ENHANCEMENT OF RELEASE FROM MHC CLASS-II ANTIGEN-POSITIVE MONOCYTES OF HEMATOPOIETIC COLONY STIMULATING FACTORS CSF-1 AND G-CSF BY RECOMBINANT HUMAN-TUMOR NECROSIS FACTOR-ALPHA - SYNERGISM WITH RECOMBINANT HUMAN INTERFERON-GAMMA
- 1 July 1988
- journal article
- research article
- Vol. 72 (1) , 34-41
Abstract
The influence of purified recombinant human tumor necrosis factor-alpha (rhu-TNF-.alpha.) was assessed alone and in combination with purified recombinant human interferon gamma (rhuIFN-.gamma.) for its effects on enhancing release from human monocytes of activities that stimulate colony formation by granulocyte-macrophage (CFU-GM), erythroid (BFU-E), and multipotential (CFU-GEMM) progenitor cells. RhuTNF-.alpha. or rhuIFN-.gamma. enhanced release of colony stimulating factors (CSFs), which were determined by a combination human and mouse colony assays, morphological assessement of colony types and neutralization studies with anti-human macrophage CSF (CSF-1) and anti-human granulocyte (G)-CSF to be CSF-1 and G-CSF. The activity in the uninduced and induced monocyte conditioned media (CM) for CFU-GM-type colonies and clusters was attributed to the presence of both CSF-1 and G-CSF, while the activity in the monocyte CM for BFU-E and CFU-GEMM colonies was attributed to the presence of G-CSF. Monocytes were separated by two-color fluorescence using a dye laser flow cytometry system with cells labeled with anti-leu M3 conjugated with fluorescein isothiocyanate and anti-HLA-DR conjugated with phycoerythrin. While "constitutive" release of CSFs from monocytes was apparent from both the leu M3+, HLA-DR+ and the leu M3+, HLA-DR- (low density or negative DR) fractions, enhanced release of CSFs in response to rhuTNF-.alpha. or rhuIFN-.gamma. was confined to the leu M3+, HLA-DR+ population of cells. RhuTNF-.alpha. and rhuIFN-.gamma. synergized to enhance release of CSFs such that low concentrations of each molecule, which were inactive when used alone, were active when the two molecules were used together. These studies suggest a role, at least in vitro, for TNF-.alpha. and IFN-.gamma. in the release of CSFs from cells of the mononuclear phagocytic lineage.This publication has 24 references indexed in Scilit:
- EFFECTS OF RECOMBINANT HUMAN-TUMOR NECROSIS FACTOR-ALPHA, RECOMBINANT HUMAN GAMMA-INTERFERON, AND PROSTAGLANDIN-E ON COLONY FORMATION OF HUMAN HEMATOPOIETIC PROGENITOR CELLS STIMULATED BY NATURAL HUMAN PLURIPOTENT COLONY-STIMULATING FACTOR, PLURIPOIETIN-ALPHA, AND RECOMBINANT ERYTHROPOIETIN IN SERUM-FREE CULTURESH1986
- The suppressive influences of human tumor necrosis factors on bone marrow hematopoietic progenitor cells from normal donors and patients with leukemia: synergism of tumor necrosis factor and interferon-gamma.The Journal of Immunology, 1986
- Interleukin 1 stimulates fibroblasts to produce granulocyte-macrophage colony-stimulating activity and prostaglandin E2.Journal of Clinical Investigation, 1986
- T cell-monocyte interactions in the production of humoral factors regulating human granulopoiesis in vitro.The Journal of Immunology, 1986
- Recombinant Human Granulocyte Colony-Stimulating Factor: Effects on Normal and Leukemic Myeloid CellsScience, 1986
- Secretion of Colony-Stimulating Factors by Human Monocytes and Bone Marrow Cells After In Vitro Treatment With Biological Response ModifiersJournal of Leukocyte Biology, 1985
- Purification and biochemical characterization of human pluripotent hematopoietic colony-stimulating factor.Proceedings of the National Academy of Sciences, 1985
- COMPARATIVE INFLUENCES OF PHYTOHEMAGGLUTININ-STIMULATED LEUKOCYTE CONDITIONED MEDIUM, HEMIN, PROSTAGLANDIN-E, AND LOW OXYGEN-TENSION ON COLONY FORMATION BY ERYTHROID PROGENITOR CELLS IN NORMAL HUMAN-BONE MARROW1985
- RELEASE OF GRANULOCYTE-MACROPHAGE COLONY STIMULATING FACTORS FROM MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II ANTIGEN-POSITIVE MONOCYTES IS ENHANCED BY HUMAN GAMMA INTERFERON1985
- COLONY-FORMING UNITS IN DIFFUSION CHAMBERS (CFU-d) AND COLONY-FORMING UNITS IN AGAR CULTURE (CFU-c) OBTAINED FROM NORMAL HUMAN BONE MARROW: A POSSIBLE PARENT–PROGENY RELATIONSHIPCell Proliferation, 1979