Suppr超能文献

细胞分裂方向通过 E-钙黏蛋白/LGN 复合物与细胞间黏附相耦合。

Cell division orientation is coupled to cell-cell adhesion by the E-cadherin/LGN complex.

机构信息

Department of Biology, Stanford University, Stanford, California 94305, USA.

Department of Molecular and Cellular Physiology, Stanford University, Stanford, California 94305, USA.

出版信息

Nat Commun. 2017 Jan 3;8:13996. doi: 10.1038/ncomms13996.

Abstract

Both cell-cell adhesion and oriented cell division play prominent roles in establishing tissue architecture, but it is unclear how they might be coordinated. Here, we demonstrate that the cell-cell adhesion protein E-cadherin functions as an instructive cue for cell division orientation. This is mediated by the evolutionarily conserved LGN/NuMA complex, which regulates cortical attachments of astral spindle microtubules. We show that LGN, which adopts a three-dimensional structure similar to cadherin-bound catenins, binds directly to the E-cadherin cytosolic tail and thereby localizes at cell-cell adhesions. On mitotic entry, NuMA is released from the nucleus and competes LGN from E-cadherin to locally form the LGN/NuMA complex. This mediates the stabilization of cortical associations of astral microtubules at cell-cell adhesions to orient the mitotic spindle. Our results show how E-cadherin instructs the assembly of the LGN/NuMA complex at cell-cell contacts, and define a mechanism that couples cell division orientation to intercellular adhesion.

摘要

细胞-细胞黏附和定向细胞分裂在建立组织架构方面发挥着重要作用,但它们如何协调尚不清楚。在这里,我们证明细胞-细胞黏附蛋白 E-钙黏蛋白可作为细胞分裂方向的指导线索。这是通过进化上保守的 LGN/NuMA 复合物介导的,该复合物调节星体纺锤体微管的皮质附着。我们表明,LGN 采用与钙黏蛋白结合连环蛋白相似的三维结构,直接结合 E-钙黏蛋白胞质尾部,从而定位于细胞-细胞连接处。在有丝分裂进入时,NuMA 从核中释放出来,并与 LGN 竞争从 E-钙黏蛋白上释放,从而局部形成 LGN/NuMA 复合物。这介导了星体微管在细胞-细胞连接处的皮质关联的稳定,以定向有丝分裂纺锤体。我们的研究结果表明 E-钙黏蛋白如何在细胞-细胞连接处指导 LGN/NuMA 复合物的组装,并定义了一种将细胞分裂方向与细胞间黏附联系起来的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b90b/5216124/0082d5548284/ncomms13996-f1.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