Human beta-migrating very low density lipoprotein induces foam cell formation in human mesangial cells

被引:12
作者
Anami, Y
Kobori, S
Sakai, M
Kasho, M
Nishikawa, T
Yano, T
Matsuda, H
Matsumura, T
Takemura, T
Shichiri, M
机构
[1] Department of Metabolic Medicine, Kumamoto Univ. School of Medicine, Kumamoto 860
关键词
human beta-VLDL; human mesangial cell; foam cell; familial type III hyperlipoproteinemia; atherosclerosis;
D O I
10.1016/S0021-9150(97)00166-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To elucidate the mechanism of foam cell formation in the mesangial region of a kidney observed in a familial type III hyperlipoproteinemic patient presenting with diabetes mellitus and nephrotic syndrome, we have examined, in the present study, the effect of human beta-VLDL (ape E2/E2) on foam cell formation in human mesangial cells, since an increase in beta-VLDL is a characteristic feature of this patient. Human beta-VLDL (ape E2/E2) induced foam cell formation in human mesangial cells. The binding of [I-125]LDL to human mesangial cells was inhibited completely by both LDL and beta-VLDL. On the other hand, the binding of [I-125]beta-VLDL was completely inhibited by beta-VLDL, but partially by LDL. The LDL receptor, but not the VLDL receptor was down-regulated by accumulation of cholesteryl esters. These results suggest that human beta-VLDL (ape E2/E2)-induced foam cell formation in mesangial cells is mediated through both the LDL receptor pathway and the beta-VLDL specific pathway, in which the VLDL receptor is one of the candidates. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:225 / 234
页数:10
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