Scientists discover how muscle stem cells "flip a switch" to rebuild damaged muscle

Researchers learned that immediately after stress, muscle stem cells temporarily slow down energy production. Instead of burning glucose for energy, they reroute it into protective repair processes to produce antioxidants that reduce inflammation. Once repairs are complete, energy production ramps back up and new muscle fibers form and strengthen.

Lauren Albrecht, UC Irvine assistant professor of pharmaceutical sciences and study's corresponding authorMuscle metabolism isn't simply about fueling growth; it's about strategic recovery. We found that muscle stem cells actively change how they use nutrients to protect themselves first, then rebuild. That metabolic timing is critical."

At the center of the discovery is an enzyme called PFKM, which helps control how cells process glucose. The team determined that cells deliberately reduce PFKM levels during early repair, creating a temporary metabolic pause. When PFKM returns, muscle building begins.

Importantly, the scientists showed that this process can be influenced. By supplying specific metabolic building blocks – nutrients that cells naturally produce later in recovery – they accelerated the transition from repair mode to growth mode in laboratory models.

The findings come as physicians and researchers grapple with increasing reports of lean muscle loss in patients using GLP-1-based weight-loss medications, as well as amid the broader challenge of age-related muscle decline.

"With the rapid rise of GLP-1 therapies and an aging population, preserving muscle mass has become a major health priority," Albrecht said. "Our work identifies a metabolic checkpoint that could one day be targeted to help people recover muscle more effectively."

The work combined advanced imaging, metabolic analysis and human muscle data to track how quickly these fuel changes occur, sometimes within minutes. Researchers from UCLA and Yale University also participated.

The study was supported by the National Institute of General Medical Sciences, the National Institute of Arthritis and Musculoskeletal and Skin Diseases, the National Cancer Institute, and the Alfred P. Sloan Foundation.

Source:

University of California - Irvine

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