Morphological and ultrastructural effects of microcystin-LR from Microcystis aeruginosa extract on a kidney cell line

被引:98
作者
Alverca, E. [1 ]
Andrade, M. [1 ]
Dias, E. [1 ,2 ,3 ]
Bento, F. Sam [1 ]
Batoreu, M. C. C. [3 ]
Jordan, P. [2 ]
Silva, M. J. [2 ]
Pereira, P. [1 ]
机构
[1] Natl Inst Hlth Dr Ricardo Jorge, Dept Environm Hlth, P-1649016 Lisbon, Portugal
[2] Natl Inst Hlth Dr Ricardo Jorge, Dept Genet, P-1649016 Lisbon, Portugal
[3] Univ Lisbon, Fac Pharm, Toxicol Lab, P-1649019 Lisbon, Portugal
关键词
Microcystin-LR; Vero cells; Cytotoxicity; Fluorescence microscopy; TEM; MITOCHONDRIAL PERMEABILITY TRANSITION; INTRACELLULAR GLUTATHIONE ALTERATION; IN-VIVO; ENDOPLASMIC-RETICULUM; INDUCED APOPTOSIS; OXIDATIVE STRESS; DRINKING-WATER; DNA-DAMAGE; CYANOBACTERIAL EXTRACT; GOLGI STRUCTURE;
D O I
10.1016/j.toxicon.2009.04.014
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
The aim of this study was to examine the toxic effects of a microcystin-LR (MCLR)-containing cyanobacteria extract on the subcellular organization of a kidney cell line (Vero-E6). Cells were exposed to different MCLR concentrations (1.3-150 mu M) for 24, 48 and 72 h and two cytotoxicity assays were performed. This information was combined with the analysis of lysosomal, mitochondrial and cytoskeleton integrity and with an ultrastructural study. Biochemical and microscopic data revealed a good agreement and demonstrated that cellular response to MCLR is dependent on the dose/exposure time. Cell viability decayed markedly after 24 h of exposure to toxin concentrations greater than 30 PM. Furthermore, it was demonstrated that lysosome destabilization precedes mitochondria dysfunction. The ultrastructural analysis showed that mild toxin incubation conditions induce endoplasmic reticulum (ER) vacuolization and assembly of large autophagic vacuoles, suggesting that autophagy is an early cellular response to the toxin. After exposure to higher MCLR doses, the number of apoptotic cells increased, as identified by microscopic observations and confirmed with TUNEL assay. Additionally, drastic exposure conditions induced the increase of necrotic cells. These results suggest that the ER is the primary microcystin target in Vero cells and that autophagy, apoptosis and necrosis are induced in a dose- and time-dependent manner. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:283 / 294
页数:12
相关论文
共 75 条
[1]
Microcystin-LR causes the collapse of actin filaments in primary human hepatocytes [J].
Batista, T ;
de Sousa, G ;
Suput, JS ;
Rahmani, R ;
Suput, DA .
AQUATIC TOXICOLOGY, 2003, 65 (01) :85-91
[2]
Autophagy delays sulindac sulfide-induced apoptosis in the human intestinal colon cancer cell line HT-29 [J].
Bauvy, C ;
Gane, P ;
Arico, S ;
Codogno, P ;
Ogier-Denis, E .
EXPERIMENTAL CELL RESEARCH, 2001, 268 (02) :139-149
[3]
ISOLATED RAT-LIVER PERFUSION STUDIES WITH CYCLIC HEPTAPEPTIDE TOXINS OF MICROCYSTIS AND OSCILLATORIA (FRESH-WATER CYANOBACTERIA) [J].
BERG, K ;
WYMAN, J ;
CARMICHAEL, W ;
DABHOLKAR, A .
TOXICON, 1988, 26 (09) :827-837
[4]
Toxic response indicators of microcystin-LR in F344 rats following a single-dose treatment [J].
Billam, Madhavi ;
Mukhi, Sandeep ;
Tang, Lili ;
Gao, Weimin ;
Wang, Jia-Sheng .
TOXICON, 2008, 51 (06) :1068-1080
[5]
Bischoff K, 2001, VET HUM TOXICOL, V43, P294
[6]
Microcystin-LR induced cellular effects in mammalian and fish primary hepatocyte cultures and cell lines: A comparative study [J].
Boaru, DA ;
Dragos, N ;
Schirmer, K .
TOXICOLOGY, 2006, 218 (2-3) :134-148
[7]
TOXICITY DETERMINED INVITRO BY MORPHOLOGICAL ALTERATIONS AND NEUTRAL RED ABSORPTION [J].
BORENFREUND, E ;
PUERNER, JA .
TOXICOLOGY LETTERS, 1985, 24 (2-3) :119-124
[8]
The role of microcystin-LR in the induction of apoptosis and oxidative stress in CaCo2 cells [J].
Botha, N ;
Gehringer, MM ;
Downing, TG ;
van de Venter, M ;
Shephard, EG .
TOXICON, 2004, 43 (01) :85-92
[9]
Microcystin-LR and nodularin induce intracellular glutathione alteration, reactive oxygen species production and lipid peroxidation in primary cultured rat hepatocytes [J].
Bouaïcha, N ;
Maatouk, I .
TOXICOLOGY LETTERS, 2004, 148 (1-2) :53-63
[10]
Cell death independent of caspases:: A review [J].
Bröker, LE ;
Kruyt, FAE ;
Giaccone, G .
CLINICAL CANCER RESEARCH, 2005, 11 (09) :3155-3162