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J. Biol. Chem., Vol. 265, Issue 22, 12869-12875, 08, 1990
H Shimano, N Yamada, S Ishibashi, K Harada, A Matsumoto, N Mori, T Inaba, K Motoyoshi, H Itakura and F Takaku
To investigate the effects of recombinant human monocyte colony-
stimulating factor (M-CSF) on plasma cholesterol metabolism, we injected
M-CSF intravenously into New Zealand White rabbits (n = 13) at a dose of
100 micrograms/day for 7 days. After the treatment, the plasma cholesterol
levels fell by 33.2% from 61.4 +/- 25.9 to 41.0 +/- 10.2 mg/dl (mean +/-
S.D.). We also injected a large dose of M-CSF (500 micrograms/day) for 6
days into Watanabe Heritable Hyperlipidemic rabbits, which are deficient in
low density lipoprotein (LDL) receptors. Again, there was a significant
reduction in plasma cholesterol levels by 36.2% from 730.5 +/- 176.4 to
466.0 +/- 104.9 mg/dl (n = 4). In the kinetic studies in New Zealand White
rabbits with very low density lipoprotein, LDL, and methylated LDL, the
removal rates of those lipoproteins were increased 1.9-, 1.7-, and
2.0-fold, respectively, after the treatment. Immunoblot analysis of LDL
receptors in the treated rabbits showed no significant changes in LDL
receptor proteins in livers but a great increase in spleens and bone
marrows compared with the controls. Messenger RNA was also estimated by
Northern blotting in both groups, and the results were compatible with
those from the immunoblot. The data suggest that M-CSF stimulates the
clearance of lipoproteins containing apolipoprotein B-100 via both LDL
receptor-dependent and -independent pathways in target cells of M-CSF and
reduces plasma cholesterol.
Human monocyte colony-stimulating factor enhances the clearance of lipoproteins containing apolipoprotein B-100 via both low density lipoprotein receptor-dependent and -independent pathways in rabbits
Third Department of Internal Medicine, Faculty of Medicine, University of Tokyo, Japan.
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