Integrin Upregulation and Localization to Focal Adhesion Sites in Pregnant Human Myometrium

被引:16
作者
Burkin, Heather R. [1 ]
Rice, Monica [1 ]
Sarathy, Apurva [1 ]
Thompson, Sara [1 ]
Singer, Cherie A. [1 ]
Buxton, Iain L. O. [1 ]
机构
[1] Univ Nevada, Sch Med, Dept Pharmacol, Ctr Mol Med, Reno, NV 89557 USA
基金
美国国家卫生研究院;
关键词
myometrium; integrin; pregnancy; RAT MYOMETRIUM; MESSENGER-RNA; SMOOTH-MUSCLE; EXPRESSION; RECEPTOR; FIBRONECTIN; ACTIVATION; PROTEINS; BINDING; LABOR;
D O I
10.1177/1933719112466303
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Focal adhesions are integrin-rich microdomains that structurally link the cytoskeleton to the extracellular matrix and transmit mechanical signals. In the pregnant uterus, increases in integrin expression and activation are thought to be critical for the formation of the mechanical syncytium required for labor. The aim of this study was to determine which integrins are upregulated and localized to focal adhesions in pregnant human myometrium. We used quantitative polymerase chain reaction, Western blotting, and confocal microscopy to determine the expression levels and colocalization with focal adhesion proteins. We observed increases in several integrin transcripts in pregnant myometrium. At the protein level, integrins such as (5)-integrin (ITGA5), ITGA7, ITGAV, and ITGB3 were significantly increased during pregnancy. The integrins ITGA3, ITGA5, ITGA7, and ITGB1 colocalized with focal adhesion proteins in term human myometrium. These data suggest that integrins 31, 51, and 71 are the most likely candidates to transmit mechanical signals from the extracellular matrix through focal adhesions in pregnant human myometrium.
引用
收藏
页码:804 / 812
页数:9
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