期刊文献+

自体脂肪间充质干细胞对大鼠肾局部缺血再灌注损伤的保护作用 被引量:2

Protective effect of autologous adipose-derived mesenchymal stem cells on renal ischemia reperfu- sion injury in rats
原文传递
导出
摘要 目的观察大鼠注射自体脂肪问充质干细胞(ADMSCs)对缺血再灌注(IR)损伤的保护作用。方法将24只成年雄性SD大鼠随机分为3组:A组(假手术正常组)、B组(IR+培养基)、c组(IR+ADMSCs),IR后1h尾静脉注射剂量为1.0×10。的白体ADMSCs。缺血时间1h,再灌注72h,接着处死大鼠观察。结果72h后,C组血清肌酐水平为(0.718±0.003)mg/dl,B组血清肌酐水平为(1.277±0.011)mg/dl,C组24h内尿量为(57.742±0.012)ml,B组24h内尿量为(23.665±0.027)ml,c组尿蛋白/肌酐的比值为1.217±0.033,B组比值为1.672±0.013,各指标两组比较差异有统计学意义(P〈0.05),c组肾组织异常程度相对于B组明显减轻;Westernblot法分析显示C组抗氧化标志物苯醌氧化还原酶基因(NQ01)和血红素氧合酶-1(HO-1)的蛋白表达水平显著高于B组(P〈0.05)。结论ADMSCs通过抑制氧化应激减轻IR诱导的肾损伤。 Objective To observe the protective effects of autologous adipose-derived mesenchy- real stem cells (ADMSCs) on the kidney in rats during renal ischemia reperfusion (IR) injury. Methods Adult male Sprague-Dawley (SD) rats (n = 24 ) were equally randomized into group A (sham control ) , group B (IR plus culture medium only) , and group C (IR plus intravenous administration of 1.0 x 106 autologous ADMSCs 1 h after IR). The duration of ischemia was 1 h, followed by 72 h of reperfusion be- fore the animals were sacrificed. Results After 72 h, serum creatinine levels in groups C and B were (0. 718 _+0.:003) and ( 1. 277 _+ 0. 011 ) mg/dL, the urine volume in group C and B was (57. 742 _+ 0.012) and (23.665 _+0.027) mL, the ratio of protein and creatinine in group C and B was 1.217 _+ 0. 033 and 1. 672 _+ 0. 013 respectively, and the comparison of all above items showed statistically significan difference ( all P 〈 0. 05 ) ; Also, apparently, the renal pathohistological lesions were aggravated in group B as compared with those in group C. Western blotting showed notably higher NAD(P) H quinone oxi- doreductase 1 (NQO1) and heine oxygenase -1 (HO-1) protein expression in group C than in group B. Conclusion ADMSCs therapy minimized kidney damage after IR injury through suppressing oxidative stress.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2012年第12期2419-2421,F0003,共4页 Chinese Journal of Experimental Surgery
基金 湖北省自然科学基金资助项目(2011CDB517)
关键词 急性肾损伤 脂肪间充质干细胞 细胞移植 Acute kidney disease Adipose-derived mesenchymal stem cells Cell transplanta- tion
  • 相关文献

参考文献10

  • 1Silva LB, Palma PV, Cury PM, et al. Evaluation of stem cell adminis- tration in a model of kidney ischemia-reperfusion injury. Int Immunop- harmaco1,2007,7 : 1609-1616.
  • 2Li B, Coiaen A, Hudson TE, et al. Mobilized human hematopoietic stem/progenitor ceils promote kidney repair after ischemia/reperfu- sion injury. Circulation ,2010,121:2211-2220.
  • 3Li B, Schmitt R, Israilova M,et al. Stromal cells protect against acute tubular injury via an endocrine effect. J Am Soc Nephrol,2007,18: 2486-2496.
  • 4李俊华,钟山,郭晖,王璐,阮永乐,张炯,向莹,陈实,陈刚.肾脏缺血再灌注损伤过程中天然免疫分子高迁移率族蛋白B1释放变化[J].中华实验外科杂志,2010(12):1809-1811. 被引量:11
  • 5邓君,崔苏萍,阮琼芳,傅斌,王共先,娄远蕾,谢安,雷琼琼,汪泱.肾缺血再灌注损伤后miR-210及其靶基因的变化[J].中华实验外科杂志,2009(11):1512-1514. 被引量:11
  • 6Marina M, Cinzia R, Tiziana M, et al. Life-sparing effect of human cord blood-mesenchymal stem cells in experimental acute kidney inju- ry. Stem Cells,2010,28:513-522.
  • 7张燊,张治明,苏泽轩.钙蛋白酶抑制剂E-64对于环孢素A诱发小鼠肾脏损伤的保护作用[J].中华实验外科杂志,2011,28(12):2083-2085. 被引量:6
  • 8Leu S, Lin YC, Yuen CM, et al. Adipose-derived mesenchymal stem cells markedly attenuate brain infarct size and improve neurological function in rats. J Transl Med,2010,8:63.
  • 9Banas A, Teratani T, Yamamoto Y, et al. IFATS collection:in vivo therapeutic potential of human adipose tissue mesenchymal stem cells after transplantation into mice with liver injury. Stem Cells ,2008,26: 2705 -2712.
  • 10Togel F, Hu Z,Weiss K, et al. Administered mesenchymal stem cells protect against ischemic acute renal failure through differentiation-in- dependent mechanisms. Am J Physiol Renal Physiol, 2005,289 : F31- F42.

