Year: 2025
Type: article
Abstract: Natural killer (NK) cells are cytotoxic innate lymphocytes that represent the first line of defense against pathogen infections and tumor growth thanks to their ability to kill cancerous or infected cells and release pro-inflammatory cytokines. NK cell activation is regulated by the expression of a wide array of inhibitory receptors for MHC-I molecules and activating receptors, including NKG2D, which recognize self-ligands upregulated on stressed and damaged cells. Even though the expression of NKG2D ligands (NKG2DL) flags the target cells for NK cell-mediated elimination, a persistent interaction of NKG2D with its ligands promotes receptor downregulation, mainly through the internalization and lysosomal degradation of NKG2D/NKG2DL complexes, thus leading to an exhausted phenotype. On both human and murine NK cells, this phenotype is characterized by the down-modulation of the cytolytic machinery and the upregulation of inhibitory receptors.In this review, we discuss the current knowledge on the contribution of the NKG2D/NKG2DL axis in both NK cell-mediated clearance of infected and transformed cells and in the dysregulation of NK cell activity due to chronic exposure to NKG2DLs during tumorigenesis.
Source: AIMS Allergy and Immunology
Institutions: Istituto Pasteur, Sapienza University of Rome
Language: English
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: diamond
OpenAlex ID: W4410328156