波复合体在负膜曲率处形成线性阵列,指导板足的形成。

IF 6.4 1区 生物学 Q1 CELL BIOLOGY
Journal of Cell Biology Pub Date : 2025-09-01 Epub Date: 2025-07-16 DOI:10.1083/jcb.202410098
Muziyue Wu, Raj Kumar Sadhu, Kirstin Meyer, Ziqi Tang, Paul Marchando, Derek N Woolfson, Nir S Gov, Orion D Weiner
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引用次数: 0

摘要

不同的肌动蛋白促核因子(NPFs)协调不同的细胞突起模式,可能反映了它们独特的自组织模式。在这里,我们利用体内生化方法来研究WAVE复合体如何指导片状板足的形成。研究人员发现,WAVE复合物是质膜上线性多层蛋白阵列的核心组成部分,有望用于构建片状肌动蛋白基突起的NPF。在上游活化剂(Rac、Arf1/6和PIP3)和WAVE2和Abi2的prd存在的情况下,负膜曲率对于WAVE复杂的线性膜结合是必要和充分的,这为板足的模板化及其紧急行为(包括屏障规避)提供了潜在的机制基础。通过计算模型,我们证明了WAVE复合体的线性组织和对负曲率的偏好在强健板足形成中都起着重要作用。我们的数据揭示了中尺度波复杂模式的关键特征,并强调了NPF自组织与细胞形态发生之间的整体关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
WAVE complex forms linear arrays at negative membrane curvature to instruct lamellipodia formation.

Different actin nucleation-promoting factors (NPFs) orchestrate different patterns of cell protrusions, likely reflecting their distinct patterns of self-organization. Here, we leveraged in vivo biochemical approaches to investigate how the WAVE complex instructs the formation of sheet-like lamellipodia. We show that the WAVE complex is a core constituent of a linear multilayered protein array at the plasma membrane, expected for an NPF that builds sheet-like actin-based protrusions. Negative membrane curvature is both necessary and sufficient for WAVE complex linear membrane association in the presence of upstream activators (Rac, Arf1/6, and PIP3) and the PRDs of both WAVE2 and Abi2, providing a potential mechanistic basis for templating of lamellipodia and their emergent behaviors, including barrier avoidance. Through computational modeling, we demonstrate that WAVE complex's linear organization and preference for negative curvature both play important roles in robust lamellipodia formation. Our data reveal key features of mesoscale WAVE complex patterning and highlight an integral relation between NPF self-organization and cell morphogenesis.

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来源期刊
Journal of Cell Biology
Journal of Cell Biology 生物-细胞生物学
CiteScore
12.60
自引率
2.60%
发文量
213
审稿时长
1 months
期刊介绍: The Journal of Cell Biology (JCB) is a comprehensive journal dedicated to publishing original discoveries across all realms of cell biology. We invite papers presenting novel cellular or molecular advancements in various domains of basic cell biology, along with applied cell biology research in diverse systems such as immunology, neurobiology, metabolism, virology, developmental biology, and plant biology. We enthusiastically welcome submissions showcasing significant findings of interest to cell biologists, irrespective of the experimental approach.
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