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The heart of the matter

Jonathan B Weitzman

Author Affiliations

Genome Biology 2002, 3:spotlight-20021218-01  doi:10.1186/gb-spotlight-20021218-01

The electronic version of this article is the complete one and can be found online at:


Published:18 December 2002

© 2002 BioMed Central Ltd

Research news

In humans, heart injury leads to the formation of scar tissue and cardiomyocyte hypertrophy, but the heart does not regenerate. In the December 13 Science Kenneth Poss and colleagues, at Harvard Medical School in Boston, show that zebrafish hearts are able to regenerate after injury without scarring (Science 2002, 298:2188-2190). Surgical removal of 20% of the ventricular myocardium from adult fish induced initial fibrin clot formation. The clot was then replaced by cardiac myofibers, and by two months after injury the hearts appeared grossly normal. Bromodeoxyuridine (BrdU) incorporation experiments showed extensive proliferation of cardiomyocytes near the surgery site. Cardiac injury in fish with a temperature-sensitive mutation in the mps1 gene, encoding a mitotic checkpoint kinase, led to the formation of large, connective-tissue scars in the absence of proliferation. These results provide an interesting model with which to investigate the molecular mechanisms underlying cardiac regeneration, and hint at the potential to manipulate cardiomyocyte proliferation in mammalian hearts.

References

  1. [http://www.sciencemag.org] webcite

    Science

  2. [http://www.harvard.edu] webcite

    Harvard University

  3. Mps1 defines a proximal blastemal proliferative compartment essential for zebrafish fin regeneration

    PubMed Abstract | Publisher Full Text OpenURL