Effects of FTY720 on Lung Injury Induced by Hindlimb Ischemia Reperfusion in Rats

Wang, Liangrong; Chen, Feifei; Pan, Yafei; Lin, Lina; Xiong, Xiangqing

doi:https://doi.org/10.1155/2017/5301312

Mediators of Inflammation

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Abstract Introduction Materials and Methods Results Discussion Conflicts of Interest Acknowledgments References Copyright Related Articles

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Sphingolipids in Inflammation

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Research Article | Open Access

Volume 2017 | Article ID 5301312 | https://doi.org/10.1155/2017/5301312

Effects of FTY720 on Lung Injury Induced by Hindlimb Ischemia Reperfusion in Rats

Liangrong Wang,¹Feifei Chen,¹Yafei Pan,¹Lina Lin,¹and Xiangqing Xiong¹

Academic Editor: Elisabetta Albi

Received21 May 2017

Revised09 Aug 2017

Accepted13 Sept 2017

Published09 Nov 2017

Abstract

Background. Sphingosine-1-phosphate (S1P) is a biologically active lysophospholipid mediator involved in modulating inflammatory process. We investigated the effects of FTY720, a structural analogue of S1P after phosphorylation, on lung injury induced by hindlimb ischemia reperfusion (IR) in rats. Methods. Fifty Sprague-Dawley rats were divided into groups SM, IR, F3, F5, and F10. Group SM received sham operation, and bilateral hindlimb IR was established in group IR. The rats in groups F3, F5, and F10 were pretreated with 3, 5, and 10 mg/kg/d FTY720 for 7 days before IR. S1P lyase (S1PL), sphingosine kinase (SphK) 1, and SphK2 mRNA expressions, wet/dry weight (W/D), and polymorphonuclear/alveolus (P/A) in lung tissues were detected, and the lung injury score was evaluated. Results. W/D, P/A, and mRNA expressions of S1PL, SphK1, and SphK2 were higher in group IR than in group SM, while these were decreased in both groups F5 and F10 as compared to IR (). The lung tissue presented severe lesions in group IR, which were attenuated in groups F5 and F10 with lower lung injury scores than in group IR (). Conclusions. FTY720 pretreatment could attenuate lung injury induced by hindlimb IR by modulating S1P metabolism and decreasing pulmonary neutrophil infiltration.

1. Introduction

Limb ischemia reperfusion (IR) injury is commonly presented in restoration of blood flow to previously hypoxic extremities following severe crush injury, vessel damage, or some surgical procedures. Limb IR injury is well demonstrated to result in various local and systemic effects, where the latter could include multiple organ failure ultimately leading to death [1, 2]. Lung tissue is very vulnerable to activated neutrophils and oxygen free radicals stimulated by limb IR [3], and lung injury is characterized by leukocyte infiltration, lung capillary barrier damage, pulmonary epithelial cell swelling, and apoptosis [4, 5]. However, the mechanisms involved in this process are complicated; accumulating evidence supports the critical role of polymorphonuclear (PMN) in the development of lung injury [6]. Therefore, strategies for limiting pulmonary PMN sequestration could serve as a promising alternative therapy to attenuate lung injury induced by limb IR.

Sphingosine-1-phosphate (S1P) is a biologically active lysophospholipid that is primarily produced by both sphingosine kinase 1 (SphK1) and sphingosine kinase 2 (SphK2) from sphingosine in response to various cellular stimuli [7], while its degradation is mainly mediated by S1P lyase (S1PL). S1PL, a pyridoxal phosphate-dependent enzyme, could irreversibly cleave S1P into ethanolamine phosphate and trans-2-hexadecenal maintaining S1P homeostasis. It has been now suggested that S1P could mediate diverse biological processes by acting on its receptors in an autocrine and paracrine manner. Functioning as an intracellular second messenger, S1P is associated with cellular proliferation, lymphocyte emigration, vascular endothelial reorganization, and apoptosis [8]. Moreover, increasing number of studies has demonstrated that S1P plays some roles in organ IR injury [9, 10]. FTY720 (fingolimod), a prodrug with promising immunoregulatory effect, is a structural analogue of S1P and could be phosphorylated by Sphk2 into FTY720-P. The phosphorylated product FTY720-P could bind to S1P receptors type 1, type 3, type 4, and type 5 and reduce lymphocyte cell trafficking by lymphocyte egress from lymphoid tissues such as lymph nodes and thymus [11]. It has been documented that FTY720 could protect organs against IR injury [12–15], and one of the potential mechanisms by which FTY720 may have exerted its protective effects was associated with its ability to reduce neutrophil priming [12]. However, the effect of FTY720 on lung injury remote to hindlimb IR remains unknown.

