inducer high fat diet versus angiotensin II between the two models.

In a double-blind, randomized, multicenter trial in patients with recent acute coronary syndrome (ACS), varespladib, a nonspecific pan-sPLA2 inhibitor, did not reduce the risk of recurrent cardiovascular events and significantly increased the risk of myocardial infarction (MI). It was thus concluded that the sPLA2 inhibition with varespladib may thus be harmful and is not a useful strategy to reduce adverse cardiovascular outcomes after ACS [79].

4. Effect of sPLA2s on Male Reproductive System

Male reproductive system consists of organs that act together to produce and deliver functional spermatozoa into the female reproductive tract. After the differentiation process of male germ cells, spermatozoa exit the seminiferous tubules of the testis through the efferent ducts towards the epididymis. During their transition from the caput to the cauda epididymidis, spermatozoa undergo significant morphological and biochemical modifications which lead to acquisition of their forward motility and ability to recognize and fertilize oocytes [80]. Ejaculated mammalian sperm must undergo a maturation process called capacitation before they are able to fertilize an egg. Different sPLA2s are expressed in male reproductive organs and in sperm cells, among which mouse GX sPLA2 is found to play an important role in sperm motility and fertilization outcome during capacitation. Several studies have suggested a role for members of sPLA2 family in capacitation, acrosome reaction (AR), and fertilization. GX sPLA2 is the major enzyme present in the acrosome of spermatozoa and it is released in an active form during capacitation through spontaneous AR in mice [81]. In their study, Escoffier et al. [81] reported that GX KO male mice produced smaller litters than wild-type male siblings when crossed with GX KO females. Further they reported that spermatozoa from GX KO mice exhibited lower rates of spontaneous AR and that this was associated with decreased in vitro fertilization (IVF) efficiency due to a drop in the fertilization potential of the sperm and an increased rate of aborted embryos. Mouse GX sPLA2 acts as a potent inhibitor of sperm motility of both capacitated and noncapacitated sperms [82]. Though the mechanism for this regulation is unclear, this effect of GX sPLA2 is dependent on its catalytic function and hence might involve changes in phospholipid metabolism. It is also found that endogenous GX sPLA2 is spontaneously released during acrosome reaction and modulates motility of capacitated sperms [82]. Mouse GX sPLA2 has a unique property of improving fertilization outcome during capacitation [83] and hence has a unique usefulness in improving outcomes in in vitro fertilization. This property of mouse GX sPLA2 is not mimicked by other sPLA2s including human GX or GV sPLA2 or progesterone; this is yet another example of how functions and specificities differ for individual sPLA2s. Deficiency of GIII sPLA2 in mice leads to defective sperm maturation and asthenozoospermia [84]. The enzyme is expressed in mouse proximal epididymal epithelium. The deficient mice had normal spermatogenesis but displayed hypomotility and demonstrated impaired fertilization efficiency. The defect was attributed to impaired phospholipids remodeling in the sperm during epididymal transit. The enzyme was also found to contribute to gonadal 12/15-lipoxygenase metabolites, indicating important role played by this enzyme in phospholipid and eicosanoid metabolism in male reproductive organs.

5. Unexpected Proteolytic Properties of sPLA2

As summarized above, sPLA2s have been associated with the development of atherosclerosis, which was related to its ability to hydrolyze phospholipids on lipoprotein particles. A novel report by Cavigiolio and Jayaraman [85] indicated that certain sPLA2s are capable of acting as proteolytic enzymes. They demonstrated the effect by hydrolyzing the apolipoprotein A1 (apoA1) on HDL. Incubation of sPLA2 (GIB, GIIA, and bee venom GIII sPLA2s) with lipid-free apoA1 produced protein fragments in the range of 6–15 suggesting specific and direct reaction of sPLA2 with apoA-I. Mass spectrometry analysis of isolated proteolytic fragments indicated at least two major cleavage sites at the C-terminal and the central domain of apoA-I. ApoA-I proteolysis by sPLA2 was Ca2+-independent, implicating a different mechanism from the Ca2+-dependent sPLA2-mediated phospholipid hydrolysis. Inhibition of proteolysis by benzamidine suggests that the proteolytic and lipolytic activities of PLA2 proceed through different mechanisms. The proteolytic potential of other sPLA2s have not yet been reported.

6. GX sPLA2 as a Regulator of Liver X Receptor Activation

Our group recently reported a novel role of GX sPLA2 in suppressing macrophage expression of ATP-binding cassette transporter A1 (ABCA1) and ATP-binding cassette transporter G1 (ABCG1) [86]. ABCA1 and ABCG1 play key roles in macrophage cholesterol homeostasis by exporting excess cellular free cholesterol to extracellular acceptors [87, 88]. The nuclear hormone receptors, liver X receptors α and β (LXRα and ) act as intracellular cholesterol sensors and induce the expression of target genes including ABCA1 and ABCG1 [89, 90]. We made the novel observation that GX sPLA2 negatively regulates expression of ABC transporters in macrophages by suppressing LXR activation [86]. Peritoneal macrophages isolated from mice deficient in GX sPLA2 exhibit significantly increased expression of ABCA1/ABCG1 and increased cellular cholesterol efflux with a consequent reduction in cellular free cholesterol content [86]. This effect of GX sPLA2 is dependent on its catalytic function and is mimicked by the exogenous addition of free arachidonic acid. Further, the effect of GX sPLA2 is abolished when LXR α- and β-expression is suppressed in macrophages. Polyunsaturated fatty acids (PUFAs) including arachidonic acid (AA) have been shown to act as antagonists for LXR activation by interacting with the ligand binding domain [91, 92]. PUFAs compete with LXR agonists to block LXR activation and hence their effects are reversed by LXR agonists including T0901317.  Like PUFAs, GX sPLA2 also suppresses LXR activation through a mechanism involving the C-terminal portion of LXR that spans the LXR binding domain. However, the effect of GX sPLA2 on LXR activity is only partially reversed by LXR agonists indicating that the hydrolytic products generated by GX sPLA2 do not act in a manner that simply involves direct competition for agonist binding. This effect of GX sPLA2 was found to be specific to LXR and not observed for other nuclear receptors tested including the glucocorticoid receptor [93].

