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血管内皮生长因子受体信号转导

VEGF receptor signal transduction.

作者信息

Li Xiujuan, Claesson-Welsh Lena, Shibuya Masabumi

机构信息

Uppsala University, Department of Genetics and Pathology, Rudbeck Laboratory, Uppsala, Sweden.

出版信息

Methods Enzymol. 2008;443:261-84. doi: 10.1016/S0076-6879(08)02013-2.

Abstract

Signal transduction by vascular endothelial growth factors (VEGFs) through their cognate VEGF receptor tyrosine kinases follows the consensus scheme for receptor tyrosine kinases. Thus, binding of ligand induces receptor dimerization and activation of the tyrosine kinase through transphosphorylation between receptor molecules, leading to initiation of intracellular signal transduction pathways. Certain signal transduction pathways are shared with most, if not all, receptor tyrosine kinases, whereas some may be unique (e.g., transduced only by VEGF receptors). Indications that such unique signaling pathways may be discerned only when VEGF receptors are expressed in their proper context (i.e., in endothelial cells of microcapillary origin). In this chapter, we describe a number of methods for the study of signal transduction in endothelial cells. We describe how to isolate and examine endothelial cell lines. We also describe the embryoid body model representing vasculogenesis and angiogenesis, the procedure for subcutaneous Matrigel plugs, and, finally, how to construct gene-targeted mouse models. We emphasize the need for validation of in vitro data in more complex models, where endothelial cells reside in their proper three-dimensional context.

摘要

血管内皮生长因子(VEGFs)通过其同源的VEGF受体酪氨酸激酶进行信号转导遵循受体酪氨酸激酶的共识模式。因此,配体的结合诱导受体二聚化,并通过受体分子之间的反式磷酸化激活酪氨酸激酶,从而引发细胞内信号转导途径。某些信号转导途径为大多数(即便不是全部)受体酪氨酸激酶所共有,而有些途径可能是独特的(例如,仅由VEGF受体转导)。有迹象表明,只有当VEGF受体在其合适的环境中(即源自微毛细血管的内皮细胞中)表达时,才能识别出这种独特的信号转导途径。在本章中,我们描述了一些用于研究内皮细胞信号转导的方法。我们描述了如何分离和检测内皮细胞系。我们还描述了代表血管发生和血管生成的胚状体模型、皮下基质胶栓的操作步骤,最后介绍了如何构建基因靶向小鼠模型。我们强调在更复杂的模型中验证体外数据的必要性,在这些模型中内皮细胞处于其合适的三维环境中。

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