Literature DB >> 33309949

Is zebrafish heart regeneration "complete"? Lineage-restricted cardiomyocytes proliferate to pre-injury numbers but some fail to differentiate in fibrotic hearts.

Alberto Bertozzi1, Chi-Chung Wu1, Phong D Nguyen2, Mohankrishna Dalvoy Vasudevarao1, Medhanie A Mulaw3, Charlotte D Koopman4, Teun P de Boer5, Jeroen Bakkers4, Gilbert Weidinger6.   

Abstract

Adult zebrafish are frequently described to be able to "completely" regenerate the heart. Yet, the extent to which cardiomyocytes lost to injury are replaced is unknown, since existing evidence for cardiomyocyte proliferation is indirect or non-quantitative. We established stereological methods to quantify the number of cardiomyocytes at several time-points post cryoinjury. Intriguingly, after cryoinjuries that killed about 1/3 of the ventricular cardiomyocytes, pre-injury cardiomyocyte numbers were restored already within 30 days. Yet, many hearts retained small residual scars, and a subset of cardiomyocytes bordering these fibrotic areas remained smaller, lacked differentiated sarcomeric structures, and displayed defective calcium signaling. Thus, a subset of regenerated cardiomyocytes failed to fully mature. While lineage-tracing experiments have shown that regenerating cardiomyocytes are derived from differentiated cardiomyocytes, technical limitations have previously made it impossible to test whether cardiomyocyte trans-differentiation contributes to regeneration of non-myocyte cell lineages. Using Cre responder lines that are expressed in all major cell types of the heart, we found no evidence for cardiomyocyte transdifferentiation into endothelial, epicardial, fibroblast or immune cell lineages. Overall, our results imply a refined answer to the question whether zebrafish can completely regenerate the heart: in response to cryoinjury, preinjury cardiomyocyte numbers are indeed completely regenerated by proliferation of lineage-restricted cardiomyocytes, while restoration of cardiomyocyte differentiation and function, as well as resorption of scar tissue, is less robustly achieved.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cardiomyocyte; Cryoinjury; Fibrosis; Heart; Lineage; Potency; Proliferation; Regeneration; Scar; Stereology; Zebrafish

Year:  2020        PMID: 33309949     DOI: 10.1016/j.ydbio.2020.12.004

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  4 in total

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Authors:  Alba Almazán; Çağrı Çevrim; Jacob M Musser; Michalis Averof; Mathilde Paris
Journal:  Sci Adv       Date:  2022-08-24       Impact factor: 14.957

2.  eif4ebp3l-A New Affector of Zebrafish Angiogenesis and Heart Regeneration?

Authors:  Lisa I Born; Theresa Andree; Svenja Frank; Judith Hübner; Sandra Link; Marion Langheine; Anne Charlet; Jennifer S Esser; Ralph Brehm; Martin Moser
Journal:  Int J Mol Sci       Date:  2022-09-03       Impact factor: 6.208

3.  Integration of multiple imaging platforms to uncover cardiovascular defects in adult zebrafish.

Authors:  Anabela Bensimon-Brito; Giulia L M Boezio; João Cardeira-da-Silva; Astrid Wietelmann; Srinath Ramkumar; Pia R Lundegaard; Christian S M Helker; Radhan Ramadass; Janett Piesker; Arno Nauerth; Clemens Mueller; Didier Y R Stainier
Journal:  Cardiovasc Res       Date:  2022-09-20       Impact factor: 13.081

4.  Histone deacetylase 1 controls cardiomyocyte proliferation during embryonic heart development and cardiac regeneration in zebrafish.

Authors:  Anja Bühler; Bernd M Gahr; Deung-Dae Park; Alberto Bertozzi; Alena Boos; Mohankrishna Dalvoy; Alexander Pott; Franz Oswald; Rhett A Kovall; Bernhard Kühn; Gilbert Weidinger; Wolfgang Rottbauer; Steffen Just
Journal:  PLoS Genet       Date:  2021-11-01       Impact factor: 5.917

  4 in total

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