The Regulation of Inflammatory Mediators in Acute Kidney 
Injury via Exogenous Mesenchymal Stem Cells

Du, Tao; Zhu, Ying-Jian

doi:https://doi.org/10.1155/2014/261697

Mediators of Inflammation

On this page

Abstract Introduction Acknowledgments References Copyright Related Articles

Review Article | Open Access

Volume 2014 | Article ID 261697 | https://doi.org/10.1155/2014/261697

The Regulation of Inflammatory Mediators in Acute Kidney Injury via Exogenous Mesenchymal Stem Cells

Tao Du^1,2and Ying-Jian Zhu¹

Academic Editor: Ronald Gladue

Received07 Jan 2014

Revised07 Mar 2014

Accepted20 Mar 2014

Published15 Apr 2014

Abstract

Acute kidney injury (AKI) remains to be an independent risk factor for mortality and morbidity. Inflammation is believed to play a major role in the pathophysiology of AKI. Exogenous mesenchymal stem cells (MSCs) are now under extensive investigation as a potential therapy for AKI. Various preclinical studies indicated the beneficial effects of MSCs in alleviating renal injury and accelerating tissue repair. However the mechanisms responsible for these effects are incompletely understood. In the recent years, anti-inflammatory/immunoregulatory properties of MSCs have become one of the important issues in the treatment of AKI. This review will summarize the current literature on the regulation of inflammatory mediators via exogenous MSCs contributing to the recovery from AKI.

1. Introduction

Acute kidney injury (AKI) is defined as a rapid decrease in glomerular filtration rate (GFR) caused by both vascular and tubular factors, including increased renal vasoconstriction, loss of autoregulation, and tubular obstruction [1–3]. Although incidence rates are decreasing, AKI is still associated with a high mortality rate [4]. Inflammation is now believed to play a major role in the pathophysiology of AKI [5, 6]. Endothelial injury can increase microvascular permeability which may lead to inflammatory cells recruitment into the injured kidney during the initial process of AKI [7]. Proximal tubular cells under hypoxia-induced damage can produce proinflammatory and profibrotic factors that result in infiltration of inflammatory cells into the injured kidney [8]. In the recent years, some anti-inflammatory therapies, such as lymphocyte or macrophage depletion, have been used against inflammatory targets for prevention and treatment of AKI [9]. Exogenous mesenchymal stem cells (MSCs) have been considered as one of the new effective strategies for AKI recently. Although the mechanisms responsible for their protective and regenerative effects are incompletely understood, anti-inflammatory/immunoregulatory properties of MSCs are recognized as one of the important mechanisms. The present brief review hopes to focus on the role of exogenous MSCs to ameliorate kidney injury and accelerate kidney repair in AKI through regulating inflammatory mediators.

2. Mesenchymal Stem Cells (MSCs)

Mesenchymal stem cells (MSCs), also known as mesenchymal stromal cells, have been the focus of great interest in regenerative medicine for their potential therapeutic applications in AKI. Since nephrons are largely of mesenchymal origin and stromal cells are of crucial importance for signaling leading to the differentiation of both nephrons and collecting ducts, MSCs are undifferentiated adult cells and may be isolated from bone marrow, umbilical cord, adipose tissue, placenta, synovium, and skeletal muscle [10–14]. They are characterized by three main criteria: (a) the ability to differentiate into osteoblasts, adipocytes, and chondroblasts in vitro; (b) the expression of surface markers CD73, CD90, and CD105; lack of expression of haematopoietic markers including CD34 and CD45; (c) plastic adherence in culture [15]. Recent studies suggested that administering exogenous MSCs could ameliorate renal injury and accelerate renal repair in AKI (Table 1). Exogenous MSCs appeared to make renoprotective effects by several mechanisms, including (a) engraftment and differentiation of MSCs into the host tissue or organ; (b) therapeutic fusion into one with existing host cells; (c) stimulation of endogenous repair by regenerating local resident SCs; and (d) release of paracrine and/or endocrine signals from MSCs. In the last decade, almost all the studies showed that the therapeutic effects of MSCs are mainly mediated through paracrine rather than differentiative mechanism. They have identified over forty growth factors, cytokines and chemokines secreted from MSCs, such as hepatocyte growth factor (HGF), insulin-like growth factor 1 (IGF-1), vascular endothelial growth factor (VEGF), interleukin-1 (IL-1), IL-4, IL-5, IL-6, KC, CXCL16, CCL2, CCL3, CX3CL1, and CCL5 [16, 17]. Some of them enhance cell proliferation, reduce cell apoptosis, modulate the inflammation, and are good candidates for therapeutic effects in AKI. Given the importance of inflammation in the pathophysiology of AKI, it is very imperative to discuss these anti-inflammatory/immunoregulatory properties of MSCs and the role they play in renoprotection [5].

3. Cytokines and Chemokines

Many cytokines and chemokines are released by leukocytes, renal tubular cells, mesangial cells, endothelial cells, and platelets into the injured tissue [29–33]. They are also important components for both the initiation and extension of inflammation. Exogenous MSCs would protect kidney from AKI by regulating the inflammatory-related cytokines and chemokines. Chemokine receptors may assist MSCs in migrating to sites of inflammation and participating in the regulation of inflammation.

3.1. Cytokines

Cisplatin-induced AKI is associated with increases in the cytokines IL-1β, IL-6, and IL-18 and neutrophil infiltration in the kidney [34]. The expression of tumor necrosis factor-α (TNF-α) is increased in cisplatin-induced AKI [35]. TNFR2 also participates in cisplatin-induced AKI and may play an important role in TNF-α mediated inflammation in kidney [36]. In the model of ischemic AKI, some proinflammatory cytokines are increased in kidney [37–39]. In response to the stimulation with noxious stimuli, endotoxin, and hypoxia in AKI, administered MSCs would reduce the expression of proinflammatory cytokines and increase the expression of anti-inflammatory factors in kidney. In the model with ischemic AKI, MSCs significantly reduced the expression of proinflammatory cytokines IL-1β, TNF-α, interferon-gamma (IFN-γ), and inducible nitric oxide synthase (iNOS) and highly upregulated the expression of anti-inflammatory cytokines IL-10, basic fibroblast growth factor (bFGF), TGF-α, and Bcl-2 in kidney [18]. In another study with ischemic AKI, the expression of IL-6 and TNF-α was significantly lower, while the expression of VEGF was significantly higher in kidney after MSCs treatment [40]. When cisplatin-treated mice were injected with MSCs, some cytokines in serum, such as MIP-2, IL-6, and IFN-γ, were significantly lowered and renal injury was ameliorated [19]. Several growth factors released from MSCs, such as VEGF, fibroblast growth factor-2 (FGF-2), HGF, and IGF-1, would improve blood flow, promote cell growth, decrease cell apoptosis, and exert a beneficial effect on neovascularization and tissue remodeling [16, 41–44]. Some studies also found that MSC-conditioned medium (MSC-CM) might protect renal cells from apoptosis induced by cisplatin in vitro [17, 45].

3.2. Chemokines

Chemokines are a family of chemotactic cytokines that were initially identified on the basis of their ability to induce the migration of different cell types [46]. A large number of proinflammatory chemokines, for example, CCL2, CCL5, CXCL8, and CXCL12, are upregulated in kidney after ischemic AKI, and chemokine receptor expressing inflammatory cells are attracted by these chemokines. These results lead to marked neutrophil infiltration in kidney [47, 48]. Some proinflammatory chemokines are controlled at the transcriptional level by nuclear factor-kB (NF-kB) and activating protein-1 (AP-1), which are activated by the phosphorylation of p38 MAPK. And pharmacological inhibition of p38 MAPK might significantly reduce proinflammatory chemokines production, attenuate leukocyte infiltration, and prevent tubular necrosis in a mouse model of ischemic AKI [49].

