I. Ishii et al., GENETIC-DIFFERENCES OF LIPID-METABOLISM IN MACROPHAGES FROM C57BL 6J AND C3H/HEN MICE/, Arteriosclerosis, thrombosis, and vascular biology, 15(8), 1995, pp. 1189-1194
Cholesterol metabolism in macrophages from atherosclerosis-prone C57BL
/6J mice was compared with that in macrophages from atherosclerosis-re
sistant C3H/HeN mice. Plasma total cholesterol levels of both types of
mice were significantly increased, but HDL cholesterol level was incr
eased only in C3H/HeN mice when a high-cholesterol diet (1% cholestero
l) was fed for 5 weeks. After incubation of macrophages from male and
female mice on the high-cholesterol diet with beta-VLDL for 24 hours,
cholesterol content in macrophages from C57BL/6J was approximately 1.5
- to 2.0-fold higher than in those from C3H/HeN mice. [H-3]Cholesterol
oleate-beta-VLDL incorporation into macrophages from C57BL/6J mice on
the high-cholesterol diet was greater than incorporation into those f
rom C3H/HeN mice. The release of [3H]cholesterol from macrophages from
C57BL/6J mice on the high-cholesterol diet was one seventh that from
macrophages from C57BL/6J mice on the basal diet or that from macropha
ges from C3H/HeN mice on the basal or high-cholesterol diet. Acid chol
esterol esterase activity was almost the same in macrophages from any
group. Acyl CoA:cholesterol acyltrans ferase activity in macrophages f
rom C57BL/6J mice on the high-cholesterol diet increased compared with
that from macrophages from C57BL/6J mice on the normal diet. Neutral
cholesterol esterase activity in macrophages from C57BL/6J mice was ab
out half of that in macrophages from C3H/HeN mice independent of the t
ype of diet. There were no sex differences in these metabolisms. Consi
dered with our previous data, these results suggested that a high-chol
esterol diet may cause metabolic changes to accumulate cholesterol est
er in macrophages from C57BL/6J mice in accordance with genetic abnorm
alities.