van der Ende A, du Maine A, Schwartz A L, Strous G J
Department of Cell Biology, University of Utrecht, The Netherlands.
Biochem J. 1989 May 1;259(3):685-92. doi: 10.1042/bj2590685.
We have recently described the transferrin-mediated uptake and release of iron by BeWo cells [van der Ende, du Maine, Simmons, Schwartz & Strous (1987) J. Biol. Chem. 262, 8910-8916]. We now extend our studies of the mechanisms responsible for uptake and release of iron by these cells. Following preloading, 59Fe release was maximal (about 12%) after about 4 h. Replacement of the extracellular medium with an equal volume of fresh medium either prior to or following the time at which equilibrium was reached further stimulated 59Fe release. Both the rate and maximum amount of iron release decreased if longer loading times were used. Preincubation of BeWo cells for 15 min with 10 mM-sodium cyanide and 50 mM-2-deoxyglucose prior to the determination of 59Fe release did not alter the amount released into medium (which did not contain a high-affinity iron chelator). However, under these conditions, the uptake of 59Fe was dramatically inhibited as a result of prolongation of the transferrin-transferrin-receptor complex recycling time. These results demonstrate that the release of iron from BeWo cells is independent of cellular ATP levels, whereas iron uptake is ATP-dependent. Rates of both 59Fe release and 59Fe uptake were temperature-dependent. Analysis of these data via an Arrhenius plot suggests a single rate-limiting step for the release and uptake processes between 0 and 37 degrees C. The apparent energies of activation of these processes are very similar (approx. 59.0 kJ/mol for iron release and 50.6 kJ/mol for iron uptake), which raises the possibility that the release and uptake of iron share a common thermodynamically rate-limiting step. Possible mechanisms involved in iron release out of the cell and out of the endosome are discussed.
我们最近描述了转铁蛋白介导的铁在BeWo细胞中的摄取和释放[范德恩德、杜缅因、西蒙斯、施瓦茨和斯特劳斯(1987年)《生物化学杂志》262卷,8910 - 8916页]。我们现在扩展对这些细胞中铁摄取和释放机制的研究。预加载后,约4小时后59Fe释放量最大(约12%)。在达到平衡之前或之后,用等体积的新鲜培养基替换细胞外培养基进一步刺激了59Fe释放。如果使用更长的加载时间,铁释放的速率和最大量都会降低。在测定59Fe释放之前,将BeWo细胞与10 mM氰化钠和50 mM 2 - 脱氧葡萄糖预孵育15分钟,并没有改变释放到培养基(其中不含高亲和力铁螯合剂)中的铁量。然而,在这些条件下,由于转铁蛋白 - 转铁蛋白受体复合物循环时间延长,59Fe的摄取受到显著抑制。这些结果表明,BeWo细胞中铁的释放与细胞ATP水平无关,而铁的摄取是ATP依赖的。59Fe释放和59Fe摄取的速率均与温度有关。通过阿累尼乌斯图分析这些数据表明,在0至37摄氏度之间,释放和摄取过程存在单一的限速步骤。这些过程的表观活化能非常相似(铁释放约为59.0 kJ/mol,铁摄取约为50.6 kJ/mol),这增加了铁的释放和摄取共享一个共同的热力学限速步骤的可能性。讨论了铁从细胞和内体释放出来可能涉及的机制。