| Literature DB >> 26556104 |
Tsuyoshi Goto1, Supaporn Naknukool2, Rieko Yoshitake2, Yuki Hanafusa2, Soshi Tokiwa2, Yongjia Li2, Tomoya Sakamoto2, Takahiro Nitta2, Minji Kim2, Nobuyuki Takahashi1, Rina Yu3, Hiromi Daiyasu4, Shigeto Seno4, Hideo Matsuda4, Teruo Kawada5.
Abstract
In this study, we investigated the effects of interleukin-1β (IL-1β), a typical proinflammatory cytokine on the β-adrenoreceptor-stimulated induction of uncoupling protein 1 (UCP1) expression in adipocytes. IL-1β mRNA expression levels were upregulated in white adipose tissues of obese mice and in RAW264.7 macrophages under conditions designed to mimic obese adipose tissue. Isoproterenol-stimulated induction of UCP1 mRNA expression was significantly inhibited in C3H10T1/2 adipocytes by conditioned medium from lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages in comparison with control conditioned medium. This inhibition was significantly attenuated in the presence of recombinant IL-1 receptor antagonist and IL-1β antibody, suggesting that activated macrophage-derived IL-1β is an important cytokine for inhibition of β-adrenoreceptor-stimulated UCP1 induction in adipocytes. IL-1β suppressed isoproterenol-induced UCP1 mRNA expression in C3H10T1/2 adipocytes, and this effect was partially but significantly abrogated by inhibition of extracellular signal-regulated kinase (ERK). IL-1β also suppressed the isoproterenol-induced activation of the UCP1 promoter and transcription factors binding to the cAMP response element. Moreover, intraperitoneal administration of IL-1β suppressed cold-induced UCP1 expression in adipose tissues. These findings suggest that IL-1β upregulated in obese adipose tissues suppresses β-adrenoreceptor-stimulated induction of UCP1 expression through ERK activation in adipocytes.Entities:
Keywords: Brown adipocyte; Brown-like adipocyte; IL-1β; Inflammation; Obesity; UCP1
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Year: 2015 PMID: 26556104 DOI: 10.1016/j.cyto.2015.11.001
Source DB: PubMed Journal: Cytokine ISSN: 1043-4666 Impact factor: 3.861