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Pericytes may improve muscle recovery

Pericyte transplantation may improve skeletal muscle recovery following limb immobilization, animal study shows

Date:
April 25, 2019
Source:
Federation of American Societies for Experimental Biology
Summary:
Extended periods of limb immobilization -- whether from long-term bed rest, casting, spaceflight, or other circumstances -- can reduce skeletal muscle mass and strength to the extent that recovery is delayed or never achieved. The biological basis for this lack of recovery, however, remains unclear. An animal study provides the first evidence that pericytes (cells integral to blood vessel formation) are important for regulating muscle mass, particularly in the context of recovery following disuse atrophy.
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Extended periods of limb immobilization -- whether from long-term bed rest, casting, spaceflight, or other circumstances -- can reduce skeletal muscle mass and strength to the extent that recovery is delayed or never achieved. The biological basis for this lack of recovery, however, remains unclear. An animal study published in The FASEB Journal provides the first evidence that pericytes (cells integral to blood vessel formation) are important for regulating muscle mass, particularly in the context of recovery following disuse atrophy.

To conduct this study, researchers used two groups of mice, both of which were subjected to unilateral hind-limb immobilization for two weeks. One group received pericyte transplantation using donor cells, while the control group received a placebo injection. After a two-week recovery period following these respective treatments, the control group continued to exhibit deficits in muscle fiber size and capillary content, while the group that received pericyte transplantation demonstrated full recovery.

These findings demonstrated that while pericytes are significantly reduced in skeletal muscle following limb immobilization, replacement of pericytes with donor cells during the recovery period can facilitate full regrowth of muscle fibers.

"Our findings suggest that pericyte-based therapies may provide an effective approach toward rebuilding skeletal muscle mass and function after loss," said Marni D. Boppart, ScD, an associate professor of kinesiology and community health at the Beckman Institute for Advanced Science and Technology at the University of Illinois, Urbana-Champaign. "We hope that this study provides the first step toward preventing devastating disabilities that can occur in older adults following long periods of inactivity."

The study's findings also suggested that perivascular support cells are responsive to mechanical cues provided by contraction. As a result, researchers are examining a role for pericytes in mediating the benefits that occur with physical activity in healthy individuals, including enhanced muscle mass, blood flow, and strength.

"Mechanical signaling has emerged as a major axis of cellular regulation and differentiation, and this study adds a novel dimension," said Thoru Pederson, PhD, Editor-in-Chief of The FASEB Journal.


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Materials provided by Federation of American Societies for Experimental Biology. Note: Content may be edited for style and length.


Journal Reference:

  1. Michael Munroe, Svyatoslav Dvoretskiy, Amber Lopez, Jiayu Leong, Michael C. Dyle, Hyunjoon Kong, Christopher M. Adams, Marni D. Boppart. Pericyte transplantation improves skeletal muscle recovery following hindlimb immobilization. The FASEB Journal, 2019; fj.201802580R DOI: 10.1096/fj.201802580R

Cite This Page:

Federation of American Societies for Experimental Biology. "Pericytes may improve muscle recovery." ScienceDaily. ScienceDaily, 25 April 2019. <www.sciencedaily.com/releases/2019/04/190425143612.htm>.
Federation of American Societies for Experimental Biology. (2019, April 25). Pericytes may improve muscle recovery. ScienceDaily. Retrieved December 21, 2024 from www.sciencedaily.com/releases/2019/04/190425143612.htm
Federation of American Societies for Experimental Biology. "Pericytes may improve muscle recovery." ScienceDaily. www.sciencedaily.com/releases/2019/04/190425143612.htm (accessed December 21, 2024).

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