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aPKC 是协调集体迁移过程中三种不同细胞极性功能的关键极性决定因素。

aPKC is a key polarity determinant in coordinating the function of three distinct cell polarities during collective migration.

机构信息

State Key Laboratory of Pharmaceutical Biotechnology and MOE Key Laboratory of Model Animals for Disease Study, Model Animal Research Center, Nanjing University, 12 Xue-fu Road, Nanjing, China 210061.

LBCMCP, Centre de Biologie Intégrative (CBI), Université de Toulouse, CNRS, UPS, 31062 Toulouse, France

出版信息

Development. 2018 May 2;145(9):dev158444. doi: 10.1242/dev.158444.

Abstract

Apical-basal polarity is a hallmark of epithelia and needs to be remodeled when epithelial cells undergo morphogenetic cell movements. Here, we analyze border cells in the ovary to address how apical-basal polarity is remodeled and turned into front-back and inside-outside as well as apical-basal polarities, during collective migration. We find that the Crumbs (Crb) complex is required for the generation of the three distinct but interconnected cell polarities of border cells. Specifically, the Crb complex, together with the Par complex and the endocytic recycling machinery, ensures the strict distribution of two distinct populations of aPKC at the inside apical junction and near the outside lateral membrane. Interestingly, aPKC distributed near the outside lateral membrane interacts with Sif and promotes Rac-induced protrusions, whereas alteration of the aPKC distribution pattern changes the pattern of protrusion formation, leading to disruption of all three polarities. Therefore, we demonstrate that aPKC, spatially controlled by the Crb complex, is a key polarity molecule coordinating the generation of three distinct but interconnected cell polarities during collective migration.

摘要

顶端-基底极性是上皮细胞的标志,当上皮细胞发生形态发生细胞运动时,需要对其进行重塑。在这里,我们分析了卵巢中的边缘细胞,以解决在集体迁移过程中,顶端-基底极性如何被重塑并转化为前后和内外以及顶端-基底极性。我们发现,Crb 复合物对于边缘细胞的三种不同但相互连接的细胞极性的产生是必需的。具体来说,Crb 复合物与 Par 复合物和内吞再循环机制一起,确保了两种不同的 aPKC 群体在内部顶端连接处和靠近外部侧膜处的严格分布。有趣的是,分布在外部侧膜附近的 aPKC 与 Sif 相互作用并促进 Rac 诱导的突起,而改变 aPKC 的分布模式会改变突起形成的模式,从而破坏所有三种极性。因此,我们证明了由 Crb 复合物空间控制的 aPKC 是在集体迁移过程中协调三种不同但相互连接的细胞极性产生的关键极性分子。

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