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Loss of FrmA leads to increased cell-cell adhesion and impaired multi-cellular development of Dictyostelium cells.FrmA的缺失导致盘基网柄菌细胞的细胞间黏附增加以及多细胞发育受损。
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引用本文的文献

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iTRAQ-Based Quantitative Proteomic Analysis of Antibacterial Mechanism of Milk-Derived Peptide BCp12 against .基于iTRAQ的乳源肽BCp12抗菌机制的定量蛋白质组学分析 针对…… (原文此处不完整)
Foods. 2022 Feb 24;11(5):672. doi: 10.3390/foods11050672.
2
Loss of FrmB results in increased size of developmental structures during the multicellular development of Dictyostelium cells.FrmB 的缺失导致了盘基网柄菌细胞在多细胞发育过程中发育结构增大。
J Microbiol. 2017 Sep;55(9):730-736. doi: 10.1007/s12275-017-7221-x. Epub 2017 Sep 2.

FrmA的缺失导致盘基网柄菌细胞的细胞间黏附增加以及多细胞发育受损。

Loss of FrmA leads to increased cell-cell adhesion and impaired multi-cellular development of Dictyostelium cells.

作者信息

Patel H, Brunton V G

机构信息

Edinburgh Cancer Research Centre, The University of Edinburgh, Crewe Road South, Edinburgh EH4 2XR, Scotland.

出版信息

Cell Mol Life Sci. 2009 Jan;66(1):145-55. doi: 10.1007/s00018-008-8527-y.

DOI:10.1007/s00018-008-8527-y
PMID:19002378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11131488/
Abstract

Cell-cell adhesion is a critical property of all multi-cellular organisms and its correct regulation is critical during development, differentiation, tissue building and maintenance, and many immune responses. The multi-talin-like FERM domain containing protein, FrmA, is required during starvation-induced multi-cellular development of Dictyostelium cells. Loss of FrmA leads to increased cell-cell adhesion and results in impaired multi-cellular development, slug migration and fruiting bodies. Further, mixing experiments show that FrmA null cells are excluded from the apex of wild-type mounds, to which cells that normally form the organising centre known as the tip sort. These data suggest a critical role for FrmA in regulating cell-cell adhesion, multi-cellular development and, in particular, the formation of the organising centre known as the tip.

摘要

细胞间黏附是所有多细胞生物的一项关键特性,其正确调控在发育、分化、组织构建与维持以及许多免疫反应过程中至关重要。含有多talin样FERM结构域的蛋白质FrmA,在盘基网柄菌细胞饥饿诱导的多细胞发育过程中是必需的。FrmA的缺失会导致细胞间黏附增加,并导致多细胞发育、蛞蝓体迁移和子实体受损。此外,混合实验表明,FrmA缺失细胞被排除在野生型丘的顶端,而正常形成被称为尖端的组织中心的细胞会聚集到该顶端。这些数据表明FrmA在调节细胞间黏附、多细胞发育,特别是在被称为尖端的组织中心的形成中起关键作用。