Efflux of Iron from the Cerebrospinal Fluid to the Blood at the Blood-CSF Barrier: Effect of Manganese Exposure

被引:29
作者
Wang, Xueqian [1 ]
Li, G. Jane [2 ]
Zheng, Wei [1 ]
机构
[1] Purdue Univ, Sch Hlth Sci, W Lafayette, IN 47907 USA
[2] Beijing Municipal Ctr Dis Prevent & Control, Beijing Municipal Hlth Bur, Beijing 100080, Peoples R China
关键词
iron; manganese; choroid plexus; blood-CSF barrier; in vitro Transwell model; ventriculo-cisternal perfusion;
D O I
10.3181/0803-RM-104
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The blood-cerebrospinal fluid (CSF) barrier (BCB) resides within the choroid plexus, with the apical side facing the CSF and the basolateral side towards the blood. Previous studies demonstrate that manganese (Mn) exposure in rats disrupts iron (Fe) homeostasis in the blood and CSF. The present study used a primary culture of rat choroidal epithelial cells grown in the two-chamber Transwell system to investigate the transepithelial transport of Fe across the BCB. Free, unbound Fe as [Fe-59] was added to the donor chamber and the radioactivity in the acceptor chamber was quantified to determine the direction of Fe fluxes. Under the normal condition, the [Fe-59] efflux (from the CSF to the blood) was 128% higher than that of the influx (P < 0.01). Mn exposure significantly increased the efflux rate of [Fe-59] (P < 0.01) and the effect was inhibited when the cells were pre-incubated with the antibody against divalent metal transport 1 (DMT1). Moreover, when the siRNA knocked down the cellular DMT1 expression, the elevated Fe uptake caused by Mn exposure in the choroidal epithelial Z310 cells was completely abolished, indicating that Mn may facilitate Fe efflux via a DMT1-mediated transport mechanism. In vivo subchronic exposure to Mn in rats reduced Fe clearance from the CSF, as demonstrated by the ventriculo-cisternal brain perfusion, along with up-regulated mRNAs encoding DMT1 and transferrin receptor (TfR) in the same animals. Taken together, these data suggest that free Fe appears to be favorably transported from the CSF toward the blood by DMT1 and this process can be facilitated by Mn exposure. Enhanced TfR-mediated influx of Fe from the blood and ferroportin-mediated expelling Fe toward the CSF may compromise DMT1-mediated efflux, leading to an increased Fe concentration in the CSF as seen in Mn-exposed animals. Exp Biol Med 233:1561-1571, 2008
引用
收藏
页码:1561 / 1571
页数:11
相关论文
共 50 条
[1]   Iron metabolism [J].
Aisen, P ;
Wessling-Resnick, M ;
Leibold, EA .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (02) :200-206
[2]   Increased brain uptake and CSF clearance of 14C-glutamate in spontaneously hypertensive rats [J].
Al-Sarraf, H ;
Philip, L .
BRAIN RESEARCH, 2003, 994 (02) :181-187
[3]   Effect of hypertension on the integrity of blood brain and blood CSF barriers, cerebral blood flow and CSF secretion in the rat [J].
Al-Sarraf, H ;
Philip, L .
BRAIN RESEARCH, 2003, 975 (1-2) :179-188
[4]   Effect of DMT1 knockdown on iron, cadmium, and lead uptake in Caco-2 cells [J].
Bannon, DI ;
Abounader, R ;
Lees, PSJ ;
Bressler, JP .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2003, 284 (01) :C44-C50
[5]   Brain iron pathways and their relevance to Parkinson's disease [J].
Berg, D ;
Gerlach, M ;
Youdim, MBH ;
Double, KL ;
Zecca, L ;
Riederer, P ;
Becker, G .
JOURNAL OF NEUROCHEMISTRY, 2001, 79 (02) :225-236
[6]  
Bradbury MWB, 1997, J NEUROCHEM, V69, P443
[7]   Effects of iron deficiency and iron overload on manganese uptake and deposition in the brain and other organs of the rat [J].
Chua, ACG ;
Morgan, EH .
BIOLOGICAL TRACE ELEMENT RESEARCH, 1996, 55 (1-2) :39-54
[8]   The choroid plexus removes β-amyloid from brain cerebrospinal fluid [J].
Crossgrove, JS ;
Li, GJ ;
Zheng, W .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2005, 230 (10) :771-776
[9]   Brain capillary endothelium and choroid plexus epithelium regulate transport of transferrin-bound and free iron into the rat brain [J].
Deane, R ;
Zheng, W ;
Zlokovic, BV .
JOURNAL OF NEUROCHEMISTRY, 2004, 88 (04) :813-820
[10]   Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter [J].
Donovan, A ;
Brownlie, A ;
Zhou, Y ;
Shepard, J ;
Pratt, SJ ;
Moynihan, J ;
Paw, BH ;
Drejer, A ;
Barut, B ;
Zapata, A ;
Law, TC ;
Brugnara, C ;
Kingsley, PD ;
Palis, J ;
Fleming, MD ;
Andrews, NC ;
Zon, LI .
NATURE, 2000, 403 (6771) :776-781