Anghileri L J, Thouvenot P
Laboratory of Biophysics, Faculty of Medicine, University of Nancy, BP 184, F-54505 Vandoeuvre les Nancy, France.
Int J Mol Med. 1998 May;1(5):869-73. doi: 10.3892/ijmm.1.5.869.
The cellular iron uptake from low molecular weight iron complexes (ferric citrate, ferric lactate and ferric ATP complex) is concentration-dependent, and only a small part of the iron penetrates the cell as shown by deferoxamine treatment. A threshold of iron concentration in the cell must be reached for the iron complex-induced increase of cellular Ca2+-uptake. ATP seems to play a key role in an iron translocation that enhances the effects of the iron complexes. A non-specific and competitive iron-binding by proteins seems to act as a buffer system that reduces the iron overload effects. Calcium channel blockers have no effects on the iron complex-cell interaction or iron-induced Ca2+-uptake modification. An iron complex concentration-dependent inhibition of the CaATPase activity, and its consequent Ca2+-extrusion impairment appear as the likely cause of calcium overload. The relevance of these findings in iron overload-induced pathologies is discussed.
细胞从低分子量铁复合物(柠檬酸铁、乳酸铁和ATP铁复合物)摄取铁是浓度依赖性的,去铁胺处理表明只有一小部分铁能穿透细胞。铁复合物诱导细胞钙摄取增加必须达到细胞内铁浓度的阈值。ATP似乎在增强铁复合物作用的铁转运中起关键作用。蛋白质的非特异性和竞争性铁结合似乎起到了减少铁过载效应的缓冲系统的作用。钙通道阻滞剂对铁复合物与细胞的相互作用或铁诱导的钙摄取改变没有影响。铁复合物对CaATPase活性的浓度依赖性抑制及其导致的Ca2+外排受损似乎是钙过载的可能原因。本文讨论了这些发现与铁过载所致病理状况的相关性。