Transferrin Receptors in Erythropoiesis

被引:43
作者
Richard, Cyrielle [1 ,2 ]
Verdier, Frederique [1 ,2 ]
机构
[1] Univ Paris, Inst Cochin, CNRS, Inserm,U1016,UMR8104, F-75014 Paris, France
[2] Univ Paris, Lab Excellence GR Ex, F-75014 Paris, France
关键词
erythropoiesis; TFR1; TFR2; iron metabolism; iron uptake; transferrin; ERYTHROID-DIFFERENTIATION; CLINICAL-SIGNIFICANCE; IRON UPTAKE; MICE LEADS; TFR2; HEPCIDIN; CELL; HFE; EXPRESSION; DELETION;
D O I
10.3390/ijms21249713
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
Erythropoiesis is a highly dynamic process giving rise to red blood cells from hematopoietic stem cells present in the bone marrow. Red blood cells transport oxygen to tissues thanks to the hemoglobin comprised of alpha- and beta-globin chains and of iron-containing hemes. Erythropoiesis is the most iron-consuming process to support hemoglobin production. Iron delivery is mediated via transferrin internalization by the endocytosis of transferrin receptor type 1 (TFR1), one of the most abundant membrane proteins of erythroblasts. A second transferrin receptor-TFR2-associates with the erythropoietin receptor and has been implicated in the regulation of erythropoiesis. In erythroblasts, both transferrin receptors adopt peculiarities such as an erythroid-specific regulation of TFR1 and a trafficking pathway reliant on TFR2 for iron. This review reports both trafficking and signaling functions of these receptors and reassesses the debated role of TFR2 in erythropoiesis in the light of recent findings. Potential therapeutic uses targeting the transferrin-TFR1 axis or TFR2 in hematological disorders are also discussed.
引用
收藏
页码:1 / 16
页数:16
相关论文
共 88 条
[1]   Comparative analysis of the efficiency and specificity of myeloid-Cre deleting strains using ROSA-EYFP reporter mice [J].
Abram, Clare L. ;
Roberge, Gray L. ;
Hu, Yongmei ;
Lowell, Clifford A. .
JOURNAL OF IMMUNOLOGICAL METHODS, 2014, 408 :89-100
[2]  
Anderson GJ, 2012, NUTR HEALTH SER, P1, DOI 10.1007/978-1-60327-485-2
[3]   Transferrin receptor 2 is a potential novel therapeutic target for β-thalassemia: evidence from a murine model [J].
Artuso, Irene ;
Lidonnici, Maria Rosa ;
Altamura, Sandro ;
Mandelli, Giacomo ;
Pettinato, Mariateresa ;
Muckenthaler, Martina U. ;
Silvestri, Laura ;
Ferrari, Giuliana ;
Camaschella, Clara ;
Nai, Antonella .
BLOOD, 2018, 132 (21) :2286-2297
[4]   Genetic hemochromatosis: Pathophysiology, diagnostic and therapeutic management [J].
Brissot, Pierre ;
Cavey, Thibault ;
Ropert, Martine ;
Guggenbuhl, Pascal ;
Loreal, Olivier .
PRESSE MEDICALE, 2017, 46 (12) :E288-E295
[5]   TfR2 localizes in lipid raft domains and is released in exosomes to activate signal transduction along the MAPK pathway [J].
Calzolari, Alessia ;
Raggi, Carla ;
Deaglio, Silvia ;
Sposi, Nadia Maria ;
Stafsnes, Marit ;
Fecchi, Katia ;
Parolini, Isabella ;
Malavasi, Fabio ;
Peschle, Cesare ;
Sargiacomo, Massimo ;
Testa, Ugo .
JOURNAL OF CELL SCIENCE, 2006, 119 (21) :4486-4498
[6]   Iron deficiency [J].
Camaschella, Clara .
BLOOD, 2019, 133 (01) :30-39
[7]   Transferrin receptor targeting nanomedicine delivering wild-type p53 gene sensitizes pancreatic cancer to gemcitabine therapy [J].
Camp, E. R. ;
Wang, C. ;
Little, E. C. ;
Watson, P. M. ;
Pirollo, K. F. ;
Rait, A. ;
Cole, D. J. ;
Chang, E. H. ;
Watson, D. K. .
CANCER GENE THERAPY, 2013, 20 (04) :222-228
[8]   Src-Mediated Phosphorylation of Dynamin and Cortactin Regulates the "Constitutive" Endocytosis of Transferrin [J].
Cao, Hong ;
Chen, Jing ;
Krueger, Eugene W. ;
McNiven, Mark A. .
MOLECULAR AND CELLULAR BIOLOGY, 2010, 30 (03) :781-792
[9]   New therapeutic targets in transfusion-dependent and-independent thalassemia [J].
Cappellini, M. Domenica ;
Motta, Irene .
HEMATOLOGY-AMERICAN SOCIETY OF HEMATOLOGY EDUCATION PROGRAM, 2017, :278-283
[10]   Correcting β-thalassemia by combined therapies that restrict iron and modulate erythropoietin activity [J].
Casu, Carla ;
Pettinato, Mariateresa ;
Liu, Alison ;
Aghajan, Mariam ;
Lo Presti, Vania ;
Lidonnici, Maria Rosa ;
Munoz, Kevin A. ;
O'Hara, Emir ;
Olivari, Violante ;
Di Modica, Simona Maria ;
Booten, Sheri ;
Guo, Shuling ;
Neil, Garry ;
Miari, Reem ;
Shapir, Nir ;
Zafir-Lavie, Inbal ;
Domev, Hagit ;
Ferrari, Giuliana ;
Sitara, Despina ;
Nai, Antonella ;
Rivella, Stefano .
BLOOD, 2020, 136 (17) :1968-1979