MSCs express several chemokines and chemokine receptors (Table 2). The chemokine receptors may assist in their migration to the sites of inflammation and participate in the regulation of inflammation. Some chemokine receptor genes, such as CXCR3, CXCR5, CCR1, CCR7, and CX3CR1, were upregulated in human bone marrow-mesenchymal stem cells (hBM-MSCs), while human umbilical cord Wharton’s jelly-mesenchymal stem cells (hUCWJ-MSCs) showed higher expression for CCR3 [50]. Short-term exposure of MSCs to low oxygen increased the expression of chemokine receptors CX3CR1 and CXCR4 and enhanced their engraftment in vivo [51]. Hypoxic preconditioning mesenchymal stem cells (HP-MSCs) enhanced the expression of CXCR4 and CXCR7, which not only improved MSCs’ chemotaxis but also stimulated the secretion of proangiogenic and mitogenic factors [52].

In response to the stimulation with noxious stimuli, endotoxin and hypoxia in AKI, administered MSCs would reduce the expression of proinflammatory chemokines and ameliorate kidney injury. MSCs could decrease the expression of MIP-2, CCL2, and KC in plasma and reduce the toxicity of cisplatin on kidney in vivo [19]. MSCs could decrease mRNA levels of CXCL1, CXCL2, CXCL5, CCL2, and CCL3 in kidney in sepsis-associated mice AKI and improve the recovery of tubular function [20]. In ischemic AKI, MSCs could also decrease the expression of CCL2, CCL3, CCL5, and KC in kidney and reduce acute tubular necrosis in injured kidney [21].

4. Adhesion Molecules

Adhesion molecules are required for leukocyte adhesion during inflammation. Leukocyte adhesion to endothelial cells leads to inflammation and extension of cellular injury [61]. Intercellular adhesion molecule-1 (ICAM-1) plays an important role in the pathophysiology of AKI [62]. The administration of a monoclonal ICAM-1 antibody or ICAM-1 deficient mice is protected against renal ischemia [63, 64]. In the model of kidney transplantation, MSCs could reduce the gene expression of proinflammatory cytokines/chemokines and ICAM-1 and ameliorate inflammation induced by prolonged cold ischemia [65]. In another study with ischemic AKI, kallikrein-modified mesenchymal stem cells (TK-MSCs) can provide enhanced protection against AKI by inhibiting apoptosis and inflammation. The expression of proinflammatory mediators CCL-2 and ICAM-1 was significantly reduced in the TK-MSCs group [66].

Selectins and their ligands are other important adhesion molecules that participate in the inflammatory response. P-selectin is expressed as part of the inflammatory stimulus in platelets and endothelial cells; L-selectin is expressed in leukocytes and lymphocytes; and E-selectin is expressed in endothelium. Renal ischemia has been shown to be associated with upregulation of endothelial P-selectin and enhanced adhesion of neutrophils [67].

Although there is no report about the expression of selectins in injured kidney after MSCs’ treatment, P-selectin and its counter-ligand were found to be involved in the extravasation of MSCs [68]. Intravenously administered MSCs can roll along the walls of the blood vessels in the ear veins of mice, and this phenomenon was significantly decreased in mice genetically deficient of P-selectin. E-selectin and L-selectin have been reported to be absent or present only in low amounts on MSCs, and their significance in MSC trafficking, compared with P-selectin, may be unimportant.

5. Inflammatory Cells

Inflammatory cells play a central role in the pathogenesis of AKI. Exogenous MSCs showed a beneficial effect on ameliorating kidney injury and accelerating kidney repair. Administrated MSCs may decrease the infiltration of neutrophils and macrophages, inhibit the dendritic cells’ differentiation and maturation, reduce the lymphocytes activities, and decline the cytotoxic activity of NK cells in injured kidney.

5.1. Neutrophils

Neutrophil recruitment is an important early step in controlling tissue infections or injury. Neutrophil chemoattractants CXCL1/CXCL2 produced by mast cells and macrophages initiate an early stage of neutrophil recruitment during tissue inflammation [69]. MSCs can decrease a panel of inflammatory cytokines and reduce the inflammatory infiltration of macrophages and neutrophils in kidney when following kidney injury [70]. The improvement of inflammatory responses in animal models was at least partially explained by the NFκB-dependent secretion of soluble tumour necrosis factor receptor-1 (sTNFR1) by MSCs. In a mouse model of sepsis-associated AKI, MSCs would alleviate kidney injury and attenuate neutrophils’ infiltration in kidney [20]. In another mouse model with cisplatin-induced AKI, infusion of MSCs ameliorated both renal function and tubular cell injury and prolonged survival. Transplanted MSCs might localize in peritubular areas and limit capillary alterations and neutrophils’ infiltration [71]. Human MSCs, pretreatment with an antioxidant, might improve the efficacy of MSCs’ transplantation [72]. Administration of these pretreated MSCs could decrease inflammation and fibrosis and reduce neutrophils’ infiltration in injured tissue.

5.2. Lymphocytes

The role of lymphocytes in AKI is an ongoing area of study. Lymphocytes have been shown to be important modulators of innate and adaptive inflammatory responses in AKI models [73].

MSCs can regulate T cells function and make their therapeutic effects in AKI [74]. MSCs can inhibit T cells activities. They can inhibit the effector T cells both in vitro and in vivo [75, 76]. MSCs could also suppress AKI-induced T cells infiltrating in ischemic kidney. When cultured with T cells, MSCs either from the same donor or from different donor can induce a G0/G1 checkpoint arrest in T cells [77, 78]. The mechanisms by which MSCs are able to mediate immunosuppression of T cells are diverse and complex; several secreted effectors have been linked to this process. Among them, indoleamine 2,3-dioxygenase (IDO), prostaglandin E2 (PGE2), TGF-β, and HGF have been described to play major roles [79–81]. MSCs can also display potent immunosuppressive effects on lymphocyte responses. These effects included the prevention of lymphocyte activation as well as the suppression of T cells proliferation. These effects were mediated through the expression of COX1/COX2 enzymes and by the production of PGE2 [82]. Moreover, MSCs can stimulate the production of regulatory T cells (Tregs), leading to self-regulation of the immune response. Through interaction with splenocyte, MSCs may induce more Tregs and attenuate ischemic AKI. Coculture of splenocytes with MSCs could increase the number of Tregs in vitro [74]. Tregs are commonly identified by their expression of CD4 and CD25 on the cell surface and upregulation of the transcription factor FoxP3. MSCs could expand CD4+CD25highFoxp3+ regulatory T cells via HLA-G5 secretion in peripheral blood lymphocytes [83].

MSCs also have an important immunosuppressive action on suppression of B cells proliferation. Mice deficient in B cells are protected against ischemic AKI [84]. In a murine model of systemic lupus erythematosus, MSCs could inhibit the activation of B cells with IFN-γ [85]. MSCs could also suppress the activation of B cells via inhibiting the production of B cell-activating factor (BAFF) [86].

