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未分化和分化的红系细胞中的铁摄取及转铁蛋白内吞作用。

Iron uptake and transferrin endocytosis in undifferentiated and differentiated erythroid cells.

作者信息

Hradilek A, Neuwirt J

出版信息

Biomed Biochim Acta. 1987;46(2-3):S141-5.

PMID:3473987
Abstract

Iron uptake from transferrin (Tf) by Friend erythroleukemia cells was studied before and after induction of the cells by dimethyl sulfoxide (DMSO) in culture. The increase in iron uptake after 5 days of induction was not accompanied by a proportional increase in the number of transferrin receptors detected by 125I-labeled Tf binding, resulting in DMSO induced cells taking up iron with the rate of about 26 iron atoms per receptor per hour, compared to 15 atoms in uninduced cells. In agreement with this finding are results of the study of cellular 125I or 59Fe-labeled Tf kinetics. In the induced cells Tf endocytosis and release proceeded with identical rates and all the endocytosed iron was retained inside the cell. Tf release by uninduced cells was slower and a part of internalized 59Fe was released. Hemin inhibits Tf-bound iron uptake by DMSO induced cells but not by the uninduced cells. Correspondingly, addition of hemin had little effect on Tf kinetics in the uninduced cells, while the release of Tf was slower in hemin-treated DMSO induced cells. Different efficiency of iron release from internalized Tf, accompanied by changes in cellular Tf kinetics is therefore proposed as a factor determining the rate of iron uptake by developing erythroid cells.

摘要

研究了在培养过程中用二甲基亚砜(DMSO)诱导前、后,Friend红白血病细胞从转铁蛋白(Tf)摄取铁的情况。诱导5天后铁摄取的增加并未伴随着通过125I标记的Tf结合检测到的转铁蛋白受体数量成比例增加,导致DMSO诱导的细胞以约每受体每小时26个铁原子的速率摄取铁,相比之下未诱导细胞为15个原子。细胞125I或59Fe标记的Tf动力学研究结果与此发现一致。在诱导细胞中,Tf内吞作用和释放以相同速率进行,并且所有内吞的铁都保留在细胞内。未诱导细胞的Tf释放较慢,并且一部分内化的59Fe被释放。血红素抑制DMSO诱导细胞摄取Tf结合的铁,但不抑制未诱导细胞。相应地,添加血红素对未诱导细胞的Tf动力学影响很小,而在血红素处理的DMSO诱导细胞中Tf的释放较慢。因此,内化Tf释放铁的效率不同,并伴随着细胞Tf动力学的变化,被认为是决定发育中的红系细胞摄取铁速率的一个因素。

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