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首页> 外文期刊>The American Journal of Pathology >Platelet-endothelial cell adhesion molecule-1 (PECAM-1/CD31) tyrosine phosphorylation state changes during vasculogenesis in the murine conceptus
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Platelet-endothelial cell adhesion molecule-1 (PECAM-1/CD31) tyrosine phosphorylation state changes during vasculogenesis in the murine conceptus

机译:鼠概念中血管生成过程中血小板-内皮细胞粘附分子-1(PECAM-1 / CD31)酪氨酸磷酸化状态的变化

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摘要

Vasculogenesis, the differentiation of mesodermal cells to angioblasts and the subsequent formation of blood islands and blood vessels by angioblasts in the conceptus, is a dynamic process modulated, in part, by cell-extracellular matrix and cell-cell interactions in the presence of a variety of growth factors and morphogens. In this report we demonstrate differential tyrosine phosphorylation of platelet-endothelial cell adhesion molecule-1 (PECAM-1) during the formation of blood islands and vessels from clusters of extraembryonic and embryonic angioblasts in the murine conceptus. In addition, we identify the phosphorylation of a particular tyrosine residue in the PECAM-1 cytoplasmic domain, Tyr686, which has the potential of mediating binding to Src homology 2 domain-containing proteins, affecting PECAM-1 cellular localization and endothelial cell migration.
机译:血管生成是中胚层中胚层细胞向成血管细胞的分化以及随后由成血管细胞形成的血岛和血管的形成,是一种动态过程,部分受多种细胞存在下细胞外基质和细胞间相互作用的调节生长因子和形态发生素在本报告中,我们证明了在鼠概念中从胚外和胚成血管细胞簇的血岛和血管形成过程中血小板-内皮细胞粘附分子1(PECAM-1)的酪氨酸磷酸化差异。此外,我们确定了PECAM-1细胞质结构域Tyr686中特定酪氨酸残基的磷酸化,该蛋白可能介导与含Src同源2域的蛋白质结合,从而影响PECAM-1细胞定位和内皮细胞迁移。

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