Mycotoxin deoxynivalenol (DON) mediates biphasic cellular response in intestinal porcine epithelial cell lines IPEC-1 and IPEC-J2

被引:114
作者
Diesing, Anne-Kathrin [1 ]
Nossol, Constanze [1 ]
Panther, Patricia [1 ]
Walk, Nicole [1 ]
Post, Andreas [1 ]
Kluess, Jeannette [1 ]
Kreutzmann, Peter [2 ]
Daenicke, Sven [3 ]
Rothkoetter, Hermann-Josef [1 ]
Kahlert, Stefan [1 ]
机构
[1] Univ Magdeburg, Inst Anat, Fac Med, D-39120 Magdeburg, Germany
[2] Univ Magdeburg, Inst Biochem & Cell Biol, Fac Med, D-39120 Magdeburg, Germany
[3] Fed Res Inst Anim Hlth, Inst Anim Nutr, FLI, D-38116 Braunschweig, Germany
关键词
Tight junction; Cell cycle; Cell proliferation; Apoptosis; Viability; PROTEIN-SYNTHESIS; IMMUNE-SYSTEM; CYCLE ARREST; IN-VITRO; CYTOTOXICITY; TRICHOTHECENES; CACO-2; SWINE; HEPATOCYTES; METABOLISM;
D O I
10.1016/j.toxlet.2010.10.006
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The Fusarium derived mycotoxin deoxynivalenol (DON) is frequently found in cereals used for human and animal nutrition. We studied effects of DON in non-transformed, non-carcinoma, polarized epithelial cells of porcine small intestinal origin (IPEC-1 and IPEC-J2) in a low (200 ng/mL) and a high (2000 ng/mL) concentration. Application of high DON concentrations showed significant toxic effects as indicated by a reduction in cell number, in cellular reduction capacity measured by MTT assay, reduced uptake of neutral red (NR) and a decrease in cell proliferation. High dose toxicity was accompanied by disintegration of tight junction protein ZO-1 and increase of cell cycle phase G2/M. Activation of caspase 3 was found as an early event in the high DON concentration with an initial maximum after 6-8 h. In contrast, application of 200 ng/mL DON exhibited a response pattern distinct from the high dose DON toxicity. The cell cycle, ZO-1 expression and distribution Ss well as caspase 3 activation were not changed. BrdU incorporation was significantly increased after 72 h incubation with 200 ng/mL DON and NR uptake was only transiently reduced after 24 h. Low dose effects of DON on intestinal epithelial cells were triggered by mechanisms different from those responsible for the high dose toxicity. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:8 / 18
页数:11
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