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在黏附连接解离时,与钙黏蛋白结合的β-连环蛋白进入Wnt信号通路:β-连环蛋白池之间存在交叉的证据。

Cadherin-bound beta-catenin feeds into the Wnt pathway upon adherens junctions dissociation: evidence for an intersection between beta-catenin pools.

作者信息

Kam Yoonseok, Quaranta Vito

机构信息

Cancer Biology Department, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.

出版信息

PLoS One. 2009;4(2):e4580. doi: 10.1371/journal.pone.0004580. Epub 2009 Feb 24.

DOI:10.1371/journal.pone.0004580
PMID:19238201
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2640460/
Abstract

Beta-catenin is an essential component of two cellular systems: cadherin-based adherens junctions (AJ) and the Wnt signaling pathway. A functional or physical connection between these beta-catenin pools has been suggested in previous studies, but not conclusively demonstrated to date. To further examine this intersection, we treated A431 cell colonies with lysophosphatidic acid (LPA), which forces rapid and synchronized dissociation of AJ. A combination of immunostaining, time-lapse microscopy using photoactivatable-GFP-tagged beta-catenin, and image analyses indicate that the cadherin-bound pool of beta-catenin, internalized together with E-cadherin, accumulates at the perinuclear endocytic recycling compartment (ERC) upon AJ dissociation, and can be translocated into the cell nucleus upon Wnt pathway activation. These results suggest that the ERC may be a site of residence for beta-catenin destined to enter the nucleus, and that dissociation of AJ may influence beta-catenin levels in the ERC, effectively affecting beta-catenin substrate levels available downstream for the Wnt pathway. This intersection provides a mechanism for integrating cell-cell adhesion with Wnt signaling and could be critical in developmental and cancer processes that rely on beta-catenin-dependent gene expression.

摘要

β-连环蛋白是两个细胞系统的重要组成部分:基于钙黏蛋白的黏附连接(AJ)和Wnt信号通路。先前的研究已提出这些β-连环蛋白池之间存在功能或物理连接,但迄今为止尚未得到确凿证实。为了进一步研究这种交叉点,我们用溶血磷脂酸(LPA)处理A431细胞集落,LPA会促使AJ快速同步解离。免疫染色、使用光激活绿色荧光蛋白标记的β-连环蛋白的延时显微镜检查以及图像分析相结合表明,与E-钙黏蛋白一起内化的与钙黏蛋白结合的β-连环蛋白池在AJ解离后积聚在核周内吞再循环区室(ERC),并且在Wnt通路激活时可转运到细胞核中。这些结果表明,ERC可能是β-连环蛋白进入细胞核的驻留位点,并且AJ的解离可能影响ERC中β-连环蛋白的水平,从而有效影响Wnt通路下游可用的β-连环蛋白底物水平。这种交叉点提供了一种将细胞间黏附与Wnt信号整合的机制,并且在依赖β-连环蛋白依赖性基因表达的发育和癌症过程中可能至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/85a06e04b604/pone.0004580.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/39c883a84784/pone.0004580.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/073797d3e54f/pone.0004580.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/df0ad67f9d52/pone.0004580.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/73afcfd14650/pone.0004580.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/91a64024ecdf/pone.0004580.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/24f6eb2530b5/pone.0004580.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/85a06e04b604/pone.0004580.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/39c883a84784/pone.0004580.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/073797d3e54f/pone.0004580.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/df0ad67f9d52/pone.0004580.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/73afcfd14650/pone.0004580.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/91a64024ecdf/pone.0004580.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/24f6eb2530b5/pone.0004580.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b570/2640460/85a06e04b604/pone.0004580.g007.jpg

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