Characterization of natural killer (NK) cells and killer (K) cells in human blood: Discrimination between NK and K cell activities

Cell suspensions enriched and depleted for rosette‐forming cells with sheep red blood cells (E‐RFC) and depleted for RFC with antibody complexes were prepared. The isolated fractions were characterized by cell surface marker analysis and tested for their natural killer (NK) and killer (K) cell activ...

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Veröffentlicht in:European journal of immunology 1978-10, Vol.8 (10), p.731-740
Hauptverfasser: Bolhuis, R. L. H., Schuit, H. R. E., Nooyen, A. M., Ronteltap, C. P. M.
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container_end_page 740
container_issue 10
container_start_page 731
container_title European journal of immunology
container_volume 8
creator Bolhuis, R. L. H.
Schuit, H. R. E.
Nooyen, A. M.
Ronteltap, C. P. M.
description Cell suspensions enriched and depleted for rosette‐forming cells with sheep red blood cells (E‐RFC) and depleted for RFC with antibody complexes were prepared. The isolated fractions were characterized by cell surface marker analysis and tested for their natural killer (NK) and killer (K) cell activity against K‐562 cells and IgG‐coated P‐815 cells, growing in suspension, and against a number of monolayer tumor cell lines. It was found that the NK cells most likely belong to the T cell lymphocyte subpopulation. Furthermore, this study indicates that several subpopulations exist, e.g. NK cells that have no IgG Fc receptor (FcR) on their surface and NK cells that bear IgG FcR, indicating that for a proportion of NK cells the IgG FcR is not involved in the NK lytic process and hence antibody‐independent. Moreover, monocytes and B lymphocytes appear not to be directly involved in the NK cell lytic process. Furthermore, cell separation procedures were used to obtain cell suspensions either bearing IgG FcR or lacking IgG FcR. Cells bearing IgG FcR were isolated in such a way that they lost their IgG FcR by shedding, as a result of the separation procedure. Again, all fractions were simultaneously characterized by cell surface marker analysis and tested for their NK and K cell lytic activity. The effect of immune complexes on the NK and K cell lytic activities was investigated. The data indicate that the IgG FcR is not involved in the NK lytic mechanism, although this receptor may be present on the NK cell. Moreover, prolonged culturing of lymphocytes increases and/or induces NK cell lytic activity.
doi_str_mv 10.1002/eji.1830081012
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Furthermore, this study indicates that several subpopulations exist, e.g. NK cells that have no IgG Fc receptor (FcR) on their surface and NK cells that bear IgG FcR, indicating that for a proportion of NK cells the IgG FcR is not involved in the NK lytic process and hence antibody‐independent. Moreover, monocytes and B lymphocytes appear not to be directly involved in the NK cell lytic process. Furthermore, cell separation procedures were used to obtain cell suspensions either bearing IgG FcR or lacking IgG FcR. Cells bearing IgG FcR were isolated in such a way that they lost their IgG FcR by shedding, as a result of the separation procedure. Again, all fractions were simultaneously characterized by cell surface marker analysis and tested for their NK and K cell lytic activity. The effect of immune complexes on the NK and K cell lytic activities was investigated. 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E.</creatorcontrib><creatorcontrib>Nooyen, A. M.</creatorcontrib><creatorcontrib>Ronteltap, C. P. M.</creatorcontrib><title>Characterization of natural killer (NK) cells and killer (K) cells in human blood: Discrimination between NK and K cell activities</title><title>European journal of immunology</title><addtitle>Eur J Immunol</addtitle><description>Cell suspensions enriched and depleted for rosette‐forming cells with sheep red blood cells (E‐RFC) and depleted for RFC with antibody complexes were prepared. The isolated fractions were characterized by cell surface marker analysis and tested for their natural killer (NK) and killer (K) cell activity against K‐562 cells and IgG‐coated P‐815 cells, growing in suspension, and against a number of monolayer tumor cell lines. It was found that the NK cells most likely belong to the T cell lymphocyte subpopulation. Furthermore, this study indicates that several subpopulations exist, e.g. NK cells that have no IgG Fc receptor (FcR) on their surface and NK cells that bear IgG FcR, indicating that for a proportion of NK cells the IgG FcR is not involved in the NK lytic process and hence antibody‐independent. Moreover, monocytes and B lymphocytes appear not to be directly involved in the NK cell lytic process. Furthermore, cell separation procedures were used to obtain cell suspensions either bearing IgG FcR or lacking IgG FcR. Cells bearing IgG FcR were isolated in such a way that they lost their IgG FcR by shedding, as a result of the separation procedure. Again, all fractions were simultaneously characterized by cell surface marker analysis and tested for their NK and K cell lytic activity. The effect of immune complexes on the NK and K cell lytic activities was investigated. The data indicate that the IgG FcR is not involved in the NK lytic mechanism, although this receptor may be present on the NK cell. 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M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of natural killer (NK) cells and killer (K) cells in human blood: Discrimination between NK and K cell activities</atitle><jtitle>European journal of immunology</jtitle><addtitle>Eur J Immunol</addtitle><date>1978-10</date><risdate>1978</risdate><volume>8</volume><issue>10</issue><spage>731</spage><epage>740</epage><pages>731-740</pages><issn>0014-2980</issn><eissn>1521-4141</eissn><abstract>Cell suspensions enriched and depleted for rosette‐forming cells with sheep red blood cells (E‐RFC) and depleted for RFC with antibody complexes were prepared. The isolated fractions were characterized by cell surface marker analysis and tested for their natural killer (NK) and killer (K) cell activity against K‐562 cells and IgG‐coated P‐815 cells, growing in suspension, and against a number of monolayer tumor cell lines. It was found that the NK cells most likely belong to the T cell lymphocyte subpopulation. Furthermore, this study indicates that several subpopulations exist, e.g. NK cells that have no IgG Fc receptor (FcR) on their surface and NK cells that bear IgG FcR, indicating that for a proportion of NK cells the IgG FcR is not involved in the NK lytic process and hence antibody‐independent. Moreover, monocytes and B lymphocytes appear not to be directly involved in the NK cell lytic process. Furthermore, cell separation procedures were used to obtain cell suspensions either bearing IgG FcR or lacking IgG FcR. Cells bearing IgG FcR were isolated in such a way that they lost their IgG FcR by shedding, as a result of the separation procedure. Again, all fractions were simultaneously characterized by cell surface marker analysis and tested for their NK and K cell lytic activity. The effect of immune complexes on the NK and K cell lytic activities was investigated. The data indicate that the IgG FcR is not involved in the NK lytic mechanism, although this receptor may be present on the NK cell. Moreover, prolonged culturing of lymphocytes increases and/or induces NK cell lytic activity.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag GmbH</pub><pmid>309395</pmid><doi>10.1002/eji.1830081012</doi><tpages>10</tpages></addata></record>
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subjects Binding Sites
Cell Line
Cells, Cultured
Cytotoxicity, Immunologic
Humans
Immunity, Innate
Immunoglobulin Fc Fragments
Immunoglobulin G - analysis
Killer Cells, Natural - immunology
Receptors, Antigen, B-Cell - analysis
Rosette Formation
T-Lymphocytes - immunology
Time Factors
title Characterization of natural killer (NK) cells and killer (K) cells in human blood: Discrimination between NK and K cell activities
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