Proteomic Analysis of Hepatic Tissue of Zebrafish (Danio rerio) Experimentally Exposed to Chronic Microcystin-LR

被引:84
作者
Wang, Minghua [1 ]
Chan, Leo L. [2 ]
Si, Mengzi [1 ]
Hong, Huasheng [1 ]
Wang, Dazhi [1 ]
机构
[1] Xiamen Univ, State Key Lab Marine Environm Sci, Xiamen 361005, Peoples R China
[2] Univ Hong Kong, Sch Biol Sci, Hong Kong, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
microcystin-LR; protein phosphatase; proteomics; chronic toxicity; ultrastructure; PROTEIN PHOSPHATASE-ACTIVITY; CARP CYPRINUS-CARPIO; CARASSIUS-AURATUS L; ARABIDOPSIS-THALIANA; OXIDATIVE STRESS; KINASE-C; LIVER; IDENTIFICATION; HEPATOCYTES; FISH;
D O I
10.1093/toxsci/kfp248
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Microcystin-LR (MCLR) is the most toxic and most frequently encountered hepatotoxin in the aquatic environment. This study investigated the protein profiles of zebrafish (Danio rerio) livers chronically exposed to MCLR concentrations (2 or 20 mu g/l) using the proteomic approach as well as cell ultrastructure, protein phosphatase (PP) activity, protein phosphatase 2A (PP2A) abundance, and toxin content analysis of the hepatic tissue. The results showed that, after 30-day exposure, the presence of MCLR strikingly enhanced toxin accumulation and the PP activity in zebrafish livers. However, the PP2A amounts were independent of toxin treatments. MCLR caused a noticeable damage to liver ultrastructure, a widespread swelling in the rough endoplasmatic reticulum and mitochondria was observed in the MCLR-exposed hepatocytes, and a honeycomb-like structure was formed in the treated nucleoli. Comparison of two-dimensional electrophoresis (2-DE) protein profiles of MCLR-exposed and nonexposed zebrafish livers revealed that the abundance of 22 proteins, measured by 2-DE, was remarkably altered in response to toxin exposure. These proteins were involved in cytoskeleton assembly, macromolecule metabolism, oxidative stress, and signal transduction, indicating that MCLR toxicity in fish liver is complex and diverse. Thus, proteomics provides a new insight into MCLR toxicity, that chronic toxicity of MCLR is different from acute toxicity, and we speculate that the reactive oxygen species pathway might be the main toxic pathway instead of the PP one. Moreover, even a low concentration of MCLR in water could significantly interrupt cellular processes, and more care should be taken in determining the criterion for MCLR content in drinking water.
引用
收藏
页码:60 / 69
页数:10
相关论文
共 59 条
[1]   SUCCINATE THIOKINASE IN PIGEON BREAST MUSCLE MITOCHONDRIA [J].
ALLEN, DA ;
OTTAWAY, JH .
FEBS LETTERS, 1986, 194 (01) :171-175
[2]   Comparative study of microcystin-LR-induced behavioral changes of two fish species, Danio rerio and Leucaspius delineatus [J].
Baganz, D ;
Staaks, G ;
Pflugmacher, S ;
Steinberg, CEW .
ENVIRONMENTAL TOXICOLOGY, 2004, 19 (06) :564-570
[3]   High crustacean toxicity of microcystin congeners does not correlate with high protein phosphatase inhibitory activity [J].
Blom, JF ;
Jüttner, F .
TOXICON, 2005, 46 (04) :465-470
[4]  
BOSCOBOINIK D, 1991, J BIOL CHEM, V266, P6188
[5]   NON-MUSCLE ALPHA-ACTININS ARE CALCIUM-SENSITIVE ACTIN-BINDING PROTEINS [J].
BURRIDGE, K ;
FERAMISCO, JR .
NATURE, 1981, 294 (5841) :565-567
[6]   CRYSTALLIZATION OF A NON-MUSCLE ACTIN [J].
CARLSSON, L ;
NYSTROM, LE ;
LINDBERG, U ;
KANNAN, KK ;
CIDDRESDNER, H ;
LOVGREN, S ;
JORNVALL, H .
JOURNAL OF MOLECULAR BIOLOGY, 1976, 105 (03) :353-366
[7]   Elucidation and short-term forecasting of microcystin concentrations in Lake Suwa (Japan) by means of artificial neural networks and evolutionary algorithms [J].
Chan, Wai Sum ;
Recknagel, Friedrich ;
Cao, Hongqing ;
Park, Ho-Dong .
WATER RESEARCH, 2007, 41 (10) :2247-2255
[8]   Identification of human liver mitochondrial aldehyde dehydrogenase as a potential target for microcystin-LR [J].
Chen, T ;
Cui, J ;
Liang, Y ;
Xin, XB ;
Young, DO ;
Chen, C ;
Shen, PP .
TOXICOLOGY, 2006, 220 (01) :71-80
[9]   MICROCYSTIN-LR INDUCED AN INHIBITION OF PROTEIN-SYNTHESIS IN ISOLATED RAT HEPATOCYTES [J].
CLAEYSSENS, S ;
FRANCOIS, A ;
CHEDEVILLE, A ;
LAVOINNE, A .
BIOCHEMICAL JOURNAL, 1995, 306 :693-696
[10]   Identification of the cDNA en coding human 6-phosphogluconolactonase, the enzyme catalyzing the second step of the pentose phosphate pathway [J].
Collard, F ;
Collet, JF ;
Gerin, I ;
Veiga-da-Cunha, M ;
Van Schaftingen, E .
FEBS LETTERS, 1999, 459 (02) :223-226