Iron regulation of transferrin synthesis in the human hepatoma cell line HepG2

被引:10
作者
Barnum-Huckins, K [1 ]
Adrian, GS [1 ]
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Cellular & Struct Biol, San Antonio, TX 78284 USA
关键词
human transferrin; iron-regulation; deferroxamine; ferritin; HepG2;
D O I
10.1006/cbir.1999.0456
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In human beings, serum transferrin levels increase during iron deficiency and decrease with iron overload. Yet, whether or not iron levels actually affect the synthesis of transferrin in human liver cells is not known. In previous studies, iron was shown to suppress the expression of chimeric human transferrin genes in livers of transgenic mice. The goal of this study was to determine if iron suppresses intact endogenous human transferrin synthesis by testing the effects of changes in iron levels on synthesis of transferrin in a human hepatoma cell line HepG2. In HepG2 cells, normalized S-35-metabolically labeled transferrin synthesis was consistently less following iron treatment with hemin or ferric citrate, than following treatment with an iron-chelator deferroxamine. Thus, this study provides new evidence that iron can regulate synthesis of intact endogenous human transferrin. (C) 2000 Academic Press.
引用
收藏
页码:71 / 77
页数:7
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