Authors: Sara C Campbell, Marko Oydanich, Jie Zhang, Candace R Longoria, Olufunmilola Ibironke, Dorothy E Vatner, David P Siderovski, Stephen F Vatner
Published: 2022-03-19
DOI: 10.1161/circ.144.suppl_1.11568
Source: Full article
The Regulator of G Protein Signaling 14 knockout (RGS14 KO) mouse strain has a unique brown adipose tissue (BAT) mechanism mediating its phenotype of healthful longevity and improved exercise performance. RGS14 KO mice demonstrated a 51 ± 8% increase in treadmill running distance before exhaustion and a 44 ± 7% increase in work to exhaustion compared to their wild type littermates (WTLs). Three days after BAT transplantation from RGS14 KO mice to WTL mice, the RGS14 KO BAT donor mice lost their enhanced exercise capacity, whereas it was gained in the WTL BAT recipients: their running distance and work to exhaustion rose by 46 ± 5% and 52 ± 7%, respectively. In contrast, when BAT was transplanted to WTL mice from other WTL mice, exercise capacity did not increase at 3 days after transplantation, but was only seen after 2 months post-transplantation. Based on these observations, our hypothesis was that the unique characteristics of RGS14 KO BAT, in inducing enhanced exercise capacity upon transplantation, are mediated by novel gene upregulation within the BAT, as well as potential interactions between the BAT and the microbiome. We found that RGS14 KO mice harbor two unique, health-beneficial strains of