Iron and Porphyrin Trafficking in Heme Biogenesis

被引:107
作者
Schultz, Iman J. [1 ,2 ]
Chen, Caiyong [3 ,4 ]
Paw, Barry H. [1 ,2 ]
Hamza, Iqbal [3 ,4 ]
机构
[1] Harvard Univ, Sch Med, Dept Med, Hematol Div,Brigham & Womens Hosp, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Med, Childrens Hosp Boston,Hemat Oncol Div, Boston, MA 02115 USA
[3] Univ Maryland, Dept Anim & Avian Sci, College Pk, MD 20742 USA
[4] Univ Maryland, Dept Cell Biol & Mol Genet, College Pk, MD 20742 USA
基金
美国国家卫生研究院;
关键词
PROTOPORPHYRINOGEN-IX OXIDASE; SULFUR CLUSTER BIOGENESIS; ENDOPLASMIC-RETICULUM; MICROCYTIC ANEMIA; HUMAN FERROCHELATASE; REGULATORY PROTEIN; IDENTIFICATION; MITOCHONDRIA; TRANSPORTER; RECEPTOR;
D O I
10.1074/jbc.R110.119503
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
Iron is an essential element for diverse biological functions. In mammals, the majority of iron is enclosed within a single prosthetic group: heme. In metazoans, heme is synthesized via a highly conserved and coordinated pathway within the mitochondria. However, iron is acquired from the environment and subsequently assimilated into various cellular pathways, including heme synthesis. Both iron and heme are toxic but essential cofactors. How is iron transported from the extracellular milieu to the mitochondria? How are heme and heme intermediates coordinated with iron transport? Although recent studies have answered some questions, several pieces of this intriguing puzzle remain unsolved.
引用
收藏
页码:26753 / 26759
页数:7
相关论文
共 99 条
[1]   Association between the endoplasmic reticulum and mitochondria of yeast facilitates interorganelle transport of phospholipids through membrane contact [J].
Achleitner, G ;
Gaigg, B ;
Krasser, A ;
Kainersdorfer, E ;
Kohlwein, SD ;
Perktold, A ;
Zellnig, G ;
Daum, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 264 (02) :545-553
[2]   Biosynthesis of heme in mammals [J].
Ajioka, Richard S. ;
Phillips, John D. ;
Kushner, James P. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2006, 1763 (07) :723-736
[3]   Forging a field: the golden age of iron biology [J].
Andrews, Nancy C. .
BLOOD, 2008, 112 (02) :219-230
[4]   Iron homeostasis: Insights from genetics and animal models [J].
Andrews, NC .
NATURE REVIEWS GENETICS, 2000, 1 (03) :208-217
[5]   PREFERENTIAL HEME TRANSPORT THROUGH ENDOPLASMIC-RETICULUM ASSOCIATED WITH MITOCHONDRIA IN RAT-LIVER [J].
ASAGAMI, H ;
HINO, Y ;
KANG, DC ;
MINAKAMI, S ;
TAKESHIGE, K .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 1994, 1193 (02) :345-352
[6]  
Bekri S, 2000, BLOOD, V96, P3256
[7]   The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload [J].
Camaschella, Clara ;
Campanella, Alessandro ;
De Falco, Luigia ;
Boschetto, Loredana ;
Merlini, Roberta ;
Silvestri, Laura ;
Levi, Sonia ;
Iolascon, Achille .
BLOOD, 2007, 110 (04) :1353-1358
[8]   Abcb10 physically interacts with mitoferrin-1 (Slc25a37) to enhance its stability and function in the erythroid mitochondria [J].
Chen, Wen ;
Paradkar, Prasad N. ;
Li, Liangtao ;
Pierce, Eric L. ;
Langer, Nathaniel B. ;
Takahashi-Makise, Naoko ;
Hyde, Brigham B. ;
Shirihai, Orian S. ;
Ward, Diane M. ;
Kaplan, Jerry ;
Paw, Barry H. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (38) :16263-16268
[9]   Submitochondrial distribution of three key steroidogenic proteins (steroidogenic acute regulatory protein and cytochrome p450(scc) and 3 beta-hydroxysteroid dehydrogenase isomerase enzymes) upon stimulation by intracellular calcium in adrenal glomerulosa cells [J].
Cherradi, N ;
Rossier, MF ;
Vallotton, MB ;
Timberg, R ;
Friedberg, I ;
Orly, J ;
Wang, XJ ;
Stocco, DM ;
Capponi, AM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (12) :7899-7907
[10]   Microcytic anemia, erythropoietic protoporphyria, and neurodegeneration in mice with targeted deletion of iron-regulatory protein 2 [J].
Cooperman, SS ;
Meyron-Holtz, EG ;
Olivierre-Wilson, H ;
Ghosh, MC ;
McConnell, JP ;
Rouault, TA .
BLOOD, 2005, 106 (03) :1084-1091