Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
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Enzyme
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Query: UNIPROT:P04141 (
granulocyte-macrophage colony-stimulating factor
)
6,790
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Colony-stimulating factors (CSFs) produced by two simian virus 40(SV40) transformed macrophage cell lines (BAM1 and BAM3), and three hybrids (
HM3
-11,
HM3
-12, and
HM3
-14) derived from fusion between BAM3 and a Chinese hamster cell line (hs222-16) were examined.
HM3
-11 and
HM3
-14 produce two molecular species of
CSF
, which are not found in the conditioned media from cultures of BAM1 and BAM3 or lipopolysaccharide (LPS), phorbolmyristate-acetate (PMA), and zymosan-stimulated BAM3.
HM3
-12, which is classified into another group in terms of
CSF
secretion, does not produce these two CSFs. On the basis of various criteria, one of these
CSF
species (peak 1-CSF) was characterized as a macrophage-colony-stimulating factor (M-CSF). The other
CSF
(peak 2-CSF) induced a group of bone marrow cells in granulocytes and macrophages as well as growth of a mast cell line, IC2. This
CSF
has an apparent molecular weight of 18,000, estimated by SDS-polyacrylamide gel electrophoresis. Unlike interleukin 3 (IL3) from WEHI-3 cells, the growth factor activity of peak 2-
CSF
binds to DEAE-Sephacel. Thus, peak 2-
CSF
is similar to a
granulocyte-macrophage colony-stimulating factor
(
GM-CSF
) rather than to IL3. The anti L cell
CSF
serum does not inhibit the
CSF
activity in Chinese hamster fibroblast conditioned medium, and the IC2 cells do not respond to Chinese hamster lung conditioned medium (CHLCM), suggesting that peak 1- and peak 2-
CSF
are of mouse origin.
...
PMID:Properties of colony-stimulating factors produced by macrophage cell lines and hybrid cells. 302 9