Primary cultured cells as sensitive in vitro model for assessment of toxicants-comparison to hepatocytes and gill epithelia

Bingsheng ZHOU, Chunsheng LIU, Jingxian WANG, Paul K. S. LAM, Shiu Sun Rudolf WU

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Abstract

In an effort to develop cultured cell models for toxicity screening and environmental biomonitoring, we compared primary cultured gill epithelia and hepatocytes from freshwater tilapia (Oreochromis niloticus) to assess their sensitivity to AhR agonist toxicants. Epithelia were cultured on permeable supports (terephthalate membranes, "filters") and bathed on the apical with waterborne toxicants (pseudo in vivo asymmetrical culture conditions). Hepatocytes were cultured in multi-well plates and exposed to toxicants in culture medium. Cytochrome P4501A (measured as 7-Ethoxyresorufin-O-deethylase, EROD) was selected as a biomarker. For cultured gill epithelia, the integrity of the epithelia remained unchanged on exposure to model toxicants, such as 1,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), benzo(a)pyrene B[a]P, polychlorinated biphenyl (PCB) mixture (Aroclor 1254), and polybrominated diphenyl ether (PBDE) mixture (DE71). A good concentration-dependent response of EROD activity was clearly observed in both cultured gill epithelia and hepatocytes. The time-course response of EROD was measured as early as 3 h, and was maximal after 6 h of exposure to TCDD, B[a]P and Aroclor 1254. The estimated 6 h EC50 for TCDD, B[a]P, and Aroclor 1254 was 1.2 × 10-9, 5.7 × 10-8 and 6.6 × 10-6 M. For the cultured hepatocytes, time-course study showed that a significant induction of EROD took place at 18 h, and the maximal induction of EROD was observed at 24 h after exposure. The estimated 24 h EC50 for TCDD, B[a]P, and Aroclor 1254 was 1.4 × 10-9, 8.1 × 10-8 and 7.3 × 10-6 M. There was no induction or inhibition of EROD in DE71 exposure to both gill epithelia and hepatocytes. The results show that cultured gill epithelia more rapidly induce EROD and are slightly more sensitive than cultured hepatocytes, and could be used as a rapid and sensitive tool for screening chemicals and monitoring environmental AhR agonist toxicants. Copyright © 2006 Elsevier B.V. All rights reserved.

Original languageEnglish
Pages (from-to)109-118
JournalAquatic Toxicology
Volume80
Issue number2
DOIs
Publication statusPublished - 16 Nov 2006

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Cytochrome P-450 CYP1A1
toxic substances
dioxin
cultured cells
hepatocytes
Hepatocytes
Cultured Cells
gills
Chlorodiphenyl (54% Chlorine)
epithelium
Epithelium
tetrachlorodibenzo-p-dioxin
Environmental Monitoring
PBDE
biomonitoring
agonists
environmental monitoring
pyrene
cytochrome
biomarker

Citation

Zhou, B., Liu, C., Wang, J., Lam, P. K. S., & Wu, R. S. S. (2006). Primary cultured cells as sensitive in vitro model for assessment of toxicants-comparison to hepatocytes and gill epithelia. Aquatic Toxicology, 80(2), 109-118. doi: 10.1016/j.aquatox.2006.07.021

Keywords

  • Primary cultured cells
  • Hepatocytes
  • Gill epithelia
  • EROD
  • Toxicity
  • Tilapia