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Toxic effects of mechlorethamine on mammalian respiratory mucociliary epithelium in primary culture

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Abstract

Mechlorethamine (HN2) is an alkylating agent usually used in cancer chemotherapy. Nevertheless, HN2 is extremely toxic and its use is accompanied by severe side-effects that may cause lung complications. Many studies report the morphological and biochemical modifications induced by sulfur mustard (SM) but no report has been published concerning the toxic effects of HN2 on the ultrastructural and functional activity of surface respiratory epithelial cells. This study was performed on rabbit tracheal epithelium (RTE) cells in primary culture. The functional activity of the culture was evaluated by measuring the ciliary beating frequency (CBF) of the ciliated cells using a videomicroscopic method, and the culture growth was determined by an image analysis system. The morphological aspects of the cells were analyzed by light, scanning electron, and transmission electron microscopy. An important inhibition of cell growth was observed associated with a detachment of the outgrowth cells. Morphological changes were expressed by vacuolization, increases in the intercellular spaces, and by disorganization of the cytoskeleton associated with a specific attack of the ciliated cells that show ciliary blebbing. The sudden CBF inhibition is more likely due to the detachment and the death of the ciliated cells than to a specific ciliotoxic effect of HN2. All these observations demonstrated the high sensitivity of respiratory epithelial cells to HN2 and showed that HN2-induced injuries were irreversible, and time- and dose-dependent.

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Abbreviations

CBF:

ciliary beating frequency

HN2:

nitrogen mustard, or mechlorethamine

RTE:

rabbit tracheal epithelium

SEM:

scanning electron microscopy

SM:

sulfur mustard

TEM:

transmission electron microscopy

References

  • Baeza-Squiban A, Romet S, Moureau A, Marano F. Progress in outgrowth culture from rabbit tracheal explants: balance between proliferation and maintenance of differentiated state in epithelial cells. In Vitro. 1991;27A:453–61.

    Google Scholar 

  • Balali M. Clinical and laboratory findings in Iranian fighters with chemical gas poisoning. Arch Belg, Suppl. 1984:254–9.

  • Breneman DL, Nartker AL, Ballman EA et al. Topical mechlorethamine in the treatment of mycosis fungoides. J Am Acad Dermatol. 1991;25:1059–64.

    Google Scholar 

  • Blanquart C, Romet S, Baeza A, Guennou C, Marano F. Primary cultures of tracheal epithelial cells for the evaluation of respiratory toxicity. Toxicol In Vitro. 1991;5(5/6):499–502.

    Google Scholar 

  • Chan PK: Cross-linkage of nucleophosmin in tumor cells by nitrogen mustard. Cancer Res. 1989;49:3271–5.

    Google Scholar 

  • Chevillard M, Lainee P, Robineau P, Puchelle E. Toxic effects of sulfur mustard on respiratory epithelial cells in culture. Cell Biol Toxicol. 1992;8(2):171–81.

    Google Scholar 

  • Colvin M. The alkylating agents. In: Chabner B, ed. Pharmacological principles of cancer treatment. Philadelphia: WB Saunders; 1982:276–308.

    Google Scholar 

  • Davison C, Rozman RS, Smith PK. Metabolism of bis-β-chloroethylsulfide (sulfur mustard gas). Biochem Pharmacol. 1961;7:64–74.

    Google Scholar 

  • Dean SW, Fox M: DNA repair, DNA synthesis and cell cycle delay in human lymphoblastoid cells differentially sensitive to the cytotoxic effects of nitrogen mustard. Mutat Res. 1984;132:63–72.

    Google Scholar 

  • Fox M, Scott D: The genetic toxicity of nitrogen and sulfur mustard. Mutat Res. 1980;75:131–68.

    Google Scholar 

  • Gamcsik MP, Hamill TG, Colvin M. NMR studies of the conjugation of mechlorethamine with glutathione. J Med Chem. 1990;33(3):1009–14.

    Google Scholar 

  • Goldenberg GJ, Vanstone CL, Bihler I. Transport of nitrogen mustard on the transport carrier of choline in L5178Y lymphoblasts. Science. 1971;172:1148–9.

    Google Scholar 

  • Gross CL, Innace JK, Hovatter RC, Meier HL, Smith WJ. Biochemical manipulation of intracellular glutathione levels influences cytotoxicity to isolated human lymphocytes by sulfur mustard. Cell Biol Toxicol. 1993;9(3):259–68.

    Google Scholar 

  • Guilianelli C, Baeza-Squiban A, Boivieux-Ulrich E et al. Effect of mineral particles containing iron on primary cultures of rabbit tracheal epithelial cells: possible implication of oxidative stress. Environ Health Perspect. 1993;101:436–42.

    Google Scholar 

  • Hansson J, Lewensohn R, Ringborg U, Nilsson B. Formation and removal of DNA cross-links induced by melphalan and nitrogen mustard in relation to drug-induced cytotoxicity in human melanoma cells. Cancer Res. 1987;47:2631–7.

    Google Scholar 

  • Jewell SA, Bellomo G, Thor H, Orrenius S: Bleb formation in hepatocytes during drug metabolism is caused by disturbances in thiol and calcium ion homeostasis. Science. 1982;217:1257–8.

    Google Scholar 

  • Khan S, Ramwani JJ, O'Brien PJ. Hepatocyte toxicity of mechlorethamine and other alkylating anticancer drugs. Biochem Pharmacol. 1992;43(9):1963–7.

