Epigenetic Control of Smooth Muscle Cell Differentiation and Phenotypic Switching in Vascular Development and Disease

被引:611
作者
Alexander, Matthew R. [1 ]
Owens, Gary K. [1 ]
机构
[1] Univ Virginia, Sch Med, Robert M Berne Cardiovasc Res Ctr, Charlottesville, VA 22908 USA
来源
ANNUAL REVIEW OF PHYSIOLOGY, VOL 74 | 2012年 / 74卷
关键词
arteriogenesis; vascular injury and repair; atherosclerosis; mesenchymal stem cells; pluripotency genes; SERUM RESPONSE FACTOR; ALPHA-ACTIN EXPRESSION; TRANSCRIPTION FACTOR-B; GROWTH FACTOR-BB; GENE-EXPRESSION; IN-VIVO; TGF-BETA; MATRIX METALLOPROTEINASES; PROGENITOR CELLS; CARG ELEMENTS;
D O I
10.1146/annurev-physiol-012110-142315
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
The vascular smooth muscle cell (SMC) in adult animals is a highly specialized cell whose principal function is contraction. However, this cell displays remarkable plasticity and can undergo profound changes in phenotype during repair of vascular injury, during remodeling in response to altered blood flow, or in various disease states. There has been extensive progress in recent years in our understanding of the complex mechanisms that control SMC differentiation and phenotypic plasticity, including the demonstration that epigenetic mechanisms play a critical role. In addition, recent evidence indicates that SMC phenotypic switching in adult animals involves the reactivation of embryonic stem cell pluripotency genes and that mesenchymal stem cells may be derived from SMC and/or pericytes. This review summarizes the current state of our knowledge in this field and identifies some of the key unresolved challenges and questions that we feel require further study.
引用
收藏
页码:13 / 40
页数:28
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