Thus, the purpose of the present study was to evaluate the treatment of FTY720 on lung injury induced by hindlimb IR in rats; histological changes, pulmonary water content, and blood gas analysis were used to assess lung injury; the PMN/alveolus ratio indicated neutrophil infiltration in lung tissue; also, the mRNA expressions of S1PL, SphK1, and SphK2 were measured.

2. Materials and Methods

2.1. Animal Preparation

All experiments were performed in accordance with the guidelines of the National Institutes of Health Guide for the Care and Use of Laboratory Animals. All experiment procedures were approved by the Animal Ethics Committee of Wenzhou Medical University.

Adult healthy male Sprague Dawley (SD) rats weighing 300 to 350 g were obtained from the Animal Experimental Center of Wenzhou Medical College. Animals were kept under standard conditions and had free access to standard rat chow and water ad libitum until the morning of the experiment. All rats were anesthetized with intraperitoneal administration of 90 mg/kg ketamine and 1 mg/kg acepromazine and placed in the supine position. Tracheotomy was established using a 15-gauge catheter, and a polyethylene catheter was inserted into the left carotid artery for direct blood pressure monitoring and blood gas sampling. A caudal vein was cannulated with a 7-gauge IV catheter for receiving an intravenous infusion of Ringer’s solution (5 mL·kg⁻¹·h⁻¹). Bilateral hindlimb ischemia was induced by applying rubber band tourniquets high around each thigh, and ischemia was verified by disappearance of blood flow signal with Doppler blood flow meter (ES-1000SPM, Hadeco Company, Japan). At the end of the 3-hour ischemia, reperfusion of the limbs was achieved by releasing the tourniquets and blood flow signal was regained.

2.2. Experimental Design

Fifty rats were divided into 5 groups, 10 in each group: (1)Group SM: the rats were treated with 2 mL distilled water lavage for 7 consecutive days before the tourniquet was put in place around the hindlimb without inflation.(2)Group IR: the rats were treated with 2 mL distilled water lavage for 7 consecutive days before hindlimb ischemia. Here, hindlimb IR model was established by 3-hour bilateral lower limb ischemia using tourniquets followed by reperfusion up to 3 h.(3)Group F3: the rats were treated with FTY720 (3 mg/kg/d, dissolved in 2 mL distilled water) for 7 consecutive days before hindlimb ischemia.(4)Group F5: the rats were preconditioned with FTY720 (5 mg/kg/d, dissolved in 2 mL distilled water) for 7 consecutive days before hindlimb ischemia.(5)Group F10: the rats were pretreated with FTY720 (10 mg/kg/d, dissolved in 2 mL distilled water) lavage for 7 consecutive days before hindlimb ischemia.

2.3. Blood Gas Analysis

Arterial blood gases were analyzed immediately using i-STAT Portable Clinical Analyzer (i-STAT Corporation, East Windsor, New Jersey) before ischemia initiation and at the end of reperfusion, respectively.

2.4. Measurement of S1PL, SphK1, and SphK2 mRNA by Real-Time PCR

The right lower lung lobe tissues were homogenized and total RNA was extracted using TRIzol reagent (Shanghai Sangon Biological Engineering Technology & Services, Shanghai, China) according to the manufacturer’s instructions. For real-time PCR, 1 μg of the total RNA from each sample was resuspended in 25 μL final volume of reaction buffer and cDNA was reverse transcribed using a synthesis kit. Housekeeping genes glyceraldehyde-3-phosphate dehydrogenase (GAPDH), β-actin, and β2 microglobulin were used for data normalization. Relative expression levels of mRNA were determined using the 2^−ΔΔCt method. The primers used for real-time PCR were listed below: S1PL forward primer 5′-GCA TCT ACG CAT CTC CAA-3′, reverse primer 5′-GCA ACC ATC TTC CTG TCA-3′; SphK1 forward primer 5′- TGG ACT TGG AGA GTG AGA A-3′, reverse primer 5′-CAG AGG AAC GAG GTA TGT G-3′, SphK2 forward primer 5′-GCT CCT ATT GGT CAA TCC TT-3′, reverse primer 5′-TGT CGT TCT GTC TGT ATG AG-3′, GAPDH forward primer 5′-AAT GCA TCC TGC ACC AA-3′, reverse primer 5′-GTA GCC ATA TTC ATT GTC ATA-3′, β-actin forward primer 5′-GAA GAT CAA GAT CAT TGC TCC T-3′, reverse primer 5′-TAC TCC TGC TTG CTG ATC CA-3′, and β2 microglobulin forward primer 5′-ATG GGA AGC CGA ACA TAC TG-3′ and reverse primer 5′-CAG TCT CAG TGG GGG TGA AT-3′.

