Department of Rheumatology, Endocrinology and Nephrology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Department of Orthopedic Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Autophagy. 2020 May;16(5):946-955. doi: 10.1080/15548627.2019.1664144. Epub 2019 Sep 8.
We aimed to investigate the involvement of macroautophagy/autophagy in autoimmunity in rheumatoid arthritis (RA) through citrullination of VIM (vimentin) and its interaction with MHC class II in synovial fibroblasts (SFs). The cell surface expression of MHC class II and B7 costimulatory molecules on SFs was analyzed by flow cytometry after treatment with IFNG/IFN-γ (interferon gamma). Intracellular citrullinated autoantigens in SFs were analyzed by immunoblotting using serum from anti-citrullinated peptide antibodies (ACPA)-positive patient as a primary antibody. SFs were incubated in serum-free medium or treated with proteasome inhibitor MG132 to induce autophagy. An autophagy inhibitor 3-methyladenin (3-MA) was used. Intracellular citrullinated VIM (cVIM) was evaluated by immunoblotting and immunocytochemistry. The interaction between MHC class II and cVIM was evaluated with co-immunoprecipitation and proximity ligation assay (PLA). We demonstrated that MHC class II, CD274/B7-H1 and PDCD1LG2/B7-DC were expressed on SFs following treatment with IFNG whereas CD276/B7-H3 was detected on SFs regardless of the presence of IFNG. ACPA-positive sera recognized a 54 kDa protein in SFs. By immunoprecipitation, the 54 kDa protein recognized by RA sera was revealed to be cVIM. Following induction of autophagy, intracellular cVIM was increased in SFs but the effect was canceled by 3-MA. The interaction between MHC class II and cVIM was demonstrated by co-immunoprecipitation. Furthermore, PLA revealed the significant increase of MHC class II-cVIM interaction following induction of autophagy. Our findings suggest that SFs may contribute to the autoimmunity in RA through citrullination of VIM and its interaction with MHC class II promoted by autophagy. 3-MA: 3-methyladenine; ACPA: anti-citrullinated peptide antibodies; anti-CCP: anti-cyclic citrullinated peptide antibody; cVIM: citrullinated VIM; BECN1: beclin1; DAPI: 4',6-diamidino-2-phenylindole; FBS: fetal bovine serum; HLA: human leukocyte antigen; IFNG/IFN-γ: interferon gamma; IL6: interleukin 6; IP: immunoprecipitation; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; MFI: mean fluorescence index; MHC: major histocompatibility complex; OA: osteoarthritis; PADI: peptidyl arginine deiminase; PepA: pepstatin A; PBS: phosphate-buffered saline; PtdIns3K: phosphatidylinositol 3-kinase; RA: rheumatoid arthritis; SFs: synovial fibroblasts; siRNA: small interfering RNA; VIM: vimentin.
我们旨在通过 VIM(波形蛋白)的瓜氨酸化及其与滑膜成纤维细胞(SFs)中 MHC Ⅱ类的相互作用来研究巨自噬/自噬在类风湿关节炎(RA)中的自身免疫作用。用 IFNG/IFN-γ(干扰素γ)处理后,通过流式细胞术分析 SFs 上 MHC Ⅱ类和 B7 共刺激分子的细胞表面表达。用抗瓜氨酸肽抗体(ACPA)阳性患者的血清作为一抗,通过免疫印迹分析 SFs 中的细胞内瓜氨酸化自身抗原。SFs 在无血清培养基中孵育或用蛋白酶体抑制剂 MG132 处理以诱导自噬。使用自噬抑制剂 3-甲基腺嘌呤(3-MA)。通过免疫印迹和免疫细胞化学评估细胞内瓜氨酸化 VIM(cVIM)。通过共免疫沉淀和邻近连接分析评估 MHC Ⅱ类和 cVIM 之间的相互作用。我们证明,IFNG 处理后 SFs 上表达 MHC Ⅱ类、CD274/B7-H1 和 PDCD1LG2/B7-DC,而 CD276/B7-H3 则无论是否存在 IFNG 均可在 SFs 上检测到。ACPA 阳性血清在 SFs 中识别出 54 kDa 蛋白。通过免疫沉淀,RA 血清识别的 54 kDa 蛋白被揭示为 cVIM。自噬诱导后,SFs 中的细胞内 cVIM 增加,但 3-MA 可消除该作用。通过共免疫沉淀证明 MHC Ⅱ类和 cVIM 之间存在相互作用。此外,PLA 显示自噬诱导后 MHC Ⅱ-cVIM 相互作用显著增加。我们的研究结果表明,SFs 可能通过自噬诱导的 VIM 瓜氨酸化及其与 MHC Ⅱ类的相互作用,促进 RA 中的自身免疫。3-MA:3-甲基腺嘌呤;ACPA:抗瓜氨酸肽抗体;抗-CCP:抗环瓜氨酸肽抗体;cVIM:瓜氨酸化 VIM;BECN1:beclin1;DAPI:4',6-二脒基-2-苯基吲哚;FBS:胎牛血清;HLA:人类白细胞抗原;IFNG/IFN-γ:干扰素γ;IL6:白细胞介素 6;IP:免疫沉淀;MAP1LC3/LC3:微管相关蛋白 1 轻链 3;MFI:平均荧光指数;MHC:主要组织相容性复合体;OA:骨关节炎;PADI:肽基精氨酸脱亚氨酶;PepA:胃蛋白酶抑制剂 A;PBS:磷酸盐缓冲盐水;PtdIns3K:磷脂酰肌醇 3-激酶;RA:类风湿关节炎;SFs:滑膜成纤维细胞;siRNA:小干扰 RNA;VIM:波形蛋白。