Role of nitric oxide in placental vascular development and function

被引:162
|
作者
Krause, B. J. [1 ]
Hanson, M. A. [2 ]
Casanello, P. [1 ]
机构
[1] Pontificia Univ Catolica Chile, Sch Med, Div Obstet & Gynecol, Santiago 391, Chile
[2] Univ Southampton, Fac Med, Acad Unit Human Dev & Hlth, Inst Dev Sci, Southampton SO16 6YD, Hants, England
关键词
Placenta; Nitric oxide; Vasculogenesis; Angiogenesis; Vascular tone; Pregnancy diseases; ENDOTHELIAL GROWTH-FACTOR; GENE-RELATED PEPTIDE; SYNTHASE EXPRESSION; SHEAR-STRESS; FACTOR RECEPTOR-1; UMBILICAL ARTERY; CELL-MIGRATION; DIFFERENTIAL EXPRESSION; INHIBITS ANGIOGENESIS; TROPHOBLAST INVASION;
D O I
10.1016/j.placenta.2011.06.025
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nitric oxide (NO) is one of the most pleiotropic signaling molecules at systemic and cellular levels, participating in vascular tone regulation, cellular respiration, proliferation, apoptosis and gene expression. Indeed NO actively participates in trophoblast invasion, placental development and represents the main vasodilator in this tissue. Despite the large number of studies addressing the role of NO in the placenta, its participation in placental vascular development and the effect of altered levels of NO on placental function remains to be clarified. This review draws a time-line of the participation of NO throughout placental vascular development, from the differentiation of vascular precursors to the consolidation of vascular function are considered. The influence of NO on cell types involved in the origin of the placental vasculature and the expression and function of the nitric oxide synthases (NOS) throughout pregnancy are described. The developmental processes involved in the placental vascular bed are considered, such as the participation of NO in placental vasculogenesis and angiogenesis through VEGF and Angiopoietin signaling molecules. The role of NO in vascular function once the placental vascular tree has developed, in normal pregnancy as well as in pregnancy-related diseases, is then discussed. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:797 / 805
页数:9
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