2.5. Histological Assessment in Lung Tissue

The left lower lung lobe was fixed in 4% buffered formalin solution overnight at room temperature, dehydrated and embedded in paraplast, and then 4 μm-thick sections were obtained. Lung histopathology was examined under a light microscope after hematoxylin and eosin (HE) staining by a pathologist who was blinded to the group allocation. The degree of lung damage was assessed using a modified histological scoring system described before in our previous study [16].

2.6. Measurement of PMN Infiltration

The PMN/alveolus ratio (P/A) was used to assess the degree of PMN infiltration. We counted PMNs and alveoli per high-power field (HPF, 400x) in ten randomly selected areas of each sample, and the PMN/alveolus ratio (P/A) was calculated.

2.7. Lung Water Content Evaluation

Freshly harvested left upper lung lobe samples were weighed to obtain “wet” weight, then placed in an oven for 24 h at 60°C and weighed again to obtain “dry” weight. The wet/dry weight ratio (W/D) was determined to indicate water content in lung tissue.

2.8. Statistical Analysis

Statistical analysis was performed with SPSS version 15.0 (SPSS, Chicago, IL). Data were analyzed for normality with the Kolmogorov-Smirnov method, and the normally distributed data were expressed as mean ± SD. To compare normally distributed data between each group, one-way ANOVA followed by the Bonferroni post hoc test was employed. A value < 0.05 was considered significant.

3. Results

3.1. The Changes in Arterial Blood Gas Parameters

The baseline arterial blood gas parameters, including pH, arterial partial pressure of oxygen (PaO₂), arterial partial pressure of carbon dioxide (PaCO₂), and base excess (BE), among these five groups, were comparable (data not shown). At the end of reperfusion, pH, PaO₂, and BE were significantly lower (), whereas PaCO₂ was higher in group IR than in group SM (; Table 1). As compared to group IR, PaCO₂ was significantly lower () and pH, PaO_2, and BE were higher in group F10 (; Table 1).

3.2. Lung W/D and P/A Ratios

As shown in Figure 1, lung W/D and P/A ratios in group SM were low, which were significantly higher in group IR (). Additionally, lung W/D and P/A ratios in both group F5 and group F10, but not in group F3, were significantly increased as compared to group IR (; Figures 1(a) and 1(b)).

(a)

(b)

Figure 1

Lung wet/dry weight ratio and PMN/alveolus ratio. Rats were divided into five groups: groups SM, IR, F3, F5, and F10. The rats in group SM received sham operation and bilateral limb IR (ischemia 3 h/reperfusion 3 h) in group IR. The rats in groups F3, F5, and F10 were treated with FTY720 3 mg/kg/d, 5 mg/kg/d, and 10 mg/kg/d, respectively, for 7 consecutive days before limb IR. Upon 3 h reperfusion, wet/dry weight ratio (W/D) and PMN/alveolus ratio (P/A) were calculated. (a) wet/dry weight ratio; (b) PMN/alveolus ratio. versus group SM; ^# versus group IR.

3.3. The Expressions of S1PL, SphK1, and SphK2 mRNA in Lung Tissues

Compared to their low levels in group SM, the mRNA expressions of S1PL, SphK1, and SphK2 were significantly upregulated in group IR (; Figure 2). As expected, the mRNA expressions of S1PL, SphK1, and SphK2 were downregulated in both group F5 and group F10 as compared to group IR (; Figure 2); no significant differences in there mRNA expressions were found between group F3 and group IR ().

