Sun Chi, Yu Zhaohui, Wang Youhua, Tao Tao
Jiangsu Province Key Laboratory for Inflammation and Molecular Drug Target, Department of Immunology, Medical College, Nantong University, Nantong, 226001, PR China.
Department of Orthopedics, Affiliated Hospital of Nantong University, Nantong, 226001, PR China.
Biochem Biophys Res Commun. 2016 Mar 18;471(4):553-9. doi: 10.1016/j.bbrc.2016.02.033. Epub 2016 Feb 12.
Karyopherin-β1 (KPNB1) which is an adaptor protein which transports several proteins to the nucleus. We study the functions and possible mechanisms of KPNB1 in collagen-induced arthritis (CIA). Western blotting and immunohistochemistry shows the protein expression of KPNB1 is increased in synovial tissue of CIA mice compared with the controls. Double immunofluorescent staining suggests that KPNB1 is expressed in CIA mice fibroblast-like synoviocytes (FLS). Moreover, the expression of KPNB1 in FLS is upregulated in time-dependent manner by IL-1β stimulation. Both immunoprecipitation and immunofluorescent staining assay reveals the interaction between KPNB1 and STAT3 and their translocation from cytoplasm to nucleus in IL-1β-treated FLS. Furthermore, suppression of KPNB1 inhibits IL-1β-induced the nucleus expression of STAT3 in FLS and decreases the expression of IL-6 and MMP-1, leading to attenuation of FLS invasion. Finally, the transport function of KPNB1 is depended on KPNA2. Therefore, we infer that KPNB1 may play a key role in the inflammation process of RA via STAT3 signal transduction pathway.
核转运蛋白-β1(KPNB1)是一种衔接蛋白,可将多种蛋白质转运至细胞核。我们研究了KPNB1在胶原诱导性关节炎(CIA)中的功能及可能机制。蛋白质印迹法和免疫组织化学显示,与对照组相比,CIA小鼠滑膜组织中KPNB1的蛋白表达增加。双重免疫荧光染色表明,KPNB1在CIA小鼠的成纤维细胞样滑膜细胞(FLS)中表达。此外,IL-1β刺激可使FLS中KPNB1的表达呈时间依赖性上调。免疫沉淀和免疫荧光染色试验均显示,在IL-1β处理的FLS中,KPNB1与信号转导和转录激活因子3(STAT3)相互作用并从细胞质转位至细胞核。此外,抑制KPNB1可抑制IL-1β诱导的FLS中STAT3的核表达,并降低白细胞介素-6(IL-6)和基质金属蛋白酶-1(MMP-1)的表达,从而减弱FLS的侵袭。最后,KPNB1的转运功能依赖于核转运蛋白α2(KPNA2)。因此,我们推断KPNB1可能通过STAT3信号转导通路在类风湿关节炎(RA)的炎症过程中起关键作用。