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超黏附:细胞间黏附的一个新概念。

Hyper-adhesion: a new concept in cell-cell adhesion.

作者信息

Garrod David, Kimura Tomomi E

机构信息

Faculty of Life Sciences, University of Manchester, Simon Building, Brunswick Street, Manchester M13 9PL, UK.

出版信息

Biochem Soc Trans. 2008 Apr;36(Pt 2):195-201. doi: 10.1042/BST0360195.

Abstract

We have developed a new concept of cell-cell adhesion termed 'hyper-adhesion', the very strong adhesion adopted by desmosomes. This uniquely desmosomal property accounts for their ability to provide the intercellular links in the desmosome-intermediate filament complex. These links are targeted by diseases, resulting in disruption of the complex with severe consequences. Hyper-adhesion is characteristic of desmosomes in tissues and is believed to result from a highly ordered arrangement of the extracellular domains of the desmosomal cadherins that locks their binding interaction so that it is highly resistant to disruption. This ordered arrangement may be reflected by and dependent upon a similarly ordered molecular structure of the desmosomal plaque. Hyper-adhesion can be down-regulated to a more weakly adhesive state by cell signalling involving protein kinase C, which translocates to the desmosomal plaque. Down-regulation takes place in wound edge epithelium and appears to be accompanied by loss of the ordered arrangement causing desmosomes to adopt the type of weaker adhesion characteristic of adherens junctions. We review the evidence for hyper-adhesion and speculate on the molecular basis of its mechanism.

摘要

我们已经提出了一种新的细胞间黏附概念,称为“超黏附”,这是桥粒所具有的极强黏附作用。这种独特的桥粒特性解释了它们在桥粒-中间丝复合体中提供细胞间连接的能力。这些连接成为疾病的攻击目标,导致复合体被破坏,产生严重后果。超黏附是组织中桥粒的特征,据信它源于桥粒钙黏蛋白细胞外结构域的高度有序排列,这种排列锁定了它们的结合相互作用,使其高度抗破坏。这种有序排列可能由桥粒斑类似的有序分子结构所反映并依赖于它。通过涉及蛋白激酶C的细胞信号传导,超黏附可以被下调至较弱的黏附状态,蛋白激酶C会转移至桥粒斑。下调发生在伤口边缘上皮细胞中,似乎伴随着有序排列的丧失,导致桥粒采用黏着连接所特有的较弱黏附类型。我们综述了超黏附的证据,并推测了其机制的分子基础。

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