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The haemopoietic growth factors interleukin 3 and colony stimulating factor‐1 stimulate proliferation but do not induce inositol lipid breakdown in murine bone‐marrow‐derived macrophages.
Author(s) -
Whetton A.D.,
Monk P.N.,
Consalvey S.D.,
Downes C.P.
Publication year - 1986
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1002/j.1460-2075.1986.tb04640.x
Subject(s) - biology , diacylglycerol kinase , inositol , growth factor , phosphatidylinositol , bone marrow , colony stimulating factor , immunology , endocrinology , microbiology and biotechnology , signal transduction , biochemistry , haematopoiesis , stem cell , receptor , protein kinase c
The haemopoietic growth factors interleukin 3 (IL‐3) and colony stimulating factor‐1 (CSF‐1) stimulate the survival and proliferation of murine normal bone‐marrow‐derived macrophages. To establish whether these growth factors elicit their effects via the hydrolysis of phosphatidylinositol(4,5)bisphosphate [PtdIns(4,5)P2] to form the second messengers inositol (1,4,5)trisphosphate [Ins(1,4,5)P3] and diacylglycerol, macrophages were labelled with tracer quantities of [3H]inositol. Treatment of these cells with either IL‐3 or CSF‐1 did not alter the levels of PtdIns(4,5)P2 or Ins(1,4,5)P3. However, addition of the chemotactic peptide N‐formyl‐methionyl‐leucyl‐phenylalanine (FMLP) which does not stimulate proliferation in macrophages caused a marked and rapid increase in the levels of Ins(1,4,5)P3, inositol bisphosphate and inositol monophosphate, and a decrease in the amount of PtdIns(4,5)P2. FMLP also evoked a rapid increase in intracellular cytosolic Ca2+ levels, as measured with quin 2 the Ca2+‐sensitive fluorescent probe, whereas IL‐3 and CSF‐1 had no such effect. These results suggest that FMLP stimulates the hydrolysis of PtdIns(4,5)P2 to form the second messenger Ins(1,4,5)P3 which acts to increase the levels of cytosolic Ca2+, and that IL‐3‐ and CSF‐1‐stimulated proliferation in macrophages is not associated with the formation of PtdIns(4,5)P2‐derived second messengers.