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诱导供者胰岛细胞高表达血红素加氧酶-1延长大鼠胰岛移植物的存活时间

HO-1 overexpression induced by CoPP in donors can prolong the survival of transplanted allogeneic islets of rats
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摘要 目的探讨钴原卟啉(CoPP)诱导大鼠胰岛细胞高表达血红素加氧酶-1(HO-1)后,对延长胰岛移植物存活时间的作用。方法(1)将分离和纯化的供者(BN大鼠)胰岛细胞分为CoPP诱导组和未诱导组。CoPP诱导组供者在分离胰岛细胞前3天和前1天腹腔注射2.5mg/kg的CoPP,未诱导组不注射CoPP。诱导后,采用免疫荧光法及Western免疫印迹法检测两组胰岛细胞中HO-1的表达情况,采用酶联免疫吸附试验(EUSA)和葡萄糖刺激试验检测胰岛细胞的胰岛素释放水平。(2)Lewis大鼠经四氧嘧啶静脉注射后建立糖尿病模型,取10只成功建立糖尿病模型的大鼠作为胰岛细胞移植的受者,随机平均将受者分为实验组和对照组,分别移植经CoPP诱导和未经诱导的供者胰岛细胞。移植后,观察和比较两组受者胰岛移植物的存活时间和发生排斥反应后胰岛移植物的组织病理学变化。结果CoPP诱导组胰岛细胞高表达HO-1,而未诱导组不表达HO-1;CoPP诱导组和未诱导组供者胰岛细胞胰岛素分泌量,在低糖刺激下分别为(15.65±0.89)mU/L和(12.28±0.89)mU/L(P〉0.05),在高糖刺激下分别为(46.60±1.13)mU/L和(19.01±1.49)mU/L(P〈0.05),刺激指数分别为2.98±0.10和1.55±0.01(P〈0.05)。实验组和对照组胰岛移植物平均存活时间分别为(12.20±5.67)d和(5.60±1.14)d(P〈0.05);当受者发生排斥反应时,对照组胰岛移植物周边可见明显的淋巴细胞、成纤维细胞以及单个核细胞浸润,而实验组细胞浸润的程度明显较轻。结论CoPP可诱导大鼠胰岛细胞高表达HO-1,其对胰岛细胞有明显保护作用。移植高表达HO-I的胰岛细胞能显著延长胰岛移植物的存活时间。 Objective To investigate the effects of the overexpression of HO-1 induced by CoPP in the donor on the survival of transplantedallogeneic islets of rats and the mechanism. Methods (1) Brown Norway rats were randomly divided into control group, and CoPP-induced group receiving intraperitoneal injection of CoPP (2. 5 mg/kg) at 3rd and 1st day prior to islet isolation. By using the cytoimmunofluorescence and Western blot, the expression of HO-1 in isolated islets was detected. The insulin level in the supernatant of the cultured islets stimulated with glucose was determined by ELISA. (2) Lewis male rat diabetic models were established by a single intravenous injection of alloxan, and then randomly divided into CoPP group and control group. Islets were transplanted under the left kidney capsule of each diabetic recipient. The survival time after transplantation, and pathological changes following rejection of the islet grafts were analyzed. Results The HO-1 was highly expressed in the islets isolated from CoPP-treated rats by cytoimmunofluorescence and Western blot. After stimulation with 16. 7 mmol/L glucose, the insulin concentration in Copp-treated and Copp-untreated groups was (46. 60 ± 1. t3) and (19. 01 ± 1.49) mIU/L respectively (P〈0. 05). The insulin concentration in Copp-treated and Copp-untreated groups in islets stimulated with 5.6 mmol/L glucose was (15.65 ± 0. 89) and (12. 28 ± 0. 89) mU/L respectively (P〉0. 05). The stimulated index in Copl-treated and Copl〉untreated groups was (2. 98 ± 0. 10) and 1.55 ± 0. 01 respectively (P〈0. 05). The survival time of islets allograft in Copp-treated and Copp-untreated groups was separately (12. 20± 5. 67) and (5.60 ± 1.14) days respectively (P〈0. 05). Histological analysis revealed the presence of more islands of insulin-positive ceils and considerably fewer lymphocytes or inflammatory infiltration than the controls. Conclusions CoPP could induce the HO-1 expression of islets, and improve thei
出处 《中华器官移植杂志》 CAS CSCD 北大核心 2009年第4期211-214,共4页 Chinese Journal of Organ Transplantation
基金 十一五国家科技支撑计划(2006BA105A07) 国家重点基础研究发展计划(2005CB522500)
关键词 胰岛移植 血红素加氧酶-1 大鼠 Islets of langerhans transplantatiomHeme oxygenase-1 Rats
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参考文献12

