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血管发育和疾病中平滑肌细胞分化和表型转换的表观遗传调控。

Epigenetic control of smooth muscle cell differentiation and phenotypic switching in vascular development and disease.

机构信息

Robert M. Berne Cardiovascular Research Center, University of Virginia School of Medicine, Charlottesville, Virginia 22908, USA.

出版信息

Annu Rev Physiol. 2012;74:13-40. doi: 10.1146/annurev-physiol-012110-142315. Epub 2011 Oct 10.

Abstract

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.

摘要

成年动物的血管平滑肌细胞(SMC)是一种高度特化的细胞,其主要功能是收缩。然而,这种细胞表现出显著的可塑性,在血管损伤修复、血流改变时的重塑,或在各种疾病状态下,其表型可以发生深刻的变化。近年来,我们在控制 SMC 分化和表型可塑性的复杂机制方面取得了广泛的进展,包括证明了表观遗传机制起着关键作用。此外,最近的证据表明,成年动物中 SMC 的表型转换涉及胚胎干细胞多能性基因的重新激活,间充质干细胞可能来源于 SMC 和/或周细胞。这篇综述总结了这一领域目前的知识状况,并确定了一些我们认为需要进一步研究的关键未解决的挑战和问题。

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