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FEBS Letters
Article . 2004 . Peer-reviewed
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Experimental and Clinical Endocrinology & Diabetes
Article . 2004 . Peer-reviewed
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FEBS Letters
Article . 2004
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Growth hormone is a positive regulator of Adiponectin Receptor 2 in 3T3-L1 Adipocytes

Authors: Ulrike Lossner; Mathias Fasshauer; Margit Klier; S Krahlisch; Ralf Paschke; Matthias Blüher; Johannes Klein;

Growth hormone is a positive regulator of Adiponectin Receptor 2 in 3T3-L1 Adipocytes

Abstract

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 α, 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.

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Keywords

Adiponectin receptor, Time Factors, Dose-Response Relationship, Drug, Reverse Transcriptase Polymerase Chain Reaction, Diabetes, Insulin resistance, Cell Differentiation, Receptors, Cell Surface, 3T3 Cells, Culture Media, Serum-Free, Mice, Gene Expression Regulation, Growth Hormone, Adipocytes, Animals, Adiponectin, Obesity, RNA, Messenger, Receptors, Adiponectin, 3T3-L1 adipocyte, Growth hormone, Cells, Cultured

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
98
Top 10%
Top 10%
Top 1%
bronze