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Organization of multiprotein complexes at cell–cell junctions

机译:细胞间连接处多蛋白复合物的组织

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摘要

The formation of stable cell–cell contacts is required for the generation of barrier-forming sheets of epithelial and endothelial cells. During various physiological processes like tissue development, wound healing or tumorigenesis, cellular junctions are reorganized to allow the release or the incorporation of individual cells. Cell–cell contact formation is regulated by multiprotein complexes which are localized at specific structures along the lateral cell junctions like the tight junctions and adherens junctions and which are targeted to these site through their association with cell adhesion molecules. Recent evidence indicates that several major protein complexes exist which have distinct functions during junction formation. However, this evidence also indicates that their composition is dynamic and subject to changes depending on the state of junction maturation. Thus, cell–cell contact formation and integrity is regulated by a complex network of protein complexes. Imbalancing this network by oncogenic proteins or pathogens results in barrier breakdown and eventually in cancer. Here, I will review the molecular organization of the major multiprotein complexes at junctions of epithelial cells and discuss their function in cell–cell contact formation and maintenance.
机译:形成上皮和内皮细胞的屏障形成片需要形成稳定的细胞间接触。在诸如组织发育,伤口愈合或肿瘤发生的各种生理过程中,细胞连接被重组以允许单个细胞的释放或掺入。细胞间的接触形成受多种蛋白复合物的调控,这些复合物位于细胞侧面的紧密连接和粘附连接等特定结构,并通过与细胞粘附分子的结合而靶向这些位置。最近的证据表明存在几种主要的蛋白质复合物,它们在连接形成过程中具有不同的功能。但是,该证据还表明,它们的组成是动态的,并会根据连接成熟的状态而发生变化。因此,细胞间的接触形成和完整性受蛋白质复合物的复杂网络调节。通过致癌蛋白或病原体使该网络失去平衡会导致屏障破坏,并最终导致癌症。在这里,我将回顾上皮细胞交界处主要多蛋白复合物的分子组织,并讨论它们在细胞间接触形成和维持中的功能。

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