5.3. Natural Killer Cells

Natural killer (NK) cells are a type of lymphocytes that mediates innate immunity against pathogens and inflammation via their ability to secrete cytokines [87]. NK cells are important participants in the early-stage innate immune responses in ischemia AKI. A recent study demonstrated that NK cells could directly kill tubular epithelial cells. NK cells induced apoptosis in tubular epithelial cells and contributed to renal ischemia-reperfusion injury (IRI). NK cells depletion in wild-type mice was protective against AKI, while adoptive transfer of NK cells worsened kidney injury in NK cell, T cell, and B cell-null Rag2 (−/−) gamma(c)(−/−) mice with IRI [88]. MSCs could inhibit NK cells proliferation and cytotoxic activity. The inhibition was mediated by a soluble factor generated upon incubation with NK cells activated by IL-15 or IL-2 [89]. MSCs can inhibit NK cells function. Through human leukocyte antigen-G5 (HLA-G5), MSCs can affect innate immunity by inhibiting both NK cell-mediated cytolysis and IFN-γ secretion [90]. MSCs can hamper the NK cells-mediated immune response by preventing their acquisition of lymphoblast characteristics, activation, and changing the expression profile of proteins with an important role in immune function [91]. Moreover, MSCs may inhibit the cytolytic functions of NK cells and have negative effects on the NK-mediated graft-versus-leukemia (GVL) [92].

5.4. Macrophages

Macrophages are important effector cells in both the adaptive and the innate immune response. They can mediate inflammation in the interstitium of the outer medulla, which has been described early in the course of ischemic AKI. Although the precise mechanisms of macrophage-mediated renal injury have yet to be determined, it is evident that macrophages can produce many molecules to cause renal damage. Some proinflammatory factors, for example, TNF-α, IL-1, TGF-β1, and PDGF secreted by macrophages, are thought to play important roles in the pathogenesis of the disease [93]. Apart from tissue destruction, macrophages can also play roles in tissue homeostasis, cellular replacement, and tissue repair [94]. Macrophages can phagocytose and remove apoptotic cells, deposited immune complexes, and fibrin. In addition, macrophages can secrete HGF and VEGF, which can promote the repair of damaged tubules and endothelium.

Some researchers reported that AKI induced kidney inflammation and fibrosis involving M1 and M2 macrophages, respectively [95, 96]. M1 macrophages predominate in the early stage of AKI and produce multiple cytokines and chemokines to recruit the immune cells and activate the innate host defense. M2 macrophages include M2a, M2b, and M2c subtypes. M2 macrophages predominate in the late stage of AKI. They are alternatively activated according to the defined stimulation and promote angiogenesis and mediate wound healing, extracellular matrix (ECM) deposition, and tissue remodeling. With ongoing injury, sustained macrophage infiltration may result in the continuous production of various wound-healing growth factors and ultimately lead to irreversible fibrosis, tissue destruction, and progressive chronic kidney disease [97]. In the recent years, some researchers proposed an alternative view to classify macrophage phenotypes as proinflammatory, anti-inflammatory, profibrotic, and fibrolytic macrophages according to their different microenvironments and functional characteristics [98]. As the injury and repair process shifts from the initial inflammatory phase to that of remodeling phase, macrophages subsequently exhibit varying polarization states and exert a diverse range of functional activities.

Several studies have demonstrated that MSCs could inhibit the expression of macrophage in the initial period of AKI. In a mouse model with cisplatin-induced AKI, infusion of mesenchymal-like progenitors (MPs) derived from human embryonic stem cells (hESCs) reduced renal macrophage infiltration through regulating MCP-1 and promoted the recovery from AKI via paracrine mechanism [99]. In a rat model of ischemic AKI, intravenous administration of allogenic fetal membrane-derived mesenchymal stem cells (FM-MSCs) could significantly suppress macrophage infiltration and renal tubular apoptosis [22]. Recent studies have also demonstrated that, in ischemic AKI, anti-inflammatory macrophages were markedly increased in kidney in the late period when human umbilical cord-derived stromal cells (hUCSCs) were injected intravenously [100, 101].

5.5. Dendritic Cells

Dendritic cells (DCs) have a dual role and can induce tolerance or immunity. In the steady state, immature DCs (iDCs) situated in the renal interstitial microenvironment are affected by autophagy of proteins from dying cells, cell-to-cell contact, danger-associated molecular patterns (DAMPS), pathogen-associated molecular patterns (PAMPS), humoral mediators, or filtered antigens [102]. Without tissue damage or local inflammation, these iDCs express low amounts of costimulatory molecules. During an infection or in the presence of maturation-inducing inflammatory signals, mature DCs will induce the development of effector T-cell responses. DCs may play an important role on the production of cytokines and chemokines that drive neutrophils’ infiltration in ischemic AKI.

MSCs are able to alter the cytokine production of DCs, resulting in a more tolerant and/or anti-inflammatory phenotype. MSCs have also been known to interact with DCs, making them become regulatory DCs [103–105]. In the mouse model of ischemic AKI, MSCs are partially mediated via DCs to induce the immune tolerance and play an important role in alleviating kidney injury [102]. MSCs, treated with 14S, 21R-dihydroxy-docosahexaenoic acid, could enhance the efficiency in improving the renal function, reducing renal tubular cell death, and inhibiting infiltration of neutrophils, macrophages, and DCs in ischemic AKI [106]. In vitro, MSCs mediated a potent inhibition on DC differentiation, and the inhibition was restricted to the early stages of cytokine-induced progression from monocytes to iDCs. The inhibition affected both the expression of informative DC surface markers and the acquisition of DC functions, such as IL-12 production. The inhibitory effect is primarily mediated by PGE2 [107, 108].

6. Microvesicles Derived from MSCs in AKI

It has been suggested that MSCs can alleviate AKI by providing a paracrine support rather than replacing renal tubular cells to the repair. Further support for the paracrine action of MSCs is provided by the experiments showing that MSC-CM can mimic the beneficial effects as the cells of origin [16, 44, 45]. Microvesicles (MVs) from MSCs, as one of the components in the cell-to-cell communication network, are involved in tissue regeneration and therefore contribute to the paracrine action of MSCs [109, 110]. MVs are vesicles composed by exosomes, shedding vesicles, and apoptotic bodies. Exosomes range from 30 to 120 nm in size, and their release depends on cytoskeleton activation, while vesicles generated by direct budding of the plasma membrane, also known as shedding vesicles, are more heterogeneous in size and ranging from 100 nm to 1 μm in size [111]. In our study, MVs derived from hUCWJ-MSCs were positive for some surface expressed molecules, such as CD9, CD44, CD63, and CD73, and negative for CD34 and CD45 [112]. MVs may influence the behavior of the target cells in several ways: (a) directly stimulate the cells by a surface interaction [113]; (b) transfer receptors from the cell of origin to the target cell [114]; (c) deliver proteins to target cells [115]; (d) mediate a horizontal transfer of mRNA and microRNA inducing epigenetic changes in the target cell [116–118]. Therefore, understanding the modulation of MVs’ therapeutic effect upon AKI may provide insight into the molecular mechanisms. For example, MVs expressing ICAM1 at their surface can interact with the lymphocyte function-associated antigen 1 (LFA1) to activate T cells [119]. MVs expressing the delta-like 4 (Dll4) may activate angiogenesis and axon growth by interacting with Notch receptors expressed by endothelial or nerve cells, respectively [120]. MVs derived from MSCs may activate a proliferative programme in tubular epithelial cells that survived injury both in vitro and in a glycerol-induced model of AKI in severe combined immunodeficiency (SCID) mice [121]. Several other studies also reported that MSCs-MVs might favor the kidney repair in nonlethal toxic and ischemic AKI. They were found to exert a prosurvival and antiapoptotic effect on renal tubular cells in vitro and in vivo [122–124].

