期刊文献+

SDF-1/CXCR4 axis modulates bone marrow mesenchymal stem cell apoptosis, migration and cytokine secretion 被引量:55

原文传递
导出
摘要 Bone marrow mesenchymal stem cells(MSCs)are considered as a promising cell source to treat the acute myocardial infarction.However,over 90%of the stem cells usually die in the first three days of transplantation.Survival potential,migration ability and paracrine capacity have been considered as the most important three factors for cell transplantation in the ischemic cardiac treatment.We hypothesized that stromal-derived factor-1(SDF-1)/CXCR4 axis plays a critical role in the regulation of these processes.In this study,apoptosis was induced by exposure of MSCs to H2O2 for 2 h.After re-oxygenation,the SDF-1 pretreated MSCs demonstrated a significant increase in survival and proliferation.SDF-1 pretreatment also enhanced the migration and increased the secretion of pro-survival and angiogenic cytokines including basic fibroblast growth factor and vascular endothelial growth factor.Western blot and RT-PCR demonstrated that SDF-1 pretreatment significantly activated the pro-survival Akt and Erk signaling pathways and up-regulated Bcl-2/Bax ratio.These protective effects were partially inhibited by AMD3100,an antagonist of CXCR4.We conclude that the SDF-1/CXCR4 axis is critical for MSC survival,migration and cytokine secretion.
出处 《Protein & Cell》 SCIE CSCD 2011年第10期845-854,共10页 蛋白质与细胞(英文版)
基金 by the National key Basic Research Program of China(Grant Nos.2011CB964903 and 2011CB606202) the National Outstanding Youth Foundation(No.30725030) the National Natural Science Foundation of China(Grant Nos.30570471 and 30970746) the National Key Scientific Program of China(No.952010).
  • 相关文献

参考文献1

二级参考文献16

  • 1Miyahara Y, Nagaya N, Kataoka M, et al. Monolayered mesenchymal stem cells repair scarred myocardium after myocardial infarction. Nat Med, 2006, 12: 459-465. 被引量:1
  • 2Stature C, Westphsd B, Kleine HD, et aL Autologous honemarrow stem-ceU transplantation for myocardial regeneration. Lancet,2003,361:45-46. 被引量:1
  • 3Berry MF, Engler AJ, Woo YJ, et al. Mesenchymal stem cell injection after myocardial infarction improves myocardial compliance. Am J Physiol Heart Circ Physiol, 2006, 290: H2196-H2203. 被引量:1
  • 4C, eng YJ. Molecular mechanisms for cardiovascular stem cell apoptosis and growth in the hearts with atherosclerotic coronary disease and ischemic heart failure. Ann N Y Acad, 2003, 1010: 687-697. 被引量:1
  • 5Mangi AA, Noiseux N, Kong D, et al. Mesenchymal stem cells modified with Akt prevent remodeling and restore performance of infarcted hearts. Nat Med, 2003,9 : 1195-1201. 被引量:1
  • 6Calabro P , Yeh ET. The pleiotropic effects of statins. Curr Opin Cardiol, 2005,20:541-546. 被引量:1
  • 7Endres M. Statins: potential new indications in inflammatory conditions. Atheroscler Suppl, 2006, 7: 31-35. 被引量:1
  • 8Hong MK, Lee CW, Kim YH, et al. Usefulness of foUow-up lowdensity lipoprotein cholesterol level as an independent predictor of changes of coronary atherosclerotic plaque size as determined by intravascular ultrasound analysis after statin (atorvastatin or simvastatin) therapy. Am J Cardiol, 2006, 98 : 866-870. 被引量:1
  • 9Chen MS, Xu FP, Wang YZ, et al. Statins initiated after hypertrophy inhibit oxidative stress and prevent heart failure in rats with aortic stenosis. J Mol Cell Cardiol, 2004, 37: 889-896. 被引量:1
  • 10Zhu W, Chen J, Cong X, et al. Hypoxia and serum deprivationinduced apoptosis in mesenchymal stem cells. Stem Cells, 2006, 24:416-425. 被引量:1

共引文献17

同被引文献384

引证文献55

二级引证文献190

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