The nature of cell division forces in epithelial monolayers

Author:

Gupta Vivek K.1ORCID,Nam Sungmin123,Yim Donghyun4ORCID,Camuglia Jaclyn5,Martin Judy Lisette6,Sanders Erin Nicole6ORCID,O’Brien Lucy Erin6ORCID,Martin Adam C.5ORCID,Kim Taeyoon4,Chaudhuri Ovijit1ORCID

Affiliation:

1. Department of Mechanical Engineering, Stanford University, Stanford, CA

2. Harvard John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA

3. Wyss Institute for Biologically Inspired Engineering, Cambridge, MA

4. Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN

5. Department of Biology, Massachusetts Institute of Technology, Cambridge, MA

6. Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA

Abstract

Epithelial cells undergo striking morphological changes during division to ensure proper segregation of genetic and cytoplasmic materials. These morphological changes occur despite dividing cells being mechanically restricted by neighboring cells, indicating the need for extracellular force generation. Beyond driving cell division itself, forces associated with division have been implicated in tissue-scale processes, including development, tissue growth, migration, and epidermal stratification. While forces generated by mitotic rounding are well understood, forces generated after rounding remain unknown. Here, we identify two distinct stages of division force generation that follow rounding: (1) Protrusive forces along the division axis that drive division elongation, and (2) outward forces that facilitate postdivision spreading. Cytokinetic ring contraction of the dividing cell, but not activity of neighboring cells, generates extracellular forces that propel division elongation and contribute to chromosome segregation. Forces from division elongation are observed in epithelia across many model organisms. Thus, division elongation forces represent a universal mechanism that powers cell division in confining epithelia.

Funder

National Science Foundation

National Institutes of Health

Stanford University

Samsung

Asan Foundation

Publisher

Rockefeller University Press

Subject

Cell Biology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3