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Global adiponectin suppress the high expression of monocyte chemotactic protein-1 induced by high glucose in NRK52E cells
Authors:Yao Tao  Wu Xiaoyan  Yu Wenli  Gao Ping  Wu Yizhe.
Affiliation:Department of Nephrology, Zhongnan Hospital of Wuhan University, Wuhan 430071, China ;Corresponding author: Wu Xiaoyan, Email: wuxiaoyan2k6@163.com
Abstract:Objective To investigate the effect of globular adiponectin on the high expression of monocyte chemotactic protein-1 (MCP-1) induced by high glucose in rat renal tubular epithelial cells(NRK52E), and its relationship with adiponectin receptors and p38MAPK. Methods NRK52E cells were cultured in vitro and divided into six groups: normal glucose group (NG, 5.6 mmol/L glucose), high glucose group(HG, 25 mmol/L glucose), gAd group1 (HG+gAd 2 mg/L), gAd group2 (HG+gAd 5 mg/L), gAd group3 (HG+gAd 10 mg/L), p38MAPK antagonist group:(SB, HG+SB203580 10 μmol/L). The protein expression of phosphorylated p38MAPK (p-p38MAPK), total p38MAPK (t-p38MAPK), MCP-1 and AdipoR1/AdipoR2 were examined by western blotting. The mRNA expression of MCP-1 and AdipoR1/AdipoR2 were detected by RT-PCR and real-time PCR respectively. Results Compared with NG group, the mRNA and protein expression of MCP-1 increased significantly in HG group (all P<0.05). The phosphorylation of p38MAPK increased (P<0.05) with no change in t-p38MAPK protein. The addition of gAd or SB203580 inhibited the unregulation of MCP-1 and p-p38MAPK induced by HG. Two kinds of adipoR,adipoR1 and adipoR2,were all detectable in NG group, and mRNA and protein expression of adipoR1 was higher than that of adipoR2 (P<0.01). Compared with NG group, the expression of adipoR decreased in HG group, but the difference had no statistical significance(P>0.05). Compared to HG group, the mRNA and protein expression of adipoR1 increased in gAd groups (all P<0.01). Conclusion The gAd can dose-dependently attenuate the overexpression of MCP-1 induced by high glucose, and this protective effect may be mediated by adipoR1 and p38MAPK.
Keywords:Adiponectin     ,Receptors, adiponectin     ,Chemokine CCL2     ,p38 mitogen-activated protein kinases,
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