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局部膜曲率引导趋化和巨吞饮细胞中的可兴奋膜波——来自创新简单模型的生物医学见解

Local Membrane Curvature Pins and Guides Excitable Membrane Waves in Chemotactic and Macropinocytic Cells - Biomedical Insights From an Innovative Simple Model.

作者信息

Hörning Marcel, Bullmann Torsten, Shibata Tatsuo

机构信息

Institute of Biomaterials and Biomolecular Systems, University of Stuttgart, Stuttgart, Germany.

Laboratory for Physical Biology, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.

出版信息

Front Cell Dev Biol. 2021 Sep 15;9:670943. doi: 10.3389/fcell.2021.670943. eCollection 2021.

Abstract

PIP3 dynamics observed in membranes are responsible for the protruding edge formation in cancer and amoeboid cells. The mechanisms that maintain those PIP3 domains in three-dimensional space remain elusive, due to limitations in observation and analysis techniques. Recently, a strong relation between the cell geometry, the spatial confinement of the membrane, and the excitable signal transduction system has been revealed by Hörning and Shibata (2019) using a novel 3D spatiotemporal analysis methodology that enables the study of membrane signaling on the entire membrane (Hörning and Shibata, 2019). Here, using 3D spatial fluctuation and phase map analysis on actin polymerization inhibited cells, we reveal a spatial asymmetry of PIP3 signaling on the membrane that is mediated by the contact perimeter of the plasma membrane - the spatial boundary around the cell-substrate adhered area on the plasma membrane. We show that the contact perimeter guides PIP3 waves and acts as a pinning site of PIP3 phase singularities, that is, the center point of spiral waves. The contact perimeter serves as a diffusion influencing boundary that is regulated by a cell size- and shape-dependent curvature. Our findings suggest an underlying mechanism that explains how local curvature can favor actin polymerization when PIP3 domains get pinned at the curved protrusive membrane edges in amoeboid cells.

摘要

在膜中观察到的磷脂酰肌醇-3,4,5-三磷酸(PIP3)动力学负责癌细胞和阿米巴样细胞中突出边缘的形成。由于观察和分析技术的限制,在三维空间中维持这些PIP3结构域的机制仍然难以捉摸。最近,Hörning和Shibata(2019年)使用一种新颖的三维时空分析方法揭示了细胞几何形状、膜的空间限制和可兴奋信号转导系统之间的紧密关系,该方法能够研究整个膜上的膜信号传导(Hörning和Shibata,2019年)。在这里,我们对肌动蛋白聚合受抑制的细胞进行三维空间波动和相位图分析,揭示了膜上PIP3信号传导的空间不对称性,这种不对称性由质膜的接触周长介导,质膜的接触周长是质膜上细胞-底物粘附区域周围的空间边界。我们表明,接触周长引导PIP3波,并作为PIP3相位奇点(即螺旋波的中心点)的固定位点。接触周长作为一个扩散影响边界,由细胞大小和形状依赖的曲率调节。我们的研究结果提出了一种潜在机制,解释了当PIP3结构域固定在阿米巴样细胞中弯曲的突出膜边缘时,局部曲率如何促进肌动蛋白聚合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f750/8479871/870ba8df89e7/fcell-09-670943-g0001.jpg

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