    Google Scholar 

  • Lepri E, Barzi A, Menconi E, Portuesi MG, Liberati M. In vitro synergistic activity of PDF-INFα and NM+INFα combinations on fresh bone-marrow samples from multiple myeloma patients. Hematol Oncol. 1991:9:79–86.

    Google Scholar 

  • Miccadei S, Kyle ME, Gilford D, Farber JL. Toxic consequence of the abrupt depletion of glutathione in cultured rat hepatocytes. Arch Biochem Biophys. 1988;265(2):311–20.

    Google Scholar 

  • Mol MAE, De Vries-Van de Ruit AMBC, Kluivers AW. NAD+ levels and glucose uptake of cultured human cells exposed to sulfur mustard. Toxicol Appl Pharmacol. 1989;98:159–65.

    Google Scholar 

  • Mol MAE, De Vries-Van de Ruit AMBC. Concentration and time related effects of sulfur mustard on human epidermal keratinocyte function. Toxicol In Vitro 1992;6(3):245–51.

    Google Scholar 

  • O'Connor PM, Ferris DK, White GA et al. Relationships between cdc-2 kinase, DNA cross-linking, and cell cycle perturbations induced by nitrogen mustard. Cell Growth Differ. 1992;3:43–52.

    Google Scholar 

  • Orrenius S, McConkey DJ, Nicotera P. Mechanisms of oxidant-induced cell damage. In: Cerutti LA, Fridovich I, McCord JM, eds. Oxy-radicals in molecular biology and pathology. New York: Alan R. Liss; 1988.

    Google Scholar 

  • Orrenius S, McConkey DJ, Bellomo G, Nicotera P. Role of Ca2+ in toxic cell killing. TIPS. 1989;10:281–5.

    Google Scholar 

  • Papirmeister B, Gross CL, Petrali JP, Hixson CJ. Pathology produced by sulfur mustard in human skin grafts on athymic nude mice. I. Gross and light microscopic changes. J Toxicol Cutan Ocul Toxicol. 1984;3:371–91.

    Google Scholar 

  • Papirmeister B, Gross CL, Meier HL, Petrali JP, Johnson JB. Molecular basis for mustard-induced vesication. Fundam Appl Toxicol. 1985;5:S134–49.

    Google Scholar 

  • Papirmeister B, Feister AJ, Robinson SI, Ford RD. Molecular mechanisms of cytotoxicity. In: Medical defense against mustard gas. Boca Raton: CRC Press; 1991:115–209.

    Google Scholar 

  • Peters RA, Wakelin RW: Observations upon a compound of mustard gas and keratin. Biochem J. 1947;41:550–55.

    Google Scholar 

  • Petrali JP, Oglesby SB, Mills KR: Ultrastructural correlates of sulfur mustard toxicity. J Toxicol Cutan Ocul Toxicol. 1990;9(3):193–214.

    Google Scholar 

  • Petrali JP, Oglesby SB, Justus TA. Morphologic effects of sulfur mustard on a human skin equivalent. Toxicol Cutan Ocul Toxicol. 1991;10(4):315–24.

    Google Scholar 

  • Pirie A. The action of mustard gas on ox cornea collagen. Biochem J. 1947;41:185–90.

    Google Scholar 

  • Romet S, Dubreuil A, Baeza A, Moreau A, Schoevaert D, Marano F. Respiratory tract epithelium in primary culture: effects of ciliotoxic compounds on the ciliary activity. Toxicol In Vitro. 1990;4:399–420.

    Google Scholar 

  • Romet S, Schoevaert D, Marano F. An original image analysis method to study the ciliary beat frequency of tracheal epithelium in culture. Biol Cell. 1991;71:183–9.

    Google Scholar 

  • Romet-Haddad S, Marano F, Blanquart C, Baeza-Squiban A. Tracheal epithelium in culture: a model for toxicity testing of inhaled molecules. Cell Biol Toxicol. 1992;8(3):141–50.

    Google Scholar 

  • Van Vloten WA, Cooijmans ACM, Poel J, Meulenbelt J. Concentrations of nitrogen mustard in the air during topical treatment of patients with mycosis fungoides. Br J Dermatol. 1993;128(4):404–6.

    Google Scholar 

  • Wada A, Nishimoto Y, Miyanishi M, Kambe S, Miller RW. Mustard gas as a cause of respiratory neoplasia in man. Lancet. 1968;1:1161–3.

    Google Scholar 

  • Whitfield D. A literature review upon the toxicology, mechanism of action and treatment of sulphur and nitrogen mustard poisoning. Porton, Wilts: Chemical Defence Establishment; 1987; CDE Technical Note no 840.

    Google Scholar 

  • Wormser U, Nyska A: Protective effect ofO-phenanthroline against mechlorethamine toxicity in the rat liver slice system and in the guinea pig skin. Arch Toxicol. 1991;65:666–70.

    Google Scholar 

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Giuliani, I., Boivieux-Ulrich, E., Houcine, O. et al. Toxic effects of mechlorethamine on mammalian respiratory mucociliary epithelium in primary culture. Cell Biol Toxicol 10, 231–246 (1994). https://doi.org/10.1007/BF00756763

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  • DOI: https://doi.org/10.1007/BF00756763

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