Myocardial Remodeling: Cellular and Extracellular Events and Targets

被引:37
作者
Dixon, Jennifer A. [1 ,2 ]
Spinale, Francis G. [1 ,2 ]
机构
[1] Med Univ S Carolina, Div Cardiothorac Surg, Charleston, SC 29425 USA
[2] Ralph H Johnson Vet Affairs Med Ctr, Charleston, SC 29401 USA
来源
ANNUAL REVIEW OF PHYSIOLOGY, VOL 73 | 2011年 / 73卷
关键词
matrix metalloproteinases; large-animal models; myocardial infarction; COLONY-STIMULATING FACTOR; MESENCHYMAL STEM-CELLS; MATRIX-METALLOPROTEINASE INHIBITION; LEFT-VENTRICULAR FUNCTION; ENDOTHELIAL PROGENITOR CELLS; BONE-MARROW-CELLS; ENHANCES COLLATERAL PERFUSION; CARDIOVASCULAR RISK-FACTORS; CARDIAC FIBROBLAST FUNCTION; RANDOMIZED CONTROLLED-TRIAL;
D O I
10.1146/annurev-physiol-012110-142230
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The focus of this review is on translational studies utilizing large-animal models and clinical studies that provide fundamental insight into cellular and extracellular pathways contributing to post myocardial infarction (MI) left ventricle (LV) remodeling. Specifically, both large-animal and clinical studies have examined the potential role of endogenous and exogenous stem cells to alter the course of LV remodeling. Interestingly, there have been alterations in LV remodeling with stem cell treatment despite a lack of long-term cell engraftment. The translation of the full potential of stem cell treatments to clinical studies has yet to be realized. The modulation of proteolytic pathways that contribute to the post-MI remodeling process has also been examined. On the basis of recent large-animal studies, there appears to be a relationship between stem cell treatment post-MI and the modification of proteolytic pathways, generating the hypothesis that stem cells leave an echo effect that moderates LV remodeling.
引用
收藏
页码:47 / 68
页数:22
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