Cholesterol accumulation in macrophages is associated with a proinflammatory phenotype [9496]. Changes in plasma membrane free cholesterol/lipid raft content modulate macrophage inflammatory responses through a myeloid differentiation primary response 88- (MyD88-) dependent signaling pathway which is independent of an ER stress response [94, 97]. In macrophages, suppressed expression of ABCA1 and ABCG1 results in decreased cholesterol efflux, increased cellular free cholesterol levels, and enhanced MyD88-dependent signaling. We determined that macrophages overexpressing GX sPLA2 have significantly increased lipid raft content consistent with GX sPLA2’s suppressive effect on ABCA1/ABCG1 expression. This increased cholesterol accumulation in macrophages was associated with enhanced macrophage inflammatory responses. Transgenic overexpression or exogenous addition of recombinant GX sPLA2 to macrophages results in increased induction of TNFα, IL6, and cyclooxygenase-2 expression in J774 macrophage-like cells in response to lipopolysaccharide (LPS) treatment [98]. This effect is abolished in macrophages that lack either toll-like receptor 4 (TLR4) or MyD88 or when cellular free cholesterol was normalized using cyclodextrin. Mice deficient in GX sPLA2 demonstrate dampened inflammatory responses as evidenced by significantly reduced plasma concentrations of inflammatory cytokines, including TNFα, IL6, and IL-1β following LPS treatment. Taken together these findings indicate that GX sPLA2 modulates plasma membrane free cholesterol and lipid raft content by suppressing the expression of LXR target genes ABCA1/ABCG1, thereby contributing to inflammatory responses in macrophages. These findings are consistent with the report by Sato et al. [99] demonstrating that pharmacological inhibition of sPLA2 significantly attenuates the acute lung inflammation and injury induced by LPS in C57BL/6J mice. The authors also concluded that the effects were most likely due to inhibition of GX sPLA2 and/or GV sPLA2. Consistent with the above observations, studies in our lab showed that deficiency of GX sPLA2 in apo mice significantly reduced abdominal aortic aneurism formation induced by angiotensin II (AngII). Apo mice lacking GX sPLA2 demonstrated significantly blunted induction of inflammatory mediators in the aorta after AngII infusion compared to apo mice [77].

Another interesting phenotype demonstrated GX KO mice related to LXR activation in adrenal glands. C57BL/6 mice deficient in GX sPLA2 have ~80% higher basal and ACTH-induced plasma corticosterone levels compared to wild-type controls [100]. GX sPLA2-deficient mice have no defect in the hypothalamic-pituitary axis as evidenced by normal ACTH levels in response to dexamethasone challenge [100]. Consistent with hypercorticosteronemia, primary adrenal cells from GX sPLA2-deficient mice showed increased corticosterone release both under basal and ACTH-stimulated conditions. Further mechanistic studies indicated that GX sPLA2 negatively regulates the expression of steroidogenic acute regulatory protein (StAR) in adrenal cells. StAR is a nuclearly encoded mitochondrial protein that mediates the rate-limiting step of steroidogenesis by delivering cholesterol to the inner mitochondrial membrane [101]. StAR mRNA expression is under positive and negative regulation by a variety of transcription factors including AP-1, SF-1, C/EBP, Sp-1, GATA, DAX-1, SREBP-1a, and LXR [102, 103]. Administration of a synthetic LXR agonist increases plasma corticosterone levels and adrenal StAR mRNA expression in mice [103, 104]. A functional LXR-response element- (LXRE-) like sequence has been identified in the StAR promoter [103]. Consistent with its effect on LXR activation as described above, GX sPLA2 suppresses LXR-mediated StAR activation through a mechanism that is dependent on GX sPLA2’s catalytic activity.  Based on luciferase reporter assays, GX sPLA2’s regulation of StAR expression requires an intact LXRE-like sequence in the StAR promoter, indicating the LXR-dependency for this effect [100].

LXR activation promotes adipogenesis and triglyceride accumulation in adipocytes [105, 106]. Consistent with the role of GX sPLA2 in suppressing LXR activation, in vitro studies indicated that GX sPLA2 suppressed triglyceride accumulation in adipocytes by blunting the expression of adipogenic genes including PPARγ, SREBP-1c, SCD1, and FAS. These genes are either direct or indirect targets of LXR. GX sPLA2-deficient mice gained more weight than WT mice when fed a normal chow diet due to increased adiposity and increased adipocyte sizes [107]. The difference in body weight was not clearly evident until the mice are at least 4-5 months of age. There was no difference in food intake, energy balance, or oxygen consumption between the wild-type and deficient mice. However, there were alterations in fat storage by adipocytes. Effect on body weight has not been shown in all studies; Fujioka et al. have observed no change in body weight between GX sPLA2-deficient mice and wild-type control mice [108]; this discrepancy could be due to differences in the type of housing of the mice in the two studies. Figure 1 shows the overall effects of GX sPLA2’s regulation of LXR activity in mice.

689815.fig.001
Figure 1: Physiological effects of suppression of LXR activity by GX sPLA2 in mice. Red arrows and lines indicate effect of GX sPLA2. LXR target genes are shown in black boxes.

7. Biological Functions of Catalytically Inactive GXIIB sPLA2

GXIIB sPLA2 is catalytically inactive due to the presence of a leucine residue in place of a canonical histidine that is essential for the enzymatic activity. GXIIB sPLA2 is abundantly expressed in liver, small intestine, and kidney in both human and mouse species. Interestingly, the expression of this sPLA2 is dramatically decreased in human tumors from the same tissues. The absence of enzymatic activity suggests that this protein may exert biological functions by acting as a ligand for as yet unidentified receptor(s) [7].

Hepatocyte nuclear factor-4 alpha (HNF-4α) is an important transcription factor governing the expression of genes involved in multiple metabolic pathways. Guan et al. reported that GXIIB sPLA2 is a target gene for HNF-4α [109]. HNF-4α agonists induce GXIIB sPLA2 expression in human hepatocarcinoma cells. Interestingly, GXIIB sPLA2-deficient mice accumulate triglyceride, cholesterol, and fatty acids in the liver and develop severe hepatosteatosis resembling some of the phenotypes of liver-specific HNF-4α-deficient mice. These defects are in part due to compromised hepatic very low density lipoprotein secretion. Overexpression of HNF-4α in liver by adenoviral vector elevates serum triglycerides level in wild-type but not GXIIB deficient mice [109]. It will be interesting to investigate whether GXIIB sPLA2 demonstrates proteolytic activity as described earlier, independent of their phospholipase activity which might account for the phenotype observed in the deficient mice.

