MRP2 and acquired tolerance to inorganic arsenic in the kidney of killifish (Fundulus heteroclitus)

被引:36
作者
Miller, David S.
Shaw, Joseph R.
Stanton, Caitlin R.
Barnaby, Roxanna
Karlson, Katherine H.
Hamilton, Joshua W.
Stanton, Bruce A.
机构
[1] Dartmouth Coll Sch Med, Dept Physiol, Hanover, NH 03755 USA
[2] Dartmouth Coll Sch Med, Dept Pharmacol & Toxicol, Hanover, NH 03755 USA
[3] NIEHS, Lab Pharmacol & Chem, NIH, Res Triangle Pk, NC 27709 USA
[4] Mt Desert Isl Biol Lab, Salsbury Cove, ME 04672 USA
[5] Dartmouth Coll, Dept Biol Sci, Hanover, NH 03755 USA
[6] Dartmouth Coll Sch Med, Ctr Environm Hlth Sci, Hanover, NH 03755 USA
关键词
adaptation; xenobiotic transport; Abcc2; environmental toxicant;
D O I
10.1093/toxsci/kfm030
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
We used proximal tubules isolated from the killifish, Fundulus heteroclitus, to examine the effect of environmentally relevant, sublethal levels of arsenic on the function and expression of MRP2, an ABC transporter that transports xenobiotics into urine, including arsenic-glutathione conjugates. Exposure of fish to arsenic as sodium arsenite (4-14 days) increased both MRP2 expression in the apical membrane of proximal tubules and MRP2-mediated transport activity. The level of MRP2 mRNA was not affected, suggesting a posttranslational mechanism of action. Acute exposure of proximal tubules isolated from control fish to 75-375 ppb arsenic decreased mitochondrial function (inner membrane electrical potential). However, in tubules from fish that were preexposed to arsenic (4-14 days), no such effect on mitochondrial function was observed. Thus, chronic in vivo exposure to arsenic induces mechanisms that protect proximal tubules during subsequent arsenic exposure. Upregulation of MRP2 expression and activity is one likely contributing factor.
引用
收藏
页码:103 / 110
页数:8
相关论文
共 33 条
[1]   Arsenic: Health effects, mechanisms of actions, and research issues [J].
Abernathy, CO ;
Liu, YP ;
Longfellow, D ;
Aposhian, HV ;
Beck, B ;
Fowler, B ;
Goyer, R ;
Menzer, R ;
Rossman, T ;
Thompson, C ;
Waalkes, M .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1999, 107 (07) :593-597
[2]   Arsenic exposure alters hepatic arsenic species composition and stress-mediated gene expression in the common killifish (Fundulus heteroclitus) [J].
Bears, H ;
Richards, JG ;
Schulte, PM .
AQUATIC TOXICOLOGY, 2006, 77 (03) :257-266
[3]   The role of multidrug, transporters in drug availability, metabolism and toxicity [J].
Bodó, A ;
Bakos, E ;
Szeri, F ;
Váradi, A ;
Sarkadi, B .
TOXICOLOGY LETTERS, 2003, 140 :133-143
[4]  
BOYLE RW, 1973, GEOCHEMISTRY ARSENIC
[5]   P-glycoprotein- and mrp2-mediated octreotide transport in renal proximal tubule [J].
Gutmann, H ;
Miller, DS ;
Droulle, A ;
Drewe, J ;
Fahr, A ;
Fricker, G .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 129 (02) :251-256
[6]   The role of protein synthesis and degradation in the post-transcriptional regulation of rat multidrug resistance-associated protein 2 (Mrp2, Abcc2) [J].
Jones, BR ;
Li, W ;
Cao, J ;
Hoffman, TA ;
Gerk, PM ;
Vore, M .
MOLECULAR PHARMACOLOGY, 2005, 68 (03) :701-710
[7]   The MRP2/cMOAT transporter and arsenic-glutathione complex formation are required for biliary excretion of arsenic [J].
Kala, SV ;
Neely, MW ;
Kala, G ;
Prater, CI ;
Atwood, DW ;
Rice, JS ;
Lieberman, MW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (43) :33404-33408
[8]   The efficiency of pooling mRNA in microarray experiments [J].
Kendziorski, CM ;
Zhang, Y ;
Lan, H ;
Attie, AD .
BIOSTATISTICS, 2003, 4 (03) :465-477
[9]   Trace analyses of arsenic in drinking water by inductively coupled plasma mass spectrometry: High resolution versus hydride generation [J].
Klaue, B ;
Blum, JD .
ANALYTICAL CHEMISTRY, 1999, 71 (07) :1408-1414
[10]   Enhanced expression of multidrug resistance-associated protein 2 and reduced expression of aquaglyceroporin 3 in an arsenic-resistant human cell line [J].
Lee, Te-Chang ;
Ho, I-Ching ;
Lu, Wen-Jen ;
Huang, Jin-Ding .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (27) :18401-18407