Like iron in the blood of the people: the requirement for heme trafficking in iron metabolism

被引:54
作者
Korolnek, Tamara [1 ,2 ]
Hamza, Iqbal [1 ,2 ]
机构
[1] Univ Maryland, Dept Anim & Avian Sci, College Pk, MD 20742 USA
[2] Univ Maryland, Dept Cell Biol & Mol Genet, College Pk, MD 20742 USA
关键词
heme; iron; transport; hematology; porphyrins; anemia; erythropoiesis; nutrition disorders; CYTOCHROME BC(1) COMPLEX; HEREDITARY MYELOPEROXIDASE DEFICIENCY; ENDOPLASMIC-RETICULUM; BINDING PROTEIN; ERYTHROLEUKEMIA-CELLS; CRYSTAL-STRUCTURE; HEMOGLOBIN-IRON; MATERNAL HEME; OXYGENASE; MITOCHONDRIA;
D O I
10.3389/fphar.2014.00126
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Heme is an iron-containing porphyrin ring that serves as a prosthetic group in proteins that function in diverse metabolic pathways. Heme is also a major source of bioavailable iron in the human diet. While the synthesis of heme has been well-characterized, the pathways for heme trafficking remain poorly understood. It is likely that heme transport across membranes is highly regulated, as free heme is toxic to cells. This review outlines the requirement for heme delivery to various subcellular compartments as well as possible mechanisms for the mobilization of heme to these compartments. We also discuss how these trafficking pathways might function during physiological events involving inter- and intra-cellular mobilization of heme, including erythropoiesis, erythrophagocytosis, heme absorption in the gut, as well as heme transport pathways supporting embryonic development. Lastly, we aim to question the current dogma that heme, in toto, is not mobilized from one cell or tissue to another, outlining the evidence for these pathways and drawing parallels to other well-accepted paradigms for copper, iron, and cholesterol homeostasis.
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页数:13
相关论文
共 114 条
[1]
ROLE OF THE GUT IN LIPID HOMEOSTASIS [J].
Abumrad, Nada A. ;
Davidson, Nicholas O. .
PHYSIOLOGICAL REVIEWS, 2012, 92 (03) :1061-1085
[2]
Bimodal targeting of cytochrome P450s to endoplasmic reticulum and mitochondria: the concept of chimeric signals [J].
Avadhani, Narayan G. ;
Sangar, Michelle C. ;
Bansal, Seema ;
Bajpai, Prachi .
FEBS JOURNAL, 2011, 278 (22) :4218-4229
[3]
Erythrophagocytosis and recycling of heme iron in normal and pathological conditions; regulation by hepcidin [J].
Beaumont, C ;
Canonne-Hergaux, F .
TRANSFUSION CLINIQUE ET BIOLOGIQUE, 2005, 12 (02) :123-130
[4]
Overlapping specificities of the mitochondrial cytochrome c and c1 heme lyases [J].
Bernard, DG ;
Gabilly, ST ;
Dujardin, G ;
Merchant, S ;
Hamel, PP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (50) :49732-49742
[5]
MEMBRANE TOPOLOGY OF THE MAMMALIAN P450-CYTOCHROMES [J].
BLACK, SD .
FASEB JOURNAL, 1992, 6 (02) :680-685
[6]
The chemistry and biochemistry of heme c: functional bases for covalent attachment [J].
Bowman, Sarah E. J. ;
Bren, Kara L. .
NATURAL PRODUCT REPORTS, 2008, 25 (06) :1118-1130
[7]
A compilation of mutations located in the cytochrome b subunit of the bacterial and mitochondrial bc(1) complex [J].
Brasseur, G ;
Saribas, AS ;
Daldal, F .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1996, 1275 (1-2) :61-69
[8]
Cellular and molecular mechanisms of senescent erythrocyte phagocytosis by macrophages. A review [J].
Bratosin, D ;
Mazurier, J ;
Tissier, JP ;
Estaquier, J ;
Huart, JJ ;
Ameisen, JC ;
Aminoff, D ;
Montreuil, J .
BIOCHIMIE, 1998, 80 (02) :173-195
[9]
BROWN EB, 1968, J LAB CLIN MED, V72, P58
[10]
STEREOSPECIFIC HEME CLEAVAGE - MODEL FOR FORMATION OF BILE-PIGMENT ISOMERS INVIVO AND INVITRO [J].
BROWN, SB .
BIOCHEMICAL JOURNAL, 1976, 159 (01) :23-27