8. Conclusions

With the increasing number of mouse strains with altered expression of individual sPLA2s, considerable progress has been made in understanding the physiological functions of each of the isoforms. However, knockout/transgenic strains for many of the isoforms and mice with tissue-specific targeting are still largely unavailable. It is now quite clear that the functions of sPLA2s are nonredundant, tissue/cell type-specific, and unique. It is therefore crucial to understand the factors contributing to the functional differences between these enzymes especially in a therapeutic point of view.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

References

  1. M. Murakami, Y. Taketomi, H. Sato, and K. Yamamoto, “Secreted phospholipase A2 revisited,” Journal of Biochemistry, vol. 150, no. 3, pp. 233–255, 2011. View at Publisher · View at Google Scholar · View at Scopus
  2. C. M. Mounier, F. Ghomashchi, M. R. Lindsay et al., “Arachidonic acid release from mammalian cells transfected with human groups IIA and X secreted phospholipase A2 occurs predominantly during the secretory process and with the involvement of cytosolic phospholipase A2-α,” Journal of Biological Chemistry, vol. 279, no. 24, pp. 25024–25038, 2004. View at Publisher · View at Google Scholar · View at Scopus
  3. M. Murakami and I. Kudo, “Diversity and regulatory functions of mammalian secretory phospholipase A2s,” Advances in Immunology, vol. 77, pp. 163–194, 2001. View at Publisher · View at Google Scholar · View at Scopus
  4. I. Kudo and M. Murakami, “Phospholipase A2 enzymes,” Prostaglandins and Other Lipid Mediators, vol. 68-69, pp. 3–58, 2002. View at Publisher · View at Google Scholar · View at Scopus
  5. M. Murakami, Y. Taketomi, Y. Miki, H. Sato, T. Hirabayashi, and K. Yamamoto, “Recent progress in phospholipase A2 research: from cells to animals to humans,” Progress in Lipid Research, vol. 50, no. 2, pp. 152–192, 2011. View at Publisher · View at Google Scholar · View at Scopus
  6. E. Valentines, F. Ghomashchi, M. H. Gelb, M. Lazdunski, and G. Lambeau, “Novel human secreted phospholipase A2 with homology to the group III bee venom enzyme,” Journal of Biological Chemistry, vol. 275, no. 11, pp. 7492–7496, 2000. View at Publisher · View at Google Scholar · View at Scopus
  7. M. Rouault, J. G. Bollinger, M. Lazdunski, M. H. Gelb, and G. Lambeau, “Novel mammalian group XII secreted phospholipase A2 lacking enzymatic activity,” Biochemistry, vol. 42, no. 39, pp. 11494–11503, 2003. View at Publisher · View at Google Scholar · View at Scopus
  8. M. Murakami, Y. Taketomi, Y. Miki, H. Sato, T. Hirabayashi, and K. Yamamoto, “Recent progress in phospholipase A2 research: from cells to animals to humans,” Progress in Lipid Research, vol. 50, no. 2, pp. 152–192, 2011. View at Publisher · View at Google Scholar · View at Scopus
  9. M. Murakami, Y. Taketomi, C. Girard, K. Yamamoto, and G. Lambeau, “Emerging roles of secreted phospholipase A2 enzymes: lessons from transgenic and knockout mice,” Biochimie, vol. 92, no. 6, pp. 561–582, 2010. View at Publisher · View at Google Scholar · View at Scopus
  10. B. B. Boyanovsky and N. R. Webb, “Biology of secretory phospholipase A2,” Cardiovascular Drugs and Therapy, vol. 23, no. 1, pp. 61–72, 2009. View at Publisher · View at Google Scholar · View at Scopus
  11. G. Lambeau and M. H. Gelb, “Biochemistry and physiology of mammalian secreted phospholipases A 2,” Annual Review of Biochemistry, vol. 77, pp. 495–520, 2008. View at Publisher · View at Google Scholar · View at Scopus
  12. T. Matsuoka, M. Hirata, H. Tanaka et al., “Prostaglandin D2 as a mediator of allergic asthma,” Science, vol. 287, no. 5460, pp. 2013–2017, 2000. View at Publisher · View at Google Scholar · View at Scopus
  13. K. Terawaki, T. Yokomizo, T. Nagase et al., “Absence of leukotriene B4 receptor 1 confers resistance to airway hyperresponsiveness and Th2-type immune responses,” Journal of Immunology, vol. 175, no. 7, pp. 4217–4225, 2005. View at Publisher · View at Google Scholar · View at Scopus
  14. A. M. Tager, S. K. Bromley, B. D. Medoff et al., “Leukotriene B4 receptor BLT1 mediates early effector T cell recruitment,” Nature Immunology, vol. 4, no. 10, pp. 982–990, 2003. View at Publisher · View at Google Scholar · View at Scopus
  15. Z. Jaffar, M. E. Ferrini, M. C. Buford, G. A. FitzGerald, and K. Roberts, “Prostaglandin I2-IP signaling blocks allergic pulmonary inflammation by preventing recruitment of CD4+ Th2 cells into the airways in a mouse model of asthma,” Journal of Immunology, vol. 179, no. 9, pp. 6193–6203, 2007. View at Publisher · View at Google Scholar · View at Scopus
  16. T. Kunikata, H. Yamane, E. Segi et al., “Suppression of allergic inflammation by the prostaglandin E receptor subtype EP3,” Nature Immunology, vol. 6, no. 5, pp. 524–531, 2005. View at Publisher · View at Google Scholar · View at Scopus
  17. C. G. Irvin, Y. Tu, J. R. Sheller, and C. D. Funk, “5-lipoxygenase products are necessary for ovalbumin-induced airway responsiveness in mice,” The American Journal of Physiology—Lung Cellular and Molecular Physiology, vol. 272, no. 6, pp. L1053–L1058, 1997. View at Google Scholar · View at Scopus
  18. B. D. Levy, G. T. De Sanctis, P. R. Devchand et al., “Multi-pronged inhibition of airway hyper-responsiveness and inflammation by lipoxin A4,” Nature Medicine, vol. 8, no. 9, pp. 1018–1023, 2002. View at Publisher · View at Google Scholar · View at Scopus
