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转铁蛋白功能与表达的调控:综述与更新

Regulation of transferrin function and expression: review and update.

作者信息

Lok C N, Loh T T

机构信息

Department of Physiology, Medical Faculty, University of Hong Kong, Hong Kong.

出版信息

Biol Signals Recept. 1998 May-Jun;7(3):157-78. doi: 10.1159/000014542.

Abstract

The cellular iron uptake is a precisely controlled process to fulfill the iron demand for the synthesis and functions of a variety of iron-containing proteins, and one of the main molecules involved is the transferrin receptor (TfR), which mediates the uptake process via the transferrin cycle. The TfR expression is tightly regulated by factors such as intracellular iron level, cell proliferation or erythropoiesis at levels of receptor recycling, transcriptional or posttranscriptional control. The iron-regulatory protein/iron-responsive element system has been widely used to explain changes in receptor expression during iron loading or depletion, oxidative stress and nitric oxide stimulation. On the other hand, transcriptional control of TfR expression appears to be more important in erythroid differentiation and general cell proliferation. There is also an increasing awareness of the clinical application and experimental therapeutics based on the TfR functioning and expression. In this review, we attempt to provide a concise account of the studies of TfR structure and function as well as those areas that have not been reviewed in depth, in particular, tissue-specific regulation of TfR, the molecular mechanisms of TfR expression, and the use of TfR as diagnostic and therapeutic tools. The regulation of TfR expression in various tissues is related to its specific cellular iron requirements. Hemoglobin-synthesizing cells exhibit distinct features of iron metabolism and TfR expression as compared to most non-erythroid cells which synthesize a much lower amount of heme. For most non-erythroid cells, iron can regulate the TfR expression in a reciprocal manner through modulating the stability of the receptor mRNA whereas in hemoglobin-synthesizing cells, the TfR expression is independent of the cellular iron loading. In spite of a wide heterogeneity in the way receptor redistribution is in response to various stimuli, regulation of the constitutive expression of TfR is one of the ways of regulating the cellular iron uptake. This expression operates on both transcriptional and posttranscriptional levels. In general, factors related to cell growth and differentiation operate on the gene transcription level, whereas iron regulates the fate of the mature mRNA.

摘要

细胞铁摄取是一个精确调控的过程,以满足多种含铁蛋白质合成及功能对铁的需求,其中涉及的主要分子之一是转铁蛋白受体(TfR),它通过转铁蛋白循环介导摄取过程。TfR的表达受到细胞内铁水平、细胞增殖或红细胞生成等因素的严格调控,调控水平涉及受体循环、转录或转录后控制。铁调节蛋白/铁反应元件系统已被广泛用于解释铁负荷或耗竭、氧化应激和一氧化氮刺激期间受体表达的变化。另一方面,TfR表达的转录控制在红细胞分化和一般细胞增殖中似乎更为重要。基于TfR功能和表达的临床应用和实验治疗也越来越受到关注。在本综述中,我们试图简要介绍TfR结构和功能的研究,以及那些尚未深入综述的领域,特别是TfR的组织特异性调控、TfR表达的分子机制,以及TfR作为诊断和治疗工具的应用。TfR在各种组织中的表达调控与其特定的细胞铁需求有关。与大多数合成血红素量低得多的非红细胞相比,合成血红蛋白的细胞表现出独特的铁代谢和TfR表达特征。对于大多数非红细胞,铁可通过调节受体mRNA的稳定性以相反的方式调节TfR表达,而在合成血红蛋白的细胞中,TfR表达与细胞铁负荷无关。尽管受体重新分布对各种刺激的反应方式存在广泛的异质性,但TfR组成型表达的调控是调节细胞铁摄取的方式之一。这种表达在转录和转录后水平上均起作用。一般来说,与细胞生长和分化相关的因素在基因转录水平上起作用,而铁则调节成熟mRNA的命运。

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