Gene Expression Analysis of Zebrafish Heart Regeneration

DSpace/Manakin Repository

Gene Expression Analysis of Zebrafish Heart Regeneration

Citable link to this page


Title: Gene Expression Analysis of Zebrafish Heart Regeneration
Author: Lien, Ching-Ling; Schebesta, Michael; Makino, Shinji; Weber, Gerhard Johannes; Keating, Mark T.

Note: Order does not necessarily reflect citation order of authors.

Citation: Lien, Ching-Ling, Michael Schebesta, Shinji Makino, Gerhard J. Weber, and Mark T. Keating. 2006. Gene expression analysis of zebrafish heart regeneration. PLoS Biology 4(8):e260.
Full Text & Related Files:
Abstract: Mammalian hearts cannot regenerate. In contrast, zebrafish hearts regenerate even when up to 20% of the ventricle is amputated. The mechanism of zebrafish heart regeneration is not understood. To systematically characterize this process at the molecular level, we generated transcriptional profiles of zebrafish cardiac regeneration by microarray analyses. Distinct gene clusters were identified based on temporal expression patterns. Genes coding for wound response/inflammatory factors, secreted molecules, and matrix metalloproteinases are expressed in regenerating heart in sequential patterns. Comparisons of gene expression profiles between heart and fin regeneration revealed a set of regeneration core molecules as well as tissue-specific factors. The expression patterns of several secreted molecules around the wound suggest that they play important roles in heart regeneration. We found that both platelet-derived growth factor-a and -b (pdgf-a and pdgf-b) are upregulated in regenerating zebrafish hearts. PDGF-B homodimers induce DNA synthesis in adult zebrafish cardiomyocytes. In addition, we demonstrate that a chemical inhibitor of PDGF receptor decreases DNA synthesis of cardiomyocytes both in vitro and in vivo during regeneration. Our data indicate that zebrafish heart regeneration is associated with sequentially upregulated wound healing genes and growth factors and suggest that PDGF signaling is required.
Published Version: doi://10.1371/journal.pbio.0040260
Other Sources:
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at
Citable link to this page:
Downloads of this work:

Show full Dublin Core record

This item appears in the following Collection(s)


Search DASH

Advanced Search