School of Basic Medical Sciences, Xi'an Jiaotong University, Xi'an, Shanxi 710061, China.
Institute of Biochemistry and Molecular Biology, School of Life Sciences, Lanzhou University, Lanzhou 730000, China.
Molecules. 2019 Aug 3;24(15):2832. doi: 10.3390/molecules24152832.
: This study aimed to investigate the protective effects of MMI-0100, a cell-penetrating peptide inhibitor of MAPK-activated protein kinase II (MK2), on acute colitis induced by dextran sodium sulfate (DSS). Mice were injected intraperitoneally with different doses of MMI-0100 (0.5 and 1 mg/kg per day, six days). The physiological indexes, the parameters for colonic pathological injury and the intensity of inflammatory responses were evaluated by histological staining, quantitative PCR, western blotting, and immunostaining. MMI-0100 attenuated DSS-induced body weight loss, colon length shortening, and colonic pathological injury, including decreased myeloperoxidase (MPO) and inhibited inflammatory cell infiltration. MMI-0100 suppressed DSS-induced activation of CD11b and F4/80 positive cell, and dramatically decreased the expression of a series of pro-inflammatory cytokines such as TNF-α, IL-6, IL-1β, TGF- β, IFN-γ, IL-17A, COX-2 and iNOS. A TUNEL assay showed that MMI-0100 protected against DSS-induced apoptosis. This is consistent with the results of Western blotting assay in apoptosis-related proteins including Bcl-2, BAX, caspase-3. The anti-inflammatory effects of MMI-0100 on DSS-induced colitis were achieved by down-regulating the phosphorylation level of MK2, IκBα and p65 protein. The current study clearly demonstrates a protective role for MMI-0100 in experimental IBD.
本研究旨在探讨细胞穿透肽 MAPK 激活蛋白激酶 II(MK2)抑制剂 MMI-0100 对葡聚糖硫酸钠(DSS)诱导的急性结肠炎的保护作用。将不同剂量的 MMI-0100(0.5 和 1 mg/kg,每天 6 次)腹腔注射到小鼠体内。通过组织学染色、定量 PCR、western blot 和免疫染色评估生理指标、结肠病理损伤参数和炎症反应强度。MMI-0100 减轻了 DSS 诱导的体重减轻、结肠缩短和结肠病理损伤,包括降低髓过氧化物酶(MPO)和抑制炎症细胞浸润。MMI-0100 抑制了 DSS 诱导的 CD11b 和 F4/80 阳性细胞的激活,并显著降低了一系列促炎细胞因子的表达,如 TNF-α、IL-6、IL-1β、TGF-β、IFN-γ、IL-17A、COX-2 和 iNOS。TUNEL 检测表明 MMI-0100 可防止 DSS 诱导的细胞凋亡。这与凋亡相关蛋白包括 Bcl-2、BAX、caspase-3 的 western blot 检测结果一致。MMI-0100 通过下调 MK2、IκBα 和 p65 蛋白的磷酸化水平,对 DSS 诱导的结肠炎发挥抗炎作用。本研究清楚地表明 MMI-0100 在实验性 IBD 中具有保护作用。