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WASp和N-WASP的酸性区域可与CDC42Hs和Rac1协同作用,诱导丝状伪足和片状伪足的形成。

The acidic regions of WASp and N-WASP can synergize with CDC42Hs and Rac1 to induce filopodia and lamellipodia.

作者信息

Hüfner Katharina, Schell Barbara, Aepfelbacher Martin, Linder Stefan

机构信息

Institut für Prophylaxe und Epidemiologie der Kreislaufkrankheiten, Ludwig-Maximilians-Universität, Pettenkoferstrasse 9, 80336 Munich, Germany.

出版信息

FEBS Lett. 2002 Mar 13;514(2-3):168-74. doi: 10.1016/s0014-5793(02)02358-x.

Abstract

The acidic (A) region of WASp family proteins is thought to represent a high-affinity binding site for Arp2/3 complex without activating properties. Here we show that GST-fused WASp-A and N-WASP-A, but not a WASP-A/W500S mutant, several truncated WASp-A constructs or WAVE1-A can pull down Arp2/3 complex from cell lysates. Significantly, WASp-A and N-WASP-A synergistically trigger formation of filopodia or lamellipodia when coinjected with sub-effective concentrations of V12CDC42Hs or V12Rac1, respectively, into macrophages. The ability of WASp family A region constructs to induce this effect is closely correlated with their ability to bind Arp2/3 complex in vitro. These results imply that (i) Arp2/3 complex is critically involved in filopodia and lamellipodia formation in macrophages and (ii) acidic regions of WASp and N-WASP are not simply binding sites for Arp2/3 complex but can prime it for RhoGTPase-triggered signals leading to actin nucleation.

摘要

WASp家族蛋白的酸性(A)区域被认为是Arp2/3复合体的高亲和力结合位点,但不具有激活特性。在此我们表明,谷胱甘肽S-转移酶(GST)融合的WASp-A和N-WASP-A,而非WASP-A/W500S突变体、几种截短的WASp-A构建体或WAVE1-A,能够从细胞裂解物中拉下Arp2/3复合体。值得注意的是,当分别与亚有效浓度的V12CDC42Hs或V12Rac1共同注射到巨噬细胞中时,WASp-A和N-WASP-A能协同触发丝状伪足或片状伪足的形成。WASp家族A区域构建体诱导这种效应的能力与其在体外结合Arp2/3复合体的能力密切相关。这些结果表明:(i)Arp2/3复合体在巨噬细胞丝状伪足和片状伪足的形成中起关键作用;(ii)WASp和N-WASP的酸性区域并非简单的Arp2/3复合体结合位点,而是能使其为RhoGTP酶触发的导致肌动蛋白成核的信号做好准备。

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