Figure 2

The expressions of S1PL, SphK1, and SphK2 mRNA in lung tissues. Rats were divided into five groups: groups SM, IR, F3, F5, and F10. The rats in group SM received sham operation and bilateral limb IR (ischemia 3 h/reperfusion 3 h) in group IR. The rats in groups F3, F5, and F10 were treated with FTY720 3 mg/kg/d, 5 mg/kg/d, and 10 mg/kg/d, respectively, for 7 consecutive days before limb IR. Upon 3 h reperfusion, the expressions of S1PL, SphK1, and SphK2 mRNA were measured. S1PL: S1P lyase; SphK1: sphingosine kinase-1; SphK2: sphingosine kinase-2. versus group SM; ^# versus group IR.

3.4. The Assessment of Histological Changes in Lung Tissues

No obvious histological abnormalities in lung tissue were noticed in group SM (Figure 3(a)). The lung presented severe lesions in group IR (Figure 3(b)); light microscope examination revealed lung interstitial edema, neutrophil infiltration, alveolar architecture destruction, and intra-alveolar hemorrhage. Treatment with a larger dose of FTY720 significantly reduced these histological damages (Figures 3(d) and 3(e)), which were also evidenced by decreased lung injury scores in both group F5 and group F10 as compared to group IR (; Figure 3(f)).

(a)

(b)

(c)

(d)

(e)

(f)

Figure 3

Histological changes in lung tissues. Rats were divided into five groups: groups SM, IR, F3, F5, and F10. The rats in group SM received sham operation and bilateral limb IR (ischemia 3 h/reperfusion 3 h) in group IR. The rats in groups F3, F5, and F10 were treated with FTY720 3 mg/kg/d, 5 mg/kg/d, and 10 mg/kg/d, respectively, for 7 consecutive days before limb IR. Upon 3 h reperfusion, lung damage was examined under a light microscope and the modified histological scoring system was evaluated. (a) Group SM; (b) group IR; (c) group F3; (d) group F5; (e) group F10; (f) histological scores. versus group SM; ^# versus group IR.

4. Discussion

The main findings of our study were that (1) pretreatment with FTY720 had beneficial effects in attenuating lung injury induced by hindlimb IR and that (2) these effects might be mediated by modulating S1P metabolism and inhibition of neutrophil infiltration in the lung tissue.

Various models are reported to simulate ischemic muscle damage, which includes the application of a tourniquet, femoral artery clamping, and iliac artery clamping. Among these, tourniquet application is the only method proven to produce complete ischemia with no residual flow [17]. During arterial occlusion of the lower limb, the tissue supplied by the occluded artery may suffer varying degrees of ischemic injury. Further complications appear during reperfusion, not only locally in necrosis and microcirculatory damage but also in remote organs such as the lung [18]. In the present study, we demonstrated that FTY720, which becomes a structural analogue of S1P following phosphorylation, could exert protective effects in alleviating lung injury induced by bilateral hindlimb IR, which was evidenced by decreased lung water content, improved oxygenation, and reduced histological injury.

Sphingosine 1-phosphate (S1P), a bioactive phospholipid, is produced by the phosphorylation of sphingosine through the action of both SphK1 and SphK2. Binding of S1P to its receptors triggers a wide array of immunological events, such as disrupting lymphocyte trafficking [19], modulating inflammatory cytokine production [20], and inhibition of apoptosis [21]. The roles of S1P signaling in modulating inflammatory response in lung tissue are complicated. Increased vascular permeability is commonly found in lung injury induced by hindlimb IR, while plasma S1P is reported to regulate the vascular tone and maintain the vascular integrity [22]. Similarly, the protective effects of S1P and FTY720 in limiting pulmonary vascular leakage were proved in a murine model of LPS-induced acute lung injury [22]. Conversely, in a dose-dependent manner, the systemic administration of S1P can induce bronchial hyperresponsiveness, increased lung resistance, and proinflammatory cytokines in mice [23], but intrapulmonary application of FTY720 and SphK inhibitors could attenuate experimental asthma acting as an antiasthmatic drug [24]. The discrepancy may attribute to the different pathogenesis including various cell types involved.

