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Growth Differentiation Factor 11 Is a Circulating Factor that Reverses Age-Related Cardiac Hypertrophy
Author(s) -
Francesco S. Loffredo,
Matthew L. Steinhauser,
Steven M. Jay,
Joseph Gan,
James R. Pancoast,
Pratyusha Yalamanchi,
Manisha Sinha,
C. Dall’Osso,
Danika Khong,
Jennifer L. Shadrach,
Christine M. Miller,
Britta Swebilius Singer,
Alexandre F.R. Stewart,
Nikolaos Psychogios,
Robert E. Gerszten,
Adam J. Hartigan,
MiJeong Kim,
Thomas Serwold,
Amy J. Wagers,
Richard Lee
Publication year - 2013
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2013.04.015
Subject(s) - parabiosis , muscle hypertrophy , biology , growth differentiation factor , medicine , cardiac hypertrophy , endocrinology , cardiac function curve , heart failure , growth factor , bone morphogenetic protein , genetics , gene , receptor
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-β 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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