ZFIN ID: ZDB-PUB-150808-11
Developmental alterations in centrosome integrity contribute to the post-mitotic state of mammalian cardiomyocytes
Zebrowski, D.C., Vergarajauregui, S., Wu, C.C., Piatkowski, T., Becker, R., Leone, M., Hirth, S., Ricciardi, F., Falk, N., Giessl, A., Just, S., Braun, T., Weidinger, G., Engel, F.B.
Date: 2015
Source: eLIFE   4: (Journal)
Registered Authors: Hirth, Sophia, Just, Steffen, Weidinger, Gilbert, Wu, Chi-Chung
Keywords: MTOC, cardiomyocyte, cell biology, centrosome, developmental biology, mouse, newt, primary cilium, rat, stem cells, terminal differentiation, zebrafish
MeSH Terms:
  • Animals
  • Cell Differentiation*
  • Cell Proliferation*
  • Centrosome/metabolism*
  • Heart/embryology*
  • Myocytes, Cardiac/cytology*
  • Myocytes, Cardiac/physiology*
  • Rats
  • Salamandridae
  • Zebrafish
PubMed: 26247711 Full text @ Elife
Mammalian cardiomyocytes become post-mitotic shortly after birth. Understanding how this occurs is highly relevant to cardiac regenerative therapy. Yet, how cardiomyocytes achieve and maintain a post-mitotic state is unknown. Here, we show that cardiomyocyte centrosome integrity is lost shortly after birth. This is coupled with relocalization of various centrosome proteins to the nuclear envelope. Consequently, postnatal cardiomyocytes are unable to undergo ciliogenesis and the nuclear envelope adopts the function as cellular microtubule organizing center. Loss of centrosome integrity is associated with, and can promote, cardiomyocyte G0/G1 cell cycle arrest suggesting that centrosome disassembly is developmentally utilized to achieve the post-mitotic state in mammalian cardiomyocytes. Adult cardiomyocytes of zebrafish and newt, which are able to proliferate, maintain centrosome integrity. Collectively, our data provide a novel mechanism underlying the post-mitotic state of mammalian cardiomyocytes as well as a potential explanation for why zebrafish and newts, but not mammals, can regenerate their heart.