TY - JOUR
T1 - Browning attenuates murine white adipose tissue expansion during postnatal development
AU - Lasar, D.
AU - Julius, A.
AU - Fromme, T.
AU - Klingenspor, M.
N1 - Funding Information:
This work was supported by the ZIEL-PhD-School “Nutritional adaptation and epigenetic mechanisms” at the Center for Nutrition and Food Sciences, the Else Kröner-Fresenius Stiftung and the EU FP7 project DIABAT (HEALTH-F2-2011-278373) . D.L. is a member of the ZIEL PhD-School and the Faculty Graduate Center Weihenstephan of TUM Graduate School at Technische Universität München, Germany. We are grateful to the animal caretaker team of the TUM Small Animal Research Center for their support and Heiko Witt at the Else Kröner-Fresenius Center for access to the PCR machine.
PY - 2013/5
Y1 - 2013/5
N2 - During postnatal development of mice distinct white adipose tissue depots display a transient appearance of brown-like adipocytes. These brite (brown in white) adipocytes share characteristics with classical brown adipocytes including a multilocular appearance and the expression of the thermogenic protein uncoupling protein 1. In this study, we compared two inbred mouse strains 129S6sv/ev and C57BL6/N known for their different propensity to diet-induced obesity. We observed transient browning in retroperitoneal and inguinal adipose tissue depots of these two strains. From postnatal day 10 to 20 the increase in the abundance of multilocular adipocytes and uncoupling protein 1 expression was higher in 129S6sv/ev than in C57BL6/N pups. The parallel increase in the mass of the two fat depots was attenuated during this browning period. Conversely, epididymal white and interscapular brown adipose tissue displayed a steady increase in mass during the first 30 days of life. In this period, 129S6sv/ev mice developed a significantly higher total body fat mass than C57BL6/N. Thus, while on a local depot level a high number of brite cells is associated with the attenuation of adipose tissue expansion the strain comparison reveals no support for a systemic impact on energy balance. This article is part of a Special Issue entitled Brown and White Fat: From Signaling to Disease.
AB - During postnatal development of mice distinct white adipose tissue depots display a transient appearance of brown-like adipocytes. These brite (brown in white) adipocytes share characteristics with classical brown adipocytes including a multilocular appearance and the expression of the thermogenic protein uncoupling protein 1. In this study, we compared two inbred mouse strains 129S6sv/ev and C57BL6/N known for their different propensity to diet-induced obesity. We observed transient browning in retroperitoneal and inguinal adipose tissue depots of these two strains. From postnatal day 10 to 20 the increase in the abundance of multilocular adipocytes and uncoupling protein 1 expression was higher in 129S6sv/ev than in C57BL6/N pups. The parallel increase in the mass of the two fat depots was attenuated during this browning period. Conversely, epididymal white and interscapular brown adipose tissue displayed a steady increase in mass during the first 30 days of life. In this period, 129S6sv/ev mice developed a significantly higher total body fat mass than C57BL6/N. Thus, while on a local depot level a high number of brite cells is associated with the attenuation of adipose tissue expansion the strain comparison reveals no support for a systemic impact on energy balance. This article is part of a Special Issue entitled Brown and White Fat: From Signaling to Disease.
KW - Brite cell
KW - Brite cell recruitment
KW - Postnatal development
KW - Retroperitoneal white adipose tissue
KW - Strain difference
UR - http://www.scopus.com/inward/record.url?scp=84875860413&partnerID=8YFLogxK
U2 - 10.1016/j.bbalip.2013.01.016
DO - 10.1016/j.bbalip.2013.01.016
M3 - Article
C2 - 23376694
AN - SCOPUS:84875860413
SN - 1388-1981
VL - 1831
SP - 960
EP - 968
JO - Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids
JF - Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids
IS - 5
ER -