Microcystin-LR induces abnormal root development by altering microtubule organization in tissue-cultured common reed (Phragmites australis) plantlets

被引:64
作者
Mathe, Csaba [1 ]
Beyer, Daniel [1 ]
Erdodi, Ferenc [2 ,3 ]
Serfozo, Zoltan [6 ]
Szekvoelgyi, Lorant [4 ]
Vasas, Gabor [1 ]
M-Hamvas, Marta [1 ]
Jambrik, Katalin [1 ]
Gonda, Sandor [1 ]
Kiss, Andrea [2 ,3 ]
Szigeti, Zsuzsa M. [5 ]
Suranyi, Gyula [1 ]
机构
[1] Univ Debrecen, Dept Bot, Fac Sci & Technol, H-4010 Debrecen, Hungary
[2] Univ Debrecen, Dept Med Chem & Cell Biol, H-4012 Debrecen, Hungary
[3] Hungarian Acad Sci, Res Ctr Mol Med, Med & Hlth Sci Ctr, Signaling Res Grp, H-4012 Debrecen, Hungary
[4] Univ Debrecen, Dept Biophys & Cell Biol, Med & Hlth Sci Ctr, H-4032 Debrecen, Hungary
[5] Univ Debrecen, Inst Food Proc Qual Control & Microbiol, Ctr Agr Sci, H-4032 Debrecen, Hungary
[6] Univ Debrecen, Dept Expt Zool, Balaton Limnol Res Inst, Hungarian Acad Sci, H-8237 Tihany, Hungary
关键词
Microcystin-LR; Protein phosphatase; Microtubules; Mitotic alterations; Phragmites australis; ABERRANT MITOTIC SPINDLES; CYANOBACTERIAL TOXINS; PROTEIN PHOSPHATASES; OKADAIC ACID; CELL-SHAPE; GROWTH; INHIBITION; ARREST; L; PHOSPHORYLATION;
D O I
10.1016/j.aquatox.2009.02.005
中图分类号
Q17 [水生生物学];
学科分类号
071004 [水生生物学];
摘要
Microcystin-LR (MC-LR) is a heptapeptide cyanotoxin, known to be a potent inhibitor of type 1 and 2A protein phosphatases in eukaryotes. Our aim was to investigate the effect of MC-LR on the organization of microtubules and mitotic chromatin in relation to its possible effects on cell and whole organ morphology in roots of common reed (Phragmites australis). P australis is a widespread freshwater and brackish water aquatic macrophyte, frequently exposed to phytotoxins in eutrophic waters. Reed plantlets regenerated from embryogenic calli were treated with 0.001-40 mu g ml(-1) (0.001-40.2 mu M) MC-LR for 2-20 days. At 0.5 mu g ml(-1) MC-LR and at higher cyanotoxin concentrations, the inhibition of protein phosphatase activity by MC-LR induced alterations in reed root growth and morphology, including abnormal lateral root development and the radial swelling of cells in the elongation zone of primary and lateral roots. Both short-term (2-5 days) and long-term (10-20 days) of cyanotoxin treatment induced microtubule disruption in meristems and in the elongation and differentiation zones. Microtubule disruption was accompanied by root cell shape alteration. At concentrations of 0.5-5 mu g ml(-1), MC-LR increased mitotic index at long-term exposure and induced the increase of the percentage of meristematic cells in prophase as well as telophase and cytokinesis of late mitosis. High cyanotoxin concentrations (10-40 mu g ml(-1)) inhibited mitosis at as short as 2 days of exposure. The alteration of microtubule organization was observed in mitotic cells at all exposure periods studied, at cyanotoxin concentrations of 0.5-40 mu g ml(-1). MC-LR induced spindle anomalies at the meta phase-anaphase transition, the formation of asymmetric anaphase spindles and abnormal sister chromatid separation. This paper reports for the first time that MC-LR induces cytoskeletal changes that lead to alterations of root architecture and development in common reed and generally, in plant cells. The MC-LR induced alterations in cells of an ecologically important aquatic macrophyte can reveal the importance of the effects of a cyanobacterial toxin in aquatic ecosystems. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:122 / 130
页数:9
相关论文
共 54 条
[11]
Effects of microcystins on the growth and the activity of superoxide dismutase and peroxidase of rape (Brassica napus L.) and rice (Oryza sativa L.) [J].
Chen, JZ ;
Song, LR ;
Dai, E ;
Gan, NQ ;
Liu, ZL .
TOXICON, 2004, 43 (04) :393-400
[12]
Cheng AY, 1998, CANCER RES, V58, P3611
[13]
Cyanobacterial toxins: risk management for health protection [J].
Codd, GA ;
Morrison, LF ;
Metcalf, JS .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2005, 203 (03) :264-272
[14]
THE BIMG GENE OF ASPERGILLUS-NIDULANS, REQUIRED FOR COMPLETION OF ANAPHASE, ENCODES A HOMOLOG OF MAMMALIAN PHOSPHOPROTEIN PHOSPHATASE-1 [J].
DOONAN, JH ;
MORRIS, NR .
CELL, 1989, 57 (06) :987-996
[15]
ENDOTHALL THIOANHYDRIDE INHIBITS PROTEIN PHOSPHATASE-1 AND PHOSPHATASE-2A IN-VIVO [J].
ERDODI, F ;
TOTH, B ;
HIRANO, K ;
HIRANO, M ;
HARTSHORNE, DJ ;
GERGELY, P .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1995, 269 (05) :C1176-C1184
[16]
Falconer I. R., 1993, Algal toxins in seafood and drinking water., P177
[17]
Falconer I.R., 1999, Toxic cyanobacteria in water, P155
[18]
Sensitive detection of apoptogenic toxins in suspension cultures of rat and salmon hepatocytes [J].
Fladmark, KE ;
Serres, MH ;
Larsen, NL ;
Yasumoto, T ;
Aune, T ;
Doskeland, SO .
TOXICON, 1998, 36 (08) :1101-1114
[19]
NUTRIENT REQUIREMENTS OF SUSPENSION CULTURES OF SOYBEAN ROOT CELLS [J].
GAMBORG, OL ;
MILLER, RA ;
OJIMA, K .
EXPERIMENTAL CELL RESEARCH, 1968, 50 (01) :151-+
[20]
Microcystin-LR and okadaic acid-induced cellular effects: a dualistic response [J].
Gehringer, MM .
FEBS LETTERS, 2004, 557 (1-3) :1-8