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Selective Harvesting of Marginating-hepatic Leukocytes
Published on: July 21, 2016
Murine non-lymphoid tumors are lysed by a combination of NK and NC cells
Abstract:
Natural cell-mediated cytotoxicity (NCMC) against a variety of tumor targets is mediated by a heterogeneous group of effector cells with the natural killer (NK) and natural cytotoxic (NC) cells being the predominant prototypes in mice. This report shows that non-lymphoid tumor targets, mostly derived from chemically induced fibrosarcomas, are susceptible to either (1) NK-mediated lysis with all the activity being the function of a poly-IC augmentable Qa-5+ effector cell; (2) NC-mediated lysis with all activity being the function of a Qa-5- cell not augmented by poly-IC; and (3) a combination of NK-and NC-mediated lysis with activity being the function of both Qa-5+ and Qa-5- cells, the NK (Qa-5+) augmented by poly-IC. These studies further support the view that murine NC and NK cells are distinct and collectively make up the NCMC system, and also that the previous association of NK cells with lymphoid tumor lysis and NC cells with non-lymphoid tumor lysis is not a valid one.
Insights
Natural cell-mediated cytotoxicity involves distinct natural killer (NK) and natural cytotoxic (NC) cells. These cells target various tumors, challenging previous assumptions about their specific roles in tumor lysis.
Area of Science:
- Immunology
- Cell Biology
Background:
- Natural cell-mediated cytotoxicity (NCMC) is crucial for tumor surveillance.
- Natural killer (NK) and natural cytotoxic (NC) cells are key effector cells in NCMC.
- Previous research suggested distinct roles for NK and NC cells in targeting lymphoid versus non-lymphoid tumors.
Purpose of the Study:
- To investigate the distinct roles and characteristics of NK and NC cells in targeting non-lymphoid tumor cells.
- To determine if poly-IC augmentation differentiates NK and NC cell activity.
- To re-evaluate the association of NK and NC cells with specific tumor types.
Main Methods:
- Utilized chemically induced fibrosarcomas as non-lymphoid tumor targets.
- Assessed susceptibility to lysis mediated by NK (Qa-5+) and NC (Qa-5-) effector cells.
- Investigated the effect of poly-IC augmentation on effector cell activity.
Main Results:
- Non-lymphoid tumors were susceptible to lysis by both NK (poly-IC augmentable, Qa-5+) and NC (non-augmentable, Qa-5-) cells.
- Three lysis patterns were observed: NK-mediated, NC-mediated, and combined NK/NC-mediated.
- NK cell activity was augmented by poly-IC, while NC cell activity was not.
Conclusions:
- Murine NK and NC cells are distinct effector cell populations within the NCMC system.
- The NCMC system comprises both NK and NC cells, which collectively mediate cytotoxicity.
- The prior association of NK cells with lymphoid tumors and NC cells with non-lymphoid tumors is not accurate.
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