Restoring Systemic GDF11 Levels Reverses Age-Related Dysfunction in Mouse Skeletal Muscle

Author:

Sinha Manisha1234,Jang Young C.124,Oh Juhyun124,Khong Danika124,Wu Elizabeth Y.124,Manohar Rohan124,Miller Christine124,Regalado Samuel G.15,Loffredo Francesco S.16,Pancoast James R.16,Hirshman Michael F.2,Lebowitz Jessica124,Shadrach Jennifer L.123,Cerletti Massimiliano12,Kim Mi-Jeong2,Serwold Thomas2,Goodyear Laurie J.27,Rosner Bernard8,Lee Richard T.16,Wagers Amy J.1234

Affiliation:

1. Harvard Stem Cell Institute and Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.

2. Joslin Diabetes Center, Boston, MA 02215, USA.

3. Howard Hughes Medical Institute, Cambridge, MA, USA.

4. Paul F. Glenn Laboratories for the Biological Mechanisms of Aging, Harvard Medical School, Boston, MA, USA.

5. University of California, Berkeley, CA, USA.

6. Cardiovascular Division, Department of Medicine, Brigham and Women’s Hospital and the Brigham Regenerative Medicine Center, Boston, MA, USA.

7. Department of Medicine, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA, USA.

8. Department of Biostatistics, Harvard School of Public Health, Boston, MA, USA.

Abstract

Help the Aged Muscle function declines with age, as does neurogenesis in certain brain regions. Two teams analyzed the effects of heterochronic parabiosis in mice. Sinha et al. (p. 649 ) found that when an aged mouse shares a circulatory system with a youthful mouse, the aged mouse sees improved muscle function, and Katsimpardi et al. (p. 630 ) observed increased generation of olfactory neurons. In both cases, Growth Differentiation Factor 11 appeared to be one of the key components of the young blood.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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