  19. O. Haworth, M. Cernadas, R. Yang, C. N. Serhan, and B. D. Levy, “Resolvin E1 regulates interleukin 23, interferon-γ and lipoxin A4 to promote the resolution of allergic airway inflammation,” Nature Immunology, vol. 9, no. 8, pp. 873–879, 2008. View at Publisher · View at Google Scholar · View at Scopus
  20. S. Offer, S. Yedgar, O. Schwob et al., “Negative feedback between secretory and cytosolic phospholipase A2 and their opposing roles in ovalbumin-induced bronchoconstriction in rats,” The American Journal of Physiology—Lung Cellular and Molecular Physiology, vol. 288, no. 3, pp. L523–L529, 2005. View at Publisher · View at Google Scholar · View at Scopus
  21. T. S. Hallstrand and W. R. Henderson Jr., “Role of leukotrienes in exercise-induced bronchoconstriction,” Current Allergy and Asthma Reports, vol. 9, no. 1, pp. 18–25, 2009. View at Publisher · View at Google Scholar · View at Scopus
  22. E. A. Capper and L. A. Marshall, “Mammalian phospholipases A2: mediators of inflammation, proliferation and apoptosis,” Progress in Lipid Research, vol. 40, no. 3, pp. 167–197, 2001. View at Publisher · View at Google Scholar · View at Scopus
  23. N. M. Muñoz, Y. J. Kim, A. Y. Meliton et al., “Human group V phospholipase A2 induces group IVA phospholipase A2-independent cysteinyl leukotriene synthesis in human eosinophils,” The Journal of Biological Chemistry, vol. 278, no. 40, pp. 38813–38820, 2003. View at Publisher · View at Google Scholar · View at Scopus
  24. N. J. Pyne, D. Tolan, and S. Pyne, “Bradykinin stimulates cAMP synthesis via mitogen-activated protein kinase-dependent regulation of cytosolic phospholipase A2 and prostaglandin E2 release in airway smooth muscle,” Biochemical Journal, vol. 328, part 2, pp. 689–694, 1997. View at Google Scholar · View at Scopus
  25. A. C. Sane, T. Mendenhall, and D. A. Bass, “Secretory phospholipase A2 activity is elevated in bronchoalveolar lavage fluid after ovalbumin sensitization of guinea pigs,” Journal of Leukocyte Biology, vol. 60, no. 6, pp. 704–709, 1996. View at Google Scholar · View at Scopus
  26. P. Vadas, “Group II phospholipases A2 are indirectly cytolytic in the presence of exogenous phospholipid,” Biochimica et Biophysica Acta, vol. 1346, no. 2, pp. 193–197, 1997. View at Publisher · View at Google Scholar · View at Scopus
  27. M. Triggiani, F. Granata, A. Petraroli et al., “Inhibition of secretory phospholipase A2-induced cytokine production in human lung macrophages by budesonide,” International Archives of Allergy and Immunology, vol. 150, no. 2, pp. 144–155, 2009. View at Publisher · View at Google Scholar · View at Scopus
  28. D. L. Bowton, M. C. Seeds, M. B. Fasano, B. Goldsmith, and D. A. Bass, “Phospholipase A2 and arachidonate increase in bronchoalveolar lavage fluid after inhaled antigen challenge in asthmatics,” The American Journal of Respiratory and Critical Care Medicine, vol. 155, no. 2, pp. 421–425, 1997. View at Publisher · View at Google Scholar · View at Scopus
  29. F. H. Chilton, F. J. Averill, W. C. Hubbard, A. N. Fonteh, M. Triggiani, and M. C. Liu, “Antigen-induced generation of lyso-phospholipids in human airways,” Journal of Experimental Medicine, vol. 183, no. 5, pp. 2235–2245, 1996. View at Publisher · View at Google Scholar · View at Scopus
  30. J. M. Stadel, K. Hoyle, R. M. Naclerio, A. Roshak, and F. H. Chilton, “Characterization of phospholipase A2 from human nasal lavage.,” American Journal of Respiratory Cell and Molecular Biology, vol. 11, no. 1, pp. 108–113, 1994. View at Publisher · View at Google Scholar · View at Scopus
  31. T. S. Hallstrand, Y. Lai, Z. Ni et al., “Relationship between levels of secreted phospholipase A2 groups IIA and X in the airways and asthma severity,” Clinical and Experimental Allergy, vol. 41, no. 6, pp. 801–810, 2011. View at Publisher · View at Google Scholar · View at Scopus
  32. A. G. Singer, F. Ghomashchi, C. Le Calvez et al., “Interfacial kinetic and binding properties of the complete set of human and mouse groups I, II, V, X, and XII secreted phospholipases A2,” Journal of Biological Chemistry, vol. 277, no. 50, pp. 48535–48549, 2002. View at Publisher · View at Google Scholar · View at Scopus
  33. W. R. Henderson Jr., E. Y. Chi, J. G. Bollinger et al., “Importance of group X-secreted phospholipase A2 in allergen-induced airway inflammation and remodeling in a mouse asthma model,” The Journal of Experimental Medicine, vol. 204, no. 4, pp. 865–877, 2007. View at Publisher · View at Google Scholar · View at Scopus
  34. T. S. Hallstrand, E. Y. Chi, A. G. Singer, M. H. Gelb, and W. R. Henderson Jr., “Secreted phospholipase A2 group X overexpression in asthma and bronchial hyperresponsiveness,” The American Journal of Respiratory and Critical Care Medicine, vol. 176, no. 11, pp. 1072–1078, 2007. View at Publisher · View at Google Scholar · View at Scopus
  35. Y. Lai, R. C. Oslund, J. G. Bollinger et al., “Eosinophil cysteinyl leukotriene synthesis mediated by exogenous secreted phospholipase A2 group X,” Journal of Biological Chemistry, vol. 285, no. 53, pp. 41491–41500, 2010. View at Publisher · View at Google Scholar · View at Scopus
  36. T. S. Hallstrand, Y. Lai, W. A. Altemeier et al., “Regulation and function of epithelial secreted phospholipase A2 group X in asthma,” The American Journal of Respiratory and Critical Care Medicine, vol. 188, no. 1, pp. 42–50, 2013. View at Publisher · View at Google Scholar · View at Scopus
  37. W. R. Henderson Jr., R. C. Oslund, J. G. Bollinger et al., “Blockade of human group X secreted phospholipase A 2 (GX-sPLA 2)-induced airway inflammation and hyperresponsiveness in a mouse asthma model by a selective GX-sPLA 2 inhibitor,” Journal of Biological Chemistry, vol. 286, no. 32, pp. 28049–28055, 2011. View at Publisher · View at Google Scholar · View at Scopus
