Liver‐originated small extracellular vesicles with TM4SF5 target brown adipose tissue for homeostatic glucose clearance. Issue 9 (5th September 2022)

• Record Type: Journal Article
• Authors: Jung, Jae Woo; Kim, Ji Eon; Kim, Eunmi; Lee, Hyejin; Lee, Haesong; Shin, Eun‐Ae; Lee, Jung Weon
• Is Part Of: Journal of extracellular vesicles. Volume 11:Issue 9(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-09-05
• Subjects: brown adipose tissue -- glucose transporter -- hepatic sEVs -- protein–protein interaction -- tetraspanin; Cells -- Mechanical properties -- Periodicals; Transport Vesicles; Cells -- Mechanical properties; Periodicals; Fulltext; Internet Resources; Periodicals; Electronic journals; Periodicals; 571.63
• DOI: 10.1002/jev2.12262
• Languages: English
• ISSNs: 2001-3078

Abstract

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 ), improved glucose tolerance in Tm4sf5 −/− KO mice and targeted brown adipose tissues (BATs), possibly allowing the clearance of blood glucose as heat independent of UCP1. Taken together, hep‐sEV Tm4sf5 might clear high extracellular glucose levels more efficiently by targeting BAT compared with hep‐sEV Control, suggesting an insulin‐like role for sEV™ 4SF5 in affecting age‐related metabolic status and thus body weight (BW).