Muscle progenitor cells are required for skeletal muscle regeneration and prevention of adipogenesis after limb ischemia

Skeletal muscle injury in peripheral artery disease (PAD) has been attributed to vascular insufficiency, however evidence has demonstrated that muscle cell responses play a role in determining outcomes in limb ischemia. Here, we demonstrate that genetic ablation of Pax7 muscle progenitor cells (MPCs...

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Bibliographic Details
Published in:Frontiers in cardiovascular medicine 2023-03, Vol.10, p.1118738-1118738
Main Authors: Abbas, Hasan, Olivere, Lindsey A, Padgett, Michael E, Schmidt, Cameron A, Gilmore, Brian F, McCord, Timothy J, Southerland, Kevin W, McClung, Joseph M, Kontos, Christopher D
Format: Article
Language:English
Subjects:
Cardiovascular Medicine
critical limb threatening ischemia
fibro/adipogenic progenitor cells
hind limb ischemia
muscle progenitor cells
peripheral artery disease
skeletal muscle regeneration
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Summary:Skeletal muscle injury in peripheral artery disease (PAD) has been attributed to vascular insufficiency, however evidence has demonstrated that muscle cell responses play a role in determining outcomes in limb ischemia. Here, we demonstrate that genetic ablation of Pax7 muscle progenitor cells (MPCs) in a model of hindlimb ischemia (HLI) inhibited muscle regeneration following ischemic injury, despite a lack of morphological or physiological changes in resting muscle. Compared to control mice (Pax7 ), the ischemic limb of Pax7-deficient mice (Pax7 ) was unable to generate significant force 7 or 28 days after HLI. A significant increase in adipose was observed in the ischemic limb 28 days after HLI in Pax7 mice, which replaced functional muscle. Adipogenesis in Pax7 mice corresponded with a significant increase in PDGFRα fibro/adipogenic progenitors (FAPs). Inhibition of FAPs with batimastat decreased muscle adipose but increased fibrosis. , Pax7 MPCs failed to form myotubes but displayed increased adipogenesis. Skeletal muscle from patients with critical limb threatening ischemia displayed increased adipose in more ischemic regions of muscle, which corresponded with fewer satellite cells. Collectively, these data demonstrate that Pax7 MPCs are required for muscle regeneration after ischemia and suggest that muscle regeneration may be an important therapeutic target in PAD.
ISSN:2297-055X
2297-055X
DOI:10.3389/fcvm.2023.1118738