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内毒素诱导肝细胞锌蓄积是由金属硫蛋白合成介导的。

Endotoxin-induced zinc accumulation by liver cells is mediated by metallothionein synthesis.

作者信息

Fukushima T, Iijima Y, Kosaka F

机构信息

Department of Anesthesiology and Resuscitology, Okayama University Medical School, Japan.

出版信息

Biochem Biophys Res Commun. 1988 Apr 29;152(2):874-8. doi: 10.1016/s0006-291x(88)80120-7.

Abstract

Endotoxin induces a decrease in zinc concentration in the serum and an increase in zinc levels in the liver. We have studied whether metallothionein (MT), which is a heavy metal-binding protein, is associated with this phenomenon in vitro. When MT of liver cells is induced by a factor secreted by endotoxin-stimulated macrophages, the cells accumulate zinc from the medium. The temporal accumulation of zinc is correlated with the induction of MT, and the accumulated zinc binds to MT. These results suggest that zinc accumulation by liver cells is mediated by metallothionein produced in response to a macrophage factor, which is elicited by endotoxin.

摘要

内毒素会导致血清中锌浓度降低,肝脏中锌水平升高。我们研究了作为重金属结合蛋白的金属硫蛋白(MT)在体外是否与这种现象相关。当内毒素刺激的巨噬细胞分泌的一种因子诱导肝细胞的MT时,细胞会从培养基中积累锌。锌的暂时积累与MT的诱导相关,并且积累的锌会与MT结合。这些结果表明,肝细胞对锌的积累是由内毒素引发的巨噬细胞因子诱导产生的金属硫蛋白介导的。

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