TY - JOUR
T1 - Characterization of a colony-stimulating factor produced by the human monocytic leukemia cell line, THP-1
AU - Gaffney, E. V.
AU - Dell'Aquila, M. L.
AU - Lingenfelter, S. E.
AU - Huffnagle, G. B.
AU - Wiest, D. L.
PY - 1986
Y1 - 1986
N2 - The human monocytic leukemia cell line, THP-1, acquires macrophage-like characteristics following exposure to mezerein. Serum-free medium conditioned by mezerein-activated cells was observed to contain colony-stimulating factor (CSF) activity in assays with murine bone marrow cultures. Isoelectrofocusing revealed that CSF activity displayed charge heterogeneity and migrated in a pl range of 4.4-5.3. Treatment with neuraminidase did not affect biological activity but did reduce charge heterogeneity. Reisofocusing of neuraminidase-treated CSF revealed a peak of activity at pl 4.9. The active component was shown to be an acidic sialoglycoprotein, resistant to proteolytic cleavage but completely inactivated by 2-mercaptoethanol. This CSF has been purified from THP-1-conditioned serum-free medium by preparative isoelectrofocusing, gel filtration through Sephacryl S-200, ion exchange chromatography on DEAE-Sephacel, neuraminidase treatment, and tris-glycinate polyacrylamide gel electrophoresis (PAGE). Elution from SDS-PAGE revealed a single peak of activity corresponding to an apparent molecular weight of 70,000 daltons. Preliminary characterization of the bone marrow cells in colonies showed that THP-1 cells produced macrophage-specific CSF.
AB - The human monocytic leukemia cell line, THP-1, acquires macrophage-like characteristics following exposure to mezerein. Serum-free medium conditioned by mezerein-activated cells was observed to contain colony-stimulating factor (CSF) activity in assays with murine bone marrow cultures. Isoelectrofocusing revealed that CSF activity displayed charge heterogeneity and migrated in a pl range of 4.4-5.3. Treatment with neuraminidase did not affect biological activity but did reduce charge heterogeneity. Reisofocusing of neuraminidase-treated CSF revealed a peak of activity at pl 4.9. The active component was shown to be an acidic sialoglycoprotein, resistant to proteolytic cleavage but completely inactivated by 2-mercaptoethanol. This CSF has been purified from THP-1-conditioned serum-free medium by preparative isoelectrofocusing, gel filtration through Sephacryl S-200, ion exchange chromatography on DEAE-Sephacel, neuraminidase treatment, and tris-glycinate polyacrylamide gel electrophoresis (PAGE). Elution from SDS-PAGE revealed a single peak of activity corresponding to an apparent molecular weight of 70,000 daltons. Preliminary characterization of the bone marrow cells in colonies showed that THP-1 cells produced macrophage-specific CSF.
KW - Animals
KW - Bone Marrow Cells
KW - Cell Adhesion/drug effects
KW - Cell Division/drug effects
KW - Cell Line
KW - Colony-Stimulating Factors/biosynthesis
KW - DNA Replication/drug effects
KW - Drug Stability
KW - Humans
KW - Isoelectric Focusing
KW - Leukemia, Myeloid/physiopathology
KW - Mice
KW - Thymidine/metabolism
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U2 - 10.1002/jlb.39.4.409
DO - 10.1002/jlb.39.4.409
M3 - Article
C2 - 3485167
SN - 0741-5400
VL - 39
SP - 409
EP - 421
JO - Journal of Leukocyte Biology
JF - Journal of Leukocyte Biology
IS - 4
ER -