SphK1 is critical in modulating inflammatory processes, which could be upregulated in several conditions. The inhibition of SphK1 expression could suppress neutrophil activation and decrease lung permeability and cytokine formation [25], and its protective effects had been elaborated in allergic asthma and sepsis-induced inflammation [26]. FTY720 is now considered as a competitive inhibitor of SphK1 [27], while some showed that FTY720 could inhibit the activities of both SphK1 and SphK2 and suppress the phosphorylation of sphingosine by SphKs, resulting in decreased S1P production [28]. FTY720 itself is a prodrug and unable to inhibit lymphocyte emigration. It is increasingly known that SphK-2, but not SphK1, mediates the phosphorylation of FTY720 into FTY720-p [28], which is responsible for its mechanism of a wide range of immunomodulatory effects through various S1P receptor types except type 2 [29]. S1PL is the only enzyme that leads to irreversible degradation of S1P to phosphoethanolamine and corresponding fatty aldehydes, and the latter can be further metabolized into fatty acids and/or alcohols [30]. Intratracheal LPS led to enhanced pulmonary S1PL expression and decreased S1P level in mice, while inhibition of S1PL activity caused an elevated S1P level and decreased neutrophils priming in lung tissue. FTY720 could not be catabolized by S1PL, but instead inhibited the activity of S1PL without affecting gene and protein expressions in mice or cell lines [25, 31]. Our results revealed that a relatively low dose of FTY720 (3 mg/kg/d, for 7 consecutive days) had no significant effects on S1PL mRNA expression but could be downregulated when the dose increased to 5 or 10 mg/kg/d. Moreover, we demonstrated that hindlimb IR resulted in a remarkable increase in mRNA expressions of SphK1 and 2; both of the SphK mRNA expressions were downregulated by a relatively large dose of FTY720 (5 and 10 mg/kg/d but not 3 mg/kg/d, for 7 days). In summary, treatment with FTY720 led to inhibition of S1PL and SphK mRNA levels, suggesting that the effects of FTY720, at least partially, depend on its action on S1P metabolism.

Although its exact underlying mechanisms were undefined, many studies have shown that pulmonary neutrophil sequestration plays a vital role in lung injury caused by hindlimb IR [32]. Recruited neutrophils in the lung tissue are activated, leading to abundant production of reactive oxygen species, proteases, and proinflammatory cytokines. Reactive oxygen species, in turn, also induces the expression of adhesion molecules on the microvessel endothelium and facilitates transendothelial migration of neutrophils; these would subsequently cause lung injury [32]. Our study demonstrated that the lung damage and infiltration of neutrophils were obviously attenuated by FTY720 preconditioning. FTY720, a S1P receptor agonist, can cause sequestration of lymphocytes into within peripheral and mesenteric lymph nodes, producing a significant decrease in circulating lymphocytes [33]. Conversely, the effects of FTY720 on neutrophil infiltration are controversial. FTY720 treatment can markedly decrease neutrophil infiltration, vascular permeability, and peripheral blood lymphocyte counts in the mouse kidney subject to IR injury [34]. In a rat transplant model, FTY720 (0.5 mg/kg) pretreatment had been shown to rescue isografts and allografts from posttransplant preservation/reperfusion injury, with lower tubular damage scores [35]. Although circulating neutrophils were unchanged, neutrophil infiltration and IL-1 were significantly reduced [35]. When FTY720 dose reaches 1 mg/kg in cats, the number of circulating neutrophils could be also reduced [36]. Moreover, depletion of CD4 T cells was demonstrated to improve liver function and reduce neutrophil infiltration in mouse liver IR injury [37]. These findings suggested a possible lymphocyte-dependent mechanism in neutrophil infiltration, and FTY720 is capable to reduce neutrophil infiltration in IR injury. In contrast, several studies suggested that neutrophil infiltration in kidney and liver IR injury was not affected by treatment with FTY720 [13–15]. Particularly, treatment with FTY720 has been demonstrated to reduce mortality and prevented secretion of proinflammatory cytokines in the lung, liver, and kidney, whereas no effect on myeloperoxidase content, an indicator for neutrophil infiltration, was detected by treatment with FTY720 [38]. However, 48-hour reperfusion itself in the abovementioned study had no effect on MPO content. Here, we established IR injury of 3-hour ischemia of bilateral hindlimb ischemia followed by 3-hour reperfusion, and our findings suggested that FTY720 inhibited neutrophil infiltration and could be considered as a potential therapy in hindlimb IR injury through limiting the inflammatory response. We assumed that the duration of the ischemia and reperfusion phase might contribute to the differences. Additionally, three different preconditioning doses of FTY720 lavage in rats were measured in our study, and a dose-dependent effect of FTY720 was found.

