PuSH - Publikationsserver des Helmholtz Zentrums München

Rohm, M.* ; Sommerfeld, A.* ; Strzoda, D.* ; Jones, A.* ; Sijmonsma, T.P.* ; Rudofsky, G.* ; Wolfrum, C.* ; Sticht, C.* ; Gretz, N.* ; Zeyda, M.* ; Leitner, L.* ; Nawroth, P.P.* ; Stulnig, T.M.* ; Berriel Diaz, M.* ; Vegiopoulos, A.* ; Herzig, S.*

Transcriptional cofactor TBLR1 controls lipid mobilization in white adipose tissue.

Cell Metab. 17, 575-585 (2013)
DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Lipid mobilization (lipolysis) in white adipose tissue (WAT) critically controls lipid turnover and adiposity in humans. While the acute regulation of lipolysis has been studied in detail, the transcriptional determinants of WAT lipolytic activity remain still largely unexplored. Here we show that the genetic inactivation of transcriptional cofactor transducin beta-like-related 1(TBLR1) blunts the lipolytic response of white adipocytes through the impairment of cAMP-dependent signal transduction. Indeed, mice lacking TBLR1 in adipocytes are defective in fasting-induced lipid mobilization and, when placed on a high-fat-diet, show aggravated adiposity, glucose intolerance, and insulin resistance. TBLR1 levels are found to increase under lipolytic conditions in WAT of both human patients and mice, correlating with serum free fatty acids (FFAs). As a critical regulator of WAT cAMP signaling and lipid mobilization, proper activity of TBLR1 in adipocytes might thus represent a critical molecular checkpoint for the prevention of metabolic dysfunction in subjects with obesity-related disorders.
Altmetric
Weitere Metriken?
Zusatzinfos bearbeiten [➜Einloggen]
Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
ISSN (print) / ISBN 1550-4131
e-ISSN 1932-7420
Zeitschrift Cell Metabolism
Quellenangaben Band: 17, Heft: 4, Seiten: 575-585 Artikelnummer: , Supplement: ,
Verlag Elsevier
Begutachtungsstatus Peer reviewed