Inhibition of prostaglandin-degrading enzyme 15-PGDH rejuvenates aged muscle mass and strength

Author:

Palla A. R.12ORCID,Ravichandran M.12ORCID,Wang Y. X.12ORCID,Alexandrova L.3,Yang A. V.12,Kraft P.12,Holbrook C. A.12,Schürch C. M.24ORCID,Ho A. T. V.12,Blau H. M.12ORCID

Affiliation:

1. Blau Laboratory, Stanford School of Medicine, Stanford, CA 94305, USA.

2. Baxter Laboratory for Stem Cell Biology, Department of Microbiology and Immunology, Institute for Stem Cell Biology and Regenerative Medicine, Stanford School of Medicine, Stanford, CA 94305, USA.

3. Vincent Coates Foundation Mass Spectrometry Laboratory, Stanford University, Stanford, CA, USA.

4. Nolan Laboratory, Stanford School of Medicine, Stanford, CA 94305, USA.

Abstract

Maintaining muscle Prostaglandin E2 (PGE2), an eicosanoid that mediates inflammatory responses, also supports the function of muscle stem cells. Palla et al. found that loss of PGE2 in aging mice contributes to loss of muscle and appears to be a consequence of increased activity of 15-hydroxyprostaglandin dehydrogenase (15-PGDH), an enzyme that degrades PGE2 (see the Perspective by Becker and Rudolph). Restoring PGE2 concentrations by inhibiting 15-PGDH in older mice improved muscle function. Decreased activity of 15-PGDH in older animals had beneficial effects that included decreased proteolysis and transforming growth factor–β signaling and increased mitochondrial function and autophagy. The findings reveal a potential therapeutic strategy to help maintain muscle mass and function during aging. Science , this issue p. eabc8059 ; see also p. 462

Funder

National Institutes of Health

California Institute for Regenerative Medicine

Li Ka Shing Foundation

Donald E. and Delia B. Baxter Foundation

Swiss National Science Foundation

Canadian Institutes of Health Research

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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