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P815-based redirected degranulation assay to study human NK cell effector functions.

Authors :
Terrén I
Astarloa-Pando G
Amarilla-Irusta A
Borrego F
Source :
Methods in cell biology [Methods Cell Biol] 2023; Vol. 173, pp. 33-48. Date of Electronic Publication: 2022 Mar 15.
Publication Year :
2023

Abstract

Natural killer (NK) cells are part of the innate immune system, the classic cytotoxic population of innate lymphoid cells (ILCs). They can directly kill virus-infected or tumor cells through different mechanisms without prior sensitization using their lytic functions in response to different signals (target cell ligands and/or inflammatory cytokines) and secreting cytokines, such as interferon gamma (IFNγ) and tumor necrosis factor (TNF). NK cells use antibody-dependent cell-mediated cytotoxicity (ADCC) to recognize and kill cells expressing target antigens when they are antibody coated. Redirected cytotoxicity is a technique used to target cells that do not per se activate NK cells. Here, we use redirected degranulation, a surrogate technique that correlates with redirected lysis. The P815 cell line (mouse mastocytoma) express fragment crystallizable gamma receptor II (FcγRII) and therefore could bind the Fc portion of mouse IgG antibodies, which through their fragment antigen-binding (Fab) may recognize NK cells activating receptors leading to target cell lysis. This technique could be used to determine the inhibitory or activating capacity of different receptors or isoforms and in immunotherapy using T cell and NK cell activators.<br />Competing Interests: Conflict of interests The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2023 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
0091-679X
Volume :
173
Database :
MEDLINE
Journal :
Methods in cell biology
Publication Type :
Academic Journal
Accession number :
36653084
Full Text :
https://doi.org/10.1016/bs.mcb.2022.02.002