TY - JOUR
T1 - Browning of white adipose tissue uncouples glucose uptake from insulin signaling
AU - Mössenböck, Karin
AU - Vegiopoulos, Alexandros
AU - Rose, Adam J.
AU - Sijmonsma, Tjeerd P.
AU - Herzig, Stephan
AU - Schafmeier, Tobias
PY - 2014/10/14
Y1 - 2014/10/14
N2 - Presence of thermogenically active adipose tissue in adult humans has been inversely associated with obesity and type 2 diabetes. While it had been shown that insulin is crucial for the development of classical brown fat, its role in development and function of inducible brown-in-white (brite) adipose tissue is less clear. Here we show that insulin deficiency impaired differentiation of brite adipocytes. However, adrenergic stimulation almost fully induced the thermogenic program under these settings. Although brite differentiation of adipocytes as well as browning of white adipose tissue entailed substantially elevated glucose uptake by adipose tissue, the capacity of insulin to stimulate glucose uptake surprisingly was not higher in the brite state. Notably, in line with the insulin-independent stimulation of glucose uptake, our data revealed that brite recruitment results in induction of solute carrier family 2 (GLUT-1) expression in adipocytes and inguinal WAT. These results for the first time demonstrate that insulin signaling is neither essential for brite recruitment, nor is it improved in cells or tissues upon browning.
AB - Presence of thermogenically active adipose tissue in adult humans has been inversely associated with obesity and type 2 diabetes. While it had been shown that insulin is crucial for the development of classical brown fat, its role in development and function of inducible brown-in-white (brite) adipose tissue is less clear. Here we show that insulin deficiency impaired differentiation of brite adipocytes. However, adrenergic stimulation almost fully induced the thermogenic program under these settings. Although brite differentiation of adipocytes as well as browning of white adipose tissue entailed substantially elevated glucose uptake by adipose tissue, the capacity of insulin to stimulate glucose uptake surprisingly was not higher in the brite state. Notably, in line with the insulin-independent stimulation of glucose uptake, our data revealed that brite recruitment results in induction of solute carrier family 2 (GLUT-1) expression in adipocytes and inguinal WAT. These results for the first time demonstrate that insulin signaling is neither essential for brite recruitment, nor is it improved in cells or tissues upon browning.
UR - http://www.scopus.com/inward/record.url?scp=84908010172&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0110428
DO - 10.1371/journal.pone.0110428
M3 - Article
C2 - 25313899
AN - SCOPUS:84908010172
VL - 9
JO - PLoS ONE
JF - PLoS ONE
SN - 1932-6203
IS - 10
M1 - e110428
ER -