Key result
Brown fat transplantation increases muscle mass and contractile force vs sham in mice.
Why the study?
Intramuscular fat accumulation correlates with poor functional outcomes, but whether paracrine cross-talk can be modified by altering fat phenotypes to support muscle regeneration was unknown.
Does transplantation of brown fat improve muscle regeneration in a mouse rotator cuff injury model?
Does transplantation of brown fat improve muscle regeneration in a mouse rotator cuff injury model?
Brown fat transplantation supports muscle regeneration in a mouse model, suggesting that the phenotype of muscle-associated fat could be a therapeutic target.
May inform adipose-targeted therapies for muscle repair; leaves open translation to human rotator cuff injury.
Accumulation of adipose tissue around and within muscles is highly correlated with reduced strength, functional limitations, and poor rehabilitative outcomes. Given the intimate physical contact between these tissues, paracrine cross-talk is a likely mediator of this association. The recent discovery that muscle-associated adipose tissue exhibits features of beige fat has suggested that this cross-talk may be modifiable, as beige fat can be stimulated to assume features of brown fat. In this work, we describe a novel intermuscular fat transplant model in the mouse rotator cuff to investigate cross-talk between muscle and adipose tissue. Specifically, we examine the role of transplanted fat phenotype on muscle regeneration by transplanting pieces of classical brown (interscapular), beige (inguinal), or white (epididymal) adipose tissue in conjunction with cardiotoxin injection to the adjacent supraspinatus muscle. Transplantation of brown fat, but not beige or white, significantly increased muscle mass, fiber cross-sectional area and contractile force production compared with sham injury. This effect was not seen when cardiotoxin was delivered to a distant muscle, or when adjacent muscles were injected with saline indicating that the effect is localized and specifically targeting the regenerative process. Thus, we conclude that local signaling between fat and muscle varies by phenotype and that brown fat supports regeneration. Clinical significance: Our findings suggest that the phenotype of muscle-associated fat could be a novel therapeutic target to modulate fat-muscle signaling.
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Bryniarski et al. (2019) studied Muscle regeneration. Transplantation of classical brown (interscapular) adipose tissue vs. Sham injury, beige (inguinal) fat, or white (epididymal) fat was evaluated on Muscle mass, fiber cross-sectional area and contractile force production. Transplantation of brown fat, but not beige or white fat, significantly increased muscle mass, fiber cross-sectional area, and contractile force production compared with sham injury in mice.
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