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. 2014 Mar 28;446(1):37-42.
doi: 10.1016/j.bbrc.2014.02.077. Epub 2014 Feb 25.

Globular adiponectin induces a pro-inflammatory response in human astrocytic cells

Zhongxiao Wan  1 , Dorrian Mah  1 , Svetlana Simtchouk  1 , Andis Klegeris  2 , Jonathan P Little  3
Affiliations

Globular adiponectin induces a pro-inflammatory response in human astrocytic cells

Zhongxiao Wan et al. Biochem Biophys Res Commun. .

Abstract

Neuroinflammation, mediated in part by activated brain astrocytes, plays a critical role in the development of neurodegenerative disorders, including Alzheimer's disease (AD). Adiponectin is the most abundant adipokine secreted from adipose tissue and has been reported to exert both anti- and pro-inflammatory effects in peripheral tissues; however, the effects of adiponectin on astrocytes remain unknown. Shifts in peripheral concentrations of adipokines, including adiponectin, could contribute to the observed link between midlife adiposity and increased AD risk. The aim of the present study was to characterize the effects of globular adiponectin (gAd) on pro-inflammatory cytokine mRNA expression and secretion in human U373 MG astrocytic cells and to explore the potential involvement of nuclear factor (NF)-κB, p38 mitogen-activated protein kinase (MAPK), extracellular signal-regulated kinase (ERK)1/2, c-Jun N-terminal kinase (JNK) and phosphatidylinositide 3-kinases (PI3K) signaling pathways in these processes. We demonstrated expression of adiponectin receptor 1 (adipoR1) and adipoR2 in U373 MG cells and primary human astrocytes. gAd induced secretion of interleukin (IL)-6 and monocyte chemoattractant protein (MCP)-1, and gene expression of IL-6, MCP-1, IL-1β and IL-8 in U373 MG cells. Using specific inhibitors, we found that NF-κB, p38MAPK and ERK1/2 pathways are involved in gAd-induced induction of cytokines with ERK1/2 contributing the most. These findings provide evidence that gAd may induce a pro-inflammatory phenotype in human astrocytes.

Keywords: Astrocytes; Extracellular signal-regulated kinase (ERK) 1/2; Globular adiponectin; Neuroinflammation.

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