Mechanical forces remodel the cardiac extracellular matrix during zebrafish development

Author:

Gentile Alessandra1ORCID,Albu Marga1ORCID,Xu Yanli1ORCID,Mortazavi Newsha23ORCID,Ribeiro da Silva Agatha1ORCID,Stainier Didier Y. R.1ORCID,Gunawan Felix23ORCID

Affiliation:

1. Max Planck Institute for Heart and Lung Research 1 Department of Developmental Genetics , , Bad Nauheim 61231 , Germany

2. Institute of Cell Biology 2 , Faculty of Medicine , , Münster 48149 , Germany

3. University of Münster 2 , Faculty of Medicine , , Münster 48149 , Germany

Abstract

ABSTRACT The cardiac extracellular matrix (cECM) is fundamental for organ morphogenesis and maturation, during which time it undergoes remodeling, yet little is known about whether mechanical forces generated by the heartbeat regulate this remodeling process. Using zebrafish as a model and focusing on stages when cardiac valves and trabeculae form, we found that altering cardiac contraction impairs cECM remodeling. Longitudinal volumetric quantifications in wild-type animals revealed region-specific dynamics: cECM volume decreases in the atrium but not in the ventricle or atrioventricular canal. Reducing cardiac contraction resulted in opposite effects on the ventricular and atrial ECM, whereas increasing the heart rate affected the ventricular ECM but had no effect on the atrial ECM, together indicating that mechanical forces regulate the cECM in a chamber-specific manner. Among the ECM remodelers highly expressed during cardiac morphogenesis, we found one that was upregulated in non-contractile hearts, namely tissue inhibitor of matrix metalloproteinase 2 (timp2). Loss- and gain-of-function analyses of timp2 revealed its crucial role in cECM remodeling. Altogether, our results indicate that mechanical forces control cECM remodeling in part through timp2 downregulation.

Funder

Max Planck Society

European Research Council

Deutsche Forschungsgemeinschaft

Westfälische Wilhelms-Universität Münster

University of Münster

Publisher

The Company of Biologists

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