4.5 Article

Interleukin-1β is a positive regulator of TIARP/STAMP2 gene and protein expression in adipocytes in vitro

Journal

FEBS LETTERS
Volume 583, Issue 7, Pages 1196-1200

Publisher

WILEY
DOI: 10.1016/j.febslet.2009.03.015

Keywords

Adipocyte; Insulin resistance; Interleukin-1 beta; Obesity; STAMP2; TIARP

Funding

  1. Deutsche Forschungsgemeinschaft (DFG), KFO 152: Atherobesity [FA476/4-1 (TP 4), BL833/1-1]
  2. Deutsche Diabetes Gesellschaft (DDG)
  3. European Section of the Aldosterone Council (ESAC) Deutschland

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The impact of interleukin (IL)-1 beta on tumor necrosis factor alpha-induced adipose-related protein (TIARP)/six-transmembrane protein of prostate 2 (STAMP2) was determined in adipocytes. TIARP/STAMP2 mRNA synthesis was significantly stimulated by IL-1 beta in a dose- and time-dependent fashion in 3T3-L1 adipocytes. Signaling studies suggested that janus kinase 2, nuclear factor kappa B, and p44/42 mitogen-activated protein kinase are involved in IL-1 beta-induced TIARP/STAMP2 mRNA expression. Furthermore, IL-1 beta, TNF alpha, and IL-6 showed synergistic stimulatory effects on TIARP/STAMP2 gene expression. Moreover, both TIARP/STAMP2 mRNA synthesis and protein expression were induced by IL-1 beta in fully differentiated human mesenchymal stem cell-derived adipocytes (hMSC-Ad). Taken together, TIARP/STAMP2 is highly upregulated in 3T3-L1 cells and hMSC-Ad by IL-1 beta and might, therefore, modulate proinflammatory and insulin resistance-inducing effects of IL-1 beta. (C) 2009 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.

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