The modulation of STAT5A/GR complexes during fat cell differentiation and in mature adipocytes

被引:25
作者
Baugh, James E., Jr. [1 ]
Floyd, Z. Elizabeth [1 ]
Stephens, Jacqueline M. [1 ]
机构
[1] Louisiana State Univ, Dept Biol Sci, Baton Rouge, LA 70803 USA
关键词
glucocorticoids; adipogenesis; adipocytes;
D O I
10.1038/oby.2007.500
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Objective: Signal transducer and activator of transcription (STAT) 5A has been shown to interact with the glucocorticoid receptor (GR) in adipocytes. The aim of this study was to investigate the subcellular locations and modulation of STAT5A/GR complexes during adipogenesis and in mature adipocytes. Research Methods and Procedures: Both 3T3-L1 and 3T3-F442A cells were studied by performing subcellular fractionations, immunoprecipitation, and Western blotting after various treatments. Results: The formation of nuclear STAT5A/GR complexes was regulated in the cytosol and in the nucleus at distinct times during adipogenesis and in mature adipocytes. STAT5A, but not STAT5B, forms a complex with GR in adipocytes. The STAT5A associated with GR in the nucleus is tyrosine phosphorylated. Discussion: The association of STAT5A with GR in the nucleus of adipocytes is modulated by the tyrosine phosphorylation of STAT5A. Both GR and STAT5A are known to have important roles in adipocyte function. Hence, our data suggest that the association of these two transcription factors may be important in the regulation of adipocyte gene expression.
引用
收藏
页码:583 / 590
页数:8
相关论文
共 26 条
[1]
STEROID-HORMONE RECEPTORS - MANY ACTORS IN SEARCH OF A PLOT [J].
BEATO, M ;
HERRLICH, P ;
SCHUTZ, G .
CELL, 1995, 83 (06) :851-857
[2]
Interleukin-2 inhibits glucocorticoid receptor transcriptional activity through a mechanism involving STATS (signal transducer and activator of transcription 5) but not AP-1 [J].
Biola, A ;
Lefebvre, P ;
Perrin-Wolff, M ;
Sturm, M ;
Bertoglio, J ;
Pallardy, M .
MOLECULAR ENDOCRINOLOGY, 2001, 15 (07) :1062-1076
[3]
Characterization of Stat5a and Stat5b homodimers and heterodimers and their association with the glucocortiocoid receptor in mammary cells [J].
Cella, N ;
Groner, B ;
Hynes, NE .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (04) :1783-1792
[4]
The N363S polymorphism of the glucocorticoid receptor: Potential contribution to central obesity in men and lack of association with other risk factors for coronary heart disease and diabetes mellitus [J].
Dobson, MG ;
Redfern, CPF ;
Unwin, N ;
Weaver, JU .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (05) :2270-2274
[5]
Expression level-dependent contribution of glucocorticoid receptor domains for functional interaction with STAT5 [J].
Doppler, W ;
Windegger, M ;
Soratroi, C ;
Tomasi, J ;
Lechner, J ;
Rusconi, S ;
Cato, ACB ;
Almlof, T ;
Liden, J ;
Okret, S ;
Gustafsson, JÅ ;
Richard-Foy, H ;
Starr, DB ;
Klocker, H ;
Edwards, D ;
Geymayer, S .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (09) :3266-3279
[6]
STAT5A promotes adipogenesis in nonprecursor cells and associates with the glucocorticoid receptor during adipocyte differentiation [J].
Floyd, ZE ;
Stephens, JM .
DIABETES, 2003, 52 (02) :308-314
[7]
The adrenal and the metabolic syndrome [J].
Golub M.S. .
Current Hypertension Reports, 2001, 3 (2) :117-120
[8]
Inactivation of the GR in the nervous system affects energy accumulation [J].
Kellendonk, C ;
Eiden, S ;
Kretz, O ;
Schütz, G ;
Schmidt, I ;
Tronche, F ;
Simon, E .
ENDOCRINOLOGY, 2002, 143 (06) :2333-2340
[9]
Signaling through the JAK/STAT pathway, recent advances and future challenges [J].
Kisseleva, T ;
Bhattacharya, S ;
Braunstein, J ;
Schindler, CW .
GENE, 2002, 285 (1-2) :1-24
[10]
CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+