Department of Molecular Pharmacology, School of Medicine and Pharmacy, Ocean University of China, Qingdao, People's Republic of China.
Mol Cell Biochem. 2010 Apr;337(1-2):277-85. doi: 10.1007/s11010-009-0309-9.
In the previous studies, MS80 was found to be able to inhibit the pulmonary fibrosis. However, the target of MS80 remains unclear. To determine the target and the antifibrosis mechanisms of MS80, affinity column, MALDITOF-MS/MS, co-immunoprecipitation, and co-localization were used. The results showed that MS80 targeting protein was receptor interacting protein 2 (RIP2), which was further confirmed by co-immunoprecipitation and co-localization. Moreover, MS80 inhibited the CD40 ligation-induced NF-kappaB activation, and subsequently inflammatory cytokines secretion, the collagen synthesis, and the excessive proliferation of fibroblasts. Thus the detailed molecular machinery was ascribed to the involvement of MS80 in targeting CD40 signal pathway via binding and blocking RIP2, the key component of CD40 signal transduction. The findings addressed here may substantially account for the effects of MS80 in combating the pulmonary fibrosis.
在之前的研究中,MS80 被发现能够抑制肺纤维化。然而,MS80 的靶点仍不清楚。为了确定 MS80 的靶点和抗纤维化机制,使用了亲和柱、MALDITOF-MS/MS、共免疫沉淀和共定位。结果表明,MS80 的靶蛋白是受体相互作用蛋白 2(RIP2),这一点通过共免疫沉淀和共定位得到了进一步证实。此外,MS80 抑制了 CD40 配体诱导的 NF-κB 激活,进而抑制了炎症细胞因子的分泌、胶原合成和纤维母细胞的过度增殖。因此,通过与 CD40 信号转导的关键组成部分 RIP2 结合和阻断,MS80 参与靶向 CD40 信号通路的详细分子机制被归因于 MS80 在抑制肺纤维化中的作用。本研究结果可能充分解释了 MS80 对抗肺纤维化的作用。