二级参考文献30

  • 1Kim BS,Chen J,Weinstein T,et al. VEGF expression in hypoxia and hyperglycemia:reciprocal effect on branching angiogenesis in epithelial-endothelial co-cultures. J Am Soc Nephrol, 2002,13 : 2027-2036.
  • 2Bhuvaneswari R, Gan YY, Lucky SS, et al. Molecular profiling of angiogenesis in hypericin mediated photodynamic therapy. Mol Cancer, 2008,13:7-56.
  • 3Kutter C, Svoboda P. miRNA, siRNA, piRNA: Knowns of the unknown. RNA Biol,2008,5 : 181-188.
  • 4Barrel DP. MicroRNAs : genomics, biogenesis, mechanism, andfunction. Cell, 2004,116:281-297.
  • 5Wightman B, Ha I, Ruvkun G. Posttranscriptional regulation of the heterochronic gene lin-14 by lin-4 medistes temporal pattern-formation in C. elegans. Cell, 1993,75:855-862.
  • 6Ritu K, Manuela F, Sylwia EW, et al. A MicroRNA signature of hypoxia. Molecular and Cellular Biology,2007,27 : 1859-1867.
  • 7Fasanaro TV,Pasquale D,Yuri DS,et al. Micro-210 modulates endothelial cell response to hypoxia and inhibits the receptor tyrosine kinase ligand Ephrin-A3. The Journal of Biological Chemistry, 2008, 283 : 15878-15883.
  • 8Galanis A, Pappa A, Giannakakis A, et al. Reactive oxygen species and HIF-1 signalling in cancer. Cancer Lett ,2008,266 : 12-20.
  • 9Ushio FM, Nakafura Y. Reactive oxygen species and angiogenesis: NADPH oxidase as target for cancer therapy. Cancer Lett,2008,266: 37-52.
  • 10Fasanaro P,D' Alessandra Y,Di SV,et al. MicroRNA-210 and endothelial cell response to hypoxia. J boil Chem, 2008,283: 15878- 15883.

共引文献23

同被引文献34

  • 1Gentile P, Orlandi A, Scioli MG, et al. Concise review : adipose-derived stromal vascular fraction cells and platelet-rich plasma : basic and clin- ical implications for tissue engineering therapies in regenerative sur- gery[ J]. Stem Cells Transl Med ,2012,1 ( 3 ) :230-236.
  • 2Qiu X, Fandel TM, Ferretti L, et al. Both immediate and delayed intra- cavernous injection of autologous adipose-derived stromal vascular fraction enhances recovery of erectile function in a rat model of cavern- ous nerve injury[J]. Eur Urol,2012,62(4) :720-727.
  • 3Bourin P, Bunnell BA, Casteilla L, et al. Stromal cells from the adipose tissue-derived stromal vascular fraction and culture expanded adipose tissue-derived stromal/stem cells : a joint statement of the International Federation for Adipose Therapeutics and Science (IFATS) and the In- ternational Society for Cellular Therapy (ISCT) [J ]. Cytotherapy, 2013,15(6) :641-648.
  • 4Banas A, Teratani T, Yamamoto Y, et al. IFATS collection:in vivo therapeutic potential of human adipose tissue nmsenchymal stem cells after transplantation into mice with liver injury [ J ]. Stem cells, 2008, 26(10) :2705-2712.
  • 5Chen YT, Sun CK, Lin YC, et al. Adipose-derived mesenchymal stem cell protects kidneys against ischemia-reperfusion injury through sup- pressing oxidative stress and inflammatory reaction [ J ]. J Transl Med, 2011,9:51.
  • 6Yasuda K,Ozaki T, Saka Y, et al. Autologous cell therapy for cispla- tin-induced acute kidney injury by using non-expanded adipose tissue- derived ceils [ J ]. Cytotherapy ,2012,14 (9) : 1089-1100.
  • 7Kim JH, Park D J, Yun JC, et at. Human adipose tissue-derived mesen- chymal stem cells protect kidneys from cisplatin nephrotoxicity in rats [ J ]. Am J Physiol Renal Physio1,2012,302 (9) : F1141-F1150.
  • 8Chen YT, Yang CC, Zhen YY, et al. Cyclosporine-assisted adipose-de- rived mesenchymal stem cell therapy to mitigate acute kidney ischemi- a-reperfusion injury [ J ]. Stem Cell Res Ther, 2013,4 ( 3 ) : 62.
  • 9Meier-Kfiesche HU, Schold JD, Sfinivas TR, et al. Lack of improve- ment in renal allograft survival despite a marked decrease in acute re- jection rates over the most recent era [ J ]. Am J Transplant, 2004,4 (3) :378-383.
  • 10Kato T, Okumi M, Tanemura M, et al. Adipose tissue-derived stem cells suppress acute cellular rejection by TSG-6 and CD44 interaction in rat kidney transplantation [ J ]. Transplantation, 2014,98 ( 3 ) : 277- 284.

引证文献2

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部