A study of the aneugenic activity of trichlorfon detected by centromere-specific probes in human lymphoblastoid cell lines

被引:41
作者
Doherty, AT
Ellard, S
Parry, EM
Parry, JM
机构
关键词
D O I
10.1016/S0027-5107(96)00142-X
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The potential of the pesticide trichlorfon to induce mitotic aneuploidy has been investigated in genetically engineered human lymphoblastoid cell lines. Trichlorfon failed to induce micronuclei in the AHH-1 and MCL-5 cell lines when treated in media at normal cell culture pH (pH 7.3). Under a treatment pH of 5.5, trichlorfon exposures resulted in the induction of both chromosome loss and chromosome non-disjunction as measured by fluorescence in situ hybridisation (FISH) using a pan-centromeric probe for all human centromeres and centromere probes specific for chromosomes 2, 7 and 18. At treatment concentrations greater than 20 mu g/ml trichlorfon also induced structural chromosome damage resulting in the production of centromere negative micronuclei.
引用
收藏
页码:221 / 231
页数:11
相关论文
共 20 条
[1]  
ADBI YA, 1991, PHARMACOL TOXICOL, V68, P137
[2]  
CHAGANTI RSK, 1993, UROL CLIN N AM, V20, P55
[3]   A METABOLICALLY COMPETENT HUMAN CELL-LINE EXPRESSING 5 CDNAS ENCODING PROCARCINOGEN-ACTIVATING ENZYMES - APPLICATION TO MUTAGENICITY TESTING [J].
CRESPI, CL ;
GONZALEZ, FJ ;
STEIMEL, DT ;
TURNER, TR ;
GELBOIN, HV ;
PENMAN, BW ;
LANGENBACH, R .
CHEMICAL RESEARCH IN TOXICOLOGY, 1991, 4 (05) :566-572
[4]   MICRONUCLEUS ASSAYS USING CYTOCHALASIN-BLOCKED MCL-5 CELLS, A PROPRIETARY HUMAN CELL-LINE EXPRESSING 5 HUMAN CYTOCHROMES P-450 AND MICROSOMAL EPOXIDE HYDROLASE [J].
CROFTONSLEIGH, C ;
DOHERTY, A ;
ELLARD, S ;
PARRY, EM ;
VENITT, S .
MUTAGENESIS, 1993, 8 (04) :363-372
[5]   PHENOTYPIC AND CYTOGENETIC STUDIES IN SELF-POISONED PATIENTS [J].
CZEIZEL, AE .
MUTATION RESEARCH-ENVIRONMENTAL MUTAGENESIS AND RELATED SUBJECTS, 1994, 313 (2-3) :175-181
[6]   ENVIRONMENTAL TRICHLORFON AND CLUSTER OF CONGENITAL-ABNORMALITIES [J].
CZEIZEL, AE ;
ELEK, C ;
GUNDY, S ;
METNEKI, J ;
NEMES, E ;
REIS, A ;
SPERLING, K ;
TIMAR, L ;
TUSNADY, G ;
VIRAGH, Z .
LANCET, 1993, 341 (8844) :539-542
[7]   An investigation into the activation and deactivation of chlorinated hydrocarbons to genotoxins in metabolically competent human cells [J].
Doherty, AT ;
Ellard, S ;
Parry, EM ;
Parry, JM .
MUTAGENESIS, 1996, 11 (03) :247-274
[8]   THE USE OF GENETICALLY ENGINEERED V79 CHINESE-HAMSTER CULTURES EXPRESSING RAT-LIVER CYP1A1, 1A2 AND 2B1 CDNAS IN MICRONUCLEUS ASSAYS [J].
ELLARD, S ;
MOHAMMED, Y ;
DOGRA, S ;
WOLFEL, C ;
DOEHMER, J ;
PARRY, JM .
MUTAGENESIS, 1991, 6 (06) :461-470
[9]   MEASUREMENT OF MICRONUCLEI IN LYMPHOCYTES [J].
FENECH, M ;
MORLEY, AA .
MUTATION RESEARCH, 1985, 147 (1-2) :29-36
[10]   INDUCTION OF MICRONUCLEI AND KARYOTYPE ABERRATIONS DURING IN-VIVO MOUSE SKIN CARCINOGENESIS [J].
HAESEN, S ;
TIMMERMANS, M ;
KIRSCHVOLDERS, M .
CARCINOGENESIS, 1993, 14 (11) :2319-2327