Volume 9 Issue 2
Mar.  2018
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Zhou Chaorong, Lyu Haijin, Sun Yao, et al. Effect of human umbilical cord mesenchymal stem cells on CD4+ T cells in liver after hepatic ischemia-reperfusion injury in mice[J]. ORGAN TRANSPLANTATION, 2018, 9(2): 103-109. doi: 10.3969/j.issn.1674-7445.2018.02.003
Citation: Zhou Chaorong, Lyu Haijin, Sun Yao, et al. Effect of human umbilical cord mesenchymal stem cells on CD4+ T cells in liver after hepatic ischemia-reperfusion injury in mice[J]. ORGAN TRANSPLANTATION, 2018, 9(2): 103-109. doi: 10.3969/j.issn.1674-7445.2018.02.003

Effect of human umbilical cord mesenchymal stem cells on CD4+ T cells in liver after hepatic ischemia-reperfusion injury in mice

doi: 10.3969/j.issn.1674-7445.2018.02.003
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  • Corresponding author: Yi Huimin, Email:ylhmin@hotmail.com
  • Received Date: 2017-12-20
    Available Online: 2021-01-19
  • Publish Date: 2018-03-15
  •   Objective  To investigate the effect of human umbilical cord mesenchymal stem cells (HUC-MSCs) on CD4+ T cells in liver after hepatic ischemia-reperfusion injury (HIRI) in mice.  Methods  Two hundred and twentyfive mice were randomly divided into sham group, control group and MSC group, with 75 mice in each group. HIRI model mice were used in MSC group and control group. HUC-MSCs were injected in MSC group through inferior vena cava. Normal saline was injected in control group through inferior vena cava. Only laparotomy and abdominal closure were performed in sham group without blood vessel clipping. At 6, 12 and 24 h after operation, 15 mice of each group were randomly selected to sample eyeball blood and liver tissues, and the 30 mice left in each group were used to extract intrahepatic mononuclear cells. The number of intrahepatic mononuclear cells, percentage, number and positive rate of CD4+ T cells in the mice of various groups at different time points were compared. The content of interleukin (IL)-17 in serum and liver tissue as well as expression levels of costimulatory molecules B7-1 and B7-2 messenger RNA (mRNA) in liver tissues of the mice at different time points were compared.  Results  At 12 and 24 h after operation, the number of intrahepatic mononuclear cells of control group was significantly higher than that of sham group, while the number of intrahepatic mononuclear cells of MSC group was significantly lower than that of control group (P < 0.01-0.05). At 6, 12 and 24 h after operation, the percentage, number and positive rate of CD4+T cells of control group were significantly higher than those of sham group (all P < 0.01), while the percentage of CD4+T cells of MSC group was significantly lower than that of control group (P < 0.01-0.05). At 12 and 24 h after operation, the number and positive rate of CD4+ T cells of MSC group were significantly lower than those of control group (P < 0.01-0.05). At 6, 12 and 24 h after operation, the IL-17 contents in serum and liver tissues of control group were higher than those of sham group (all P < 0.01), while the IL-17 contents in serum and liver tissues of MSC group were lower than those of control group (all P < 0.01). At 6 h after operation, the mRNA expression level of B7-2 of control group was higher than that of sham group (P < 0.05). At 12 and 24 h after operation, the mRNA expression levels of B7-1 and B7-2 of control group were higher than those of sham group (all P < 0.01), while the mRNA expression levels of B7-1 and B7-2 of MSC group were lower than those of control group (all P < 0.01).  Conclusions  HUC-MSCs inhibits the number of CD4+T cells and the secretion of IL-17 in liver after HIRI, as well as decreases the number of intrahepatic mononuclear cells and the mRNA expression of B7-1 and B7-2, thereby alleviating HIRI.

     

