Hori Arisa, Toyoura Saori, Fujiwara Miyu, Taniguchi Ren, Kano Yasutaka, Yamano Tomoyoshi, Hanayama Rikinari, Nakayama Masafumi
Laboratory of Immunology and Microbiology, College of Pharmaceutical Sciences, Ritsumeikan University, Kusatsu, Shiga 525-8577, Japan.
Department of Immunology, Kanazawa University Graduate School of Medical Sciences, 13-1 Takara-machi, Kanazawa, Ishikawa 920-8640, Japan.
iScience. 2024 Apr 10;27(5):109704. doi: 10.1016/j.isci.2024.109704. eCollection 2024 May 17.
In addition to cross-presentation, cross-dressing plays an important role in the induction of CD8 T cell immunity. In the process of cross-dressing, conventional dendritic cells (DCs) acquire major histocompatibility complex class I (MHCI) from other cells and subsequently prime CD8 T cells via the pre-formed antigen-MHCI complexes without antigen processing. However, the mechanisms underlying the cross-dressing pathway, as well as the relative contributions of cross-presentation and cross-dressing to CD8 T cell priming are not fully understood. Here, we demonstrate that DCs rapidly acquire MHCI-containing membrane fragments from dead cells via the phosphatidylserine recognition-dependent mechanism for cross-dressing. The MHCI dressing is enhanced by a TLR3 ligand polyinosinic-polycytidylic acid (polyI:C). Further, polyI:C promotes not only cross-presentation but also cross-dressing . Taken together, these results suggest that cross-dressing as well as cross-presentation is involved in inflammatory diseases associated with cell death and type I IFN production.
除了交叉呈递外,交叉着装在CD8 T细胞免疫的诱导中也起着重要作用。在交叉着装过程中,常规树突状细胞(DCs)从其他细胞获取主要组织相容性复合体I类(MHCI),随后通过预先形成的抗原-MHCI复合物激活CD8 T细胞,而无需进行抗原加工。然而,交叉着装途径的潜在机制以及交叉呈递和交叉着装对CD8 T细胞激活的相对贡献尚未完全了解。在这里,我们证明DCs通过依赖磷脂酰丝氨酸识别的交叉着装机制从死细胞中快速获取含MHCI的膜片段。TLR3配体聚肌苷酸-聚胞苷酸(polyI:C)可增强MHCI着装。此外,polyI:C不仅促进交叉呈递,还促进交叉着装。综上所述,这些结果表明交叉着装以及交叉呈递与与细胞死亡和I型干扰素产生相关的炎症性疾病有关。