Abstract
Colony-stimulating factor-1 (CSF-1) regulates mononuclear cell proliferation, differentiation, and survival. The functions of CSF-1 are well documented in mammals; however, little is known about CSF-1 biology in lower vertebrates. This is the first report on the identification and functional characterization of a fish CSF-1 molecule expressed highly in the spleen and in phorbol 12-myristate 13-acetate-stimulated monocytes. Goldfish CSF-1 is a 199-amino acid protein that possesses the required cysteine residues to form important intra-chain and inter-chain disulfide bonds that allow CSF-1 to form a functional homodimer and to interact with its high affinity receptor, CSF-1R. Recombinant goldfish CSF-1 formed a homodimer and bound to the soluble goldfish CSF-1R. The addition of the recombinant CSF-1 to sorted goldfish progenitor cells, monocytes, and macrophages induced the differentiation of monocytes into macrophages and the proliferation of monocyte-like cells. The proliferation of these cells was abrogated by addition of an anti-CSF-1R antibody as well as the soluble CSF-1R. The ability of the soluble CSF-1R to inhibit CSF-1-induced proliferation represents a novel mechanism for the regulation of CSF-1 function.
Original language | English |
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Pages (from-to) | 31865-31872 |
Number of pages | 8 |
Journal | The Journal of Biological Chemistry |
Volume | 282 |
Issue number | 44 |
Early online date | 6 Sep 2007 |
DOIs | |
Publication status | Published - 2 Nov 2007 |
Keywords
- Amino Acid Sequence
- Animals
- Base Sequence
- Cell Differentiation
- Fish Proteins
- Goldfish
- Kidney
- Macrophage Colony-Stimulating Factor
- Macrophages
- Molecular Sequence Data
- Monocytes
- Receptor, Macrophage Colony-Stimulating Factor
- Spleen
- factor-receptor
- M-CSF, langsdorfii kidney, cells, proliferation, cultures, vitro