Multipotent human stromal cells improve cardiac function after myocardial infarction in mice without long-term engraftment

被引:330
作者
Iso, Yoshitaka
Spees, Jeffrey L.
Serrano, Claudia
Bakondi, Benjamin
Pochampally, Radhika
Song, Yao-Hua
Sobel, Burton E.
Delafontaine, Patrick
Prockop, Darwin J.
机构
[1] Tulane Univ, Hlth Sci Ctr, Ctr Gene Therapy, New Orleans, LA 70112 USA
[2] Univ Vermont, Cardiovasc Res Inst, Dept Med, Colchester, VT 05446 USA
[3] Tulane Univ, Hlth Sci Ctr, Dept Med, Cardiol Sect, New Orleans, LA 70112 USA
关键词
multipotent stromal cells; myocardial infarction; cellular engraftment; secreted factors; cytoprotection; MESENCHYMAL STEM-CELLS; PROGENITOR CELLS; REPAIR; HEART; FEASIBILITY; PROTECTION; INJECTION; MIGRATION; THERAPY; MUSCLE;
D O I
10.1016/j.bbrc.2007.01.045
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of this study was to determine whether intravenously administered multipotent stromal cells from human bone marrow (hMSCs) can improve cardiac function after myocardial infarction (MI) without long-term engraftment and therefore whether transitory paracrine effects or secreted factors are responsible for the benefit conferred. hMSCs were injected systemically into immunodeficient mice with acute MI. Cardiac function and fibrosis after MI in the hMSC-treated group were significantly improved compared with controls. However, despite the cardiac improvement, there was no evident hMSC engraftment in the heart 3 weeks after MI. Microarray assays and ELISAs demonstrated that multiple protective factors were expressed and secreted from the hMSCs in culture. Factors secreted by hMSCs prevented cell death of cultured cardiomyocytes and endothelial cells under conditions that mimicked tissue ischemia. The favorable effects of hMSCs appear to reflect the impact of secreted factors rather than engraftment, differentiation, or cell fusion. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:700 / 706
页数:7
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