Chan W Y, Garnica A D, Rennert O M
Clin Chim Acta. 1978 Sep 15;88(3):495-507. doi: 10.1016/0009-8981(78)90284-x.
The dose response as well as kinetics of uptake and retention of copper and cadmium of normal and Menkes kinky hair disease (MKHD) cultured fibroblasts are described. In basal culture medium, intracellular copper concentration in MKHD fibroblasts was approximately 3 times that of control cultures. The intracellular copper concentration of MKHD cells was significantly higher than that of normal fibroblasts at medium copper concentrations below 20 microgram/ml. Death of MKHD cells occurred at medium copper concentrations between 15 and 20 microgram/ml with an intracellular copper level 3 times that at basal medium. Normal cells died at medium copper concentration above 30 microgram/ml with an intracellular copper concentration 19 times that at basal medium. These observations suggested the existence of a regulatory mechanism for maintenance and control of intracellular copper in normal fibroblasts which is effective at medium copper concentrations below 30 microgram/ml. This system is defective in MKHD fibroblasts. In basal medium MKHD and normal fibroblasts had similar intracellular cadmium concentrations; however, at higher medium cadmium concentrations MKHD cells had increased intracellular cadmium levels. The uptake of both 64Cu and 109Cd was significantly higher in MKHD cells than in normal cells, indicating that the uptake of 64Cu and 109Cd is not impaired in MKHD cells. A higher retention of 64Cu was observed in MKHD cells at both 37 degrees C and 4 degrees C. No obvious trend, however, was observed in the difference of retention of 109Cd between MKHD and normal cells. An impairment of egress of copper in MKHD cells is implicated by these results.
描述了正常和成Menkes卷发疾病(MKHD)培养的成纤维细胞对铜和镉的剂量反应以及摄取和保留的动力学。在基础培养基中,MKHD成纤维细胞内的铜浓度约为对照培养物的3倍。在铜浓度低于20微克/毫升的培养基中,MKHD细胞的细胞内铜浓度显著高于正常成纤维细胞。MKHD细胞在铜浓度为15至20微克/毫升之间时死亡,细胞内铜水平是基础培养基中的3倍。正常细胞在铜浓度高于30微克/毫升时死亡,细胞内铜浓度是基础培养基中的19倍。这些观察结果表明,正常成纤维细胞中存在一种维持和控制细胞内铜的调节机制,该机制在铜浓度低于30微克/毫升的培养基中有效。该系统在MKHD成纤维细胞中存在缺陷。在基础培养基中,MKHD和成纤维细胞的细胞内镉浓度相似;然而,在较高的培养基镉浓度下,MKHD细胞的细胞内镉水平增加。MKHD细胞对64Cu和109Cd的摄取均显著高于正常细胞,表明MKHD细胞对64Cu和109Cd的摄取未受损。在37℃和4℃下,MKHD细胞中均观察到64Cu的保留率较高。然而,在MKHD细胞和正常细胞之间,109Cd保留率的差异未观察到明显趋势。这些结果提示MKHD细胞中铜的流出存在障碍。