Cytotoxic effects of environmentally relevant chlorophenols on L929 cells and their mechanisms

被引:50
作者
Chen, J
Jiang, J
Zhang, F [1 ]
Yu, H
Zhang, J
机构
[1] Nanjing Univ, State Key Lab Pharmaceut Biotechnol, Dept Biochem, Nanjing 210093, Peoples R China
[2] Nanjing Univ, State Key Lab Pollut Control & Resources Reuse, Sch Environm, Nanjing 210093, Peoples R China
基金
中国国家自然科学基金;
关键词
apoptosis; chlorophenol chemicals; cytotoxicity; fibroblast cells; structure-activity relationship; tumor promotion;
D O I
10.1023/B:CBTO.0000029468.89746.64
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The chlorophenol chemicals (CPs) are a major class of widely distributed and frequently occurring persistent environmental pollutants. Pentachlorophenol (PCP) has been proposed to be procarcinogen in rodents and in possibly human beings. Human beings also easily expose to other chlorophenol chemicals, including 4-chlorophenol (CP), 2,4-dichlorophenol (DCP), 2,3,4-trichlorophenol (TCP), prompting this investigation of their comparative cytotoxic effects and cell death mechanisms, assayed in fibroblast L929 cells. The effective concentration for half-maximal response (EC50) values at 24 h for CP, DCP, TCP, and PCP are 2.18, 0.83, 0.46, and 0.11 mmol/L respectively and the EC50 values at 48 h are 1.18, 0.13, 0.08, and 0.06 mmol/L respectively by using 3-(4,5-dimethylthiazd-2-yl)-2,5-diphenyltentrazolium bromide (MTT) reduction assay. A clear structure-activity relationship was observed between toxicity of CPs and their octanol water partition coefficients. The further studies indicate that CP, DCP, and TCP induce apoptosis in L929 cells in a concentration or time-dependent manner, but PCP mediates cell death more characteristic of necrosis than apoptosis. These results not only demonstrate that L929 cell growth inhibition bioassay may be useful to provide the comparative evaluation of toxicity of CPs in vitro, but also implicate that CP, DCP, TCP, in comparison with PCP, can induce L929 cell death by apoptosis, resulting in lower procarcinogensis, which may help to elucidate the molecular basis for the adverse health effects associated with CPs exposure.
引用
收藏
页码:183 / 196
页数:14
相关论文
共 33 条
  • [1] CHLORINATED PHENOLS - OCCURRENCE, TOXICITY, METABOLISM, AND ENVIRONMENTAL-IMPACT
    AHLBORG, UG
    THUNBERG, TM
    [J]. CRC CRITICAL REVIEWS IN TOXICOLOGY, 1980, 7 (01): : 1 - 35
  • [2] APOPTOSIS AND NECROSIS - 2 DISTINCT EVENTS INDUCED, RESPECTIVELY, BY MILD AND INTENSE INSULTS WITH N-METHYL-D-ASPARTATE OR NITRIC-OXIDE SUPEROXIDE IN CORTICAL CELL-CULTURES
    BONFOCO, E
    KRAINC, D
    ANKARCRONA, M
    NICOTERA, P
    LIPTON, SA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) : 7162 - 7166
  • [3] CELL-DEATH BY APOPTOSIS AND ITS PROTECTIVE ROLE AGAINST DISEASE
    BURSCH, W
    OBERHAMMER, F
    SCHULTEHERMANN, R
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 1992, 13 (06) : 245 - 251
  • [4] Toxicology and carcinogenesis studies of pentachlorophenol in rats
    Chhabra, RS
    Maronpot, RM
    Bucher, JR
    Haseman, JK
    Toft, JD
    Hejtmancik, MR
    [J]. TOXICOLOGICAL SCIENCES, 1999, 48 (01) : 14 - 20
  • [5] Oxidative DNA lesions in V79 cells mediated by pentachlorophenol metabolites
    Dahlhaus, M
    Almstadt, E
    Henschke, P
    Luttgert, S
    Appel, KE
    [J]. ARCHIVES OF TOXICOLOGY, 1996, 70 (07) : 457 - 460
  • [6] IMPAIRED IN-VITRO LYMPHOCYTE-RESPONSES IN PATIENTS WITH ELEVATED PENTACHLOROPHENOL (PCP) BLOOD-LEVELS
    DANIEL, V
    HUBER, W
    BAUER, K
    OPELZ, G
    [J]. ARCHIVES OF ENVIRONMENTAL HEALTH, 1995, 50 (04): : 287 - 292
  • [7] DARZYNKIEWICZ Z, 1997, CYTOMETRY, V7, P120
  • [8] Deichmann WB, 1981, PATTYS IND HYGIENE T, P2567
  • [9] Apoptosis: Molecular regulation of cell death
    Hale, AJ
    Smith, CA
    Sutherland, LC
    Stoneman, VEA
    Longthorne, VL
    Culhane, AC
    Williams, GT
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 236 (01): : 1 - 26
  • [10] Jensen J, 1996, REV ENVIRON CONTAM T, V146, P25