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Regulation of zebrafish heart regeneration by miR-133.
Yin, Viravuth P; Lepilina, Alexandra; Smith, Ashley; Poss, Kenneth D.
Afiliación
  • Yin VP; Department of Cell Biology, Howard Hughes Medical Institute, Duke University Medical Center, Durham, NC 27710, USA.
Dev Biol ; 365(2): 319-27, 2012 May 15.
Article en En | MEDLINE | ID: mdl-22374218
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Regeneración / Pez Cebra / Miocitos Cardíacos / MicroARNs / Corazón Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Dev Biol Año: 2012 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Regeneración / Pez Cebra / Miocitos Cardíacos / MicroARNs / Corazón Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Dev Biol Año: 2012 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos