Regulatory effects of T cell lymphokines on cytokine gene expression in monocytes
Cluitmans, F.H.; Esendam, B.H.; Landegent, J.E.; Willemze, R.; Falkenburg, J.H.
Lymphokine and Cytokine Research 12(6): 457-464
1993
ISSN/ISBN: 1056-5477 PMID: 8123762 Document Number: 406715
Hematopoiesis is regulated by colony-stimulating factors (CSF) and many other cytokines. T helper cell and monocyte/macrophage interactions that take place in the immune response, resulting in the production of many cytokines, probably can influence inducible hematopoiesis. We investigated the effect of the T helper cell-derived lymphokines IL-2, IL-3, GM-CSF, and IFN-gamma, on the expression of cytokine genes in monocytes and compared this to LPS-induced cytokine gene expression in monocytes. To avoid inadvertent activation of monocytes, cells were purified by elutriation and cultured under serum-free, LPS-free, and nonadherent conditions. Similar to LPS, IL-2, IL-3, and GM-CSF induced the expression of IL-1-beta, IL-6, IL-8, TNF-alpha, and IL-1-RA genes in monocytes, but with some differences in the amount and kinetics of cytokine mRNA accumulation. Unlike LPS, IL-2, IL-3, and GM-CSF did not induce G-CSF gene expression in monocytes. GM-CSF and IL-3 were the only inducers capable of expressing the M-CSF gene in monocytes. IL-2, IL-3, and GM-CSF showed no effect on the IL-10 gene while IFN-gamma appeared to have no effect on any of the cytokine genes studied in monocytes. These data indicate that in the immune response expression of the proinflammatory cytokine genes, IL-1-beta, IL-6, IL-8, and TNF-alpha, can occur and that autoregulatory control mechanisms, like the expression of IL-1-RA gene, are also activated. It is not likely that the immune response has a direct effect on inducible granulopoiesis, because no induction of G-CSF was found in monocytes stimulated with T helper lymphokines. The induction of G-CSF and, to a lesser extent, GM-CSF gene expression in monocytes by the microbial product LPS suggests that the pathogen itself is of greater importance in regulating granulopoiesis.