Dynamic mechanobiology of cardiac cells and tissues: Current status and future perspective

Author:

Wang Chenyan12,Ramahdita Ghiska3,Genin Guy45ORCID,Huebsch Nathaniel367ORCID,Ma Zhen12ORCID

Affiliation:

1. Department of Biomedical and Chemical Engineering, Syracuse University 1 , Syracuse, New York 13244, USA

2. BioInspired Institute for Material and Living Systems, Syracuse University 2 , Syracuse, New York 13244, USA

3. Department of Biomedical Engineering, Washington University in St. Louis 3 , St. Louis, Missouri 63130, USA

4. Department of Mechanical Engineering and Materials Science, Washington University in St. Louis, St. Louis 4 , Missouri 63130, USA

5. NSF Science and Technology Center for Engineering Mechanobiology, McKelvey School of Engineering, Washington University in St. Louis, St. Louis 5 , Missouri 63130, USA

6. Center for Regenerative Medicine, Washington University in St. Louis, St. Louis 6 , Missouri 63130, USA

7. Center for Investigation of Membrane Excitability Diseases, Center for Cardiovascular Research, Washington University in St. Louis, St. Louis 7 , Missouri 63130, USA

Abstract

Mechanical forces impact cardiac cells and tissues over their entire lifespan, from development to growth and eventually to pathophysiology. However, the mechanobiological pathways that drive cell and tissue responses to mechanical forces are only now beginning to be understood, due in part to the challenges in replicating the evolving dynamic microenvironments of cardiac cells and tissues in a laboratory setting. Although many in vitro cardiac models have been established to provide specific stiffness, topography, or viscoelasticity to cardiac cells and tissues via biomaterial scaffolds or external stimuli, technologies for presenting time-evolving mechanical microenvironments have only recently been developed. In this review, we summarize the range of in vitro platforms that have been used for cardiac mechanobiological studies. We provide a comprehensive review on phenotypic and molecular changes of cardiomyocytes in response to these environments, with a focus on how dynamic mechanical cues are transduced and deciphered. We conclude with our vision of how these findings will help to define the baseline of heart pathology and of how these in vitro systems will potentially serve to improve the development of therapies for heart diseases.

Funder

National Science Foundation

National Heart, Lung, and Blood Institute

Publisher

AIP Publishing

Subject

General Medicine

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