7. Summary

Inflammation is now believed to play a major role in the pathophysiology of AKI. Inflammatory mediators are produced to regulate the inflammation in injured kidney. If tubular epithelial and endothelial injury exceeds over the regenerative potential, injured kidney might progress to interstitial fibrosis and even chronic kidney disease. Therefore, controlling kidney inflammation and promoting epithelial/endothelial repair are probably the best ways to target AKI and to maintain renal function. The role of MSCs in cell-based therapies for AKI is under intensive investigation. Preclinical studies indicate that administered MSCs can both ameliorate renal injury and accelerate renal repair. The mechanisms responsible for their protective and regenerative effects are incompletely understood. However, a concept is now clearer that exogenous MSCs likely involve paracrine effects in regulating the inflammatory mediators to ameliorate kidney injury (Figure 1). Some researchers also found that MVs derived from MSCs can alleviate AKI. By regulating inflammatory mediators like cytokines, chemokines, neutrophils, lymphocytes, NK cells, DCs, and macrophages, MSCs could reduce the kidney inflammation, restore the healthy epithelium and endothelium, and ultimately improve the kidney structure and function.

Conflict of Interests

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

Acknowledgments

This study is supported by Grants from the Research Program of Science and Technology Commission of Shanghai Municipality (10411967200) and the National Natural Science Foundation of China (81170642) and the fund of Shanghai First People’s Hospital (12RC04).

