Retracted: S100A9 gene silencing inhibits the release of pro‐inflammatory cytokines by blocking the IL ‐17 signalling pathway in mice with acute pancreatitis

• Published in: Journal of cellular and molecular medicine Vol. 22; no. 4; pp. 2378 - 2389
• Main Authors: Wu, Dong‐Mei, Wang, Shan, Shen, Min, Wang, Yong‐Jian, Zhang, Bo, Wu, Zi‐Qi, Lu, Jun, Zheng, Yuan‐Lin
• Format: Journal Article
• Language: English
• Published: Chichester John Wiley & Sons, Inc 01.04.2018
• Subjects: Animal tissues; Apoptosis; Cell cycle; Cell proliferation; Cytokines; Enzyme-linked immunosorbent assay; Flow cytometry; G1 phase; Gene silencing; HMGB1 protein; Immunoglobulin G; Inflammation; Mice; Pancreatitis; Signal transduction; TLR4 protein; Toll-like receptors; Tumor necrosis factor-α; Western blotting; Beijing China; United States > US; China
• ISSN: 1582-1838; 1582-4934
• DOI: 10.1111/jcmm.13532

The study aimed to investigate whether S100A9 gene silencing mediating the IL‐17 pathway affected the release of pro‐inflammatory cytokines in acute pancreatitis (AP). Kunming mice were assigned to the normal, AP, AP + negative control (NC), AP + shRNA, AP + IgG and AP + anti IL‐17 groups. ELISA was applied to measure expressions of AMY, LDH, CRP, TNF‐α, IL‐6 and IL‐8. The cells were distributed into the control, blank, NC, shRNA1 and shRNA2 groups. MTT assay, flow cytometry, RT‐qPCR and Western blotting were used to evaluate cell proliferation, cell cycle and apoptosis, and expressions of S100A9, TLR4, RAGE, IL‐17, HMGB1 and S100A12 in tissues and cells. Compared with the normal group, the AP group displayed increased expressions of AMY, LDH, CRP, TNFα, IL‐6, IL‐8, S100A9, TLR4, RAGE, IL‐17, HMGB1 and S100A12. The AP + shRNA and AP + anti IL‐17 groups exhibited an opposite trend. The in vivo results: Compare with the control group, the blank, NC, shRNA1 and shRNA2 groups demonstrated increased expressions of S100A9, TLR4, RAGE, IL‐17, HMGB1 and S100A12, as well as cell apoptosis and cells at the G1 phase, with reduced proliferation. Compared with the blank and NC groups, the shRNA1 and shRNA2 groups had declined expressions of S100A9, TLR4, RAGE, IL‐17, HMGB1 and S100A12, as well as cell apoptosis and cells at the G1 phase, with elevated proliferation. The results indicated that S100A9 gene silencing suppressed the release of pro‐inflammatory cytokines through blocking of the IL‐17 pathway in AP.