Thorstensen K, Romslo I
Scand J Clin Lab Invest. 1986 Apr;46(2):107-13. doi: 10.3109/00365518609083645.
The mechanism by which utilization of transferrin-bound iron is linked with cellular metabolism has been studied in isolated rat hepatocytes. The initial binding of transferrin to the hepatocyte is not dependent on metabolic energy, but the subsequent progressive binding of transferrin and uptake of iron depend on metabolic energy and the drainage of reducing equivalents from the respiratory chain. When respiration is completely blocked with cyanide a limiting energy level for the uptake of iron is found at an intracellular concentration of ATP of approximately 0.2 mmol/l. The iron uptake process utilizes ATP hydrolysis, substrate oxidation and dissipation of ionic gradients as energy sources interchangeably.
已在分离的大鼠肝细胞中研究了转铁蛋白结合铁的利用与细胞代谢相关的机制。转铁蛋白与肝细胞的初始结合不依赖于代谢能量,但随后转铁蛋白的逐步结合和铁的摄取依赖于代谢能量以及呼吸链中还原当量的消耗。当用氰化物完全阻断呼吸时,在细胞内ATP浓度约为0.2 mmol/l时发现了铁摄取的能量限制水平。铁摄取过程可交替利用ATP水解、底物氧化和离子梯度耗散作为能量来源。