  38. N. Degousee, D. J. Kelvin, G. Geisslinger et al., “Group V phospholipase A2 in bone marrow-derived myeloid cells and bronchial epithelial cells promotes bacterial clearance after Escherichia coli pneumonia,” The Journal of Biological Chemistry, vol. 286, no. 41, pp. 35650–35662, 2011. View at Publisher · View at Google Scholar · View at Scopus
  39. N. M. Muñoz, A. Y. Meliton, J. P. Arm, J. V. Bonventre, W. Cho, and A. R. Leff, “Deletion of secretory group V phospholipase A2 attenuates cell migration and airway hyperresponsiveness in immunosensitized mice,” Journal of Immunology, vol. 179, no. 7, pp. 4800–4807, 2007. View at Publisher · View at Google Scholar · View at Scopus
  40. G. Giannattasio, D. Fujioka, W. Xing, H. R. Katz, J. A. Boyce, and B. Balestrieri, “Group v secretory phospholipase A2 reveals its role in house dust mite-induced allergic pulmonary inflammation by regulation of dendritic cell function,” Journal of Immunology, vol. 185, no. 7, pp. 4430–4438, 2010. View at Publisher · View at Google Scholar · View at Scopus
  41. B. Balestrieri, A. Maekawa, W. Xing, M. H. Gelb, H. R. Katz, and J. P. Arm, “Group V secretory phospholipase A2 modulates phagosome maturation and regulates the innate immune response against Candida albicans,” Journal of Immunology, vol. 182, no. 8, pp. 4891–4898, 2009. View at Publisher · View at Google Scholar · View at Scopus
  42. S. Lapointe, A. Brkovic, I. Cloutier, J. Tanguay, J. P. Arm, and M. G. Sirois, “Group V secreted phospholipase A2 contributes to LPS-induced leukocyte recruitment,” Journal of Cellular Physiology, vol. 224, no. 1, pp. 127–134, 2010. View at Publisher · View at Google Scholar · View at Scopus
  43. M. Ohtsuki, Y. Taketomi, S. Arata et al., “Transgenic expression of group V, but not group X, secreted phospholipase A2 in mice leads to neonatal lethality because of lung dysfunction,” Journal of Biological Chemistry, vol. 281, no. 47, pp. 36420–36433, 2006. View at Publisher · View at Google Scholar · View at Scopus
  44. A. A. Kelvin, N. Degousee, D. Banner et al., “Lack of group X secreted phospholipase A2 increases survival following pandemic H1N1 influenza infection,” Virology, vol. 454-455, pp. 78–92, 2014. View at Google Scholar
  45. A. Enomoto, M. Murakami, E. Valentin, G. Lambeau, M. H. Gelb, and I. Kudo, “Redundant and segregated functions of granule-associated heparin-binding group II subfamily of secretory phospholipases A2 in the regulation of degranulation and prostaglandin D2 synthesis in mast cells,” The Journal of Immunology, vol. 165, no. 7, pp. 4007–4014, 2000. View at Publisher · View at Google Scholar · View at Scopus
  46. M. A. Balboa, J. Balsinde, M. V. Winstead, J. A. Tischfield, and E. A. Dennis, “Novel group V phospholipase A2 involved in arachidonic acid mobilization in murine P388D1 macrophages,” Journal of Biological Chemistry, vol. 271, no. 50, pp. 32381–32384, 1996. View at Publisher · View at Google Scholar · View at Scopus
  47. S. Masuda, M. Murakami, M. Mitsuishi et al., “Expression of secretory phospholipase A2 enzymes in lungs of humans with pneumonia and their potential prostaglandin-synthetic function in human lung-derived cells,” Biochemical Journal, vol. 387, no. 1, pp. 27–38, 2005. View at Publisher · View at Google Scholar · View at Scopus
  48. K. Hamaguchi, H. Kuwata, K. Yoshihara et al., “Induction of distinct sets of secretory phospholipase A2 in rodents during inflammation,” Biochimica et Biophysica Acta—Molecular and Cell Biology of Lipids, vol. 1635, no. 1, pp. 37–47, 2003. View at Publisher · View at Google Scholar · View at Scopus
  49. E. Movert, Y. Wu, G. Lambeau, F. Kahn, L. Touqui, and T. Areschoug, “Secreted group iia phospholipase a2 protects humans against the group b streptococcus: experimental and clinical evidence,” The Journal of Infectious Diseases, vol. 208, pp. 2025–2035, 2013. View at Publisher · View at Google Scholar
  50. A. Piris-Gimenez, M. Paya, G. Lambeau et al., “In vivo protective role of human group IIA phospholipase A2 against experimental anthrax,” The Journal of Immunology, vol. 175, no. 10, pp. 6786–6791, 2005. View at Publisher · View at Google Scholar · View at Scopus
  51. F. Granata, A. Frattini, S. Loffredo et al., “Signaling events involved in cytokine and chemokine production induced by secretory phospholipase A2 in human lung macrophages,” European Journal of Immunology, vol. 36, no. 7, pp. 1938–1950, 2006. View at Publisher · View at Google Scholar · View at Scopus
  52. B. Balestrieri and J. P. Arm, “Group V sPLA2: classical and novel functions,” Biochimica et Biophysica Acta: Molecular and Cell Biology of Lipids, vol. 1761, no. 11, pp. 1280–1288, 2006. View at Publisher · View at Google Scholar · View at Scopus
  53. M. Mitsuishi, S. Masuda, I. Kudo, and M. Murakami, “Group V and X secretory phospholipase A2 prevents adenoviral infection in mammalian cells,” Biochemical Journal, vol. 393, no. 1, pp. 97–106, 2006. View at Publisher · View at Google Scholar · View at Scopus
  54. M. Kimura-Matsumoto, Y. Ishikawa, K. Komiyama et al., “Expression of secretory phospholipase A2s in human atherosclerosis development,” Atherosclerosis, vol. 196, no. 1, pp. 81–91, 2008. View at Publisher · View at Google Scholar · View at Scopus
  55. K. Hanasaki, K. Yamada, S. Yamamoto et al., “Potent modification of low density lipoprotein by group X secretory phospholipase A2 is linked to macrophage foam cell formation,” Journal of Biological Chemistry, vol. 277, no. 32, pp. 29116–29124, 2002. View at Publisher · View at Google Scholar · View at Scopus
