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Dephosphorylation of the adaptor LAT and phospholipase C-γ by SHP-1 inhibits natural killer cell cytotoxicity.SHP-1介导的衔接蛋白LAT和磷脂酶C-γ的去磷酸化作用可抑制自然杀伤细胞的细胞毒性。
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Cytotoxic T Cells Use Mechanical Force to Potentiate Target Cell Killing.细胞毒性T细胞利用机械力增强对靶细胞的杀伤作用。
Cell. 2016 Mar 24;165(1):100-110. doi: 10.1016/j.cell.2016.01.021. Epub 2016 Feb 25.
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Adaptive rheology and ordering of cell cytoskeleton govern matrix rigidity sensing.细胞骨架的适应性流变学和有序排列调控基质硬度感知。
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Matrix stiffness drives epithelial-mesenchymal transition and tumour metastasis through a TWIST1-G3BP2 mechanotransduction pathway.基质硬度通过TWIST1-G3BP2机械转导途径驱动上皮-间质转化和肿瘤转移。
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Modulation of the tumor microenvironment for cancer treatment: a biomaterials approach.用于癌症治疗的肿瘤微环境调控:一种生物材料方法。
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F-actin flow drives affinity maturation and spatial organization of LFA-1 at the immunological synapse.F-肌动蛋白流驱动免疫突触处LFA-1的亲和力成熟和空间组织。
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The extracellular matrix modulates the hallmarks of cancer.细胞外基质调节癌症的特征。
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WASp family verprolin-homologous protein-2 (WAVE2) and Wiskott-Aldrich syndrome protein (WASp) engage in distinct downstream signaling interactions at the T cell antigen receptor site.WASp家族维普洛林同源蛋白2(WAVE2)和威斯科特-奥尔德里奇综合征蛋白(WASp)在T细胞抗原受体位点参与不同的下游信号相互作用。
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肌动蛋白逆行流通过调节 SHP-1 的构象状态控制自然杀伤细胞的反应。

Actin retrograde flow controls natural killer cell response by regulating the conformation state of SHP-1.

机构信息

The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.

The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel

出版信息

EMBO J. 2018 Mar 1;37(5). doi: 10.15252/embj.201696264. Epub 2018 Feb 15.

DOI:10.15252/embj.201696264
PMID:29449322
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5830919/
Abstract

Natural killer (NK) cells are a powerful weapon against viral infections and tumor growth. Although the actin-myosin (actomyosin) cytoskeleton is crucial for a variety of cellular processes, the role of mechanotransduction, the conversion of actomyosin mechanical forces into signaling cascades, was never explored in NK cells. Here, we demonstrate that actomyosin retrograde flow (ARF) controls the immune response of primary human NK cells through a novel interaction between β-actin and the SH2-domain-containing protein tyrosine phosphatase-1 (SHP-1), converting its conformation state, and thereby regulating NK cell cytotoxicity. Our results identify ARF as a master regulator of the NK cell immune response. Since actin dynamics occur in multiple cellular processes, this mechanism might also regulate the activity of SHP-1 in additional cellular systems.

摘要

自然杀伤 (NK) 细胞是对抗病毒感染和肿瘤生长的强大武器。尽管肌动蛋白-肌球蛋白 (actomyosin) 细胞骨架对于各种细胞过程至关重要,但机械转导(将肌动蛋白-肌球蛋白机械力转化为信号级联的过程)的作用从未在 NK 细胞中得到探索。在这里,我们证明肌动蛋白逆行流 (ARF) 通过β-肌动蛋白和含 SH2 结构域的蛋白酪氨酸磷酸酶-1 (SHP-1) 之间的新相互作用控制原代人 NK 细胞的免疫反应,改变其构象状态,从而调节 NK 细胞的细胞毒性。我们的结果确定 ARF 是 NK 细胞免疫反应的主要调节剂。由于肌动蛋白动力学发生在多个细胞过程中,因此该机制也可能调节其他细胞系统中 SHP-1 的活性。