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首页> 外文期刊>Molecular biology of the cell >CRB3 Binds Directly to Par6 and Regulates the Morphogenesis of the Tight Junctions in Mammalian Epithelial Cells
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CRB3 Binds Directly to Par6 and Regulates the Morphogenesis of the Tight Junctions in Mammalian Epithelial Cells

机译:CRB3直接绑定到Par6,并调节哺乳动物上皮细胞中紧密连接的形态发生。

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摘要

Crumbs is an apical transmembrane protein crucial for epithelial morphogenesis in Drosophila melanogaster embryos. A protein with all the characteristics for a Crumbs homologue has been identified from patients suffering from retinitis pigmentosa group 12, but this protein (CRB1) is only expressed in retina and some parts of the brain, both in human and mouse. Here, we describe CRB3, another Crumbs homologue that is preferentially expressed in epithelial tissues and skeletal muscles in human. CRB3 shares the conserved cytoplasmic domain with other Crumbs but exhibits a very short extracellular domain without the EGF- and laminin A-like G repeats present in the other Crumbs. CRB3 is localized to the apical and subapical area of epithelial cells from the mouse and human intestine, suggesting that it could play a role in epithelial morphogenesis. Indeed, expression of CRB3 or of a chimera containing the extracellular domain of the neurotrophin receptor p75NTR and the transmembrane and cytoplasmic domains of CRB3 led to a slower development of functional tight junctions in Madin-Darby canine kidney cells. This phenotype relied on the presence of CRB3 four last amino acids (ERLI) that are involved in a direct interaction with Par6, a regulator of epithelial polarity and tight junction formation. Thus, CRB3, through its cytoplasmic domain and its interactors, plays a role in apical membrane morphogenesis and tight junction regulation.
机译:面包屑是一种顶端果糖跨膜蛋白,对果蝇胚胎果蝇的上皮形态发生至关重要。从患有色素性视网膜炎的第12组患者中已鉴定出具有Crumbs同源物所有特征的蛋白质,但是该蛋白质(CRB1)仅在人和小鼠的视网膜和大脑的某些部位表达。在这里,我们描述了CRB3,这是另一种Crumbs同源物,优先在人的上皮组织和骨骼肌中表达。 CRB3与其他面包屑共享保守的胞质结构域,但表现出非常短的细胞外结构域,而其他面包屑中不存在EGF和层粘连蛋白A样G重复序列。 CRB3位于小鼠和人肠上皮细胞的顶端和顶端区域,提示它可能在上皮形态发生中起作用。实际上,CRB3或含有神经营养蛋白受体p75NTR的胞外域以及CRB3的跨膜和胞质域的嵌合体的表达导致Madin-Darby犬肾细胞中功能性紧密连接的发展变慢。此表型依赖于CRB3的最后四个氨基酸(ERLI)的存在,后者与上皮极性和紧密连接形成的调节因子Par6直接相互作用。因此,CRB3通过其胞质结构域和其相互作用物,在顶膜形态发生和紧密连接调节中起作用。

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