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血小板内皮细胞黏附分子-1(PECAM-1/CD31)酪氨酸磷酸化状态在小鼠胚胎血管生成过程中发生变化。

Platelet-endothelial cell adhesion molecule-1 (PECAM-1/CD31) tyrosine phosphorylation state changes during vasculogenesis in the murine conceptus.

作者信息

Pinter E, Barreuther M, Lu T, Imhof B A, Madri J A

机构信息

Department of Pathology, Yale University School of Medicine, New Haven, CT 06520-8023, USA.

出版信息

Am J Pathol. 1997 May;150(5):1523-30.

Abstract

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.

摘要

血管生成是指中胚层细胞分化为成血管细胞,并随后由胚胎中的成血管细胞形成血岛和血管的过程,它是一个动态过程,部分受到多种生长因子和形态发生素存在下细胞与细胞外基质以及细胞间相互作用的调节。在本报告中,我们展示了在小鼠胚胎中,从胚外和成血管细胞簇形成血岛和血管的过程中血小板内皮细胞黏附分子-1(PECAM-1)的酪氨酸磷酸化存在差异。此外,我们确定了PECAM-1细胞质结构域中一个特定酪氨酸残基Tyr686的磷酸化,它有可能介导与含Src同源2结构域蛋白的结合,影响PECAM-1的细胞定位和内皮细胞迁移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9928/1858227/ba78a9c93c8f/amjpathol00029-0023-a.jpg

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