Department of Life Sciences, National Chung Hsing University (NCHU), Taichung, 40227, Taiwan.
Ph.D. Program in Tissue Engineering and Regenerative Medicine, National Chung Hsing University, Taichung, 40227, Taiwan.
Cell Mol Biol Lett. 2022 Mar 2;27(1):19. doi: 10.1186/s11658-022-00312-0.
Peptididylarginine deiminase type 2 (PADI2) catalyzes the conversion of arginine residues to citrulline residues on proteins. We demonstrate that PADI2 induces T cell activation and investigate how PADI2 promotes activated T cell autonomous death (ACAD). In activated Jurkat T cells, overexpression of PADI2 significantly increases citrullinated proteins and induces endoplasmic reticulum (ER) stress and unfolded protein response (UPR) signaling, ultimately resulting in the expression of autophagy-related proteins and autophagy. PADI2 promoted autophagy and resulted in the early degradation of p62 and the light chain 3B (LC3B)-II accumulation. In Jurkat T cells, silencing the autophagy-related gene (Atg) 12 protein inhibits PADI2-mediated autophagy and promotes ER stress and apoptosis, whereas overexpression of Atg12 decreased ER stress and prolonged autophagy to promote cell survival. Additionally, PADI2 regulates T cell activation and the production of Th17 cytokines in Jurkat T cells (interleukins 6, IL-17A, IL-17F, IL-21, and IL-22). In Jurkat T cells, silencing IL-6 promotes autophagy mediated by PADI2 and inhibits PADI2-induced apoptosis, whereas silencing Beclin-1 increases the activation and survival of Th17-like T cells while decreasing autophagy and apoptosis. PADI2 silencing alleviates ER stress caused by PADI2 and decreases cytokine expression associated with Th17-like T cell activation and ACAD. We propose that PADI2 was involved in Th17 lymphocyte ACAD via a mechanism involving ER stress and autophagy that was tightly regulated by PADI2-mediated citrullination. These findings suggest that inhibiting Th17 T cell activation and the development of severe autoimmune diseases may be possible through the use of novel antagonists that specifically target PADI2.
肽基精氨酸脱亚氨酶 2(PADI2)催化蛋白质上精氨酸残基向瓜氨酸残基的转化。我们证明 PADI2 诱导 T 细胞活化,并研究了 PADI2 如何促进活化 T 细胞自主死亡(ACAD)。在活化的 Jurkat T 细胞中,过表达 PADI2 可显著增加瓜氨酸化蛋白,并诱导内质网(ER)应激和未折叠蛋白反应(UPR)信号转导,最终导致自噬相关蛋白和自噬的表达。PADI2 促进自噬,并导致 p62 和轻链 3B(LC3B)-II 积累的早期降解。在 Jurkat T 细胞中,沉默自噬相关基因(Atg)12 蛋白抑制 PADI2 介导的自噬并促进 ER 应激和细胞凋亡,而 Atg12 的过表达则降低 ER 应激并延长自噬以促进细胞存活。此外,PADI2 调节 Jurkat T 细胞中的 T 细胞活化和 Th17 细胞因子的产生(白细胞介素 6、IL-17A、IL-17F、IL-21 和 IL-22)。在 Jurkat T 细胞中,沉默 IL-6 促进 PADI2 介导的自噬并抑制 PADI2 诱导的细胞凋亡,而沉默 Beclin-1 增加 Th17 样 T 细胞的活化和存活,同时减少自噬和细胞凋亡。PADI2 沉默减轻了由 PADI2 引起的 ER 应激,并降低了与 Th17 样 T 细胞活化和 ACAD 相关的细胞因子表达。我们提出,PADI2 通过一种由 PADI2 介导的瓜氨酸化严格调控的 ER 应激和自噬机制参与 Th17 淋巴细胞的 ACAD。这些发现表明,通过使用专门针对 PADI2 的新型拮抗剂抑制 Th17 T 细胞活化和严重自身免疫性疾病的发展是可能的。