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Stonin1介导蛋白聚糖NG2的内吞作用,并调节粘着斑动力学和细胞运动。

Stonin1 mediates endocytosis of the proteoglycan NG2 and regulates focal adhesion dynamics and cell motility.

作者信息

Feutlinske Fabian, Browarski Marietta, Ku Min-Chi, Trnka Philipp, Waiczies Sonia, Niendorf Thoralf, Stallcup William B, Glass Rainer, Krause Eberhard, Maritzen Tanja

机构信息

Leibniz-Institut für Molekulare Pharmakologie (FMP), Robert-Rössle-Strasse 10, 13125 Berlin, Germany.

Berlin Ultrahigh Field Facility (B.U.F.F.), Max-Delbrueck Center for Molecular Medicine, Robert-Rössle-Strasse 10, 13125 Berlin, Germany.

出版信息

Nat Commun. 2015 Oct 5;6:8535. doi: 10.1038/ncomms9535.

Abstract

Cellular functions, ranging from focal adhesion (FA) dynamics and cell motility to tumour growth, are orchestrated by signals cells receive from outside via cell surface receptors. Signalling is fine-tuned by the exo-endocytic cycling of these receptors to control cellular responses such as FA dynamics, which determine cell motility. How precisely endocytosis regulates turnover of the various cell surface receptors remains unclear. Here we identify Stonin1, an endocytic adaptor of unknown function, as a regulator of FA dynamics and cell motility, and demonstrate that it facilitates the internalization of the oncogenic proteoglycan NG2, a co-receptor of integrins and platelet-derived growth factor receptor. Embryonic fibroblasts obtained from Stonin1-deficient mice display a marked surface accumulation of NG2, increased cellular signalling and defective FA disassembly as well as altered cellular motility. These data establish Stonin1 as a specific adaptor for the endocytosis of NG2 and as an important factor for FA dynamics and cell migration.

摘要

细胞功能,从粘着斑(FA)动态变化和细胞运动性到肿瘤生长,均由细胞通过细胞表面受体从外部接收的信号精心调控。信号通过这些受体的胞吐 - 内吞循环进行微调,以控制细胞反应,如决定细胞运动性的FA动态变化。内吞作用如何精确调节各种细胞表面受体的周转仍不清楚。在这里,我们鉴定出功能未知的内吞衔接蛋白Stonin1作为FA动态变化和细胞运动性的调节因子,并证明它促进致癌蛋白聚糖NG2的内化,NG2是整合素和血小板衍生生长因子受体的共受体。从Stonin1缺陷小鼠获得的胚胎成纤维细胞显示出NG2在表面的显著积累、细胞信号增强、FA解体缺陷以及细胞运动性改变。这些数据确立了Stonin1作为NG2内吞作用的特异性衔接蛋白以及FA动态变化和细胞迁移的重要因子的地位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5539/4600748/f480684a3308/ncomms9535-f1.jpg

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