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Arp2/3 complex inhibition radically alters lamellipodial actin architecture, suspended cell shape, and the cell spreading process

机译:Arp2 / 3复合物抑制作用从根本上改变了片状脂蛋白的肌动蛋白结构,悬浮的细胞形状和细胞扩散过程

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Recent studies have investigated the dendritic actin cytoskeleton of the cell edge's lamellipodial (LP) region by experimentally decreasing the activity of the actin filament nucleator and branch former, the Arp2/3 complex. Here we extend these studies via pharmacological inhibition of the Arp2/3 complex in sea urchin coelomocytes, cells that possess an unusually broad LP region and display correspondingly exaggerated centripetal flow. Using light and electron microscopy, we demonstrate that Arp2/3 complex inhibition via the drug CK666 dramatically altered LP actin architecture, slowed centripetal flow, drove a lamellipodial-to-filopodial shape change in suspended cells, and induced a novel actin structural organization during cell spreading. A general feature of the CK666 phenotype in coelomocytes was transverse actin arcs, and arc generation was arrested by a formin inhibitor. We also demonstrate that CK666 treatment produces actin arcs in other cells with broad LP regions, namely fish keratocytes and Drosophila S2 cells. We hypothesize that the actin arcs made visible by Arp2/3 complex inhibition in coelomocytes may represent an exaggerated manifestation of the elongate mother filaments that could possibly serve as the scaffold for the production of the dendritic actin network.
机译:最近的研究已经通过实验降低肌动蛋白丝成核剂和分支形成子Arp2 / 3复合物的活性,研究了细胞边缘的层状脂质体(LP)区域的树突肌动蛋白细胞骨架。在这里,我们通过药理抑制海胆体白细胞中的Arp2 / 3复合物扩展了这些研究,这些细胞具有异常宽的LP区域并显示了相应的向心血流。使用光镜和电子显微镜,我们证明通过药物CK666抑制Arp2 / 3复合物显着改变了LP肌动蛋白的结构,减慢了向心流动,驱动了悬浮细胞中纤毛状体到丝状的形状变化,并诱导了新的肌动蛋白结构传播。结肠细胞中CK666表型的一般特征是横向肌动蛋白弧,并且电弧的形成被福明抑制剂抑制。我们还证明,CK666治疗在其他具有宽LP区的细胞(即鱼角膜细胞和果蝇S2细胞)中产生肌动蛋白弧。我们假设,通过Arp2 / 3复合物抑制在内皮细胞中可见的肌动蛋白弧可能代表了细长的母丝的夸大表现,而这些母丝可能充当树突状肌动蛋白网络产生的支架。

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