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  • [1]
    CALDWELL CC, TSCHOEP J, LENTSCH AB, et al. Lymphocyte function during hepatic ischemia/reperfusion injury[J]. J Leukoc Biol, 2007, 82(3): 457-464. doi: 10.1189/jlb.0107062
    [2]
    SHEN X, WANG Y, GAO F, et al. CD4 T cells promote tissue inflammation via CD40 signaling without de novo activation in a murine model of liver ischemia/reperfusion injury[J]. Hepatology, 2009, 50(5): 1537-1546. DOI: 10.1002/hep.23153.
    [3]
    CALDWELL CC, OKAYA T, MARTIGNONI A, et al. Divergent functions of CD4+ T lymphocytes in acute liver inflammation and injury after ischemia-reperfusion[J]. Am J Physiol Gastrointest Liver Physiol, 2005, 289(5): G969-G976. doi: 10.1152/ajpgi.00223.2005
    [4]
    REIFART J, RENTSCH M, MENDE K, et al. Modulating CD4+ T cell migration in the postischemic liver: hepatic stellate cells as new therapeutic target?[J]. Transplantation, 2015, 99(1): 41-47. DOI: 10.1097/TP.0000000000000461.
    [5]
    MAGGI U, FORNONI G, CENTONZE L, et al. Ischemia time and liver transplantation, today[J]. Transplant Proc, 2014, 46(7): 2295-2299. DOI: 10.1016/j.transproceed.2014.07.040.
    [6]
    HAGA H, YAN IK, BORRELLI DA, et al. Extracellular vesicles from bone marrow-derived mesenchymal stem cells protect against murine hepatic ischemia/reperfusion injury[J]. Liver Transpl, 2017, 23(6): 791-803. DOI: 10.1002/lt.24770.
    [7]
    ROWART P, ERPICUM P, DETRY O, et al. Mesenchymal stromal cell therapy in ischemia/reperfusion injury[J]. J Immunol Res, 2015: 602597. DOI: 10.1155/2015/602597.
    [8]
    UCHIDA Y, FREITAS MC, ZHAO D, et al. The protective function of neutrophil elastase inhibitor in liver ischemia/reperfusion injury[J]. Transplantation, 2010, 89(9): 1050-1056. DOI: 10.1097/TP.0b013e3181d45a98.
    [9]
    VAN GOLEN RF, REINIERS MJ, VRISEKOOP N, et al. The mechanisms and physiological relevance of glycocalyx degradation in hepatic ischemia/reperfusion injury[J]. Antioxid Redox Signal, 2014, 21(7): 1098-1118. DOI: 10.1089/ars.2013.5751.
    [10]
    ZWACKA RM, ZHANG Y, HALLDORSON J, et al. CD4(+) T-lymphocytes mediate ischemia/reperfusion-induced inflammatory responses in mouse liver[J]. J Clin Invest, 1997, 100(2): 279-289. doi: 10.1172/JCI119533
    [11]
    YAO Z, PAINTER SL, FANSLOW WC, et al. Human IL-17: a novel cytokine derived from T cells[J]. J Immunol, 1995, 155(12): 5483-5486. http://www.jimmunol.org/content/155/12/5483.full.pdf
    [12]
    KONO H, FUJⅡ H, OGIKU M, et al. Role of IL-17A in neutrophil recruitment and hepatic injury after warm ischemia-reperfusion mice[J]. J Immunol, 2011, 187(9): 4818-4825. DOI: 10.4049/jimmunol.1100490.
    [13]
    KOJIMA N, SATO M, SUZUKI A, et al. Enhanced expression of B7-1, B7-2, and intercellular adhesion molecule 1 in sinusoidal endothelial cells by warm ischemia/reperfusion injury in rat liver[J]. Hepatology, 2001, 34(4 Pt 1): 751-757. doi: 10.1053/jhep.2001.27804?scrollTo=references
    [14]
    TAKADA M, CHANDRAKER A, NADEAU KC, et al. The role of the B7 costimulatory pathway in experimental cold ischemia/reperfusion injury[J]. J Clin Invest, 1997, 100(5): 1199-1203. doi: 10.1172/JCI119632
    [15]
    LENTSCH AB. Regulatory mechanisms of injury and repair after hepatic ischemia/reperfusion[J]. Scientifica (Cairo), 2012: 513192. DOI: 10.6064/2012/513192.
    [16]
    FEISST V, BROOKS AE, CHEN CJ, et al. Characterization of mesenchymal progenitor cell populations directly derived from human dermis[J]. Stem Cells Dev, 2014, 23(6): 631-642. DOI: 10.1089/scd.2013.0207.
    [17]
    徐土炳, 李莉, 罗兴迪, 等.骨髓间充质干细胞在肝细胞损伤恢复中的作用[J].实用医学杂志, 2017, 33(5): 687-692. DOI: 10.3969/j.issn.1006-5725.2017.05.004.

    XU TB, LI L, LUO XD, et al. Role of bone marrow mesenchymal stem cells in recovery process of hepatocyte injury[J]. J Pract Med, 2017, 33(5): 687-692. DOI: 10.3969/j.issn.1006-5725.2017.05.004.
    [18]
    ROSSIGNOL J, BOYER C, THINARD R, et al. Mesenchymal stem cells induce a weak immune response in the rat striatum after allo or xenotransplantation[J]. J Cell Mol Med, 2009, 13(8B): 2547-2558. DOI: 10.1111/j.1582-4934.2009.00657.x.
    [19]
    唐飞龙, 栾佐, 吴南海, 等.脐带间充质干细胞治疗儿童移植相关并发症的疗效观察[J].转化医学杂志, 2017, 6(3): 132-136. DOI: 10.3969/j.issn.2095-3097.2017.03.002.

    TANG FL, LUAN Z, WU NH, et al. Therapeutic effect of umbilical cord-mesenchymal stem cell on transplantation-related complications in children[J]. Translat Med J, 2017, 6(3): 132-136. DOI: 10.3969/j.issn.2095-3097.2017.03.002.
    [20]
    BLOOM DD, CENTANNI JM, BHATIA N, et al. A reproducible immunopotency assay to measure mesenchymal stromal cell-mediated T-cell suppression[J]. Cytotherapy, 2015, 17(2): 140-151. DOI: 10.1016/j.jcyt.2014.10.002.
    [21]
    DANCHUK S, YLOSTALO JH, HOSSAIN F, et al. Human multipotent stromal cells attenuate lipopolysaccharide-induced acute lung injury in mice via secretion of tumor necrosis factor-α-induced protein 6[J]. Stem Cell Res Ther, 2011, 2(3): 27. DOI: 10.1186/scrt68.
    [22]
    HSU WT, LIN CH, CHIANG BL, et al. Prostaglandin E2 potentiates mesenchymal stem cell-induced IL-10+IFN-γ+CD4+ regulatory T cells to control transplant arteriosclerosis[J]. J Immunol, 2013, 190(5): 2372-2380. DOI: 10.4049/jimmunol.1202996.
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