4.8 Article

Growth Differentiation Factor 11 Is a Circulating Factor that Reverses Age-Related Cardiac Hypertrophy

期刊

CELL
卷 153, 期 4, 页码 828-839

出版社

CELL PRESS
DOI: 10.1016/j.cell.2013.04.015

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资金

  1. NIH [P30DK036836, 1RO1 AG033053, 1DP2 OD004345, 5U01 HL100402, R01 AG032977 1R01 AG040019, KO8 DK090147]
  2. American Heart Association
  3. Glenn Foundation
  4. Watkins Cardiovascular Leadership Award

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The most common form of heart failure occurs with normal systolic function and often involves cardiac hypertrophy in the elderly. To clarify the biological mechanisms that drive cardiac hypertrophy in aging, we tested the influence of circulating factors using heterochronic parabiosis, a surgical technique in which joining of animals of different ages leads to a shared circulation. After 4 weeks of exposure to the circulation of young mice, cardiac hypertrophy in old mice dramatically regressed, accompanied by reduced cardiomyocyte size and molecular remodeling. Reversal of age-related hypertrophy was not attributable to hemodynamic or behavioral effects of parabiosis, implicating a blood-borne factor. Using modified aptamer-based proteomics, we identified the TGF-beta superfamily member GDF11 as a circulating factor in young mice that declines with age. Treatment of old mice to restore GDF11 to youthful levels recapitulated the effects of parabiosis and reversed age-related hypertrophy, revealing a therapeutic opportunity for cardiac aging.

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