Yoshida Tadashi, Owens Gary K
Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville 22908, USA.
Circ Res. 2005 Feb 18;96(3):280-91. doi: 10.1161/01.RES.0000155951.62152.2e.
Although the primary role of vascular smooth muscle cells (SMCs) is contraction, they exhibit extensive phenotypic diversity and plasticity during normal development, during repair of vascular injury, and in disease states. Results of recent studies indicate that there are unique as well as common transcriptional regulatory mechanisms that control expression of various SMC marker genes in distinct SMC subtypes, and that these mechanisms are complex and dynamic even at the single cell level. This article will review recent progress in our understanding of the transcriptional regulatory mechanisms involved in controlling expression of SMC marker genes with a particular focus on examination of processes that contribute to the phenotypic diversity of SMCs. In addition, because of considerable controversy in the literature regarding the relationship between phenotypically modulated SMCs and myofibroblasts, we will briefly consider both similarities and differences in regulation of gene expression between these cell types.
尽管血管平滑肌细胞(SMC)的主要功能是收缩,但它们在正常发育过程、血管损伤修复过程以及疾病状态下表现出广泛的表型多样性和可塑性。最近的研究结果表明,存在独特的以及共同的转录调控机制,这些机制控制着不同SMC亚型中各种SMC标记基因的表达,并且即使在单细胞水平上,这些机制也是复杂且动态的。本文将综述我们在理解控制SMC标记基因表达的转录调控机制方面的最新进展,特别关注对导致SMC表型多样性的过程的研究。此外,由于文献中关于表型调节的SMC与肌成纤维细胞之间关系存在相当大的争议,我们将简要探讨这两种细胞类型在基因表达调控方面的异同。