Seattle Children's Research Institute, University of Washington, 1900 Ninth Ave, M/S C9S-5, Seattle, WA 98101, USA.
Circ Res. 2011 Feb 4;108(3):365-77. doi: 10.1161/CIRCRESAHA.110.223800.
Molecular pathways that control the specification, migration, and number of available smooth muscle progenitor cells play key roles in determining blood vessel size and structure, capacity for tissue repair, and progression of age-related disorders. Defects in these pathways produce malformations of developing blood vessels, depletion of smooth muscle progenitor cell pools for vessel wall maintenance and repair, and aberrant activation of alternative differentiation pathways in vascular disease. A better understanding of the molecular mechanisms that uniquely specify and maintain vascular smooth muscle cell precursors is essential if we are to use advances in stem and progenitor cell biology and somatic cell reprogramming for applications directed to the vessel wall.
控制平滑肌祖细胞的特化、迁移和数量的分子途径在决定血管大小和结构、组织修复能力以及与年龄相关的疾病进展方面起着关键作用。这些途径的缺陷会导致发育中血管的畸形、血管壁维持和修复所需的平滑肌祖细胞池的耗竭,以及血管疾病中替代分化途径的异常激活。如果我们要将干细胞和祖细胞生物学以及体细胞重编程的进展应用于血管壁,就必须更好地了解特化和维持血管平滑肌细胞前体的分子机制。