The effect of colony stimulating factor on the synthesis of ribonucleic acid by mouse bone marrow cells in vitro

✍ Scribed by Antony W. Burgess; Donald Metcalf

• Publisher: John Wiley and Sons
• Year: 1977
• Tongue: English
• Weight: 919 KB
• Volume: 90
• Category: Article
• ISSN: 0021-9541
• DOI: 10.1002/jcp.1040900311

✦ Synopsis

Abstract

The effect of granulocyte‐macrophage colony stimulating factor (GM‐CSF) on the synthesis of RNA in liquid cultures of mouse bone marrow, spleen, thymus, peritoneal, peripheral blood leukocytes and lymph node cells was investigated. GM‐CSF appeared to stimulate RNA‐synthesis in syngeneic bone marrow cells within ten minutes of adding it to the culture. In the presence of GM‐CSF bone marrow cultures maintained their initial rate of RNA synthesis for approximately ten hours. GM‐CSF had no apparent effect on the uptake of ^3^H‐uridine into bone marrow cells. This stimulation was still observed in the presence of puromycin and cycloheximide, but was abrogated by actinomycin D. The magnitude of the stimulation was not affected by the density of cells between 1 and 20 × 10^6^ cells/ml but was slightly smaller at 0.1 and 40 × 10^6^ cells/ml. Increasing concentration of GM‐CSF (up to 2 × 10^5^ units per ml) led to increased stimulation of RNA synthesis in bone marrow cells, but a significant stimulation could be detected at concentrations as low as 800 units/ml.

GM‐CSF did not significantly stimulate RNA synthesis in spleen, thymus, mesenteric or subcutaneous lymph node cells. However a small stimulation was observed in peripheral blood leukocytes and peritoneal cells.

Autoradiographic studies showed that GM‐CSF stimulated RNA synthesis in blast cells, myelocytes, metamyelocytes and polymorphs. Nucleated erythroid cells showed no increased labeling with GM‐CSF. Labeling in lymphoid‐like cells was highly variable but the level of labeling did not appear to be influenced by GM‐CSF.