Pericyte Rho GTPase mediates both pericyte contractile phenotype and capillary endothelial growth state

被引:69
|
作者
Kutcher, Matthew E.
Kolyada, Alexey Y.
Surks, Howard K.
Herman, Ira M.
机构
[1] Tufts Univ, Sch Med, Dept Physiol, Boston, MA 02111 USA
[2] Tufts Univ, Sch Med, Boston, MA USA
[3] Caritas St Elizabeth Med Ctr, Kidney & Dialysis Res Lab, Boston, MA USA
[4] Tufts Univ, New England Med Ctr, Boston, MA 02111 USA
[5] Tufts Univ, Mol Cardiol Res inst, Boston, MA 02111 USA
来源
AMERICAN JOURNAL OF PATHOLOGY | 2007年 / 171卷 / 02期
关键词
D O I
10.2353/ajpath.2007.070102
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Pericytes regulate microvascular development and maturation through the control of endothelial cell motility, proliferation, and differentiation. The Rho GTPases have recently been described as key regulators of pericyte shape and contractile phenotype by signaling through the actin cytoskeleton in an isoactin-specific manner. In this report, we reveal that Rho GTPase-dependent signal transduction not only influences pericyte shape and contractile potential but also modulates capillary endothelial proliferative status and pericyte-endothelial interactions in vitro. We provide evidence that overexpression of mutant Rho GTPases, but not other Ras-related small GTPases, significantly alters pericyte shape, contractility, and endothelial growth state in microvascular cell co-cultures. In particular, we describe the use of a silicon substrate deformation assay to demonstrate that pericyte contractility is Rho GTP- and Rho kinase-dependent, further, we describe a novel in vitro system for examining pericyte-mediated endothelial growth arrest and show that control pericytes are capable of growth-arresting capillary endothelial cells in a cell contact-dependent manner, whereas pericytes overexpressing dominant-active and -negative Rho GTPase are comparably incompetent. These data strongly suggest that signaling through the pericyte Rho GTPase pathway may provide critical cues to the processes of microvascular stabilization, maturation, and contractility during development and disease.
引用
收藏
页码:693 / 701
页数:9
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