'Longevity Protein' Rejuvenates Muscle Healing in Old Mice

December 3, 2018

One of the downsides to getting older is that skeletal muscle loses its ability to heal after injury. New research from the University of Pittsburgh implicates the so-called “longevity protein” Klotho, both as culprit and therapeutic target.

Klotho HR

In young muscle, high levels of Klotho maintain mitochondia, which aids regeneration after injury. Age-related Klotho declines lead to mitochondrial damage and impaired healing in older animals.

Klotho
Klotho (green) is expressed around an injury site in muscle tissue (red) in young mice.
Credit: Sahu et al. (2018), Nature Communications.


The paper, published in Nature Communications, showed that, in young animals, Klotho expression soars after a muscle injury, whereas in old animals, it remains flat. By raising Klotho levels in old animals, or by mitigating downstream effects of Klotho deficiency, the researchers could restore muscle regeneration after injury.

“We found that we were able to rescue, at least in part, the regenerative defect of aged skeletal muscle,” said lead author Fabrisia Ambrosio, PhD, director of rehabilitation for UPMC International, associate professor of physical medicine and rehabilitation at Pitt, and core faculty at the McGowan Institute of Regenerative Medicine. “We saw functional levels of muscle regeneration in old animals that paralleled those of their young counterparts, suggesting that this could potentially be a therapeutic option down the road.”

Suspecting that Klotho acts through mitochondria dysfunction, the researchers gave Klotho-deficient animals a mitochondria-targeting drug called SS-31, which is currently in phase III clinical trials. Treated animals grew more new muscle tissue at the site of injury compared to untreated controls, and their strength after recovery rivaled that of genetically normal mice. 

Similarly, injecting Klotho into older animals a few days after injury resulted in greater muscle mass and better functional recovery than their saline-treated counterparts. Normal, healthy mice did not benefit from SS-31 after injury.

Clinically, these findings could translate to older adults who either sustained a muscle injury or underwent muscle-damaging surgery. Giving them Klotho at the appropriate timepoint could boost their muscle regeneration and lead to a more complete recovery.

Ambrosio cautions that the timing, dosage and route of administration will require future research. 

“If you just bombard the muscle with Klotho, we do not expect to observe any functional benefit,” Ambrosio said. “We’ve found that mimicking the timing profile we see in young animals seems to be critical. We think that this gives some insight into the therapeutic window.”

Additional authors from Pitt include Amrita Sahu, MS, Hikaru Mamiya, BS, Sunita Shinde, MS, Amin Cheikhi, PhD, Lia Winter, BS, Nam Vo, PhD, Donna Stolz, PhD, Vera Roginskaya, BS, Claudette St. Croix, PhD, Ben Van Houten, PhD, and Aaron Barchowsky, PhD. Collaborators outside Pitt include Winnie Tang, PhD, of Johns Hopkins Bloomberg School of Public Health; Laurie Sanders, PhD, of Duke University School of Medicine; Michael Franti, PhD, of Boehringer-Ingelheim, and Thomas Rando, MD, PhD, of Stanford University School of Medicine.

This research was funded by National Institutes of Health grant R01-AG052978 from the National Institute on Aging and grant R01-ES023696 from the National Institute of Environmental Health Science. Boehringer-Ingelheim did not influence the interpretation of the results.