References

M. Legrand, E. G. Mik, T. Johannes, D. Payen, and C. Ince, “Renal hypoxia and dysoxia after reperfusion of the ischemic kidney,” Molecular Medicine, vol. 14, no. 7-8, pp. 502–516, 2008.
View at: Publisher Site | Google Scholar
R. Bellomo, L. Wan, C. Langenberg, and C. May, “Septic acute kidney injury: new concepts,” Nephron: Experimental Nephrology, vol. 109, no. 4, pp. e95–e100, 2008.
View at: Publisher Site | Google Scholar
N. Pannu and M. K. Nadim, “An overview of drug-induced acute kidney injury,” Critical Care Medicine, vol. 36, no. 4, pp. S216–S223, 2008.
View at: Publisher Site | Google Scholar
J. V. Bonventre and L. Yang, “Cellular pathophysiology of ischemic acute kidney injury,” The Journal of Clinical Investigation, vol. 121, no. 11, pp. 4210–4221, 2011.
View at: Publisher Site | Google Scholar
J. V. Bonventre and A. Zuk, “Ischemic acute renal failure: an inflammatory disease?” Kidney International, vol. 66, no. 2, pp. 480–485, 2004.
View at: Publisher Site | Google Scholar
J. J. Friedewald and H. Rabb, “Inflammatory cells in ischemic acute renal failure,” Kidney International, vol. 66, no. 2, pp. 486–491, 2004.
View at: Publisher Site | Google Scholar
H. Umehara, S. Goda, T. Imai et al., “Fractalkine, a CX₃C-chemokine, functions predominantly as an adhesion molecule in monocytic cell line THP-1,” Immunology and Cell Biology, vol. 79, no. 3, pp. 298–302, 2001.
View at: Publisher Site | Google Scholar
B. Rodríguez-Iturbe and G. G. García, “The role of tubulointerstitial inflammation in the progression of chronic renal failure,” Nephron: Clinical Practice, vol. 116, no. 2, pp. 81–88, 2010.
View at: Publisher Site | Google Scholar
R. Yalavanthy and C. L. Edelstein, “Therapeutic and predictive targets of AKI,” Clinical Nephrology, vol. 70, no. 6, pp. 453–463, 2008.
View at: Google Scholar
A. Malgieri, E. Kantzari, M. P. Patrizi, and S. Gambardella, “Bone marrow and umbilical cord blood human mesenchymal stem cells: state of the art,” International Journal of Clinical and Experimental Medicine, vol. 3, no. 4, pp. 248–269, 2010.
View at: Google Scholar
J. Gao, R. Liu, J. Wu et al., “The use of chitosan based hydrogel for enhancing the therapeutic benefits of adipose-derived MSCs for acute kidney injury,” Biomaterials, vol. 33, no. 14, pp. 3673–3681, 2012.
View at: Publisher Site | Google Scholar
S. F. Zhu, Z. N. Zhong, X. F. Fu et al., “Comparison of cell proliferation, apoptosis, cellular morphology and ultrastructure between human umbilical cord and placenta-derived mesenchymal stem cells,” Neuroscience Letters, vol. 541, pp. 77–82, 2013.
View at: Publisher Site | Google Scholar
B. A. Jones and M. Pei, “Synovium-derived stem cells: a tissue-specific stem cell for cartilage engineering and regeneration,” Tissue Engineering B: Reviews, vol. 18, no. 4, pp. 301–311, 2012.
View at: Publisher Site | Google Scholar
T. Tamaki, S. Soeda, H. Hashimoto et al., “3D reconstitution of nerve-blood vessel networks using skeletal muscle-derived multipotent stem cell sheet pellets,” Regenerative Medicine, vol. 8, no. 4, pp. 437–451, 2013.
View at: Google Scholar
M. Dominici, K. le Blanc, I. Mueller et al., “Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement,” Cytotherapy, vol. 8, no. 4, pp. 315–317, 2006.
View at: Publisher Site | Google Scholar
F. Tögel, K. Weiss, Y. Yang, Z. Hu, P. Zhang, and C. Westenfelder, “Vasculotropic, paracrine actions of infused mesenchymal stem cells are important to the recovery from acute kidney injury,” American Journal of Physiology: Renal Physiology, vol. 292, no. 5, pp. F1626–F1635, 2007.
View at: Publisher Site | Google Scholar
K. Cheng, P. Rai, A. Plagov et al., “Transplantation of bone marrow-derived MSCs improves cisplatinum-induced renal injury through paracrine mechanisms,” Experimental and Molecular Pathology, vol. 94, no. 3, pp. 466–473, 2013.
View at: Google Scholar
F. Tögel, Z. Hu, K. Weiss, J. Isaac, C. Lange, and C. Westenfelder, “Administered mesenchymal stem cells protect against ischemic acute renal failure through differentiation-independent mechanisms,” American Journal of Physiology: Renal Physiology, vol. 289, no. 1, pp. F31–F42, 2005.
View at: Publisher Site | Google Scholar
N. Eliopoulos, J. Zhao, M. Bouchentouf et al., “Human marrow-derived mesenchymal stromal cells decrease cisplatin renotoxicity in vitro and in vivo and enhance survival of mice post-intraperitoneal injection,” American Journal of Physiology: Renal Physiology, vol. 299, no. 6, pp. F1288–F1298, 2010.
View at: Publisher Site | Google Scholar
C. J. Luo, F. J. Zhang, L. Zhang et al., “Mesenchymal stem cells ameliorate sepsis-associated acute kidney injury in mice,” Shock, vol. 41, no. 2, pp. 123–129, 2014.
View at: Publisher Site | Google Scholar
K. Furuichi, H. Shintani, Y. Sakai et al., “Effects of adipose-derived mesenchymal cells on ischemia-reperfusion injury in kidney,” Clinical and Experimental Nephrology, vol. 16, no. 5, pp. 679–689, 2012.
View at: Publisher Site | Google Scholar
H. Tsuda, K. Yamahara, K. Otani et al., “Transplantation of allogenic fetal membrane-derived mesenchymal stem cells protect against ischemia-reperfusion-induced acute kidney injury,” Cell Transplantation. In press.
View at: Google Scholar
P. Semedo, C. G. Palasio, C. D. Oliveira et al., “Early modulation of inflammation by mesenchymal stem cell after acute kidney injury,” International Immunopharmacology, vol. 9, no. 6, pp. 677–682, 2009.
View at: Publisher Site | Google Scholar
H. L. Cao, H. Qian, W. R. Xu et al., “Mesenchymal stem cells derived from human umbilical cord ameliorate ischemia/reperfusion-induced acute renal failure in rats,” Biotechnology Letters, vol. 32, no. 5, pp. 725–732, 2010.
View at: Publisher Site | Google Scholar
P. Semedo, P. M. Wang, T. H. Andreucci et al., “Mesenchymal stem cells ameliorate tissue damages triggered by renal ischemia and reperfusion injury,” Transplantation Proceedings, vol. 39, no. 2, pp. 421–423, 2007.
View at: Publisher Site | Google Scholar
L. A. Reis, F. T. Borges, M. J. Simões et al., “Bone marrow-derived mesenchymal stem cells repaired but did not prevent gentamicin-induced acute kidney injury through paracrine effects in rats,” PLoS ONE, vol. 7, no. 9, article e44092, 2012.
View at: Publisher Site | Google Scholar
T. Du, J. Cheng, L. Zhong et al., “The alleviation of acute and chronic kidney injury by human Wharton's jelly-derived mesenchymal stromal cells triggered by ischemia-reperfusion injury via an endocrine mechanism,” Cytotherapy, vol. 14, no. 10, pp. 1215–1227, 2012.
View at: Publisher Site | Google Scholar
Y.-T. Chen, C.-K. Sun, Y.-C. Lin et al., “Adipose-derived mesenchymal stem cell protects kidneys against ischemia-reperfusion injury through suppressing oxidative stress and inflammatory reaction,” Journal of Translational Medicine, vol. 9, article 51, 2011.
View at: Publisher Site | Google Scholar
E. Karshovska, C. Weber, and P. von Hundelshausen, “Platelet chemokines in health and disease,” Thrombosis and Haemostasis, vol. 110, no. 5, pp. 894–902, 2013.
View at: Publisher Site | Google Scholar
T. Imaizumi, T. Aizawa-Yashiro, K. Tsuruga et al., “Melanoma differentiation-associated gene 5 regulates the expression of a chemokine CXCL10 in human mesangial cells: implications for chronic inflammatory renal diseases,” The Tohoku Journal of Experimental Medicine, vol. 228, no. 1, pp. 17–26, 2012.
View at: Publisher Site | Google Scholar
K. Furuichi, T. Wada, H. Yokoyama, and K.-I. Kobayashi, “Role of cytokines and chemokines in renal ischemia-reperfusion injury,” Drug News & Perspectives, vol. 15, no. 8, pp. 477–482, 2002.
View at: Publisher Site | Google Scholar
A. Akcay, Q. Nguyen, and C. L. Edelstein, “Mediators of inflammation in acute kidney injury,” Mediators of Inflammation, vol. 2009, Article ID 137072, 12 pages, 2009.
View at: Publisher Site | Google Scholar
J. Patel, N. Pancholi, K. P. Gudehithlu et al., “Stem cells from foreign body granulation tissue accelerate recovery from acute kidney injury,” Nephrology Dialysis Transplantation, vol. 27, no. 5, pp. 1780–1786, 2012.
