Breuer W, Ronson A, Slotki I N, Abramov A, Hershko C, Cabantchik Z I
Department of Biological Chemistry, Institute of Life Sciences, Hebrew University of Jerusalem, Jerusalem, Israel.
Blood. 2000 May 1;95(9):2975-82.
Nontransferrin-bound iron (NTBI) appears in the serum of individuals with iron overload and in a variety of other pathologic conditions. Because NTBI constitutes a labile form of iron, it might underlie some of the biologic damage associated with iron overload. We have developed a simple method for NTBI determination, which operates in a 96-well enzyme-linked immunosorbent assay format with sensitivity comparable to that of previous assays. A weak ligand, oxalic acid, mobilizes the NTBI and mediates its transfer to the iron chelator deferoxamine (DFO) immobilized on the plate. The amount of DFO-bound iron, originating from NTBI, is quantitatively revealed in a fluorescence plate reader by the fluorescent metallosensor calcein. No NTBI is found in normal sera because transferrin-bound iron is not detected in the assay. Thalassemic sera contained NTBI in 80% of the cases (range, 0.9-12.8 micromol/L). In patients given intravenous infusions of DFO, NTBI initially became undetectable due to the presence of DFO in the sera, but reappeared in 55% of the cases within an hour of cessation of the DFO infusion. This apparent rebound was attributable to the loss of DFO from the circulation and the possibility that a major portion of NTBI was not mobilized by DFO. NTBI was also found in patients with end-stage renal disease who were treated for anemia with intravenous iron supplements and in patients with hereditary hemochromatosis, at respective frequencies of 22% and 69%. The availability of a simple assay for monitoring NTBI could provide a useful index of iron status during chelation and supplementation treatments. (Blood. 2000;95:2975-2982)
非转铁蛋白结合铁(NTBI)出现在铁过载个体的血清以及多种其他病理状况中。由于NTBI构成一种不稳定的铁形式,它可能是与铁过载相关的一些生物损伤的基础。我们开发了一种简单的NTBI测定方法,该方法以96孔酶联免疫吸附测定形式进行,灵敏度与先前的测定方法相当。一种弱配体草酸可动员NTBI,并介导其转移至固定在平板上的铁螯合剂去铁胺(DFO)。源自NTBI的与DFO结合的铁的量,通过荧光金属传感器钙黄绿素在荧光酶标仪中进行定量检测。正常血清中未发现NTBI,因为在该测定中未检测到转铁蛋白结合铁。80%的地中海贫血血清中含有NTBI(范围为0.9 - 12.8微摩尔/升)。在接受静脉输注DFO的患者中,由于血清中存在DFO,NTBI最初无法检测到,但在停止DFO输注后一小时内,55%的病例中NTBI再次出现。这种明显的反弹归因于循环中DFO的流失以及大部分NTBI未被DFO动员的可能性。在接受静脉补铁治疗贫血的终末期肾病患者以及遗传性血色素沉着症患者中也发现了NTBI,其出现频率分别为22%和69%。一种用于监测NTBI的简单测定方法的可用性,可为螯合和补充治疗期间的铁状态提供有用指标。(《血液》。2000年;95:2975 - 2982)