There are several limitations to our study. First, FTY720 was chosen because we acknowledged the critical role of S1P signaling in modulating inflammation and attempted to investigate the possible therapy, but FTY720 is just one of various S1P receptor agonists; the effects of other S1P receptor agonists in attenuating lung inflammation were not evaluated. Second, the long-term effects of FTY720 on lung injury and survival of rats remained unknown. Finally, we did not detect S1P levels due to technical unavailability.

In conclusion, through modulating S1P metabolism and inhibiting pulmonary neutrophil infiltration, pretreatment with FTY720 could attenuate lung injury induced by hindlimb IR.

Conflicts of Interest

The authors declare that there are no conflicts of interest in connection with this paper.

Acknowledgments

The study was funded by the Natural Science Foundation of Zhejiang Province (no. LY16H070004) and the Medical Science and Technology Fund of Zhejiang Province (no. 2013KYA131). The authors gratefully acknowledge the assistance of Han Lin in preparing the photomicrographs.

References

M. M. Yassin, D. W. Harkin, D. Barros, A. A. Sa, M. I. Halliday, and B. J. Rowlands, “Lower limb ischemia-reperfusion injury triggers a systemic inflammatory response and multiple organ dysfunction,” World Journal of Surgery, vol. 26, no. 1, pp. 115–121, 2002.
View at: Publisher Site | Google Scholar
M. D. Bianco-Batlles, A. Sosunov, R. A. Polin, and V. S. Ten, “Systemic inflammation following hind-limb ischemia-reperfusion affects brain in neonatal mice,” Developmental Neuroscience, vol. 30, no. 6, pp. 367–373, 2008.
View at: Publisher Site | Google Scholar
T. C. Peng, W. C. Jan, P. S. Tsai, and C. J. Huang, “Heme oxygenase-1 mediates the protective effects of ischemic preconditioning on mitigating lung injury induced by lower limb ischemia-reperfusion in rats,” Journal of Surgical Research, vol. 167, no. 2, pp. e245–e253, 2011.
View at: Publisher Site | Google Scholar
M. C. Kao, W. C. Jan, P. S. Tsai, T. Y. Wang, and C. J. Huang, “Magnesium sulfate mitigates lung injury induced by bilateral lower limb ischemia-reperfusion in rats,” Journal of Surgical Research, vol. 171, no. 1, pp. e97–106, 2011.
View at: Publisher Site | Google Scholar
K. Y. Hsu, P. S. Tsai, J. J. Lee, T. Y. Wang, and C. J. Huang, “Platonin mitigates acute lung injury induced by bilateral lower limb ischemia-reperfusion in rats,” Journal of Surgical Research, vol. 167, no. 2, pp. e255–e262, 2011.
View at: Publisher Site | Google Scholar
W. Gao, J. Zhao, H. Kim et al., “α1-Antitrypsin inhibits ischemia reperfusion-induced lung injury by reducing inflammatory response and cell death,” The Journal of Heart and Lung Transplantation, vol. 33, no. 3, pp. 309–315, 2014.
View at: Publisher Site | Google Scholar
N. Gellings Lowe, J. S. Swaney, K. M. Moreno, and R. A. Sabbadini, “Sphingosine-1-phosphate and sphingosine kinase are critical for transforming growth factor-β-stimulated collagen production by cardiac fibroblasts,” Cardiovascular Research, vol. 82, no. 2, pp. 303–312, 2009.
View at: Publisher Site | Google Scholar
H. C. Tsai and M. H. Han, “Sphingosine-1-phosphate (S1P) and S1P signaling pathway: therapeutic targets in autoimmunity and inflammation,” Drugs, vol. 76, no. 11, pp. 1067–1079, 2016.
View at: Publisher Site | Google Scholar
M. Kim, S. W. Park, S. M. Pitson, and H. T. Lee, “Isoflurane protects human kidney proximal tubule cells against necrosis via sphingosine kinase and sphingosine-1-phosphate generation,” American Journal of Nephrology, vol. 31, no. 4, pp. 353–362, 2010.
View at: Publisher Site | Google Scholar