View at: Publisher Site | Google Scholar
S. Faubel, E. C. Lewis, L. Reznikov et al., “Cisplatin-induced acute renal failure is associated with an increase in the cytokines interleukin (IL)-1β, IL-18, IL-6, and neutrophil infiltration in the kidney,” The Journal of Pharmacology and Experimental Therapeutics, vol. 322, no. 1, pp. 8–15, 2007.
View at: Publisher Site | Google Scholar
B. Zhang, G. Ramesh, S. Uematsu, S. Akira, and W. B. Reeves, “TLR4 signaling mediates inflammation and tissue injury in nephrotoxicity,” Journal of the American Society of Nephrology, vol. 19, no. 5, pp. 923–932, 2008.
View at: Publisher Site | Google Scholar
G. Ramesh and W. B. Reeves, “TNFR2-mediated apoptosis and necrosis in cisplatin-induced acute renal failure,” American Journal of Physiology: Renal Physiology, vol. 285, no. 4, pp. F610–F618, 2003.
View at: Google Scholar
N. Goes, J. Urmson, V. Ramassar, and P. F. Halloran, “Ischemic acute tubular necrosis induces an extensive local cytokine response: evidence for induction of interferon-γ, transforming growth factor-β1, granulocyte-macrophage colony-stimulating factor, interleukin-2, and interleukin-10,” Transplantation, vol. 59, no. 4, pp. 565–572, 1995.
View at: Google Scholar
J. M. Thurman, A. M. Lenderink, P. A. Royer et al., “C3a is required for the production of CXC chemokines by tubular epithelial cells after renal ishemia/reperfusion,” The Journal of Immunology, vol. 178, no. 3, pp. 1819–1828, 2007.
View at: Google Scholar
J. C. Rice, J. S. Spence, D. L. Yetman, and R. L. Safirstein, “Monocyte chemoattractant protein-1 expression correlates with monocyte infiltration in the post-ischemic kidney,” Renal Failure, vol. 24, no. 6, pp. 703–723, 2002.
View at: Publisher Site | Google Scholar
J. J. Zhao, J. L. Liu, L. Liu, and H. Y. Jia, “Protection of mesenchymal stem cells on acute kidney injury,” Molecular Medicine Reports, vol. 9, no. 1, pp. 91–96, 2014.
View at: Publisher Site | Google Scholar
B. Bi, R. Schmitt, M. Israilova, H. Nishio, and L. G. Cantley, “Stromal cells protect against acute tubular injury via an endocrine effect,” Journal of the American Society of Nephrology, vol. 18, no. 9, pp. 2486–2496, 2007.
View at: Google Scholar
B. Imberti, M. Morigi, S. Tomasoni et al., “Insulin-like growth factor-1 sustains stem cell-mediated renal repair,” Journal of the American Society of Nephrology, vol. 18, no. 11, pp. 2921–2928, 2007.
View at: Publisher Site | Google Scholar
A. Uccelli, V. Pistoia, and L. Moretta, “Mesenchymal stem cells: a new strategy for immunosuppression?” Trends in Immunology, vol. 28, no. 5, pp. 219–226, 2007.
View at: Publisher Site | Google Scholar
A. Oskowitz, H. McFerrin, M. Gutschow, M. L. Carter, and R. Pochampally, “Serum-deprived human multipotent mesenchymal stromal cells (MSCs) are highly angiogenic,” Stem Cell Research, vol. 6, no. 3, pp. 215–225, 2011.
View at: Publisher Site | Google Scholar
S. Qi and D. Wu, “Bone marrow-derived mesenchymal stem cells protect against cisplatin-induced acute kidney injury in rats by inhibiting cell apoptosis,” International Journal of Molecular Medicine, vol. 32, no. 6, pp. 1262–1272, 2013.
View at: Publisher Site | Google Scholar
S. Segerer, P. J. Nelson, and D. Schlondorff, “Chemokines, chemokine receptors, and renal disease: from basic science to pathophysiologic and therapeutic studies,” Journal of the American Society of Nephrology, vol. 11, no. 1, pp. 152–176, 2000.
View at: Google Scholar
K. Furuichi, S. Kaneko, and T. Wada, “Chemokine/chemokine receptor-mediated inflammation regulates pathologic changes from acute kidney injury to chronic kidney disease,” Clinical and Experimental Nephrology, vol. 13, no. 1, pp. 9–14, 2009.
View at: Publisher Site | Google Scholar
F. Togel, J. Isaac, Z. M. Hu, K. Weiss, and C. Westenfelder, “Renal SDF-1 signals mobilization and homing of CXCR4-positive cells to the kidney after ischemic injury,” Kidney International, vol. 67, no. 5, pp. 1772–1784, 2005.
View at: Publisher Site | Google Scholar
K. Furuichi, T. Wada, Y. Iwata et al., “Administration of FR167653, a new anti-inflammatory compound, prevents renal ischaemia/reperfusion injury in mice,” Nephrology Dialysis Transplantation, vol. 17, no. 3, pp. 399–407, 2002.
View at: Google Scholar
S. Balasubramanian, P. Venugopal, S. Sundarraj, Z. Zakaria, A. S. Majumdar, and M. Ta, “Comparison of chemokine and receptor gene expression between Wharton's jelly and bone marrow-derived mesenchymal stromal cells,” Cytotherapy, vol. 14, no. 1, pp. 26–33, 2012.
View at: Publisher Site | Google Scholar
S.-C. Hung, R. R. Pochampally, S.-C. Hsu et al., “Short-term exposure of multipotent stromal cells to low oxygen increases their expression of CX3CR1 and CXCR4 and their engraftment in vivo,” PLoS ONE, vol. 2, no. 5, article e416, 2007.
View at: Publisher Site | Google Scholar
H. Liu, S. Liu, Y. Li et al., “The role of SDF-1-CXCR4/CXCR7 axis in the therapeutic effects of hypoxia-preconditioned mesenchymal stem cells for renal ischemia/ reperfusion injury,” PLoS ONE, vol. 7, no. 4, article e34608, 2012.
View at: Publisher Site | Google Scholar
M. Honczarenko, Y. Le, M. Swierkowski, I. Ghiran, A. M. Glodek, and L. E. Silberstein, “Human bone marrow stromal cells express a distinct set of biologically functional chemokine receptors,” Stem Cells, vol. 24, no. 4, pp. 1030–1041, 2006.
View at: Publisher Site | Google Scholar
D. S. Kim, M. W. Lee, K. H. Yoo et al., “Gene expression profiles of human adipose tissue-derived mesenchymal stem cells are modified by cell culture density,” PLoS ONE, vol. 9, no. 1, article e83363, 2014.
View at: Publisher Site | Google Scholar
S. J. Baek, S. K. Kang, and J. C. Ra, “In vitro migration capacity of human adipose tissue-derived mesenchymal stem cells reflects their expression of receptors for chemokines and growth factors,” Experimental & Molecular Medicine, vol. 43, no. 10, pp. 596–603, 2011.
View at: Publisher Site | Google Scholar
V. Sordi, M. L. Malosio, F. Marchesi et al., “Bone marrow mesenchymal stem cells express a restricted set of functionally active chemokine receptors capable of promoting migration to pancreatic islets,” Blood, vol. 106, no. 2, pp. 419–427, 2005.
View at: Publisher Site | Google Scholar
A. L. Ponte, E. Marais, N. Gallay et al., “The in vitro migration capacity of human bone marrow mesenchymal stem cells: comparison of chemokine and growth factor chemotactic activities,” Stem Cells, vol. 25, no. 7, pp. 1737–1745, 2007.
View at: Publisher Site | Google Scholar
J. Ringe, S. Strassburg, K. Neumann et al., “Towards in situ tissue repair: human mesenchymal stem cells express chemokine receptors CXCR1, CXCR2 and CCR2, and migrate upon stimulation with CXCL8 but not CCL2,” Journal of Cellular Biochemistry, vol. 101, no. 1, pp. 135–146, 2007.
View at: Publisher Site | Google Scholar
H. Zhang, H. Ning, L. Banie et al., “Adipose tissue-derived stem cells secrete CXCL5 cytokine with chemoattractant and angiogenic properties,” Biochemical and Biophysical Research Communications, vol. 402, no. 3, pp. 560–564, 2010.
View at: Publisher Site | Google Scholar
J. M. Fox, G. Chamberlain, B. A. Ashton, and J. Middleton, “Recent advances into the understanding of mesenchymal stem cell trafficking,” British Journal of Haematology, vol. 137, no. 6, pp. 491–502, 2007.
View at: Publisher Site | Google Scholar
S. M. Albelda, C. W. Smith, and P. A. Ward, “Adhesion molecules and inflammatory injury,” The FASEB Journal, vol. 8, no. 8, pp. 504–512, 1994.
View at: Google Scholar
B. A. Molitoris and J. Marrs, “The role of cell adhesion molecules in ischemic acute renal failure,” American Journal of Medicine, vol. 106, no. 5, pp. 583–592, 1999.
View at: Publisher Site | Google Scholar
K. J. Kelly, W. W. Williams Jr., R. B. Colvin, and J. V. Bonventre, “Antibody to intercellular adhesion molecule 1 protects the kidney against ischemic injury,” Proceedings of the National Academy of Sciences of the United States of America, vol. 91, no. 2, pp. 812–816, 1994.
