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"Young at heart": Regenerative potential linked to immature cardiac phenotypes.
Gomes, Renata S M; Skroblin, Philipp; Munster, Alex B; Tomlins, Hannah; Langley, Sarah R; Zampetaki, Anna; Yin, Xiaoke; Wardle, Fiona C; Mayr, Manuel.
Afiliação
  • Gomes RS; King's British Heart Foundation Centre, King's College London, London, UK.
  • Skroblin P; King's British Heart Foundation Centre, King's College London, London, UK.
  • Munster AB; King's British Heart Foundation Centre, King's College London, London, UK.
  • Tomlins H; King's British Heart Foundation Centre, King's College London, London, UK.
  • Langley SR; King's British Heart Foundation Centre, King's College London, London, UK.
  • Zampetaki A; King's British Heart Foundation Centre, King's College London, London, UK.
  • Yin X; King's British Heart Foundation Centre, King's College London, London, UK.
  • Wardle FC; Cardiovascular Development, Randall Division, King's College London, UK.
  • Mayr M; King's British Heart Foundation Centre, King's College London, London, UK. Electronic address: manuel.mayr@kcl.ac.uk.
J Mol Cell Cardiol ; 92: 105-8, 2016 Mar.
Article em En | MEDLINE | ID: mdl-26827899
The adult human myocardium is incapable of regeneration; yet, the zebrafish (Danio rerio) can regenerate damaged myocardium. Similar to the zebrafish heart, hearts of neonatal, but not adult mice are capable of myocardial regeneration. We performed a proteomics analysis of adult zebrafish hearts and compared their protein expression profile to hearts from neonatal and adult mice. Using difference in-gel electrophoresis (DIGE), there was little overlap between the proteome from adult mouse (>8weeks old) and adult zebrafish (18months old) hearts. Similarly, there was a significant degree of mismatch between the protein expression in neonatal and adult mouse hearts. Enrichment analysis of the selected proteins revealed over-expression of DNA synthesis-related proteins in the cardiac proteome of the adult zebrafish heart similar to neonatal and 4days old mice, whereas in hearts of adult mice there was a mitochondria-related predominance in protein expression. Importantly, we noted pronounced differences in the myofilament composition: the adult zebrafish heart lacks many of the myofilament proteins of differentiated adult cardiomyocytes such as the ventricular isoforms of myosin light chains and nebulette. Instead, troponin I and myozenin 1 were expressed as skeletal isoforms rather than cardiac isoforms. The relative immaturity of the adult zebrafish heart was further supported by cardiac microRNA data. Our assessment of zebrafish and mammalian hearts challenges the assertions on the translational potential of cardiac regeneration in the zebrafish model. The immature myofilament composition of the fish heart may explain why adult mouse and human cardiomyocytes lack this endogenous repair mechanism.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regeneração / Peixe-Zebra / Proteoma / Proteômica / Coração Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Regeneração / Peixe-Zebra / Proteoma / Proteômica / Coração Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article