Failla M L, Cousins R J, Mascenik M J
Biochim Biophys Acta. 1979 Feb 19;583(1):63-72. doi: 10.1016/0304-4165(79)90310-6.
Primary cultures of adult rat liver parenchymal cells, isolated by the collagenase perfusion technique and maintained as a monolayer, were used to investigate the characteristics of hepatic cadmium accumulation and metabolism. Cadmium accumulation was found to be a temperature- and concentration-dependent process that required sulfhydryl groups and was significantly stimulated by the addition of dexamethasone to the medium. Once taken up, cadmium was less available for exit-exchange processes than its biologically required congener, zinc. Moreover, cadmium influx enhanced zinc efflux. While most of the intracellular cadmium was located in the cytosol, its distribution within this fraction was altered with time. Initially the metal was bound to both high molecular weight species (less than 50 000) and metallothionein. As the incubation period increased, the cytosol concentration of cadmium and the percentage of this metal associated with metallothionein was likewise increased. [3H]Amino acid incorporation studies indicated that the accumulation of cadmium resulted in de novo synthesis of the 1 and 2 forms of metallothionein.
采用胶原酶灌注技术分离并维持为单层培养的成年大鼠肝实质细胞原代培养物,用于研究肝脏镉积累和代谢的特征。发现镉积累是一个温度和浓度依赖性过程,需要巯基,并且向培养基中添加地塞米松可显著刺激该过程。一旦被摄取,镉比其生物学必需的同类物锌更不易用于出-交换过程。此外,镉流入增强了锌流出。虽然大部分细胞内镉位于细胞质中,但其在该部分内的分布随时间而改变。最初,金属与高分子量物质(小于50000)和金属硫蛋白结合。随着孵育期增加,镉的细胞质浓度以及与金属硫蛋白相关的该金属百分比同样增加。[3H]氨基酸掺入研究表明,镉的积累导致金属硫蛋白1和2型的从头合成。