Literature DB >> 30131170

Spatial Proliferation of Epithelial Cells Is Regulated by E-Cadherin Force.

Abhinav Mohan1, Kyle T Schlue1, Alex F Kniffin1, Carl R Mayer1, Ashley A Duke1, Vani Narayanan1, Paul T Arsenovic1, Kranthidhar Bathula1, Brooke E Danielsson1, Sandeep P Dumbali2, Venkat Maruthamuthu2, Daniel E Conway3.   

Abstract

Cell proliferation and contact inhibition play a major role in maintaining epithelial cell homeostasis. Prior experiments have shown that externally applied forces, such as stretch, result in increased proliferation in an E-cadherin force-dependent manner. In this study, the spatial regulation of cell proliferation in large epithelial colonies was examined. Surprisingly, cells at the center of the colony still had increased proliferation as compared to cells in confluent monolayers. E-cadherin forces were found to be elevated for both cells at the edge and center of these larger colonies when compared to confluent monolayers. To determine if high levels of E-cadherin force were necessary to induce proliferation at the center of the colony, a lower-force mutant of E-cadherin was developed. Cells with lower E-cadherin force had significantly reduced proliferation for cells at the center of the colony but minimal differences for cells at the edges of the colony. Similarly, increasing substrate stiffness was found to increase E-cadherin force and increase the proliferation rate across the colony. Taken together, these results show that forces through cell-cell junctions regulate proliferation across large groups of epithelial cells. In addition, an important finding of this study is that junction forces are dynamic and modulate cellular function even in the absence of externally applied loads.
Copyright © 2018 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2018        PMID: 30131170      PMCID: PMC6127877          DOI: 10.1016/j.bpj.2018.07.030

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  32 in total

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6.  Protrusive activity guides changes in cell-cell tension during epithelial cell scattering.

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4.  Characterization of 3D Printed Stretching Devices for Imaging Force Transmission in Live-Cells.

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6.  Alteration of calcium signalling in cardiomyocyte induced by simulated microgravity and hypergravity.

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8.  Mechanical disruption of E-cadherin complexes with epidermal growth factor receptor actuates growth factor-dependent signaling.

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Review 10.  The Cross-Talk Between EGFR and E-Cadherin.

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  10 in total

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