Quantitative analysis of the effect of CD16 ligation on human NK cell proliferation.

CD16 (Fc gammaRIIIA), the low affinity receptor for IgG, is expressed on the majority of human peripheral blood NK cells. Ligation of CD16 with mAb or immune complexes activates NK cell cytotoxicity and cytokine secretion, and stimulates death of activated NK cells by apoptosis. This study uses NK cells labeled with the stable intracytoplasmic fluorescent dye 5- and 6-carboxyfluorescein diacetate succinimidyl ester to provide quantitative data on the effect of CD16 ligation on NK cell division and NK cell survival. When NK cells are cultured with rIL-2 and CD16 is ligated, NK cell division is stimulated, but there also is a substantial loss of NK progenitor cells. When NK cell proliferation is stimulated by coculture with gamma-irradiated MM-170 malignant melanoma cells and rIL-2, CD16 ligation enhances entry of NK cells into division. In some cases, CD16 ligation is essential for NK cell proliferation stimulated by MM-170 cells. In these cultures, there is no loss of NK progenitor cells. This study demonstrates that CD16 is an activation receptor for NK cell proliferation, and suggests that cellular costimulation alters the balance between NK cell death and NK cell proliferation stimulated by CD16 ligation.

[1]  E. C. Snow,et al.  Strength of signal through BCR determines the fate of cycling B cells by regulating the expression of the Bcl-2 family of survival proteins. , 1998, Cellular immunology.

[2]  B. Wollenberg,et al.  Absence of B7.1‐CD28/CTLA‐4‐mediated co‐stimulation in human NK cells , 1998, European journal of immunology.

[3]  C. Rabourdin-Combe,et al.  Hepatocytes induce functional activation of naive CD8+ T lymphocytes but fail to promote survival , 1998, European journal of immunology.

[4]  H. Gudmundsdottir,et al.  Following the fate of individual T cells throughout activation and clonal expansion. Signals from T cell receptor and CD28 differentially regulate the induction and duration of a proliferative response. , 1997, The Journal of clinical investigation.

[5]  C. Ware,et al.  Fas involvement in human NK cell apoptosis: lack of a requirement for CD16‐mediated events , 1997, Journal of leukocyte biology.

[6]  Eric O Long,et al.  Killer cell inhibitory receptors: diversity, specificity, and function , 1997, Immunological reviews.

[7]  J. Bluestone,et al.  CD28/B7 interactions deliver a unique signal to naive T cells that regulates cell survival but not early proliferation. , 1996, Journal of immunology.

[8]  H. Warren NK cell proliferation and inflammation , 1996, Immunology and cell biology.

[9]  J. H. Lee,et al.  B cell differentiation and isotype switching is related to division cycle number , 1996, The Journal of experimental medicine.

[10]  T. Whiteside,et al.  Divergent effects of FcγRIIIA ligands on the functional activities of human natural killer cells in vitro , 1996, European journal of immunology.

[11]  L. Lanier,et al.  Analysis of the costimulatory role of IL-2 and IL-15 in initiating proliferation of resting (CD56dim) human NK cells. , 1996, Journal of immunology.

[12]  P. Krammer,et al.  Fc receptor-induced expression of Fas ligand on activated NK cells facilitates cell-mediated cytotoxicity and subsequent autocrine NK cell apoptosis. , 1996, Journal of immunology.

[13]  G. Mills,et al.  CD28 costimulation inhibits TCR-induced apoptosis during a primary T cell response. , 1996, Journal of immunology.

[14]  D. Green,et al.  Early redistribution of plasma membrane phosphatidylserine is a general feature of apoptosis regardless of the initiating stimulus: inhibition by overexpression of Bcl-2 and Abl , 1995, The Journal of experimental medicine.

[15]  S. Fortune,et al.  Opposing roles of CD95 (Fas/APO-1) and CD40 in the death and rescue of human low density tonsillar B cells. , 1995, Journal of immunology.

[16]  R. Abraham,et al.  Interaction between lck and syk Family Tyrosine Kinases in Fcγ Receptor-initiated Activation of Natural Killer Cells (*) , 1995, The Journal of Biological Chemistry.

[17]  C. Thompson,et al.  CD28 costimulation can promote T cell survival by enhancing the expression of Bcl-XL. , 1995, Immunity.

