Anghileri L J, Maincent P, Córdova-Martínez A, Escanero J F
Laboratory of Biophysics, Faculty of Medicine, University of Nancy, France.
Biol Trace Elem Res. 1994 Jan;40(1):83-8. doi: 10.1007/BF02916823.
Ferric lactate is known to modify Ca2+ uptake by the cells. To enlighten the role of protein and ATP in this phenomenon, iron transfer from ferric lactate to albumin and adenosine polyphosphates was determined by electrophoresis. The order of iron affinity was ATP > ADP > AMP for the polyphosphates, and albumin does not compete for iron binding with the polyphosphates. The iron transfer to ATP was also observed in vivo by adsorption chromatography of the adenosine polyphosphates fraction from blood plasma of mice injected with ferric lactate plus ATP. In vitro iron and calcium uptake by Ehrlich ascites tumor cells showed that albumin and ATP decreased iron uptake, whereas calcium incorporation is diminished by albumin but augmented by ATP. This difference might be explained by albumin binding of ferric lactate that is inhibited from reaching cell structures, whereas ATP, known to be an inhibitor of iron polymerization, facilitates it.
已知乳酸铁可改变细胞对Ca2+的摄取。为了阐明蛋白质和ATP在此现象中的作用,通过电泳测定了铁从乳酸铁向白蛋白和多聚腺苷酸的转移。对于多聚磷酸盐,铁亲和力的顺序为ATP > ADP > AMP,并且白蛋白不与多聚磷酸盐竞争铁结合。通过对注射了乳酸铁加ATP的小鼠血浆中的多聚腺苷酸部分进行吸附色谱分析,也在体内观察到了铁向ATP的转移。艾氏腹水肿瘤细胞的体外铁和钙摄取表明,白蛋白和ATP降低了铁摄取,而白蛋白减少了钙掺入,但ATP增加了钙掺入。这种差异可能是由于乳酸铁与白蛋白结合而被阻止到达细胞结构,而ATP已知是铁聚合的抑制剂,却促进了铁摄取。