Literature DB >> 22374218

Regulation of zebrafish heart regeneration by miR-133.

Viravuth P Yin1, Alexandra Lepilina, Ashley Smith, Kenneth D Poss.   

Abstract

Zebrafish regenerate cardiac muscle after severe injuries through the activation and proliferation of spared cardiomyocytes. Little is known about factors that control these events. Here we investigated the extent to which miRNAs regulate zebrafish heart regeneration. Microarray analysis identified many miRNAs with increased or reduced levels during regeneration. miR-133, a miRNA with known roles in cardiac development and disease, showed diminished expression during regeneration. Induced transgenic elevation of miR-133 levels after injury inhibited myocardial regeneration, while transgenic miR-133 depletion enhanced cardiomyocyte proliferation. Expression analyses indicated that cell cycle factors mps1, cdc37, and PA2G4, and cell junction components cx43 and cldn5, are miR-133 targets during regeneration. Using pharmacological inhibition and EGFP sensor interaction studies, we found that cx43 is a new miR-133 target and regeneration gene. Our results reveal dynamic regulation of miRNAs during heart regeneration, and indicate that miR-133 restricts injury-induced cardiomyocyte proliferation.
Copyright © 2012. Published by Elsevier Inc.

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Year:  2012        PMID: 22374218      PMCID: PMC3342384          DOI: 10.1016/j.ydbio.2012.02.018

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


  45 in total

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5.  Connexin 43 expression and distribution in compensated and decompensated cardiac hypertrophy in patients with aortic stenosis.

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Authors:  Kenneth D Poss; Alex Nechiporuk; Ann M Hillam; Stephen L Johnson; Mark T Keating
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  92 in total

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Review 5.  Concise review: new frontiers in microRNA-based tissue regeneration.

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Review 7.  MicroRNAs in myocardial ischemia: identifying new targets and tools for treating heart disease. New frontiers for miR-medicine.

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Review 9.  Functions of microRNAs in cardiovascular biology and disease.

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Review 10.  Roles of the canonical myomiRs miR-1, -133 and -206 in cell development and disease.

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