  56. S. A. I. Ghesquiere, M. J. J. Gijbels, M. Anthonsen et al., “Macrophage-specific overexpression of group IIa sPLA2 increases atherosclerosis and enhances collagen deposition,” Journal of Lipid Research, vol. 46, no. 2, pp. 201–210, 2005. View at Publisher · View at Google Scholar · View at Scopus
  57. S. A. Karabina, I. Brochériou, G. le Naour et al., “Atherogenic properties of LDL particles modified by human group X secreted phospholipase A2 on human endothelial cell function.,” The FASEB Journal, vol. 20, no. 14, pp. 2547–2549, 2006. View at Publisher · View at Google Scholar · View at Scopus
  58. A. Jönsson-Rylander, S. Lundin, B. Rosengren, C. Pettersson, and E. Hurt-Camejo, “Role of secretory phospholipases in atherogenesis,” Current Atherosclerosis Reports, vol. 10, no. 3, pp. 252–259, 2008. View at Publisher · View at Google Scholar · View at Scopus
  59. B. Boyanovsky, M. Zack, K. Forrest, and N. R. Webb, “The capacity of group V sPLA2 to increase atherogenicity of ApoE-/- and LDLR-/- mouse LDL in vitro predicts its atherogenic role in vivo,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 29, no. 4, pp. 532–538, 2009. View at Publisher · View at Google Scholar · View at Scopus
  60. H. Sato, R. Kato, Y. Isogai et al., “Analyses of group III secreted phospholipase A2 transgenic mice reveal potential participation of this enzyme in plasma lipoprotein modification, macrophage foam cell formation, and atherosclerosis,” The Journal of Biological Chemistry, vol. 283, no. 48, pp. 33483–33497, 2008. View at Publisher · View at Google Scholar
  61. M. A. Bostrom, B. B. Boyanovsky, C. T. Jordan et al., “Group V secretory phospholipase A2 promotes atherosclerosis: evidence from genetically altered mice,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 27, no. 3, pp. 600–606, 2007. View at Publisher · View at Google Scholar · View at Scopus
  62. F. C. De Beer and N. R. Webb, “Inflammation and atherosclerosis: group iia and group v spla2 are not redundant,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 26, no. 7, pp. 1421–1422, 2006. View at Publisher · View at Google Scholar · View at Scopus
  63. B. B. Boyanovsky, D. R. van der Westhuyzen, and N. R. Webb, “Group V secretory phospholipase A2-modified low density lipoprotein promotes foam cell formation by a SR-A- and CD36-independent process that involves cellular proteoglycans,” Journal of Biological Chemistry, vol. 280, no. 38, pp. 32746–32752, 2005. View at Publisher · View at Google Scholar · View at Scopus
  64. M. Romano, E. Romano, S. Björkerud, and E. Hurt-Camejo, “Ultrastructural localization of secretory type II phospholipase A2 in atherosclerotic and nonatherosclerotic regions of human arteries,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 18, no. 4, pp. 519–525, 1998. View at Publisher · View at Google Scholar · View at Scopus
  65. P. Sartipy, G. Camejo, L. Svensson, and E. Hurt-Camejo, “Phospholipase A2 modification of low density lipoproteins forms small high density particles with increased affinity for proteoglycans and glycosaminoglycans,” The Journal of Biological Chemistry, vol. 274, no. 36, pp. 25913–25920, 1999. View at Publisher · View at Google Scholar · View at Scopus
  66. K. Kugiyama, Y. Ota, K. Takazoe et al., “Circulating levels of secretory type II phospholipase A2 predict coronary events in patients with coronary artery disease,” Circulation, vol. 100, no. 12, pp. 1280–1284, 1999. View at Publisher · View at Google Scholar · View at Scopus
  67. B. P. Kennedy, P. Payette, J. Mudgett et al., “A natural disruption of the secretory group II phospholipase A2 gene in inbred mouse strains,” The Journal of Biological Chemistry, vol. 270, no. 38, pp. 22378–22385, 1995. View at Publisher · View at Google Scholar · View at Scopus
  68. B. Ivandic, L. W. Castellani, X. Wang et al., “Role of group II secretory phospholipase A2 in atherosclerosis: 1. Increased atherogenesis and altered lipoproteins in transgenic mice expressing group IIa phospholipase A2,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 19, no. 5, pp. 1284–1290, 1999. View at Publisher · View at Google Scholar · View at Scopus
  69. U. J. F. Tietge, C. Maugeais, W. Cain et al., “Overexpression of secretory phospholipase A2 causes rapid catabolism and altered tissue uptake of high density lipoprotein cholesteryl ester and apolipoprotein A-I,” Journal of Biological Chemistry, vol. 275, no. 14, pp. 10077–10084, 2000. View at Publisher · View at Google Scholar · View at Scopus
  70. F. C. de Beer, P. M. Connell, J. Yu, M. C. de Beer, N. R. Webb, and D. R. van der Westhuyzen, “HDL modification by secretory phospholipase A2 promotes scavenger receptor class B type I interaction and accelerates HDL catabolism,” Journal of Lipid Research, vol. 41, no. 11, pp. 1849–1857, 2000. View at Google Scholar · View at Scopus
  71. N. R. Webb, M. A. Bostrom, S. J. Szilvassy, D. R. van der Westhuyzen, A. Daugherty, and F. C. de Beer, “Macrophage-expressed group IIA secretory phospholipase A2 increases atherosclerotic lesion formation in LDL receptor-deficient mice,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 23, no. 2, pp. 263–268, 2003. View at Publisher · View at Google Scholar · View at Scopus
  72. B. Rosengren, H. Peilot, M. Umaerus et al., “Secretory phospholipase A2 group V: lesion distribution, activation by arterial proteoglycans, and induction in aorta by a western diet,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 26, no. 7, pp. 1579–1585, 2006. View at Publisher · View at Google Scholar · View at Scopus