View at: Google Scholar
K. J. Kelly, W. W. Williams Jr., R. B. Colvin et al., “Intercellular adhesion molecule-1-deficient mice are protected against ischemic renal injury,” The Journal of Clinical Investigation, vol. 97, no. 4, pp. 1056–1063, 1996.
View at: Google Scholar
Y. Hara, M. Stolk, J. Ringe et al., “In vivo effect of bone marrow-derived mesenchymal stem cells in a rat kidney transplantation model with prolonged cold ischemia,” Transplant International, vol. 24, no. 11, pp. 1112–1123, 2011.
View at: Publisher Site | Google Scholar
M. Hagiwara, B. Shen, L. Chao, and J. Chao, “Kallikrein-modified mesenchymal stem cell implantation provides enhanced protection against acute ischemic kidney injury by inhibiting apoptosis and inflammation,” Human Gene Therapy, vol. 19, no. 8, pp. 807–819, 2008.
View at: Publisher Site | Google Scholar
D. Dragun, U. Hoff, J. K. Park et al., “Ischemia-reperfusion injury in renal transplantation is independent of the immunologic background,” Kidney International, vol. 58, no. 5, pp. 2166–2177, 2000.
View at: Publisher Site | Google Scholar
B. Rüster, S. Göttig, R. J. Ludwig et al., “Mesenchymal stem cells display coordinated rolling and adhesion behavior on endothelial cells,” Blood, vol. 108, no. 12, pp. 3938–3944, 2006.
View at: Publisher Site | Google Scholar
K. de Filippo, A. Dudeck, M. Hasenberg et al., “Mast cell and macrophage chemokines CXCL1/CXCL2 control the early stage of neutrophil recruitment during tissue inflammation,” Blood, vol. 121, no. 24, pp. 4930–4937, 2013.
View at: Publisher Site | Google Scholar
H. Yagi, A. Soto-Gutierrez, N. Navarro-Alvarez et al., “Reactive bone marrow stromal cells attenuate systemic inflammation via sTNFR1,” Molecular Therapy, vol. 18, no. 10, pp. 1857–1864, 2010.
View at: Publisher Site | Google Scholar
M. Morigi, C. Rota, T. Montemurro et al., “Life-sparing effect of human cord blood-mesenchymal stem cells in experimental acute kidney injury,” Stem Cells, vol. 28, no. 3, pp. 513–522, 2010.
View at: Publisher Site | Google Scholar
Q. Wang, H. Zhu, W. G. Zhou et al., “N-acetylcysteine- pretreated human embryonic mesenchymal stem cell administration protects against bleomycin-induced lung injury,” The American Journal of the Medical Sciences, vol. 346, no. 2, pp. 113–122, 2013.
View at: Publisher Site | Google Scholar
H. Rabb, “The T cell as a bridge between innate and adaptive immune systems: implications for the kidney,” Kidney International, vol. 61, no. 6, pp. 1935–1946, 2002.
View at: Publisher Site | Google Scholar
J. Hu, L. Zhang, N. Wang et al., “Mesenchymal stem cells attenuate ischemic acute kidney injury by inducing regulatory T cells through splenocyte interactions,” Kidney International, vol. 84, no. 3, pp. 521–531, 2013.
View at: Publisher Site | Google Scholar
M.-G. Kim, S. Y. Lee, Y. S. Ko et al., “CD4⁺ CD25⁺ regulatory T cells partially mediate the beneficial effects of FTY720, a sphingosine-1-phosphate analogue, during ischaemia/reperfusion-induced acute kidney injury,” Nephrology Dialysis Transplantation, vol. 26, no. 1, pp. 111–124, 2011.
View at: Publisher Site | Google Scholar
Y. M. Wang, G. Y. Zhang, M. Hu et al., “CD8⁺ regulatory T cells induced by T cell vaccination protect against autoimmune nephritis,” Journal of the American Society of Nephrology, vol. 23, no. 6, pp. 1058–1067, 2012.
View at: Publisher Site | Google Scholar
Z. Ye, Y. Wang, H.-Y. Xie, and S.-S. Zheng, “Immunosuppressive effects of rat mesenchymal stem cells: involvement of CD4⁺CD25⁺ regulatory T cells,” Hepatobiliary & Pancreatic Diseases International, vol. 7, no. 6, pp. 608–614, 2008.
View at: Google Scholar
J.-A. Kim, S. Hong, B. Lee et al., “The inhibition of T-cells proliferation by mouse mesenchymal stem cells through the induction of ${p16}^{INK4A}$ -cyclin D1/cdk4 and ${p 21}^{waf1}$ , ${p 27}^{kip1}$ -cyclin E/cdk2 pathways,” Cellular Immunology, vol. 245, no. 1, pp. 16–23, 2007.
View at: Publisher Site | Google Scholar
A. J. Nauta and W. E. Fibbe, “Immunomodulatory properties of mesenchymal stromal cells,” Blood, vol. 110, no. 10, pp. 3499–3506, 2007.
View at: Publisher Site | Google Scholar
M. M. Duffy, J. Pindjakova, S. A. Hanley et al., “Mesenchymal stem cell inhibition of T-helper 17 cell- differentiation is triggered by cell-cell contact and mediated by prostaglandin E2 via the EP4 receptor,” European Journal of Immunology, vol. 41, no. 10, pp. 2840–2851, 2011.
View at: Publisher Site | Google Scholar
R. Yañez, A. Oviedo, M. Aldea, J. A. Bueren, and M. L. Lamana, “Prostaglandin E2 plays a key role in the immunosuppressive properties of adipose and bone marrow tissue-derived mesenchymal stromal cells,” Experimental Cell Research, vol. 316, no. 19, pp. 3109–3123, 2010.
View at: Publisher Site | Google Scholar
M. Najar, G. Raicevic, H. I. Boufker et al., “Mesenchymal stromal cells use PGE2 to modulate activation and proliferation of lymphocyte subsets: combined comparison of adipose tissue, Wharton's jelly and bone marrow sources,” Cellular Immunology, vol. 264, no. 2, pp. 171–179, 2010.
View at: Publisher Site | Google Scholar
S. Sakaguchi, T. Yamaguchi, T. Nomura, and M. Ono, “Regulatory T cells and immune tolerance,” Cell, vol. 133, no. 5, pp. 775–787, 2008.
View at: Publisher Site | Google Scholar
M. J. Burne-Taney, D. B. Ascon, F. Daniels, L. Racusen, W. Baldwin, and H. Rabb, “B cell deficiency confers protection from renal ischemia reperfusion injury,” The Journal of Immunology, vol. 171, no. 6, pp. 3210–3215, 2003.
View at: Google Scholar
F. Schena, C. Gambini, A. Gregorio et al., “Interferon-γ-dependent inhibition of B cell activation by bone marrow-derived mesenchymal stem cells in a murine model of systemic lupus erythematosus,” Arthritis & Rheumatism, vol. 62, no. 9, pp. 2776–2786, 2010.
View at: Publisher Site | Google Scholar
X. Ma, N. Che, Z. Gu et al., “Allogenic mesenchymal stem cell transplantation ameliorates nephritis in lupus mice via inhibition of B-cell activation,” Cell Transplantation, vol. 22, no. 12, pp. 2279–2290, 2012.
View at: Publisher Site | Google Scholar
A. Cerwenka and L. L. Lanier, “Natural killer cells, viruses and cancer,” Nature Reviews Immunology, vol. 1, no. 1, pp. 41–49, 2001.
View at: Google Scholar
Z.-X. Zhang, S. Wang, X. Huang et al., “NK cells induce apoptosis in tubular epithelial cells and contribute to renal ischemia-reperfusion injury,” The Journal of Immunology, vol. 181, no. 11, pp. 7489–7498, 2008.
View at: Google Scholar
A. Pradier, J. Passweg, J. Villard, and V. Kindler, “Human bone marrow stromal cells and skin fibroblasts inhibit natural killer cell proliferation and cytotoxic activity,” Cell Transplantation, vol. 20, no. 5, pp. 681–691, 2011.
View at: Publisher Site | Google Scholar
Z. Selmani, A. Naji, I. Zidi et al., “Human leukocyte antigen-G5 secretion by human mesenchymal stem cells is required to suppress T lymphocyte and natural killer function and to induce CD4⁺ ${CD25}^{high}$ FOXP3⁺ regulatory T cells,” Stem Cells, vol. 26, no. 1, pp. 212–222, 2008.
View at: Publisher Site | Google Scholar
A. Ribeiro, P. Laranjeira, S. Mendes et al., “Mesenchymal stem cells from umbilical cord matrix, adipose tissue and bone marrow exhibit different capability to suppress peripheral blood B, natural killer and T cells,” Stem Cell Research & Therapy, vol. 4, no. 5, article 125, 2013.
View at: Publisher Site | Google Scholar
Z. G. Zhao, Z. Cao, W. Xu et al., “Immune protection function of multipotent mesenchymal stromal cells: role of transforming growth factor-β1,” Cancer Investigation, vol. 30, no. 9, pp. 646–656, 2012.
View at: Publisher Site | Google Scholar
D. J. Nikolic-Paterson and R. C. Atkins, “The role of macrophages in glomerulonephritis,” Nephrology Dialysis Transplantation, vol. 16, supplement 5, pp. 3–7, 2001.
View at: Google Scholar
