Key role for Rac in the early transcriptional response to extracellular matrix stiffness and stiffness-dependent repression of ATF3

Author:

Dang Irène1,Brazzo Joseph A.2,Bae Yongho2ORCID,Assoian Richard K.1ORCID

Affiliation:

1. University of Pennsylvania 1 Department of Systems Pharmacology and Translational Therapeutics , , Philadelphia, PA 19104 , USA

2. Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York 2 Department of Pathology and Anatomical Sciences , , Buffalo, NY 14203 , USA

Abstract

ABSTRACT The Rho family GTPases Rac and Rho play critical roles in transmitting mechanical information contained within the extracellular matrix (ECM) to the cell. Rac and Rho have well-described roles in regulating stiffness-dependent actin remodeling, proliferation and motility. However, much less is known about the relative roles of these GTPases in stiffness-dependent transcription, particularly at the genome-wide level. Here, we selectively inhibited Rac and Rho in mouse embryonic fibroblasts cultured on deformable substrata and used RNA sequencing to elucidate and compare the contribution of these GTPases to the early transcriptional response to ECM stiffness. Surprisingly, we found that the stiffness-dependent activation of Rac was dominant over Rho in the initial transcriptional response to ECM stiffness. We also identified activating transcription factor 3 (ATF3) as a major target of stiffness- and Rac-mediated signaling and show that ATF3 repression by ECM stiffness helps to explain how the stiffness-dependent activation of Rac results in the induction of cyclin D1.

Funder

National Institutes of Health

National Science Foundation

EMBO

American Heart Association

Publisher

The Company of Biologists

Subject

Cell Biology

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