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S6K是一种形态发生蛋白,其作用机制涉及细丝蛋白A磷酸化和磷脂酸结合。

S6K is a morphogenic protein with a mechanism involving Filamin-A phosphorylation and phosphatidic acid binding.

作者信息

Henkels Karen M, Mallets Elizabeth R, Dennis Patrick B, Gomez-Cambronero Julian

机构信息

*Wright State University School of Medicine, Department of Biochemistry and Molecular Biology, Dayton, Ohio, USA; and Materials and Manufacturing Directorate, Air Force Research Laboratory, Wright-Patterson Air Force Base, Ohio, USA.

*Wright State University School of Medicine, Department of Biochemistry and Molecular Biology, Dayton, Ohio, USA; and Materials and Manufacturing Directorate, Air Force Research Laboratory, Wright-Patterson Air Force Base, Ohio, USA

出版信息

FASEB J. 2015 Apr;29(4):1299-313. doi: 10.1096/fj.14-260992. Epub 2014 Dec 15.

Abstract

Change of cell shape in vivo plays many roles that are central to life itself, such as embryonic development, inflammation, wound healing, and pathologic processes such as cancer metastasis. Nonetheless, the spatiotemporal mechanisms that control the concerted regulation of cell shape remain understudied. Here, we show that ribosomal S6K, which is normally considered a protein involved in protein translation, is a morphogenic protein. Its presence in cells alters the overall organization of the cell surface and cell circularity [(4π × area)/(perimeter)(2)] from 0.47 ± 0.06 units in mock-treated cells to 0.09 ± 0.03 units in S6K-overexpressing macrophages causing stellation and arborization of cell shape. This effect was partially reversed in cells expressing a kinase-inactive S6K mutant and was fully reversed in cells silenced with small interference RNA. Equally important is that S6K is itself regulated by phospholipids, specifically phosphatidic acid, whereby 300 nM 1,2-dioleoyl-sn-glycero-3-phosphate (DOPA), but not the control 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC), binds directly to S6K and causes an ∼ 2.9-fold increase in S6K catalytic activity. This was followed by an increase in Filamin A (FLNA) functionality as measured by phospho-FLNA (S(2152)) expression and by a subsequent elevation of actin nucleation. This reliance of S6K on phosphatidic acid (PA), a curvature-inducing phospholipid, explained the extra-large perimeter of cells that overexpressed S6K. Furthermore, the diversity of the response to S6K in several unrelated cell types (fibroblasts, leukocytes, and invasive cancer cells) that we report here indicates the existence of an underlying common mechanism in mammalian cells. This new signaling set, PA-S6K-FLNA-actin, sheds light for the first time into the morphogenic pathway of cytoskeletal structures that are crucial for adhesion and cell locomotion during inflammation and metastasis.

摘要

体内细胞形状的变化发挥着许多对生命本身至关重要的作用,如胚胎发育、炎症、伤口愈合以及诸如癌症转移等病理过程。尽管如此,控制细胞形状协同调节的时空机制仍未得到充分研究。在此,我们表明核糖体S6K,通常被认为是一种参与蛋白质翻译的蛋白质,是一种形态发生蛋白。它在细胞中的存在改变了细胞表面的整体组织和细胞圆形度[(4π×面积)/(周长)²],从模拟处理细胞中的0.47±0.06单位变为S6K过表达巨噬细胞中的0.09±0.03单位,导致细胞形状呈星状和分支状。在表达激酶失活的S6K突变体的细胞中,这种效应部分逆转,而在用小干扰RNA沉默的细胞中则完全逆转。同样重要的是,S6K本身受磷脂调节,特别是磷脂酸,由此300 nM的1,2 - 二油酰 - sn - 甘油 - 3 - 磷酸(DOPA),而不是对照1,2 - 二油酰 - sn - 甘油 - 3 - 磷酸胆碱(DOPC),直接结合到S6K上,并使S6K催化活性增加约2.9倍。随后通过磷酸化丝状肌动蛋白A(FLNA)(S(2152))表达以及随后肌动蛋白成核作用的升高来衡量,丝状肌动蛋白A(FLNA)功能增强。S6K对磷脂酸(PA)(一种诱导曲率的磷脂)的这种依赖性解释了过表达S6K的细胞的超大周长。此外,我们在此报道的几种不相关细胞类型(成纤维细胞、白细胞和侵袭性癌细胞)对S6K反应的多样性表明哺乳动物细胞中存在潜在的共同机制。这个新的信号传导组,PA - S6K - FLNA - 肌动蛋白,首次揭示了细胞骨架结构的形态发生途径,这些结构在炎症和转移过程中对粘附和细胞运动至关重要。

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