Q. Cao, D. Zheng, Y. P. Wang, and D. C. Harris, “Macrophages and dendritic cells for treating kidney disease,” Nephron: Experimental Nephrology, vol. 117, no. 3, pp. e47–e52, 2011.
View at: Publisher Site | Google Scholar
H. Lu, D. Huang, N. Saederup, I. F. Charo, R. M. Ransohoff, and L. Zhou, “Macrophages recruited via CCR2 produce insulin-like growth factor-1 to repair acute skeletal muscle injury,” The FASEB Journal, vol. 25, no. 1, pp. 358–369, 2011.
View at: Publisher Site | Google Scholar
D. M. Mosser and J. P. Edwards, “Exploring the full spectrum of macrophage activation,” Nature Reviews Immunology, vol. 8, no. 12, pp. 958–969, 2008.
View at: Publisher Site | Google Scholar
S. D. Ricardo, H. van Goor, and A. A. Eddy, “Macrophage diversity in renal injury and repair,” The Journal of Clinical Investigation, vol. 118, no. 11, pp. 3522–3530, 2008.
View at: Publisher Site | Google Scholar
H.-J. Anders and M. Ryu, “Renal microenvironments and macrophage phenotypes determine progression or resolution of renal inflammation and fibrosis,” Kidney International, vol. 80, no. 9, pp. 915–925, 2011.
View at: Publisher Site | Google Scholar
J. Luo, X. Zhao, Z. Tan, Z. Su, F. Meng, and M. Zhang, “Mesenchymal-like progenitors derived from human embryonic stem cells promote recovery from acute kidney injury via paracrine actions,” Cytotherapy, vol. 15, no. 6, pp. 649–662, 2013.
View at: Publisher Site | Google Scholar
S. Lee, S. Huen, H. Nishio et al., “Distinct macrophage phenotypes contribute to kidney injury and repair,” Journal of the American Society of Nephrology, vol. 22, no. 2, pp. 317–326, 2011.
View at: Publisher Site | Google Scholar
W. Li, Q. Zhang, M. Wang et al., “Macrophages are involved in the protective role of human umbilical cord-derived stromal cells in renal ischemia-reperfusion injury,” Stem Cell Research, vol. 10, no. 3, pp. 405–416, 2013.
View at: Publisher Site | Google Scholar
M. D. Okusa and L. Li, “Dendritic cells in acute kidney injury: cues from the microenvironment,” Transactions of the American Clinical and Climatological Association, vol. 123, pp. 54–62, 2012.
View at: Google Scholar
M. G. Kim, S. H. Kim, H. Noh et al., “CD11c⁺ cells partially mediate the renoprotective effect induced by bone marrow-derived mesenchymal stem cells,” PLoS ONE, vol. 8, no. 8, article e72544, 2013.
View at: Publisher Site | Google Scholar
Y. Zhang, W. Cai, Q. Huang et al., “Mesenchymal stem cells alleviate bacteria-induced liver injury in mice by inducing regulatory dendritic cells,” Hepatology, vol. 59, no. 2, pp. 671–682, 2014.
View at: Publisher Site | Google Scholar
Z. Han, Y. Jing, S. Zhang et al., “The role of immunosuppression of mesenchymal stem cells in tissue repair and tumor growth,” Cell & Bioscience, vol. 2, no. 1, article 8, 2012.
View at: Publisher Site | Google Scholar
H. Tian, Y. Lu, S. P. Shah, Q. Wang, and S. Hong, “14S,21R-dihydroxy-docosahexaenoic acid treatment enhances mesenchymal stem cell amelioration of renal ischemia/reperfusion injury,” Stem Cells and Development, vol. 21, no. 7, pp. 1187–1199, 2012.
View at: Publisher Site | Google Scholar
B. Kronsteiner, A. Peterbauer-Scherb, R. Grillari-Voglauer et al., “Human mesenchymal stem cells and renal tubular epithelial cells differentially influence monocyte-derived dendritic cell differentiation and maturation,” Cellular Immunology, vol. 267, no. 1, pp. 30–38, 2011.
View at: Publisher Site | Google Scholar
G. M. Spaggiari, H. Abdelrazik, F. Becchetti, and L. Moretta, “MSCs inhibit monocyte-derived DC maturation and function by selectively interfering with the generation of immature DCs: central role of MSC-derived prostaglandin E2,” Blood, vol. 113, no. 26, pp. 6576–6583, 2009.
View at: Publisher Site | Google Scholar
J. Ratajczak, K. Miekus, M. Kucia et al., “Embryonic stem cell-derived microvesicles reprogram hematopoietic progenitors: evidence for horizontal transfer of mRNA and protein delivery,” Leukemia, vol. 20, no. 5, pp. 847–856, 2006.
View at: Publisher Site | Google Scholar
G. Camussi, M. C. Deregibus, S. Bruno, V. Cantaluppi, and L. Biancone, “Exosomes/microvesicles as a mechanism of cell-to-cell communication,” Kidney International, vol. 78, no. 9, pp. 838–848, 2010.
View at: Publisher Site | Google Scholar
G. Camussi, M. C. Deregibus, and V. Cantaluppi, “Role of stem-cell-derived microvesicles in the paracrine action of stem cells,” Biochemical Society Transactions, vol. 41, no. 1, pp. 283–287, 2013.
View at: Publisher Site | Google Scholar
S. Wu, G. Q. Ju, T. Du et al., “Microvesicles derived from human umbilical cord Wharton's jelly mesenchymal stem cells attenuate bladder tumor cell growth in vitro and in vivo,” PLoS ONE, vol. 8, no. 4, article e61366, 2013.
View at: Publisher Site | Google Scholar
J. Polgar, J. Matuskova, and D. D. Wagner, “The P-selectin, tissue factor, coagulation triad,” Journal of Thrombosis and Haemostasis, vol. 3, no. 8, pp. 1590–1596, 2005.
View at: Publisher Site | Google Scholar
J. W. Kim, E. Wieckowski, D. D. Taylor, T. E. Reichert, S. Watkins, and T. L. Whiteside, “Fas ligand-positive membranous vesicles isolated from sera of patients with oral cancer induce apoptosis of activated T lymphocytes,” Clinical Cancer Research, vol. 11, no. 3, pp. 1010–1020, 2005.
View at: Google Scholar
J. Ratajczak, M. Wysoczynski, F. Hayek, A. Janowska-Wieczorek, and M. Z. Ratajczak, “Membrane-derived microvesicles: important and underappreciated mediators of cell-to-cell communication,” Leukemia, vol. 20, no. 9, pp. 1487–1495, 2006.
View at: Publisher Site | Google Scholar
F. Collino, M. C. Deregibus, S. Bruno et al., “Microvesicles derived from adult human bone marrow and tissue specific mesenchymal stem cells shuttle selected pattern of miRNAs,” PLoS ONE, vol. 5, no. 7, article e11803, 2010.
View at: Publisher Site | Google Scholar
H. Valadi, K. Ekstrom, A. Bossios, M. Sjöstrand, J. J. Lee, and J. O. Lötvall, “Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells,” Nature Cell Biology, vol. 9, no. 6, pp. 654–659, 2007.
View at: Publisher Site | Google Scholar
S. Ramachandran and V. Palanisamy, “Horizontal transfer of RNAs: exosomes as mediators of intercellular communication,” Wiley Interdisciplinary Reviews: RNA, vol. 3, no. 2, pp. 286–293, 2012.
View at: Publisher Site | Google Scholar
E. N. Nolte-'t Hoen, S. I. Buschow, S. M. Anderton, W. Stoorvogel, and M. H. M. Wauben, “Activated T cells recruit exosomes secreted by dendritic cells via LFA-1,” Blood, vol. 113, no. 9, pp. 1977–1981, 2009.
View at: Publisher Site | Google Scholar
H. Sheldon, E. Heikamp, H. Turley et al., “New mechanism for Notch signaling to endothelium at a distance by Delta-like 4 incorporation into exosomes,” Blood, vol. 116, no. 13, pp. 2385–2394, 2010.
View at: Publisher Site | Google Scholar
S. Bruno, C. Grange, M. C. Deregibus et al., “Mesenchymal stem cell-derived microvesicles protect against acute tubular injury,” Journal of the American Society of Nephrology, vol. 20, no. 5, pp. 1053–1067, 2009.
View at: Publisher Site | Google Scholar
S. Bruno, C. Grange, F. Collino et al., “Microvesicles derived from mesenchymal stem cells enhance survival in a lethal model of acute kidney injury,” PLoS ONE, vol. 7, no. 3, article e33115, 2012.
View at: Publisher Site | Google Scholar
Y. Zhou, H. Xu, W. Xu et al., “Exosomes released by human umbilical cord mesenchymal stem cells protect against cisplatin-induced renal oxidative stress and apoptosis in vivo and in vitro,” Stem Cell Research & Therapy, vol. 4, no. 2, article 34, 2013.
View at: Publisher Site | Google Scholar
S. Gatti, S. Bruno, M. C. Deregibus et al., “Microvesicles derived from human adult mesenchymal stem cells protect against ischaemia-reperfusion-induced acute and chronic kidney injury,” Nephrology Dialysis Transplantation, vol. 26, no. 5, pp. 1474–1483, 2011.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2014 Tao Du and Ying-Jian Zhu. 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.

PDF Download Citation

Download other formats

Order printed copies

Views

2082

Downloads

1175

Citations