New insights into erythropoiesis:: The roles of folate, vitamin B12, and iron

被引:308
作者
Koury, MJ [1 ]
Ponka, P
机构
[1] Vanderbilt Univ, Sch Med, Dept Med, Nashville, TN 37232 USA
[2] Vet Affairs Tennessee Valley Healthcare Syst, Nashville, TN 37232 USA
[3] McGill Univ, Jewish Gen Hosp, Lady Davis Inst Med Res, Dept Physiol, Montreal, PQ H3T 1E2, Canada
[4] McGill Univ, Jewish Gen Hosp, Lady Davis Inst Med Res, Dept Med, Montreal, PQ H3T 1E2, Canada
关键词
apoptosis; heme; erythrocytes; iron deficiency anemia; megaloblastic anemia;
D O I
10.1146/annurev.nutr.24.012003.132306
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Erythropoiesis is the process in which new erythrocytes are produced. These new erythrocytes replace the oldest erythrocytes (normally about one percent) that are phagocytosed and destroyed each day. Folate, vitamin B-12, and iron have crucial roles in erythropoiesis. Erythroblasts require folate and vitamin B-12 for proliferation during their differentiation. Deficiency of folate or vitamin B-12 inhibits purine and thymidylate syntheses, impairs DNA synthesis, and causes erythroblast apoptosis, resulting in anemia from ineffective erythropoiesis. Erythroblasts require large amounts of iron for hemoglobin synthesis. Large amounts of iron are recycled daily with hemoglobin breakdown from destroyed old erythrocytes. Many recently identified proteins are involved in absorption, storage, and cellular export of nonheme iron and in erythroblast uptake and utilization of iron. Erythroblast heme levels regulate uptake of iron and globin synthesis such that iron deficiency causes anemia by retarded production rates with smaller, less hemoglobinized erythrocytes.
引用
收藏
页码:105 / 131
页数:29
相关论文
共 124 条
[1]   A novel mammalian iron-regulated protein involved in intracellular iron metabolism [J].
Abboud, S ;
Haile, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (26) :19906-19912
[2]   Chemistry and biology of eukaryotic iron metabolism [J].
Aisen, P ;
Enns, C ;
Wessling-Resnick, M .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2001, 33 (10) :940-959
[3]   The ceruloplasmin homolog hephaestin and the control of intestinal iron absorption [J].
Anderson, GJ ;
Frazer, DM ;
McKie, AT ;
Vulpe, CD .
BLOOD CELLS MOLECULES AND DISEASES, 2002, 29 (03) :367-375
[4]  
Antony A.C., 2000, HEMATOLOGY BASIC PRI, P446
[5]   MEGALOBLASTIC HEMATOPOIESIS INVITRO - INTERACTION OF ANTIFOLATE RECEPTOR ANTIBODIES WITH HEMATOPOIETIC PROGENITOR CELLS LEADS TO A PROLIFERATIVE RESPONSE INDEPENDENT OF MEGALOBLASTIC CHANGES [J].
ANTONY, AC ;
BRIDDELL, RA ;
BRANDT, JE ;
STRANEVA, JE ;
VERMA, RS ;
MILLER, ME ;
KALASINSKI, LA ;
HOFFMAN, R .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (01) :313-325
[6]   EFFECT OF PERTURBATION OF SPECIFIC FOLATE RECEPTORS DURING INVITRO ERYTHROPOIESIS [J].
ANTONY, AC ;
BRUNO, E ;
BRIDDELL, RA ;
BRANDT, JE ;
VERMA, RS ;
HOFFMAN, R .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 80 (06) :1618-1623
[7]   Ferritin, iron homeostasis, and oxidative damage [J].
Arosio, P ;
Levi, S .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 33 (04) :457-463
[8]   Vitamin B12 deficiency in the elderly [J].
Baik, HW ;
Russell, RM .
ANNUAL REVIEW OF NUTRITION, 1999, 19 :357-377
[9]  
BESTWICK RK, 1982, J BIOL CHEM, V257, P9300
[10]  
BILLS ND, 1992, BLOOD, V79, P2273