z-logo
open-access-imgOpen Access
Stimulation of 3T3-L1 Adipogenesis by Signal Transducer and Activator of Transcription 5
Author(s) -
Rika Nanbu-Wakao,
Yoshihiro Morikawa,
Itaru Matsumura,
Yasuhiko Masuho,
Masaaki Muramatsu,
Emiko Senba,
Hiroshi Wakao
Publication year - 2002
Publication title -
molecular endocrinology
Language(s) - English
Resource type - Journals
eISSN - 1944-9917
pISSN - 0888-8809
DOI - 10.1210/mend.16.7.0862
Subject(s) - adipogenesis , biology , stat5 , adipocyte , stat protein , ectopic expression , microbiology and biotechnology , transcription factor , 3t3 l1 , activator (genetics) , peroxisome proliferator activated receptor , receptor , cell culture , adipose tissue , endocrinology , signal transduction , stat3 , gene , biochemistry , genetics
Signal transducer and activator of transcription 5 (Stat5) mediates signaling of many cytokines and growth factors. Here we show that Stat5 functions as an initial mediator of adipogenesis. The preadipocyte cell line 3T3-L1 undergoes adipocyte differentiation upon appropriate hormonal induction. We found that Stat5A and Stat5B were strongly activated at an early stage of 3T3-L1 differentiation. To investigate physiological roles of Stat5 in adipogenesis, we have constructed 3T3-L1 cell lines in which either an exogenous wild type (wt) or dominant negative (dn) form of Stat5A expression was controlled under the doxycycline-regulatable promoter. Precocious induction of wt-Stat5A in adipocyte differentiation promoted accumulation of triglycerides within the cells. In contrast, induction of dn-Stat5A attenuated lipid accumulation. Northern blot analyses revealed that the expression of proadipogenic transcription factors was influenced in a complementary fashion by ectopic expression of either wt- or dn-Stat5A. Notably, Stat5 regulated expression of peroxisome proliferator-activated receptor-gamma, which plays crucial roles in adipogenesis. We have also generated transgenic mice in which dn-Stat5A is expressed in an adipose tissue-specific fashion and found attenuation of peroxisome proliferator-activated receptor-gamma and of many adipocyte-related genes. These results highlight a novel role of Stat5 in adipocyte differentiation.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom