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Onset of apoprotein E secretion during differentiation of mouse bone marrow-derived mononuclear phagocytes

Journal Article · · J. Cell Biol.; (United States)
A number of macrophage functions were sequentially expressed when the bone marrow precursors of mononuclear phagocytes differentiated in culture in the presence of a specific growth factor, colony-stimulating factor-1. The authors defined the expression of apoprotein E (ApoE), a major secreted protein of resident peritoneal macrophages, during maturation of adherent bone marrow-derived mononuclear phagocytes into macrophages. By 5 d the bone marrow macrophages were active secretory cells, but few cells contained intracellular immunoreactive ApoE, and little, if any, ApoE was secreted. ApoE secretion was initiated at 9 d, and this correlated with an increase in the percentage of macrophages containing intracellular ApoE. The onset of ApoE secretion was selective, and little change occurred in the other major secreted proteins detected by (/sup 35/S)methionine incorporation. In parallel, the high rate of plasminogen activator secretion, which peaked at 7 d, decreased markedly. ApoE secretion was not associated with altered expression of the macrophage surface antigen, la, or with secretion of fibronectin. Virtually all cells in independent colonies of bone marrow-derived macrophages eventually expressed ApoE. The proliferating monocyte/macrophage-like cell lines P388D1, J774.2, WHEI-3, RAW 264.1, and MGI.D/sup +/ secreted little or no ApoE. These data establish that ApoE secretion is developmentally regulated.
Research Organization:
Univ. of California, San Francisco
DOE Contract Number:
AC03-76SF01012
OSTI ID:
6350073
Journal Information:
J. Cell Biol.; (United States), Journal Name: J. Cell Biol.; (United States) Vol. 97; ISSN JCLBA
Country of Publication:
United States
Language:
English