  • 1Shapiro AM, Lakey JR, Ryan EA,et al. Islet transplantation in seven patients with type 1 diabetes mellitus using a glucocortieoid free immunosuppressive regimen. N Engl J Med, 2000, 343(4):230-238. 被引量:1
  • 2McCarter SD, Akyea TG, Lu X, et al. Endogenous heme oxygenase induction is a critical mechanism attenuating apoptosis and restoring microvascular perfusion following limb ischemia/reperfusion. Surgery, 2004, 136(1): 67-75. 被引量:1
  • 3Woo J, Iyer S, Mori N, et al. Alleviation of graft-versus-host disease after conditioning with cobalt-protoporphyrin, an inducer of heine oxygenase-1. Transplantation, 2000, 69 (4) : 623-633. 被引量:1
  • 4Shapiro AM, Hao E, Rajotte RV, et al. High yield of rodent islets with intraductal collagenase and stationary digestion-a comparison with standard technique. Cell Transplantation, 1996, 5(6) :631-638. 被引量:1
  • 5Nishio J, Gaglia JL, Turvey SE, et al. Islet recovery and reversal of murine type 1 diabetes in the absence of any infused spleen cell contribution. Science, 2006, 311 ( 5768 ) : 1775- 1778. 被引量:1
  • 6李永翔,李戈,董维平,陈静,王煜非,陈晓波,卢大儒,谭建明.腺病毒载体转染人HO-1基因增强成人胰岛细胞抗凋亡和胰岛素释放功能的研究[J].中华医学杂志,2006,86(13):915-918. 被引量:7
  • 7Lee TS, Chau LY. Heme oxygenase-1 mediates the anti-inflammatory effect of interleukin-10 in mice. Nat Med, 2002, 8(3):240-246. 被引量:1
  • 8Otterbein LE, Bach FH, Alam J, et al. Carbon monoxide has anti-inflammatory effects involving the mitogen-activated protein kinase pathway. Nat Med, 2000, 6(4):422-428. 被引量:1
  • 9Ginther L, Berberat PO, Haga M, et al. Carbon monoxide protects pancreatic beta-cells from apoptosis and improves islet function/ survival after transplantation. Diabetes, 2002, 51 (4) : 994-999. 被引量:1
  • 10Tobiasch E, Ginther L, Bach FH. Heme oxygenase-1 protects pancreatic beta cells from apoptosis caused by various stimuli. J Investig Med, 2001, 49(6) :566-571. 被引量:1

二级参考文献16

  • 1蔡锦全,谭建明,董维平,王煜菲,王鉴波.免疫抑制剂对成人胰岛细胞的毒性作用的体外观察[J].中华医学杂志,2005,85(10):654-656. 被引量:8
  • 2Ye J, Laychock SG. A protective role for heme oxygenase expression in pancreatic islets exposed to interleukin-1beta. Endocrinology,1998,139:4155-4163. 被引量:1
  • 3Juan SH, Lee TS, Tseng KW, et al. Adenovirus-mediated heme oxygenase-1 gene transfer inhibits the development of aiberosclerosis in apolipoprotein E-deficient mice. Circulation, 2001,104: 1519-1525. 被引量:1
  • 4Abraham NG, Jiang S, Yang L, et al. Adenoviral vector-mediated transfer of human heme oxygenase in mrs decreases renal heme-dependent arachidonic acid epoxygenase activity. J Phannacol Exp Ther, 2000,293:494-500. 被引量:1
  • 5Lundquist I, Aim P, Salehi A, et al. Carbon monoxide stimulates insulin release and propagates Ca^2+ signals between pancreatic beta-cells. Am J Physiol Endocrinol Metab ,2003, 285 : E1055-E1063. 被引量:1
  • 6Amersi F, shen XD, Anselmo D, et al. Ex vivo exposure to carbon monoxide prevents hepatic ischemia/reperfusion injury through p38 MAP kinase pathway. Hepatology ,2002,35:815-823. 被引量:1
  • 7Fujimoto H, Ohno M, Ayabe S, et al. Carlton monoxide protects against cardiac ischemia-reperfusion injury in vivo via MAPK and Akt-eNOS pathways. Arterioscler Thromb Vase Biol,2004,24 : 1848-1853. 被引量:1
  • 8Zhang YC, Pileggi A, Agarwal A, et al. Adeno-essociated virus-mediated IL-10 gene therapy inhibits diabetes recurrence in syngeneic islet cell transplantation of NOD mice. Diabetes,2003,52:708-716. 被引量:1
  • 9Shapiro AM, Lakey JR, Ryan EA, et al. Islet transplantation in seven patients with type 1 diabetes mellitus using a glucocorficoid-free immunosuppressive regimen. N Engl J Med, 2000, 343 : 230-238. 被引量:1
  • 10Biarnes M, Montolio M, Nacher V, et al. Beta-cell death and mass in syngeneically transplanted islets exposed to short-and long-term hyperglycemia. Diabetes,2002, 51: 66-72. 被引量:1

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