Purified colony-stimulating factor (CSF-1) (or macrophage colony stimulating factor [M-CSF]) stimulated the glucose uptake of murine bone marrow-derived macrophages (BMM) and resident peritoneal macrophages (RPM) as measured by 3H-2-deoxyglucose (2-DOG) uptake. Similar concentrations of CSF-1 stimul
Proliferation of rat liver macrophages in vitro: Influence of hemopoietic growth factors
β Scribed by Rein M. J. Hoedemakers; Gerrit L. Scherphof; Dr. Toos Daemen
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 984 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0270-9139
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β¦ Synopsis
We examined the effects of several hemopoietic growth factors on proliferation of rat liver macrophages in &FO. The proliferative response of liver macrophages to hemopoietic growth factors was assayed on the basis of [methyl-'Hlthymidine uptake. Macrophage colony-stimulating factor and recombinant murine granulocyte-macrophage colony-stimulating factor stimulated [rnethyl-'H]thymidine incorporation in a concentration-dependent manner. With granulocyte-macrophage colony-stimulating factor, maximum incorporation was observed at 50 U/ml, whereas with macrophage colony-stimulating factor no incorporation plateau was observed up to 50% L929-conditioned medium. Incubation of liver macrophages with various concentrations of recombinant human interleukin-2, recombinant murine interleukin-3 and recombinant human interleukin-6 or culture medium alone did not result in significant incorporation of [methyl-SHlthymidine. When liver macrophages were fractionated according to cell size, highest incorporation was observed in the large macrophages. Proliferating cells in cultures of all subfractions were microscopically identified as typical macrophages by the use of macrophage-specific monoclonal antibodies. After 6 days in culture, these macrophages had functional properties similar to those of resident liver macrophages with respect to phagocytosis and in U ~~F O activation with immunomodulators to tumorcytotoxicity and secretion of nitric oxide and tumor necrosis factor-a. These results suggest that macrophage colony-stimulating factor and granulocyte-macrophage colony-stimulating factor play important roles among the regulatory factors that support local proliferation of rat liver macrophages. (HEPATOLOGY 1994;
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