Simpson R J, Cooper C E, Raja K B, Halliwell B, Evans P J, Aruoma O I, Singh S, Konijn A M
Department of Clinical Biochemistry, King's College School of Medicine and Dentistry, London, UK.
Biochim Biophys Acta. 1992 Dec 8;1156(1):19-26. doi: 10.1016/0304-4165(92)90090-h.
Serum from homozygous hypotransferrinaemic mice (a mixed group of males and females, aged 6-8 wk) was found to contain low levels of iron (mean 0.9 +/- 0.5 microM (SEM, n = 4), as assayed by conventional serum iron assays. Similarly, low levels of non-transferrin-bound iron were determined with a nitrilotriacetate chelation assay (1.3 +/- 0.4 microM, n = 4) (Singh, S., Hider, R.C. and Porter, J.B. (1990) Analytical Biochemistry 186, 320-323). Mononuclear Fe (citrate) was undectable by electron paramagnetic resonance spectroscopy (EPR). Significantly larger quantities of iron (16 +/- 5 microM, n = 8) were detected by the bleomycin assay (Gutteridge, J.M.C., Rowley, D.A. and Halliwell, B. (1981) Biochemical Journal 199, 263-265), while non-haem iron assay or atomic absorption spectrophotometry revealed up to 96 microM iron. Haemoglobin iron was detectable at approximately 10 microM by spectrophotometry. Ferri-haem was undetectable by EPR spectroscopy. Serum ferritin levels of 641 +/- 128 micrograms/l (n = 14) in hypotransferrinaemic mice (wild-types 44 +/- 6 micrograms/l, n = 14) were observed and these cannot account for the non-transferrin-bound iron. Hypotransferrinaemic mouse serum therefore contains large quantities of non-transferrin-bound iron which is unreactive in some assays used to detect such iron in human iron overload. Fractionation by Sephadex G200 chromatography revealed three distinct species with apparent molecular weights of > or = 150 kDa, 40-80 kDa and 1-5 kDa. The iron may be distinguished from known extracellular iron proteins and haem-proteins by its availability to hot acid extractions.
在纯合子低转铁蛋白血症小鼠(6 - 8周龄的雄性和雌性混合组)的血清中,通过传统血清铁检测法测定发现其铁含量较低(平均值为0.9±0.5微摩尔/升(标准误,n = 4))。同样,通过次氮基三乙酸螯合测定法测定的非转铁蛋白结合铁水平也较低(1.3±0.4微摩尔/升,n = 4)(辛格,S.,希德,R.C.和波特,J.B.(1990年)《分析生物化学》186卷,320 - 323页)。通过电子顺磁共振光谱法(EPR)未检测到单核铁(柠檬酸盐)。通过博来霉素测定法检测到大量铁(16±5微摩尔/升,n = 8)(古特里奇,J.M.C.,罗利,D.A.和哈利威尔,B.(1981年)《生物化学杂志》199卷,263 - 265页),而非血红素铁测定法或原子吸收分光光度法显示铁含量高达96微摩尔/升。通过分光光度法可检测到血红蛋白铁约为10微摩尔/升。通过EPR光谱法未检测到高铁血红素。观察到低转铁蛋白血症小鼠的血清铁蛋白水平为641±128微克/升(n = 14)(野生型为44±6微克/升,n = 14),而这些水平无法解释非转铁蛋白结合铁的情况。因此,低转铁蛋白血症小鼠血清中含有大量非转铁蛋白结合铁,在用于检测人类铁过载中此类铁的一些检测方法中,这些铁无反应性。通过葡聚糖G200柱色谱法分离显示出三种不同的组分,其表观分子量分别≥150 kDa、40 - 80 kDa和1 - 5 kDa。通过热酸提取法可将该铁与已知的细胞外铁蛋白和血红素蛋白区分开来。