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锌激发后金属硫蛋白基因敲除小鼠的肝脏锌:体内和体外研究

Hepatic zinc in metallothionein-null mice following zinc challenge: in vivo and in vitro studies.

作者信息

Coyle P, Philcox J C, Rofe A M

机构信息

Division of Clinical Biochemistry, Institute of Medical and Veterinary Science, Adelaide, Australia.

出版信息

Biochem J. 1995 Jul 1;309 ( Pt 1)(Pt 1):25-31. doi: 10.1042/bj3090025.

Abstract

Hepatic zinc uptake and accumulation were compared in freshly isolated and cultured hepatocytes prepared from control (MT+/+) and metallothionein (MT)-null (MT-/-) mice. In freshly isolated hepatocytes, rapid (10-15 min) exchange of 65Zn was proportional to the Zn concentration in the medium and occurred to the same extent in hepatocytes from MT+/+ and MT-/- mice. In 24 h culture experiments with MT+/+ and MT-/- hepatocytes it was shown that approx. 40% of newly acquired cell-associated Zn was attached to the cell surface and not internalized. In MT+/+ and MT-/- hepatocyte cultures, internalized Zn (intZn) increased in proportion to extracellular Zn. Zn accumulation in MT-/- hepatocytes was only 60% that of MT+/+ cells. Addition of 1 microM dexamethasone (Dex) and recombinant mouse interleukin-6 (IL-6; 100 units/ml) increased MT accumulation by 8.6-fold in MT+/+ hepatocytes (at 50 microM Zn) and there was an associated parallel increase in intZn. Dex and IL-6 did not increase intZn in the MT-/- hepatocytes. At 16 h after an intraperitoneal injection of 5 micrograms/g Zn, plasma and urine Zn concentrations were 69 +/- 10 microM and 86 +/- 25 microM respectively in MT-/- mice (n = 10) and 27 +/- 1 microM and 23 +/- 4 microM respectively in MT+/+ controls (n = 9) (P < 0.001, plasma; P < 0.05, urine). Hepatic cytosolic Zn concentrations doubled in MT+/+ mice and increased by a significant 15% in MT-/- mice. There was no increase in hepatic Zn (dry wt.) concentrations or in total hepatic Zn, demonstrating that the increase in cytosolic Zn in MT-/- mice was due to hepatic water loss rather than net Zn uptake. It appears that even at extreme plasma concentrations of Zn, little if any accumulates within the liver when there is no MT available for its sequestration. That this is not fully demonstrated in vitro is probably due to nature of cell culture, where organ architecture is lost and the external protein binding milieu is less complex.

摘要

比较了从对照(MT+/+)和金属硫蛋白(MT)基因敲除(MT-/-)小鼠制备的新鲜分离和培养的肝细胞中肝锌摄取和积累情况。在新鲜分离的肝细胞中,65Zn的快速(10 - 15分钟)交换与培养基中的锌浓度成正比,并且在MT+/+和MT-/-小鼠的肝细胞中发生程度相同。在对MT+/+和MT-/-肝细胞进行的24小时培养实验中发现,约40%新获得的细胞相关锌附着在细胞表面而未内化。在MT+/+和MT-/-肝细胞培养物中,内化锌(intZn)与细胞外锌成比例增加。MT-/-肝细胞中的锌积累仅为MT+/+细胞的60%。添加1 microM地塞米松(Dex)和重组小鼠白细胞介素-6(IL-6;100单位/毫升)使MT+/+肝细胞(在50 microM锌时)中的MT积累增加了8.6倍,并且intZn相应平行增加。Dex和IL-6并未增加MT-/-肝细胞中的intZn。腹腔注射5微克/克锌16小时后,MT-/-小鼠(n = 10)的血浆和尿液锌浓度分别为69±10 microM和86±25 microM,MT+/+对照小鼠(n = 9)的血浆和尿液锌浓度分别为27±1 microM和23±4 microM(血浆,P < 0.001;尿液,P < 0.05)。MT+/+小鼠肝细胞质锌浓度翻倍,MT-/-小鼠肝细胞质锌浓度显著增加15%。肝锌(干重)浓度和肝总锌均未增加,表明MT-/-小鼠细胞质锌增加是由于肝水分流失而非净锌摄取。似乎即使在血浆锌浓度极高时,如果没有MT用于螯合,肝脏中几乎不会积累锌。这在体外未得到充分证明可能是由于细胞培养的性质,即器官结构丧失且外部蛋白质结合环境不太复杂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c054/1135795/fef3119e84ea/biochemj00060-0036-a.jpg

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