R. Ding, J. Han, Y. Tian, R. Guo, and X. Ma, “Sphingosine-1-phosphate attenuates lung injury induced by intestinal ischemia/reperfusion in mice: role of inducible nitric-oxide synthase,” Inflammation, vol. 35, no. 1, pp. 158–166, 2012.
View at: Publisher Site | Google Scholar
M. Mansoor and A. J. Melendez, “Recent trials for FTY720 (fingolimod): a new generation of immunomodulators structurally similar to sphingosine,” Reviews on Recent Clinical Trials, vol. 3, no. 1, pp. 62–69, 2008.
View at: Publisher Site | Google Scholar
M. L. Stone, A. K. Sharma, Y. Zhao et al., “Sphingosine-1-phosphate receptor 1 agonism attenuates lung ischemia-reperfusion injury,” American Journal of Physiology Lung Cellular and Molecular Physiology, vol. 308, no. 12, pp. 1245–1252, 2015.
View at: Publisher Site | Google Scholar
D. M. Anselmo, F. F. Amersi, X. D. Shen et al., “FTY720 pretreatment reduces warm hepatic ischemia reperfusion injury through inhibition of T-lymphocyte infiltration,” American Journal of Transplantation, vol. 2, no. 9, pp. 843–849, 2002.
View at: Publisher Site | Google Scholar
D. Anselmo, F. F. Amersi, X. D. Shen et al., “FTY720: a novel approach to the treatment of hepatic ischemia-reperfusion injury,” Transplantation Proceedings, vol. 34, no. 5, pp. 1467-1468, 2002.
View at: Publisher Site | Google Scholar
P. Troncoso, M. Ortiz, L. Martinez, and B. D. Kahan, “FTY 720 prevents ischemic reperfusion damage in rat kidneys,” Transplantation Proceedings, vol. 33, no. 1-2, pp. 857–859, 2001.
View at: Publisher Site | Google Scholar
X. Q. Xiong, L. N. Lin, L. R. Wang, and L. D. Jin, “Sevoflurane attenuates pulmonary inflammation and ventilator-induced lung injury by upregulation of HO-1 mRNA expression in mice,” International Journal of Nanomedicine, vol. 8, no. 1, pp. 1075–1081, 2013.
View at: Publisher Site | Google Scholar
P. S. Barie and R. J. Mullins, “Experimental methods in the pathogenesis of limb ischemia,” Journal of Surgical Research, vol. 44, no. 3, pp. 284–307, 1988.
View at: Publisher Site | Google Scholar
E. Gyurkovics, P. Aranyi, R. Stangl et al., “Postconditioning of the lower limb—protection against the reperfusion syndrome,” Journal of Surgical Research, vol. 169, no. 1, pp. 139–147, 2011.
View at: Publisher Site | Google Scholar
V. Brinkmann, “FTY720: mechanism of action and potential benefit in organ transplantation,” Yonsei Medical Journal, vol. 45, no. 6, pp. 991–997, 2004.
View at: Publisher Site | Google Scholar
D. T. Bolick, S. Srinivasan, K. W. Kim et al., “Sphingosine-1-phosphate prevents tumor necrosis factor-α-mediated monocyte adhesion to aortic endothelium in mice,” Arteriosclerosis Thrombosis and Vascular Biology, vol. 25, no. 5, pp. 976–981, 2005.
View at: Publisher Site | Google Scholar
A. J. Melendez, “Sphingosine kinase signalling in immune cells: potential as novel therapeutic targets,” Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics, vol. 1784, no. 1, pp. 66–75, 2008.
View at: Publisher Site | Google Scholar
E. Camerer, J. B. Regard, I. Cornelissen et al., “Sphingosine-1-phosphate in the plasma compartment regulates basal and inflammation-induced vascular leak in mice,” The Journal of Clinical Investigation, vol. 119, no. 7, pp. 1871–1879, 2009.
View at: Publisher Site | Google Scholar
F. Roviezzo, B. D'Agostino, V. Brancaleone et al., “Systemic administration of sphingosine-1-phosphate increases bronchial hyperresponsiveness in the mouse,” American Journal of Respiratory Cell and Molecular Biology, vol. 42, no. 5, pp. 572–577, 2010.
View at: Publisher Site | Google Scholar
M. Idzko, H. Hammad, M. van Nimwegen et al., “Local application of FTY720 to the lung abrogates experimental asthma by altering dendritic cell function,” The Journal of Clinical Investigation, vol. 116, no. 11, pp. 2935–2944, 2006.
