Skip to main content
Log in

Effect of toluene diisocyanate and its corresponding amines on viability and growth of human lung fibroblasts in culture

  • Published:
Cell Biology and Toxicology Aims and scope Submit manuscript

Abstract

Toluene diisocyanate (TDI) is a highly volatile chemical known to cause occupational asthma in exposed workers. TDI-induced asthma is associated with airway epithelium injury and repair, and subepithelial fibrosis. We investigated the effect of TDI and its hydrolysis products, the 2,4- and 2,6-toluenediamines (TDA), on viability and growth of human lung fibroblasts (HLFs) in culture, using a tetrazolium-based cell viability assay. The effects of increasing concentrations of each of these chemicals were evaluated on quiescent cells seeded at two densities (2500 and 5000 cells/well) and treated for 24 or 48 h. TDI (10–4–10–5 mol/L, as a mixture of 80% 2,4-TDI and 20% 2,6-TDI) exhibited a partial but significant cytotoxic effect (10–24%, p<0.05) on HLFs. This effect was observed at both cell densities, and was time- and concentration-dependent. 2,4-TDA, at lower concentrations (10–8–10–6 mol/L) applied for 48 h, also partially reduced HLF viability (10–15%, p<0.05), whereas it tended to trigger cell growth at concentrations higher than 10–5 mol/L. 2,6-TDA exhibited both a cytotoxic and a proliferative effect on HLFs that depended on concentration, time of exposure and cell culture density. Significant cytotoxicity was only observed after 24 h of treatment with 10–7–10–6 mol/L 2,6-TDA, and reached greater intensity in cells cultured at the highest density. In contrast, 2,6-TDA stimulated HLF growth only after 48 h of incubation at 10–4 mol/L on cells cultured at the lowest density. Taken together, our results showed that TDI and 2,4-TDA somewhat decreased HLF viability, whereas 2,6-TDA appeared to exhibit both a cytotoxic and a growth stimulatory effect on these cells. TDI and 2,4-TDA are thus suggested to contribute to airway epithelium damage associated with TDI-induced asthma, whereas 2,6-TDA might either trigger epithelial damage or induce cell proliferation that could contribute to epithelium repair or subepithelial fibrosis.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Barnes PJ. Airway epithelial receptors. Eur Respir Rev. 1994;4:371–9.

    Google Scholar 

  • Baur X, Marek W, Ammon J et al. Respiratory and other hazards of isocyanates. Int Arch Occup Environ Health. 1994;66:141–52.

    Google Scholar 

  • Chan-Yeung M, Malo J-L. Aetiological agents in occupational asthma. Eur Respir J. 1994;7:346–71.

    Google Scholar 

  • Dieter MP, Boorman GA, Jameson CW, Matthews HB, Huff JE. The carcinogenic activity of commercial grade toluene diisocyanate in rats and mice in relation to the metabolism of the 2,4-and 2,6-TDI isomers. Toxicol Ind Health. 1990;6:599–621.

    Google Scholar 

  • Gordon T, Sheppard D, McDonald D, Di Stefano S, Scypinski L. Airway hyperresponsiveness and inflammation induced by toluene diisocyanate in guinea pigs. Am Rev Respir Dis. 1985;132:1106–12.

    Google Scholar 

  • Jordana M, Särnstrand B, Sime PJ, Ramis I. Immune-inflammatory functions of fibroblasts. Eur Respir J. 1994;7:2212–22.

    Google Scholar 

  • Karol MH. Respiratory effects of inhaled isocyanates. CRC Crit Rev Toxicol. 1986;16:349–79.

    Google Scholar 

  • Kassel O, Schmidlin F, Duvernelle C, De Blay F, Frossard N. Up-and down-regulation by glucocorticoids of the constitutive expression of the mast cell growth factor stem cell factor by human lung fibroblasts in culture. Mol Pharmacol. 1998;54:1073–9.

    Google Scholar 

  • Kovacs EJ. Fibrogenic cytokines: the role of immune mediators in the development of scar tissue. Immunol Today. 1991;12:17–23.

    Google Scholar 

  • Mapp CE, Saetta M, Maestrelli P et al. Mechanisms and pathology of occupational asthma. Eur Respir J. 1994;7:544–54.

    Google Scholar 

  • Mattoli S, Miante S, Calabro F, Mezzetti M, Fasoli A, Allegra L. Bronchial epithelial cells exposed to isocyanates potentiate activation and proliferation of T-cells. Am J Physiol. 1990;259:L320–7.

    Google Scholar 

  • Mattoli S, Colotta F, Fincato G et al. Time course of IL1 and IL6 synthesis and release in human bronchial epithelial cell cultures exposed to toluene diisocyanate. J Cell Physiol. 1991;149:260–8.

    Google Scholar 

  • Mosman T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 1983;65:55–63.

    Google Scholar 

  • Saetta M, Maestrelli P, Turato G et al. Airway wall remodeling after cessation of exposure to isocyanates in sensitized asthmatic subjects. Am J Respir Crit Care Med. 1995;151:489–94.

    Google Scholar 

  • Vandenplas O, Malo J-L, Saetta M, Mapp CE, Fabbri LM. Occupational asthma and extrinsic alveolitis due to isocyanates: current status and perspectives. Br J Ind Med. 1993; 50:213–28.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Pons, F., Fischer, A., Frossard, N. et al. Effect of toluene diisocyanate and its corresponding amines on viability and growth of human lung fibroblasts in culture. Cell Biol Toxicol 15, 333–340 (1999). https://doi.org/10.1023/A:1007671903406

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1007671903406

Navigation