4.2 Article

Macrophages are involved in the protective role of human umbilical cord-derived stromal cells in renal ischemia-reperfusion injury

期刊

STEM CELL RESEARCH
卷 10, 期 3, 页码 405-416

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.scr.2013.01.005

关键词

-

资金

  1. Major Research Plan of the National Natural Science Foundation of China [91129718]
  2. National Natural Science Foundation of China [31140063, 81000181, 81272481, 81071421]
  3. Scientific and Technological Supporting Program of Jiangsu Province [BE2010703]
  4. Transfer of Scientific and Technological Achievements Foundation of Jiangsu Province [BA2009124]
  5. Jiangsu Province's Project of Scientific and Technological Innovation and Achievements Transformation [BL2012055]
  6. Jiangsu Province's Outstanding Medical Academic Leader and Sci-tech Innovation Team Program [LJ201117]

向作者/读者索取更多资源

Administration of fibroblastic cells derived from a number of tissues (collectively called mesenchymal stem cells) has been suggested to be beneficial for renal repair and mortality reduction in renal ischemia reperfusion injury (IRO, but the underlying mechanism is not fully understood. In the present study, our objective was to investigate the involvement of macrophages in the therapeutic effect of human umbilical cord-derived stromal cells (hUCSCs) on renal IRI. Twenty-four hours after reperfusion, hUCSCs were injected intravenously and resulted in significant improvements in renal function, with a lower tubular injury score together with more proliferative and fewer apoptotic tubular cells in kidney tissue. Moreover, hUCSCs reduced the infiltration of macrophages into renal interstitium especially at 5 days post-reperfusion, while the proportion of anti-inflammatory M2 macrophages was markedly increased. HUCSCs also alleviated the local inflammatory response in kidneys. The absence of macrophages during the early phase of reperfusion enhanced the therapeutic effect of hUCSCs, whereas macrophage depletion during the late repair phase eliminated the renoprotective role of hUCSCs. In vitro, macrophages cocultured with hUCSCs were switched to the alternatively activated M2 phenotype. Our data indicate that hUCSCs are capable of promoting the M2 polarization of macrophages at injury sites, suggesting a new mechanism for hUCSC-mediated protection in renal IRI. (C) 2013 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据