Ferritin: a novel mechanism for delivery of iron to the brain and other organs

被引:165
作者
Fisher, J.
Devraj, K.
Ingram, J.
Slagle-Webb, B.
Madhankumar, A. B.
Liu, X.
Klinger, M.
Simpson, I. A.
Connor, J. R.
机构
[1] Penn State Univ, Milton S Hershey Med Ctr, Dept Neurosurg H110, Hershey, PA 17033 USA
[2] Penn State Univ, Milton S Hershey Med Ctr, Coll Med, Dept Neural & Behav Sci, Hershey, PA 17033 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2007年 / 293卷 / 02期
关键词
blood-brain barrier; iron transport; H-ferritin;
D O I
10.1152/ajpcell.00599.2006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Traditionally, transferrin has been considered the primary mechanism for cellular iron delivery, despite suggestive evidence for additional iron delivery mechanisms. In this study we examined ferritin, considered an iron storage protein, as a possible delivery protein. Ferritin consists of H- and L-subunits, and we demonstrated iron uptake by ferritin into multiple organs and that the uptake of iron is greater when the iron is delivered via H-ferritin compared with L-ferritin. The delivery of iron via H-ferritin but not L-ferritin was significantly decreased in mice with compromised iron storage compared with control, indicating that a feedback mechanism exists for H-ferritin iron delivery. To further evaluate the mechanism of ferritin iron delivery into the brain, we used a cell culture model of the blood-brain barrier to demonstrate that ferritin is transported across endothelial bells. There are receptors that prefer H-ferritin on the endothelial cells in culture and on rat brain microvasculature. These studies identify H-ferritin as an iron transport protein and suggest the presence of an H-ferritin receptor for mediating iron delivery. The relative amount of iron that could be delivered via H-ferritin could make this protein a predominant player in cellular iron delivery.
引用
收藏
页码:C641 / C649
页数:9
相关论文
共 46 条
[1]   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
[2]   Hydrocortisone decreases retinal endothelial cell water and solute flux coincident with increased content and decreased phosphorylation of occludin [J].
Antonetti, DA ;
Wolpert, EB ;
DeMaio, L ;
Harhaj, NS ;
Scaduto, RC .
JOURNAL OF NEUROCHEMISTRY, 2002, 80 (04) :667-677
[3]   Brain iron uptake in hypotransferrinemic mice: Influence of systemic iron status [J].
Beard, JL ;
Wiesinger, JA ;
Li, N ;
Connor, JR .
JOURNAL OF NEUROSCIENCE RESEARCH, 2005, 79 (1-2) :254-261
[4]   Ultrastructural and morphometric investigation of human brain capillaries in normal and peritumoral tissues [J].
Bertossi, M ;
Virgintino, D ;
Maiorano, E ;
Occhiogrosso, M ;
Roncali, L .
ULTRASTRUCTURAL PATHOLOGY, 1997, 21 (01) :41-49
[5]   Regulation of the profile of iron-management proteins in brain microvasculature [J].
Burdo, JR ;
Simpson, IA ;
Menzies, S ;
Beard, J ;
Connor, JR .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2004, 24 (01) :67-74
[6]   Mechanisms and regulation of transferrin and iron transport in a model blood-brain barrier system [J].
Burdo, JR ;
Antonetti, DA ;
Wolpert, EB ;
Connor, JR .
NEUROSCIENCE, 2003, 121 (04) :883-890
[7]   Brain iron uptake and homeostatic mechanisms: An overview [J].
Burdo, JR ;
Connor, JR .
BIOMETALS, 2003, 16 (01) :63-75
[8]  
BUYS SS, 1991, BLOOD, V78, P3288
[9]   Nuclear ferritin protects DNA from UV damage in corneal epithelial cells [J].
Cai, CX ;
Birk, DE ;
Linsenmayer, TF .
MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (05) :1037-1051
[10]   Effect of vascular endothelial growth factor on cultured endothelial cell monolayer transport properties [J].
Chang, YS ;
Munn, LL ;
Hillsley, MV ;
Dull, RO ;
Yuan, J ;
Lakshminarayanan, S ;
Gardner, TW ;
Jain, RK ;
Tarbell, JM .
MICROVASCULAR RESEARCH, 2000, 59 (02) :265-277