Suppr超能文献

Dbnl 和 β-连环蛋白促进前 N-钙黏蛋白的加工,以维持顶底极性。

Dbnl and β-catenin promote pro-N-cadherin processing to maintain apico-basal polarity.

机构信息

Instituto de Biología Molecular de Barcelona, Parc Científic de Barcelona, Barcelona, Spain.

出版信息

J Cell Biol. 2021 Jun 7;220(6). doi: 10.1083/jcb.202007055. Epub 2021 May 3.

Abstract

The neural tube forms when neural stem cells arrange into a pseudostratified, single-cell-layered epithelium, with a marked apico-basal polarity, and in which adherens junctions (AJs) concentrate in the subapical domain. We previously reported that sustained β-catenin expression promotes the formation of enlarged apical complexes (ACs), enhancing apico-basal polarity, although the mechanism through which this occurs remained unclear. Here, we show that β-catenin interacts with phosphorylated pro-N-cadherin early in its transit through the Golgi apparatus, promoting propeptide excision and the final maturation of N-cadherin. We describe a new β-catenin-dependent interaction of N-cadherin with Drebrin-like (Dbnl), an actin-binding protein that is involved in anterograde Golgi trafficking of proteins. Notably, Dbnl knockdown led to pro-N-cadherin accumulation and limited AJ formation. In brief, we demonstrate that Dbnl and Drebrin-like β-catenin assist in the maturation of pro-N-cadherin, which is critical for AJ formation and for the recruitment AC components like aPKC and, consequently, for the maintenance of apico-basal polarity.

摘要

神经管形成时,神经干细胞排列成假复层、单细胞层上皮,具有明显的顶底极性,其中黏附连接(AJs)集中在亚顶域。我们之前的研究报告表明,持续的β-连环蛋白表达促进了扩大的顶端复合物(ACs)的形成,增强了顶底极性,尽管其发生的机制仍不清楚。在这里,我们表明β-连环蛋白在其通过高尔基体早期与磷酸化的原 N-钙粘蛋白相互作用,促进前肽的切除和 N-钙粘蛋白的最终成熟。我们描述了一种新的β-连环蛋白依赖的 N-钙粘蛋白与 Drebrin 样(Dbnl)的相互作用,Dbnl 是一种参与蛋白正向高尔基运输的肌动蛋白结合蛋白。值得注意的是,Dbnl 敲低导致原 N-钙粘蛋白的积累和 AJ 的形成受限。简而言之,我们证明 Dbnl 和 Drebrin 样β-连环蛋白有助于原 N-钙粘蛋白的成熟,这对于 AJ 的形成以及 aPKC 等 AC 成分的募集至关重要,从而维持顶底极性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c14a/8097490/139c53e1ef85/JCB_202007055_Fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验