The transferrin receptor: role in health and disease

被引:440
作者
Ponka, P
Lok, CN
机构
[1] Sir Mortimer B Davis Jewish Hosp, Lady Davis Inst Med Res, Montreal, PQ H3T 1E2, Canada
[2] McGill Univ, Dept Physiol, Montreal, PQ, Canada
[3] McGill Univ, Dept Med, Montreal, PQ, Canada
基金
英国医学研究理事会;
关键词
D O I
10.1016/S1357-2725(99)00070-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The transferrin receptor is a membrane glycoprotein whose only clearly defined function is to mediate cellular uptake of iron from a plasma glycoprotein, transferrin. Iron uptake from transferrin involves the binding of transferrin to the transferrin receptor, internalization of transferrin within an endocytic vesicle by receptor-mediated endocytosis and the release of iron from the protein by a decrease in endosomal pH. With the exception of highly differentiated cells, transferrin receptors are probably expressed on all cells but their levels vary greatly. Transferrin receptors are highly expressed on immature erythroid cells, placental tissue, and rapidly dividing cells, both normal and malignant. In proliferating nonerythroid cells the expression of transferrin receptors is negatively regulated post-transcriptionally by intracellular iron through iron responsive elements (IREs) in the 3' untranslated region of transferrin receptor mRNA. IREs are recognized by specific cytoplasmic proteins (IRPs; iron regulatory proteins) that, in the absence of iron in the labile pool, bind to the IREs of transferrin receptor mRNA, preventing its degradation. On the other hand, the expansion of the labile iron pool leads to a rapid degradation of transferrin receptor mRNA that is not protected since IRPs are not bound to it. However, some cells and tissues with specific requirements for iron probably evolved mechanisms that can override the IRE/IRP-dependent control of transferrin receptor expression. Erythroid cells, which are the most avid consumers of iron in the organism, use a transcriptional mechanism to maintain very high transferrin receptor levels. Transcriptional regulation is also involved in the receptor expression during T and B lymphocyte activation. Macrophages are another example of a cell type that shows 'unorthodox' responses in terms of IRE/IRP paradigm since in these cells elevated iron levels increase (rather than decrease) transferrin receptor mRNA and protein levels, Erythroid cells contain the highest mass of the total organismal transferrin receptors which are released from reticulocytes during their maturation to erythrocytes. Hence, plasma contains small amounts of transferrin receptors which represent a soluble fragment of the extracellular receptor domain. Measurements of serum transferrin receptor concentrations are clinically useful since their levels correlate with the total mass of immature erythroid cells. (C) 1999 Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1111 / 1137
页数:27
相关论文
共 186 条
  • [41] Exon/intron structure of the human transferrin receptor gene
    Evans, P
    Kemp, J
    [J]. GENE, 1997, 199 (1-2) : 123 - 131
  • [42] SPECIFIC MEMBRANE-RECEPTORS FOR DIFERRIC-TRANSFERRIN IN CULTURED RAT SKELETAL MYOCYTES AND CHICK-EMBRYO CARDIAC MYOCYTES
    FAVA, RA
    COMEAU, RD
    WOODWORTH, RC
    [J]. BIOSCIENCE REPORTS, 1981, 1 (05) : 377 - 385
  • [43] The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding
    Feder, JN
    Penny, DM
    Irrinki, A
    Lee, VK
    Lebrón, JA
    Watson, N
    Tsuchihashi, Z
    Sigal, E
    Bjorkman, PJ
    Schatzman, RC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (04) : 1472 - 1477
  • [44] A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
    Feder, JN
    Gnirke, A
    Thomas, W
    Tsuchihashi, Z
    Ruddy, DA
    Basava, A
    Dormishian, F
    Domingo, R
    Ellis, MC
    Fullan, A
    Hinton, LM
    Jones, NL
    Kimmel, BE
    Kronmal, GS
    Lauer, P
    Lee, VK
    Loeb, DB
    Mapa, FA
    McClelland, E
    Meyer, NC
    Mintier, GA
    Moeller, N
    Moore, T
    Morikang, E
    Prass, CE
    Quintana, L
    Starnes, SM
    Schatzman, RC
    Brunke, KJ
    Drayna, DT
    Risch, NJ
    Bacon, BR
    Wolff, RK
    [J]. NATURE GENETICS, 1996, 13 (04) : 399 - 408
  • [45] FERGUSON BJ, 1992, J LAB CLIN MED, V119, P385
  • [46] FILLET G, 1989, BLOOD, V74, P844
  • [47] A structurally novel transferrin-like protein accumulates in the plasma membrane of the unicellular green alga Dunaliella salina grown in high salinities
    Fisher, M
    Gokhman, I
    Pick, U
    Zamir, A
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (03) : 1565 - 1570
  • [48] Iron uptake by the halotolerant alga Dunaliella is mediated by a plasma membrane transferrin
    Fisher, M
    Zamir, A
    Pick, U
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (28) : 17553 - 17558
  • [49] Fleming MD, 1997, NAT GENET, V16, P383, DOI 10.1038/ng0897-383
  • [50] Nramp2 is mutated in the anemic Belgrade (b) rat:: Evidence of a role for Nramp2 in endosomal iron transport
    Fleming, MD
    Romano, MA
    Su, MA
    Garrick, LM
    Garrick, MD
    Andrews, NC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (03) : 1148 - 1153