Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1986 Feb;83(3):669-73.
doi: 10.1073/pnas.83.3.669.

High-affinity binding of granulocyte-macrophage colony-stimulating factor to normal and leukemic human myeloid cells

High-affinity binding of granulocyte-macrophage colony-stimulating factor to normal and leukemic human myeloid cells

J C Gasson et al. Proc Natl Acad Sci U S A. 1986 Feb.

Abstract

Purified natural and biosynthetic (recombinant) human granulocyte-macrophage colony-stimulating factor (GM-CSF) stimulate colony formation by myeloid progenitor cells and enhance the function of mature neutrophils. Both of these actions occur at concentrations between 1 and 100 pM, with half-maximal stimulation at 10-20 pM. We have examined specific binding of 125I-labeled GM-CSF to responsive target cells in this range of concentrations. The results show a low number (50-250) of high-affinity (15-30 pM) binding sites on GM-CSF-responsive leukemic cells (KG-1, HL-60), as well as on peripheral blood neutrophils from normal donors. This high-affinity binding component was absent from unresponsive cell lines (KG-1a, K562). These results suggest that this binding site mediates the biological activities of GM-CSF on both proliferation and function of myeloid cells.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Steroids. 1975 Oct;26(4):538-42 - PubMed
    1. Nature. 1977 Nov 24;270(5635):347-9 - PubMed
    1. Science. 1978 Jun 9;200(4346):1153-4 - PubMed
    1. Blood. 1975 Mar;45(3):321-34 - PubMed
    1. J Cell Biol. 1980 Apr;85(1):153-9 - PubMed

Publication types

MeSH terms

Substances