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Proteomic analysis of macrophage differentiation
journal contribution
posted on 2001-07-13, 00:00 authored by X Csar, N Wilson, K A McMahon, D Marks, T Beecroft, Alister WardAlister Ward, G Whitty, V Kanangasundarum, J HamiltonProteomic analysis of macrophage differentiation
History
Journal
Journal of Biological ChemistryVolume
276Issue
28Pagination
26211 - 26217Publisher
American Society for Biochemistry and Molecular BiologyLocation
United StatesPublisher DOI
Link to full text
ISSN
0021-9258eISSN
1083-351XLanguage
engNotes
Macrophage colony stimulating factor (M-CSF or CSF-1) acts to regulate the development and function of cells of the macrophage lineage. Murine myeloid FDC-P1 cells transfected with the CSF-1 receptor (FD/WT) adopt a macrophage-like morphology when cultured in CSF-1. This process is abrogated in FDC-P1 cells transfected with the CSF-1 receptor with a tyrosine to phenyalanine substitution at position 807 (FD/807), suggesting that a molecular interaction critical to differentiation signaling is lost (Bourette, R. P., Myles, G. M., Carlberg, K., Chen, A. R., and Rohrschneider, L. R. (1995) Cell Growth Differ. 6, 631-645). A detailed examination of lysates of CSF-1-treated FD/807 cells by two-dimensional SDS-polyacrylamide gel electrophoresis (PAGE) revealed a number of proteins whose degree of tyrosine phosphorylation was modulated by the Y807F mutation. Included in this category were three phosphorylated proteins that co-migrated with p46/52Shc. Immunoprecipitation, Western blotting, and in vitro binding studies suggest that they are indeed p46/52Shc. A key regulator of differentiation in a number of cell systems, ERK was observed to exhibit an activity that correlated with the relative degree of differentiation induced by CSF-1 in the two cell types. Transfection of cells with a non-tyrosine-phosphorylatable form of p46/52Shc prevented the normally observed CSF-1-mediated macrophage differentiation as determined by adoption of macrophage-like morphology and expression of the monocyte/macrophage lineage cell surface marker, Mac-1. These results are the first to suggest that p46/52Shc may play a role in CSF-1-induced macrophage differentiation. Additionally, a number of proteins were identified by two-dimensional SDS-PAGE whose degree of tyrosine phosphorylation is also modulated by the Y807F substitution. This group of molecules may contain novel signaling molecules important in macrophage differentiation.Publication classification
C1.1 Refereed article in a scholarly journalCopyright notice
2001 by the American Society for Biochemistry and Molecular Biology.Usage metrics
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