Takada A, Bannai S
J Biol Chem. 1984 Feb 25;259(4):2441-5.
Uptake of cystine and factors affecting the transport were investigated in adult rat hepatocytes in primary monolayer culture. The cystine uptake was initially mediated by Na+-dependent route(s). However, the activity of Na+-dependent uptake decreased markedly during the culture, and Na+-independent uptake emerged with a lag period of 12 h in response to insulin and dexamethasone in the culture medium. After 48 h in culture, cystine was mainly transported into the cells through this Na+-independent route. The action of insulin and dexamethasone on the enhancement of the Na+-independent uptake was apparently additive, and the enhancement was completely blocked by cycloheximide or actinomycin D. Emergence of the Na+-independent uptake of cystine was also regulated by cell density; at lower density, the uptake tended to be elevated. The transport of cystine through the Na+-independent system was pH sensitive and was inhibited by some anionic amino acids, such as glutamate and homocysteate, but not by aspartate. These results suggest that the emerging system is similar to the ones reported in fibroblasts and in some hepatoma cell lines; the anionic form of cystine is transported through the system.
在原代单层培养的成年大鼠肝细胞中研究了胱氨酸的摄取及其影响因素。胱氨酸的摄取最初由钠依赖性途径介导。然而,在培养过程中,钠依赖性摄取活性显著下降,并且在培养基中存在胰岛素和地塞米松的情况下,非钠依赖性摄取在12小时的延迟期后出现。培养48小时后,胱氨酸主要通过这种非钠依赖性途径转运进入细胞。胰岛素和地塞米松对增强非钠依赖性摄取的作用明显具有加和性,并且这种增强被环己酰亚胺或放线菌素D完全阻断。胱氨酸非钠依赖性摄取的出现也受细胞密度调节;在较低密度下,摄取倾向于升高。胱氨酸通过非钠依赖性系统的转运对pH敏感,并受到一些阴离子氨基酸(如谷氨酸和高半胱氨酸)的抑制,但不受天冬氨酸的抑制。这些结果表明,新出现的系统与成纤维细胞和一些肝癌细胞系中报道的系统相似;胱氨酸的阴离子形式通过该系统转运。