交叉展示
CTL公司*
细胞毒性T细胞
抗原
细胞生物学
MHC I级
抗原处理
CD8型
免疫系统
抗原呈递
免疫学
生物
内吞循环
T细胞
T淋巴细胞
抗原提呈细胞
树突状细胞
内体
表位
免疫
调节器
主要组织相容性复合体
化学
内生
获得性免疫系统
MHC II级
淋巴细胞
细胞
作者
Zhi-kai Zha,Cheng-jie Deng,Ling-jun Shen,Ling‐Zhen Liu,Yun-Xiao Huang,Yan-hong Li,Li Lv,Ke Zhang,Lin-shuang CHEN,Fei-er Chen,Sheng‐An Li
标识
DOI:10.1038/s41419-026-08705-1
摘要
Abstract Antigen cross-presentation is essential for initiating CD8 + cytotoxic T lymphocyte (CTL) response. Perforin-2 (P2), a pore-forming protein constitutively expressed in dendritic cells (DCs), has been implicated in endocytic cargo escape, but its role in cross-presentation remains poorly defined. Here, we show that loss of P2 markedly impairs DC-mediated cross-presentation of both soluble and particulate antigens, leading to weakened antigen-specific CD8 + T cell responses. Additionally, P2 -/- mice exhibited defective endogenous CTL responses and diminished anti-tumor immunity in melanoma models. Mechanistically, oligomerization of plasma membrane P2 promotes antigen uptake via membrane-repair-mediated macropinocytosis. In parallel, P2 limits excessive endosomal acidification, preserving antigens for efficient loading onto MHC class I molecules. These findings identify P2 as a key regulator that coordinates antigen uptake and processing to support effective cross-presentation and CD8 + T cell immunity.
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