  73. L. Gesquiere, W. Cho, and P. V. Subbaiah, “Role of group IIa and group V secretory phospholipases A2 in the metabolism of lipoproteins. Substrate specificities of the enzymes and the regulation of their activities by sphingomyelin,” Biochemistry, vol. 41, no. 15, pp. 4911–4920, 2002. View at Publisher · View at Google Scholar · View at Scopus
  74. C. R. Wooton-Kee, B. B. Boyanovsky, M. S. Nasser, W. J. S. de Villiers, and N. R. Webb, “Group V spla2 hydrolysis of low-density lipoprotein results in spontaneous particle aggregation and promotes macrophage foam cell formation,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 24, no. 4, pp. 762–767, 2004. View at Publisher · View at Google Scholar · View at Scopus
  75. B. B. Boyanovsky and N. R. Webb, “Biology of secretory phospholipase A2,” Cardiovascular Drugs and Therapy, vol. 23, no. 1, pp. 61–72, 2009. View at Publisher · View at Google Scholar · View at Scopus
  76. B. Boyanovsky, M. Zack, K. Forrest, and N. R. Webb, “The capacity of group V sPLA2 to increase atherogenicity of ApoE-/- and LDLR-/- mouse LDL in vitro predicts its atherogenic role in vivo,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 29, no. 4, pp. 532–538, 2009. View at Publisher · View at Google Scholar · View at Scopus
  77. M. Zack, B. B. Boyanovsky, P. Shridas et al., “Group X secretory phospholipase A2 augments angiotensin II-induced inflammatory responses and abdominal aortic aneurysm formation in apoE-deficient mice,” Atherosclerosis, vol. 214, no. 1, pp. 58–64, 2011. View at Publisher · View at Google Scholar · View at Scopus
  78. H. Ait-Oufella, O. Herbin, C. Lahoute et al., “Group X secreted phospholipase a2 limits the development of atherosclerosis in LDL receptor-null mice,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 33, no. 3, pp. 466–473, 2013. View at Publisher · View at Google Scholar · View at Scopus
  79. S. J. Nicholls, J. J. Kastelein, G. G. Schwartz et al., “Varespladib and cardiovascular events in patients with an acute coronary syndrome: the vista-16 randomized clinical trial,” The Journal of the American Medical Association, vol. 311, pp. 252–262, 2014. View at Google Scholar
  80. T. G. Cooper, “Role of the epididymis in mediating changes in the male gamete during maturation,” Advances in Experimental Medicine and Biology, vol. 377, pp. 87–101, 1995. View at Publisher · View at Google Scholar · View at Scopus
  81. J. Escoffier, I. Jemel, A. Tanemoto et al., “Group X phospholipase A2 is released during sperm acrosome reaction and controls fertility outcome in mice,” The Journal of Clinical Investigation, vol. 120, no. 5, pp. 1415–1428, 2010. View at Publisher · View at Google Scholar · View at Scopus
  82. J. Escoffier, V. J. Pierre, I. Jemel et al., “Group X secreted phospholipase A2 specifically decreases sperm motility in mice,” Journal of Cellular Physiology, vol. 226, no. 10, pp. 2601–2609, 2011. View at Publisher · View at Google Scholar · View at Scopus
  83. R. Abi Nahed, J. Escoffier, C. Revel et al., “The effect of group X secreted phospholipase A2 on fertilization outcome is specific and not mimicked by other secreted phospholipases A2 or progesterone,” Biochimie, vol. 99, pp. 88–95, 2014. View at Publisher · View at Google Scholar
  84. H. Sato, Y. Taketomi, Y. Isogai et al., “Group III secreted phospholipase A2 regulates epididymal sperm maturation and fertility in mice,” Journal of Clinical Investigation, vol. 120, no. 5, pp. 1400–1414, 2010. View at Publisher · View at Google Scholar · View at Scopus
  85. G. Cavigiolio and S. Jayaraman, “Proteolysis of apolipoprotein a-i by secretory phospholipase a2: a new link between inflammation and atherosclerosis,” The Journal of Biological Chemistry, vol. 289, pp. 10011–10023, 2014. View at Google Scholar
  86. P. Shridas, W. M. Bailey, F. Gizard et al., “Group X secretory phospholipase A2 negatively regulates ABCA1 and ABCG1 expression and cholesterol efflux in macrophages,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 30, no. 10, pp. 2014–2021, 2010. View at Publisher · View at Google Scholar · View at Scopus
  87. A. D. Attie, J. P. Kastelein, and M. R. Hayden, “Pivotal role of ABCA1 in reverse cholesterol transport influencing HLD levels and susceptibility to atherosclerosis,” Journal of Lipid Research, vol. 42, no. 11, pp. 1717–1726, 2001. View at Google Scholar · View at Scopus
  88. N. Wang, D. Lan, W. Chen, F. Matsuura, and A. R. Tall, “ATP-binding cassette transporters G1 and G4 mediate cellular cholesterol efflux to high-density lipoproteins,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 26, pp. 9774–9779, 2004. View at Publisher · View at Google Scholar · View at Scopus
  89. P. Costet, Y. Luo, N. Wang, and A. R. Tall, “Sterol-dependent transactivation of the ABC1 promoter by the liver X receptor/retinoid X receptor,” Journal of Biological Chemistry, vol. 275, no. 36, pp. 28240–28245, 2000. View at Publisher · View at Google Scholar · View at Scopus
  90. A. Venkateswaran, B. A. Laffitte, S. B. Joseph et al., “Control of cellular cholesterol efflux by the nuclear oxysterol receptor LXR α,” Proceedings of the National Academy of Sciences of the United States of America, vol. 97, no. 22, pp. 12097–12102, 2000. View at Publisher · View at Google Scholar · View at Scopus
  91. T. Yoshikawa, H. Shimano, N. Yahagi et al., “Polyunsaturated fatty acids suppress sterol regulatory element-binding protein 1c promoter activity by inhibition of liver X receptor (LXR) binding to LXR response elements,” Journal of Biological Chemistry, vol. 277, no. 3, pp. 1705–1711, 2002. View at Publisher · View at Google Scholar · View at Scopus
