The effect of metabolic inhibitors on transferrin and iron uptake and transferrin release from reticulocytes.
The effect of metabolic inhibitors on transferrin and iron uptake and transferrin release from reticulocytes.
复制标题
代谢抑制剂对转铁蛋白和网织红细胞铁摄取和转铁蛋白释放的影响。
DOI:
10.1016/0304-4165(69)90048-8
复制
发表时间:
1969
期刊:
影响因子:
--
通讯作者:
E. Baker
中科院分区:
文献类型:
--
作者:
E. Morgan;E. Baker
Metabolic inhibitors were broadly classified into three groups on the basis of their effect on the uptake of [125I]transferrin and59Fe and the release of [125I]transferrin by rabbit reticulocytesin vitro:1.1. Inhibitors which had no effect on transferrin or iron uptake (sodium malonate and ouabain).2.2. Those which blocked iron uptake more than transferrin uptake (retonone, 2,4-dinitrophenol, oligomycin, NaCN, NaN3, NaF and cycloheximide). The effect of these compounds was attributed to inhibition of the mitochondrial electron transfer chain.3.3. Those which inhibited iron and transferrin uptake to approximately the same degree (sodium arsenite, iodoacetamide,N-ethylmaleimide,p-chloromercuribenzoate (PCMB),p-chloromercuribenzenesulfonate (PCMBS) and lead acetate). The onset of inhibition by all the inhibitors studied was immediate, but the effects of iodoacetamide,N-ethylmaleimide, PCMB and PCMBS were largely prevented by prior addition of cysteine in 1–4 times the molar concentration of inhibitor. Sodium arsenite, iodoacetamide andN-ethylmaleimide also inhbited transferrin release. These compounds (all sulfhydryl reagents) may act by altering reticulocyte membrane structure, reducing transferrin and hence iron uptake.