View at: Publisher Site | Google Scholar
L. P. Vlasenko and A. J. Melendez, “A critical role for sphingosine kinase in anaphylatoxin-induced neutropenia, peritonitis, and cytokine production in vivo,” The Journal of Immunology, vol. 174, no. 10, pp. 6456–6461, 2005.
View at: Publisher Site | Google Scholar
W. Q. Lai, H. H. Goh, Z. Bao, W. S. Wong, A. J. Melendez, and B. P. Leung, “The role of sphingosine kinase in a murine model of allergic asthma,” The Journal of Immunology, vol. 180, no. 6, pp. 4323–4329, 2008.
View at: Publisher Site | Google Scholar
N. J. Pyne and S. Pyne, “Sphingosine 1-phosphate and cancer,” Nature Reviews Cancer, vol. 10, no. 7, pp. 489–503, 2010.
View at: Publisher Site | Google Scholar
S. W. Paugh, S. G. Payne, S. E. Barbour, S. Milstien, and S. Spiegel, “The immunosuppressant FTY720 is phosphorylated by sphingosine kinase type 2,” FEBS Letters, vol. 554, no. 1-2, pp. 189–193, 2003.
View at: Publisher Site | Google Scholar
B. Zemann, B. Kinzel, M. Muller et al., “Sphingosine kinase type 2 is essential for lymphopenia induced by the immunomodulatory drug FTY720,” Blood, vol. 107, no. 4, pp. 1454–1458, 2006.
View at: Publisher Site | Google Scholar
P. P. Van Veldhoven and G. P. Mannaerts, “Subcellular localization and membrane topology of sphingosine-1-phosphate lyase in rat liver,” Journal of Biological Chemistry, vol. 266, no. 19, pp. 12502–12507, 1991.
View at: Google Scholar
P. Bandhuvula, Y. Y. Tam, B. Oskouian, and J. D. Saba, “The immune modulator FTY720 inhibits sphingosine-1-phosphate lyase activity,” Journal of Biological Chemistry, vol. 280, no. 40, pp. 33697–33700, 2005.
View at: Publisher Site | Google Scholar
E. Abraham, “Neutrophils and acute lung injury,” Critical Care Medicine, vol. 31, Supplement 4, pp. S195–S199, 2003.
View at: Publisher Site | Google Scholar
M. Suleiman, P. M. Cury, J. O. Pestana, E. A. Burdmann, and V. Bueno, “FTY720 prevents renal T-cell infiltration after ischemia/reperfusion injury,” Transplantation Proceedings, vol. 37, no. 1, pp. 373-374, 2005.
View at: Publisher Site | Google Scholar
A. S. Awad, H. Ye, L. Huang, L. Li, and F. W. Foss JrT. L. Macdonald, K. R. Lynch, and M. D. Okusa, “Selective sphingosine 1-phosphate 1 receptor activation reduces ischemia-reperfusion injury in mouse kidney,” American Journal of Physiology Renal Physiology, vol. 290, no. 6, pp. F1516–F1524, 2006.
View at: Publisher Site | Google Scholar
D. Dragun, T. Bohler, M. Nieminen-Kelha et al., “FTY720-induced lymphocyte homing modulates post-transplant preservation/reperfusion injury,” Kidney International, vol. 65, no. 3, pp. 1076–1083, 2004.
View at: Publisher Site | Google Scholar
S. Downes, Y. J. Chen, A. Kyles, and C. Gregory, “Oral pharmacokinetic and pharmacodynamic effects of FTY720 in cats,” Journal of Veterinary Pharmacology and Therapeutics, vol. 30, no. 1, pp. 55–61, 2007.
View at: Publisher Site | Google Scholar
R. M. Zwacka, Y. Zhang, J. Halldorson, H. Schlossberg, L. Dudus, and J. F. Engelhardt, “CD4⁺ T-lymphocytes mediate ischemia/reperfusion-induced inflammatory responses in mouse liver,” Journal Clinical Investigation, vol. 100, no. 2, pp. 279–289, 1997.
View at: Publisher Site | Google Scholar
M. Frink, C. P. Kaudel, F. Hildebrand et al., “FTY720 improves survival after transient ischemia and reperfusion of the hind limbs,” The Journal of Trauma and Care Surgery, vol. 63, no. 2, pp. 263–267, 2007.
View at: Publisher Site | Google Scholar

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Copyright © 2017 Liangrong Wang et al. 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.

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