细胞毒性T细胞
免疫系统
细胞生物学
CD8型
MHC I级
生物
主要组织相容性复合体
免疫学
化学
遗传学
体外
作者
Shiyu Ayukawa,Nagisa Kamoshita,Jun Nakayama,Ryohei Teramoto,Novalia Pishesha,Kenji Ohba,Nanami Sato,Kei Kozawa,Hikari Abe,Kentaro Semba,Nobuhito Goda,Yasuyuki Fujita,Takeshi Maruyama
出处
期刊:Nature Immunology
[Nature Portfolio]
日期:2021-10-22
卷期号:22 (11): 1391-1402
被引量:44
标识
DOI:10.1038/s41590-021-01045-6
摘要
Epithelial cells have an ability termed ‘cell competition’, which is an immune surveillance-like function that extrudes precancerous cells from the epithelial layer, leading to apoptosis and clearance. However, it remains unclear how epithelial cells recognize and extrude transformed cells. Here, we discovered that a PirB family protein, leukocyte immunoglobulin-like receptor B3 (LILRB3), which is expressed on non-transformed epithelial cells, recognizes major histocompatibility complex class I (MHC class I) that is highly expressed on transformed cells. MHC class I interaction with LILRB3 expressed on normal epithelial cells triggers an SHP2–ROCK2 pathway that generates a mechanical force to extrude transformed cells. Removal of transformed cells occurs independently of natural killer (NK) cell or CD8+ cytotoxic T cell-mediated activity. This is a new mechanism in that the immunological ligand–receptor system generates a mechanical force in non-immune epithelial cells to extrude precancerous cells in the same epithelial layer. Epithelial cells can use an immune-like mechanism to extrude neighboring precancerous cells; however, the recognition and control mechanisms of this process are unclear. Maruyama and colleagues demonstrate that LILRB3 on normal epithelial cells recognizes elevated MHC class I on transformed cells and triggers the extrusion process.
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