Globular Adiponectin Exerts a Pro-Inflammatory Effect via IκB/NF-κB Pathway Activation and Anti-Inflammatory Effect by IRAK-1 Downregulation

• Published in: Molecules and cells 2018, 41(8), , pp.762-770
• Main Authors: Lee, Kyoung-Hee, Jeong, Jiyeong, Woo, Jisu, Lee, Chang-Hoon, Yoo, Chul-Gyu
• Format: Article
• Language: English
• Subjects: Adiponectin - pharmacology; Animals; Down-Regulation; Humans; I-kappa B Proteins - metabolism; Interleukin-1 Receptor-Associated Kinases - genetics; Interleukin-1 Receptor-Associated Kinases - metabolism; Mice; Neovascularization, Pathologic - metabolism; NF-kappa B - metabolism; Oleanolic Acid - metabolism; Proto-Oncogene Proteins c-akt - metabolism; RAW 264.7 Cells; Receptors, Vascular Endothelial Growth Factor - metabolism; Signal Transduction - drug effects; 생물학
• ISSN: 1016-8478; 0219-1032
• DOI: 10.14348/molcells.2018.0005

Adiponectin, a hormone produced by adipose tissue, is very abundant in plasma, and its anti- and pro-inflammatory effects are reported. However, the mechanisms of these pro- and anti-inflammatory effects are not fully defined. Herein, we evaluated the dual inflammatory response mechanism of adiponectin in macrophages. Short-term globular adiponectin (gAd) treatment induced IκBα degradation, NF-κB nuclear translocation, and TNF-α production in RAW 264.7 cells. Polymyxin B pretreatment did not block gAd-induced IκBα degradation, and heated gAd was unable to degrade IκBα, suggesting that the effects of gAd were not due to endotoxin contamination. gAd activated IKK and Akt, and inhibition of either IKK or Akt by dominant-negative IKKβ (DN-IKKβ) or DN-Akt overexpression blocked gAd-induced IκBα degradation, suggesting that short-term incubation with gAd mediates inflammatory responses by activating the IκB/NF-κB and PI3K/Akt pathways. Contrastingly, long-term stimulation with gAd induced, upon subsequent stimulation, tolerance to gAd, lipopolysaccharide, and CpG-oligodeoxynucleotide, which is associated with gAd-induced downregulation of IL-receptor-associated kinase-1 (IRAK-1) due to IRAK-1 transcriptional repression. Conclusively, our findings demonstrate that the pro- and anti-inflammatory responses to gAd in innate immune cells are time-dependent, and mediated by the activation of the IκB/NF-κB pathway, and IRAK-1 downregulation, respectively.