  92. J. Ou, H. Tu, B. Shan et al., “Unsaturated fatty acids inhibit transcription of the sterol regulatory element-binding protein-1c (SREBP-1c) gene by antagonizing ligand-dependent activation of the LXR,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 11, pp. 6027–6032, 2001. View at Publisher · View at Google Scholar · View at Scopus
  93. P. Shridas, W. M. Bailey, F. Gizard et al., “Group X secretory phospholipase A2 negatively regulates ABCA1 and ABCG1 expression and cholesterol efflux in macrophages,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 30, no. 10, pp. 2014–2021, 2010. View at Publisher · View at Google Scholar · View at Scopus
  94. X. Zhu, J. Lee, J. M. Timmins et al., “Increased cellular free cholesterol in macrophage-specific Abca1 knock-out mice enhances pro-inflammatory response of macrophages,” Journal of Biological Chemistry, vol. 283, no. 34, pp. 22930–22941, 2008. View at Publisher · View at Google Scholar · View at Scopus
  95. Y. Li, R. F. Schwabe, T. DeVries-Seimon et al., “Free cholesterol-loaded macrophages are an abundant source of tumor necrosis factor-α and interleukin-6: model of NF-κB- and map kinase-dependent inflammation in advanced atherosclerosis,” Journal of Biological Chemistry, vol. 280, no. 23, pp. 21763–21772, 2005. View at Publisher · View at Google Scholar · View at Scopus
  96. M. Koseki, K. Hirano, D. Masuda et al., “Increased lipid rafts and accelerated lipopolysaccharide-induced tumor necrosis factor-α secretion in Abca1-deficient macrophages,” Journal of Lipid Research, vol. 48, no. 2, pp. 299–306, 2007. View at Publisher · View at Google Scholar · View at Scopus
  97. L. Yvan-Charvet, C. Welch, T. A. Pagler et al., “Increased inflammatory gene expression in ABC transporter-deficient macrophages: free cholesterol accumulation, increased signaling via toll-like receptors, and neutrophil infiltration of atherosclerotic lesions,” Circulation, vol. 118, no. 18, pp. 1837–1847, 2008. View at Publisher · View at Google Scholar · View at Scopus
  98. P. Shridas, W. M. Bailey, K. R. Talbott, R. C. Oslund, M. H. Gelb, and N. R. Webb, “Group X secretory phospholipase A2 enhances TLR4 signaling in macrophages,” Journal of Immunology, vol. 187, no. 1, pp. 482–489, 2011. View at Publisher · View at Google Scholar · View at Scopus
  99. R. Sato, S. Yamaga, K. Watanabe et al., “Inhibition of secretory phospholipase A2 activity attenuates lipopolysaccharide-induced acute lung injury in a mouse model,” Experimental Lung Research, vol. 36, no. 4, pp. 191–200, 2010. View at Publisher · View at Google Scholar · View at Scopus
  100. P. Shridas, W. M. Bailey, B. B. Boyanovsky, R. C. Oslund, M. H. Gelb, and N. R. Webb, “Group X secretory phospholipase A2 regulates the expression of steroidogenic acute regulatory protein (StAR) in mouse adrenal glands,” Journal of Biological Chemistry, vol. 285, no. 26, pp. 20031–20039, 2010. View at Publisher · View at Google Scholar · View at Scopus
  101. D. M. Stocco, “StAR protein and the regulation of steroid hormone biosynthesis,” Annual Review of Physiology, vol. 63, pp. 193–213, 2001. View at Publisher · View at Google Scholar · View at Scopus
  102. A. Rigotti, E. R. Edelman, P. Seifert et al., “Regulation by adrenocorticotropic hormone of the in vivo expression of scavenger receptor class B type I (SR-BI), a high density lipoprotein receptor, in steroidogenic cells of the murine adrenal gland,” Journal of Biological Chemistry, vol. 271, no. 52, pp. 33545–33549, 1996. View at Publisher · View at Google Scholar · View at Scopus
  103. C. L. Cummins, D. H. Volle, Y. Zhang et al., “Liver X receptors regulate adrenal cholesterol balance,” Journal of Clinical Investigation, vol. 116, no. 7, pp. 1902–1912, 2006. View at Publisher · View at Google Scholar · View at Scopus
  104. K. R. Steffensen, S. Y. Neo, T. M. Stulnig et al., “Genome-wide expression profiling; a panel of mouse tissues discloses novel biological functions of liver X receptors in adrenals,” Journal of Molecular Endocrinology, vol. 33, no. 3, pp. 609–622, 2004. View at Publisher · View at Google Scholar · View at Scopus
  105. L. K. Juvet, S. M. Andresen, G. U. Schuster et al., “On the role of liver X receptors in lipid accumulation in adipocytes,” Molecular Endocrinology, vol. 17, no. 2, pp. 172–182, 2003. View at Publisher · View at Google Scholar · View at Scopus
  106. J. B. Seo, H. M. Moon, W. S. Kim et al., “Activated liver x receptors stimulate adipocyte differentiation through induction of peroxisome proliferator-activated receptor γexpression,” Molecular and Cellular Biology, vol. 24, no. 8, pp. 3430–3444, 2004. View at Publisher · View at Google Scholar · View at Scopus
  107. X. Li, P. Shridas, K. Forrest, W. Bailey, and N. R. Webb, “Group X secretory phospholipase a2 negatively regulates adipogenesis in murine models,” FASEB Journal, vol. 24, no. 11, pp. 4313–4324, 2010. View at Publisher · View at Google Scholar · View at Scopus
  108. D. Fujioka, Y. Saito, T. Kobayashi et al., “Reduction in myocardial ischemia/reperfusion injury in group X secretory phospholipase A2-deficient mice,” Circulation, vol. 117, no. 23, pp. 2977–2985, 2008. View at Publisher · View at Google Scholar · View at Scopus
  109. M. Guan, L. Qu, W. Tan, L. Chen, and C. Wong, “Hepatocyte nuclear factor-4 alpha regulates liver triglyceride metabolism in part through secreted phospholipase A2 GXIIB,” Hepatology, vol. 53, no. 2, pp. 458–466, 2011. View at Publisher · View at Google Scholar · View at Scopus