Growth hormone is a positive regulator of adiponectin receptor 2 in 3T3-L1 adipocytes

被引:95
作者
Fasshauer, M
Klein, J
Kralisch, S
Klier, M
Lössner, U
Blüher, M
Paschke, R
机构
[1] Univ Leipzig, Dept Internal Med 3, D-04103 Leipzig, Germany
[2] Med Univ Lubeck, Dept Internal Med 1, D-23538 Lubeck, Germany
关键词
3T3-L1; adipocyte; adiponectin; adiponectin receptor; diabetes; growth hormone; insulin resistance; obesity;
D O I
10.1016/S0014-5793(03)01525-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The fat-derived protein adiponectin is an important insulin-sensitizing adipocytokine which is downregulated in insulin resistance and obesity. Recently, two receptors of this adipose-expressed protein called adiponectin receptor 1 (AdipoR1) and 2 (AdipoR2) have been cloned. To clarify expression and regulation of these receptors in fat cells, AdipoR1 and AdipoR2 mRNA was measured by quantitative real-time reverse transcription-polymerase chain reaction during differentiation of 3T3-L1 adipocytes and after treatment with various hormones known to induce insulin resistance. Interestingly, AdipoR2 synthesis was significantly increased up to 4.8-fold during differentiation of 3T3-L1 preadipocytes, whereas AdipoR1 expression was only augmented up to 1.4-fold. Furthermore, growth hormone (GH) induced AdipoR2, but not AdipoR1 mRNA by up to 2.4-fold in a dose- and time-dependent fashion with significant stimulation detectable at concentrations as low as 5 ng/ml GH and as early as 2 h after effector addition. The positive effect of GH on AdipoR2 expression could be reversed by withdrawal of the hormone for 24 h. In contrast, other key hormones involved in the regulation of insulin resistance and energy metabolism such as insulin, isoproterenol, dexamethasone, triiodothyronine, angiotensin 2, tumor necrosis factor alpha and interleukin-6 did not influence AdipoR1 and AdipoR2 synthesis in vitro. Taken together, our results suggest that AdipoR2 expression is differentiation-dependent and selectively regulated by GH implying a potential role of this hormone in adiponectin-associated alterations of insulin sensitivity and energy homeostasis. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:27 / 32
页数:6
相关论文
共 44 条
[1]
The adipocyte-secreted protein Acrp30 enhances hepatic insulin action [J].
Berg, AH ;
Combs, TP ;
Du, XL ;
Brownlee, M ;
Scherer, PE .
NATURE MEDICINE, 2001, 7 (08) :947-953
[2]
Björntorp P, 1999, DRUGS, V58, P13
[3]
PATHOGENESIS OF THE DAWN PHENOMENON IN PATIENTS WITH INSULIN-DEPENDENT DIABETES-MELLITUS - ACCELERATED GLUCOSE-PRODUCTION AND IMPAIRED GLUCOSE-UTILIZATION DUE TO NOCTURNAL SURGES IN GROWTH-HORMONE SECRETION [J].
CAMPBELL, PJ ;
BOLLI, GB ;
CRYER, PE ;
GERICH, JE .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 312 (23) :1473-1479
[4]
Essential role of insulin receptor substrate-2 in insulin stimulation of Glut4 translocation and glucose uptake in brown adipocytes [J].
Fasshauer, M ;
Klein, J ;
Ueki, K ;
Kriauciunas, KM ;
Benito, M ;
White, MF ;
Kahn, CR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (33) :25494-25501
[5]
Interleukin (IL)-6 mRNA expression is stimulated by insulin, isoproterenol, tumour necrosis factor alpha, growth hormone, and IL-6 in 3T3-L1 adipocytes [J].
Fasshauer, M ;
Klein, J ;
Lossner, U ;
Paschke, R .
HORMONE AND METABOLIC RESEARCH, 2003, 35 (03) :147-152
[6]
Adiponectin gene expression and secretion is inhibited by interleukin-6 in 3T3-L1 adipocytes [J].
Fasshauer, M ;
Kralisch, S ;
Klier, M ;
Lossner, U ;
Bluher, M ;
Klein, J ;
Paschke, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 301 (04) :1045-1050
[7]
Hormonal regulation of adiponectin gene expression in 3T3-L1 adipocytes [J].
Fasshauer, M ;
Klein, J ;
Neumann, S ;
Eszlinger, M ;
Paschke, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 290 (03) :1084-1089
[8]
Adiponectin gene expression is inhibited by β-adrenergic stimulation via protein kinase A in 3T3-L1 adipocytes [J].
Fasshauer, M ;
Klein, J ;
Neumann, S ;
Eszlinger, M ;
Paschke, R .
FEBS LETTERS, 2001, 507 (02) :142-146
[9]
Tumor necrosis factor α is a negative regulator of resistin gene expression and secretion in 3T3-L1 adipocytes [J].
Fasshauer, M ;
Klein, J ;
Neumann, S ;
Eszlinger, M ;
Paschke, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 288 (04) :1027-1031
[10]
Isoproterenol inhibits resistin gene expression through a GS-protein-coupled pathway in 3T3-L1 adipocytes [J].
Fasshauer, M ;
Klein, J ;
Neumann, S ;
Eszlinger, M ;
Paschke, R .
FEBS LETTERS, 2001, 500 (1-2) :60-63