Liver-originated small extracellular vesicles with TM4SF5 target brown adipose tissue for homeostatic glucose clearance.

ABSTRACT: Transmembrane 4 L six family member 5 (TM4SF5) is involved in chronic liver disease, although its role in glucose homeostasis remains unknown. TM4SF5 deficiency caused age-dependent glucose (in)tolerance with no link to insulin sensitivity. Further, hepatic TM4SF5 binding to GLUT1 promoted glucose uptake and glycolysis. Excessive glucose repletion caused hepatocytes to secrete small extracellular vesicles (sEVs) loaded with TM4SF5 (hep-sEV^Tm4sf5 ), suggesting a role for sEV^Tm4sf5 in glucose metabolism and homeostasis. Hep-sEV^Tm4sf5 were smaller than sEV^Control and recruit proteins for efficient organ tropism. Liver-derived sEVs, via a liver-closed vein circuit (LCVC) using hepatic TM4SF5-overexpressing (Alb-Tm4sf5 TG) mice (liv-sEV^Tm4sf5

SUBMITTER: Jung JW 

PROVIDER: S-EPMC9443943 | biostudies-literature | 2022 Sep

REPOSITORIES: biostudies-literature