[18]  L. Lanier,et al.  Production of IL-5 by human NK cells and regulation of IL-5 secretion by IL-4, IL-10, and IL-12. , 1995, Journal of immunology.

[19]  C. Thompson,et al.  The role of bcl‐xL in CD40‐mediated rescue from anti‐μ‐induced apoptosis in WEHI‐231 B lymphoma cells , 1995, European journal of immunology.

[20]  B. Calabretta,et al.  Ligand binding to Fc gamma R induces c-myc-dependent apoptosis in IL-2-stimulated NK cells. , 1995, Journal of immunology.

[21]  J. Ortaldo,et al.  Receptor-induced death in human natural killer cells: involvement of CD16 , 1995, The Journal of experimental medicine.

[22]  H. Warren,et al.  Differential expression of CD45R0 on natural killer (NK) cells in patients with an NK lymphocytosis , 1994, Immunology and cell biology.

[23]  A. B. Lyons,et al.  Determination of lymphocyte division by flow cytometry. , 1994, Journal of immunological methods.

[24]  M. Hibbs,et al.  Membrane-proximal Ig-like domain of Fc gamma RIII (CD16) contains residues critical for ligand binding. , 1994, Journal of immunology.

[25]  P. Anderson,et al.  Association of a 70‐kDa tyrosine phosphoprotein with the CD16:ζ:γ complex expressed in human natural killer cells , 1993 .

[26]  T. Kurosaki,et al.  Physical and functional association of p56lck with Fc gamma RIIIA (CD16) in natural killer cells , 1993, The Journal of experimental medicine.

[27]  H. Warren,et al.  Human natural killer (NK) cells: Requirements for cell proliferation and expansion of phenotypically novel subpopulations , 1993, Immunology and cell biology.

[28]  J. Ritz,et al.  Costimulatory signals are required for optimal proliferation of human natural killer cells. , 1993, Journal of immunology.

[29]  L. Azzoni,et al.  Stimulation of Fc gamma RIIIA results in phospholipase C-gamma 1 tyrosine phosphorylation and p56lck activation , 1992, The Journal of experimental medicine.

[30]  E. Reinherz,et al.  Characterization of FcεRIγ in human natural killer cells , 1992 .

[31]  K. Oshimi,et al.  Activation via the CD3 and CD16 pathway mediates interleukin-2-dependent autocrine proliferation of granular lymphocytes in patients with granular lymphocyte proliferative disorders. , 1991, Blood.

[32]  J. Kinet,et al.  Characterization of the family of dimers associated with Fc receptors (Fc epsilon RI and Fc gamma RIII). , 1991, Journal of immunology.

[33]  L. Lanier,et al.  Analysis of Fc gamma RIII (CD16) membrane expression and association with CD3 zeta and Fc epsilon RI-gamma by site-directed mutation. , 1991, Journal of immunology.

[34]  D. Harris,et al.  Induction of activation antigens on human natural killer cells mediated through the Fc-gamma receptor. , 1989, Journal of immunology.

[35]  L. Lanier,et al.  Functional and biochemical analysis of CD16 antigen on natural killer cells and granulocytes. , 1988, Journal of immunology.

[36]  G. Trinchieri,et al.  Interaction of Fc receptor (CD16) ligands induces transcription of interleukin 2 receptor (CD25) and lymphokine genes and expression of their products in human natural killer cells , 1988, The Journal of experimental medicine.

[37]  G. Trinchieri,et al.  Antibody 3G8, specific for the human neutrophil Fc receptor, reacts with natural killer cells. , 1984, Journal of immunology.

[38]  G. Trinchieri,et al.  Human natural killer cells analyzed by B73.1, a monoclonal antibody blocking Fc receptor functions. I. Characterization of the lymphocyte subset reactive with B73.1. , 1983, Journal of immunology.

[39]  P. Anderson,et al.  Structure and function of the CD16:zeta:gamma complex expressed on human natural-killer cells. , 1992, International journal of cancer. Supplement = Journal international du cancer. Supplement.

[40]  H. Warren,et al.  Phenotypic analysis of a resting subpopulation of human peripheral blood NK cells: the FcR gamma III (CD16) molecule and NK cell differentiation. , 1991, Immunology.

[41]  V. McGovern,et al.  Mechanisms in pigmentation , 1973 .