Yin, Hang2; Pasut, Alessandra2; Soleimani, Vahab D2; Bentzinger, C Florian2; Antoun, Ghadi2; Thorn, Stephanie2; Seale, Patrick2; Fernando, Pasan2; van Ijcken, Wilfred2; Grosveld, Frank2; Dekemp, Robert A2; Boushel, Robert1; Harper, Mary-Ellen2; Rudnicki, Michael A2
1 Anæstesiologisk Afdeling Z, Bispebjerg and Frederiksberg Hospital, The Capital Region of Denmark2 unknown
Brown adipose tissue (BAT) is an energy-dispensing thermogenic tissue that plays an important role in balancing energy metabolism. Lineage-tracing experiments indicate that brown adipocytes are derived from myogenic progenitors during embryonic development. However, adult skeletal muscle stem cells (satellite cells) have long been considered uniformly determined toward the myogenic lineage. Here, we report that adult satellite cells give rise to brown adipocytes and that microRNA-133 regulates the choice between myogenic and brown adipose determination by targeting the 3'UTR of Prdm16. Antagonism of microRNA-133 during muscle regeneration increases uncoupled respiration, glucose uptake, and thermogenesis in local treated muscle and augments whole-body energy expenditure, improves glucose tolerance, and impedes the development of diet-induced obesity. Finally, we demonstrate that miR-133 levels are downregulated in mice exposed to cold, resulting in de novo generation of satellite cell-derived brown adipocytes. Therefore, microRNA-133 represents an important therapeutic target for the treatment of obesity.