Alteration at translational but not transcriptional level of transferrin receptor expression following manganese exposure at the blood-CSF barrier in vitro

被引:39
作者
Li, GJ [1 ]
Zhao, QQ [1 ]
Zheng, W [1 ]
机构
[1] Purdue Univ, Sch Hlth Sci, W Lafayette, IN 47907 USA
关键词
manganese (Mn); iron (Fe); influx; choroid plexus; Z310; cells; blood-CSF barrier (BCB); transferrin receptor (TfR); ferritin; heterogeneous nuclear RNA (hnRNA); iron regulatory protein (IRP); iron response element (IRE); nuclear run-off assay; gel shift assay; reverse transcriptase polymerase chain reaction (RT-PCR); quantitative real-time RT-PCR;
D O I
10.1016/j.taap.2004.10.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Manganese exposure alters iron homeostasis in blood and cerebrospinal fluid (CSF), possibly by acting on iron transport mechanisms localized at the blood-brain barrier and/or blood-CSF barrier. This study was designed to test the hypothesis that manganese exposure may change the binding affinity of iron regulatory proteins (IRPs) to rnRNAs encoding transferrin receptor (TfR), thereby influencing iron transport at the blood-CSF barrier. A primary culture of choroidal epithelial cells was adapted to grow on a permeable membrane sandwiched between two culture chambers to mimic blood-CSF barrier. Trace Fe-59 was used to determine the transepithelial transport of iron. Following manganese treatment (100 mu M for 24 h), the initial flux rate constant (K-i) of iron was increased by 34%, whereas the storage of iron in cells was reduced by 58%, as compared to controls. A gel shift assay demonstrated that manganese exposure increased the binding of IRP1 and IRP2 to the stein loop-containing mRNAs. Consequently, the cellular concentrations of TfR proteins were increased by 84% in comparison to controls. Assays utilizing RT-PCR, quantitative real-time reverse traiiscriptase-PCR, and nuclear run off techniques showed that manganese treatment did not affect the level of heterogeneous nuclear RNA (hnRNA) encoding TfR, nor did it affect the level of nascent TfR mRNA. However, manganese exposure resulted in a significantly increased level of TfR mRNA and reduced levels of ferritin mRNA. Taken together, these results suggest that manganese exposure increases iron transport at the blood-CSF barrier; the effect is likely due to manganese action on translational events relevant to the production of TfR, but not due to its action on transcriptional, gene expression of TfR. The disrupted protein-TfR rnRNA interaction in the choroidal epithelial cells may explain the toxicity of manganese at the blood-CSF barrier. (c) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:188 / 200
页数:13
相关论文
共 52 条
[31]   Effects of hemoglobin on heme oxygenase gene expression and viability of cultured smooth muscle cells [J].
Marton, LS ;
Wang, XY ;
Kowalczuk, A ;
Zhang, ZD ;
Windmeyer, E ;
Macdonald, RL .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2000, 279 (05) :H2405-H2413
[32]   Post-transcriptional control via iron-responsive elements:: the impact of aberrations in hereditary disease [J].
Mikulits, W ;
Schranzhofer, M ;
Beug, H ;
Müllner, EW .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 1999, 437 (03) :219-230
[33]   Transferrin and transferrin receptor function in brain barrier systems [J].
Moos, T ;
Morgan, EH .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2000, 20 (01) :77-95
[34]  
MUNRO H, 1993, NUTR REV, V51, P65, DOI 10.1111/j.1753-4887.1993.tb03072.x
[35]   Activation of transcription of the human presenilin 1 gene by 12-O-tetradecanoylphorbol 13-acetate [J].
Pastorcic, M ;
Das, HK .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2002, 269 (23) :5956-5962
[36]   The transferrin receptor: role in health and disease [J].
Ponka, P ;
Lok, CN .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1999, 31 (10) :1111-1137
[37]  
Ponka P, 1998, SEMIN HEMATOL, V35, P35
[38]   Inhaled iron, unlike manganese, is not transported to the rat brain via the olfactory pathway [J].
Rao, DB ;
Wong, BA ;
McManus, BE ;
McElveen, AM ;
James, AR ;
Dorman, DC .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2003, 193 (01) :116-126
[39]  
Rouault T A, 1996, EXS, V77, P183
[40]   Real-time and quantitative PCR: Applications to mechanism-based toxicology [J].
Walker, NJ .
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2001, 15 (03) :121-127