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受体 - 配体结合与脂域形成之间的相互作用取决于细胞 - 底物黏附中配体的流动性。

Interplay Between Receptor-Ligand Binding and Lipid Domain Formation Depends on the Mobility of Ligands in Cell-Substrate Adhesion.

作者信息

Li Long, Wang Xiaohuan, Wu Helong, Shao Yingfeng, Wu Huaping, Song Fan

机构信息

State Key Laboratory of Nonlinear Mechanics (LNM) and Beijing Key Laboratory of Engineered Construction and Mechanobiology, Institute of Mechanics, Chinese Academy of Sciences, Beijing, China.

School of Engineering Science, University of Chinese Academy of Sciences, Beijing, China.

出版信息

Front Mol Biosci. 2021 Apr 12;8:655662. doi: 10.3389/fmolb.2021.655662. eCollection 2021.

DOI:10.3389/fmolb.2021.655662
PMID:33987204
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8112205/
Abstract

Cell-cell adhesion and the adhesion of cells to extracellular matrix are mediated by the specific binding of receptors on the cell membrane to their cognate ligands on the opposing surface. The adhesion receptors can exhibit affinity for nanoscale lipid clusters that form in the cell membrane. Experimental studies of such adhesion systems often involve a cell adhering either to a solid surface with immobile ligands or a supported lipid bilayer with mobile ligands. A central question in these cell-substrate adhesions is how the mobility of the ligands physically affects their binding to the adhesion receptors and thereby the behavior of the nanoscale lipid clusters associated with the receptors. Using a statistical mechanical model and Monte Carlo simulations for the adhesion of cells to substrates with ligands, we find that, for mobile ligands, binding to adhesion receptors can promote the formation of mesoscale lipid domains, which in turn enhances the receptor-ligand binding. However, in the case of immobile ligands, the receptor-ligand binding and the tendency for the nanoscale lipid clusters to further coalesce depend on the distribution of the ligands on the substrate. Our findings help to explain why different adhesion experiments for identifying the interplay between receptor-ligand binding and heterogeneities in cell membranes led to contradictory results.

摘要

细胞间黏附以及细胞与细胞外基质的黏附是由细胞膜上的受体与其相对表面上的同源配体的特异性结合介导的。黏附受体可对细胞膜中形成的纳米级脂质簇表现出亲和力。此类黏附系统的实验研究通常涉及细胞黏附于带有固定配体的固体表面或带有可移动配体的支持脂质双层。这些细胞-底物黏附中的一个核心问题是配体的流动性如何在物理上影响它们与黏附受体的结合,进而影响与受体相关的纳米级脂质簇的行为。通过使用统计力学模型和蒙特卡罗模拟来研究细胞与带有配体的底物的黏附,我们发现,对于可移动配体,与黏附受体的结合可促进中尺度脂质结构域的形成,这反过来又增强了受体-配体的结合。然而,在固定配体的情况下,受体-配体的结合以及纳米级脂质簇进一步聚结的趋势取决于配体在底物上的分布。我们的研究结果有助于解释为什么用于确定受体-配体结合与细胞膜异质性之间相互作用的不同黏附实验会得出相互矛盾的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef4/8112205/3726bc96cf5a/fmolb-08-655662-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef4/8112205/f9fc327c186e/fmolb-08-655662-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef4/8112205/ead0629631da/fmolb-08-655662-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef4/8112205/ba386e9250e9/fmolb-08-655662-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef4/8112205/0b2b37cb0d01/fmolb-08-655662-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef4/8112205/3726bc96cf5a/fmolb-08-655662-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef4/8112205/f9fc327c186e/fmolb-08-655662-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef4/8112205/ead0629631da/fmolb-08-655662-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef4/8112205/ba386e9250e9/fmolb-08-655662-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef4/8112205/0b2b37cb0d01/fmolb-08-655662-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef4/8112205/3726bc96cf5a/fmolb-08-655662-g005.jpg

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