Influence of cadmium speciation for the evaluation of in vitro cadmium toxicity on LLC-PK1 cells

Citation
Mp. Barrouillet et al., Influence of cadmium speciation for the evaluation of in vitro cadmium toxicity on LLC-PK1 cells, TOX VITRO, 15(4-5), 2001, pp. 525-529
Citations number
10
Categorie Soggetti
Pharmacology & Toxicology
Journal title
TOXICOLOGY IN VITRO
ISSN journal
08872333 → ACNP
Volume
15
Issue
4-5
Year of publication
2001
Pages
525 - 529
Database
ISI
SICI code
0887-2333(200108/10)15:4-5<525:IOCSFT>2.0.ZU;2-5
Abstract
The main objective of the present work was to assess the potentiality of in vitro models to improve our understanding of cadmium-induced toxicity, esp ecially on epithelial renal cells. Indeed cadmium, a potent toxic metal, po ses a serious environmental threat and the mechanisms of its renal toxicity need to be clarified. Cytotoxicity studies presented here were performed i n a tubular proximal original established porcine kidney cell line (LLC-PK1 ). We have compared cytotoxicity induced by different chemical cadmium form s in LLC-PK1 cells as a function of media cell culture pH and protein conte nt. Cadmium stock solutions were prepared either by dissolving cadmium chlo ride or cadmium sulphate with increasing protein concentrations in the medi a cell culture. Its pH was monitored during experiments. Cytotoxicity was m easured by neutral red uptake after 24 h of exposure. Dose-dependent cytoto xicity curves, calculated with REGTOX, were systematically correlated with pH and protein content. Experiments in vitro revealed that cadmium was dose -dependently toxic for LLC-PK1 for concentrations ranging from 10(-4) to 10 (-6) M. We have noticed a lack of influence of the media cell culture pH on the cadmium cytotoxicity. REGTOX determines closely the EC50 values but EC 50CdCl2 > EC50CdSO4 and cadmium have been assayed with an inductively coupl ed atomic emission spectrometer (ICP/AES) directly in the media cell cultur e and the cellular pellet. (C) 2001 Elsevier Science Ltd. All rights reserv ed.