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Neutral red (NR) assay for cell viability and xenobiotic-induced cytotoxicity in primary cultures of human and rat hepatocytes

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Abstract

Neutral red (NR) in medium was absorbed and concentrated in lysosomes of cultured rat and human hepatocytes. NR uptake increased with the time of incubation and reached a plateau in 2 hr. Uptake was proportional to the concentration of the NR solution and the numbers of viable liver cells. Prolonged culture of hepatocytes increased the numbers of lysosomes, and thus, the dye accumulation. The NR can be extracted from lysosomes for quantitative measurement of hepatocyte viability and cytotoxicity of xenobiotics. With this assay, several serum-free media (e.g., Waymouth's, MEM, LHC-8, etc.) were compared for the maintenance of viable hepatocytes in vitro. Interestingly, LHC-8 medium, which is used to grow human bronchial epithelial cells, best preserved viable rat hepatocytes. The cytotoxic effects of dimethylnitrosamine (DMN) and aflatoxin B1 (AFB1) were examined by NR assay on rat and human hepatocyte cultures and were found to be dependent on dose and time of the exposures. NR50 was 20 mM for DMN and 0.072 µM for AFB1 in rat hepatocytes with 24 hr of exposures and reduced to 12.5 mM for DMN and 0.053 µ uM for AFB1 with 48 fr exposures. Human hepatocytes were more resistant to the toxicity of both chemicals; NR50 values were 100 mM DMN and 1.8 µM AFB1 respectively, for 24 hr treatments. Compared with lactate dehydrogenase (LDH) leakage test, the NR assay was simpler and more sensitive in determining the viability and cytotoxicity of xenobiotics in primary cultures of hepatocytes.

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Abbreviations

NR:

Neutral Red

MEM:

Eagle's Minimum Essential Medium

DMN:

dimethylnitrosamine

AFB1 :

aflatoxin B1

LDH:

lactate dehydrogenase

HBSS:

Hanks balanced salt solution;

EDTA:

ethylene bis (oxyethylenenitrilo)-tetraacetic acid

L-15:

Leibovitz's 15

NADH:

B-nicotinamide adenine dinu

FBS:

fetal bovine serum

IA:

immediate autopsy

References

  • ANUFORO, D.C., ACOSTA, D. and SMITH, R.V. (1978). Hepatoxicity studies with primary cultures of rat liver cells. In Vitro 14:981–988.

    Google Scholar 

  • BABICH, H. and BORENFREUND, E. (1987). Structure-activity relationship (SAR) models established in vitro with the neutral red cytotoxicity assay. Toxic. In Vitro 1:3–9.

    Google Scholar 

  • BABICH, H., SARDANA, M.K. and BORENFREUND, E. (1988). Acute cytotoxicities of polynuclear aromatic hydrocarbons determined in vitro with the human liver tumor cell line, HepG2. Cell Biol. Toxicol. 4(3):295–309.

    Google Scholar 

  • BERGMEYER, H.U. and BERNT, E. (1974). Lactate dehydrogenase. In: Methods of Enzymatic Analysis (H.U. Bergmeyer, ed.), Vol. 11, pp 574–579. Academic Press, New York.

    Google Scholar 

  • BORENFREUND, E. and BORRERO, O. (1984). In vitro cytotoxicity assays: Potential alternatives to the Draize ocular irritancy test. Cell Biol. Toxicol. 1:55–65.

    Google Scholar 

  • BORENFREUND, E. and PUERNER, J.A. (1984). A simple quantitative procedure using monolayer culture for cytotoxicity assays (HTD/ NR-90). J. Tissue Cult. Methods 9:7–9.

    Google Scholar 

  • BORENFREUND, E. and PUERNER, J.A. (1986). Cytotoxicity of metals, metal-metal and metal-chelator combinations assayed in vitro. Toxicology 39:121–134.

    Google Scholar 

  • BORENFREUND, E. and SHOPSIS, C. (1985). Toxicity monitored with a correlated set of cell culture assays. Xenobiotica 15:705–711.

    Google Scholar 

  • DAVIES, D. S. (1981). Drug hepatoxicity: formation and importance of reactive metabolites. In: Drug Reactions and the Liver (M. Davis, J.M. Tredger, and R. Williams, eds.), pp 12–18. Pitman Medical, London.

    Google Scholar 

  • FIENNES, A., WALTON, J., WINTERBOURNE, D., McGLASHAN, D. and HERMONTAYLOR, J. (1987). Quantitative correlation of neutral red dye uptake with cell number in human cancer cell cultures. Cell Biol. Int. Rep. 11(5):373–378.

    Google Scholar 

  • FINTER, N.B. (1969). Dye uptake methods for assessing vital cytopathogenicity and their application to interferon assays. J. Gen. Vitol. 5:419–427.

    Google Scholar 

  • FLICK, D.A. and GEORGE, E.G. (1984). Comparison of in vitro cell cytotoxic assays for tumor necrosis factor. J. Immunol. Methods 68(1/2):167–176.

    Google Scholar 

  • GOMEZ-LECHON, M.J., MONTOYA, A., LOPEZ, P., DONATO, T., LARRAURI, A. and CASTELL, J.V. (1988). The potential use of cultured hepatocytes in predicting the hepatotoxicity of xenobiotics. Xenobiotics 18(6):725–735.

    Google Scholar 

  • GUILLOUZO, A. (1986). Use of isolated and cultured hepatocytes for xenobiotic metabolism and cytotoxicity studies. In: Isolated and Cultured Hepatocytes (A. Guillouzo and C. Guguen-Guillouzo, eds.), pp 313–332. John Libbery and Company Ltd., London.

    Google Scholar 

  • HAMMOND, M.E., GOODWIN, J. and DVORAK, H.F. (1980). Quantitative measurements of neutral red uptake and excretion by mammalian cells. J. Reticuloendothel. Soc. 27:337–346.

    Google Scholar 

  • HOLME, J. (1985). Xenobiotic metabolism and toxicity in primary monolayer cultures of hepatocytes. NIPH Ann. 8:49–63.

    Google Scholar 

  • HOLME, J.A., SODERLUND, E.J., CHRISTENSEN, T., TRYGG, B. and BJORNSTAD, C. (1986). Modulation of cytotoxic and genotoxic effects of 2-acetylaminofluorene in rat and hamster hepatocytes by 3-methylcholanthrene pre-treatment. Carcinogenesis 7:1561–1567.

    Google Scholar 

  • HSU, I.C., HARRIS, C.C., SNYDER, S., LIPSKY, M.M. and TRUMP, B.F. (1987). Cell and species difference in metabolic activation of procarcinogens. Mutation Res. 177:1–7.

    Google Scholar 

  • HSU, I.C., HARRIS, C.C., SU, C.H., HOLDERNESS, K.E. and TRUMP, B.F. (1985). Isolation and culture of human hepatocytes from liver of immediate autopsy. In Vitro Cell. Dev. Biol. 21:154–160.

    Google Scholar 

  • JACQUES, P.J. (1973). Endocytosis. In: Lysosomes in Biology and Pathology (J.T. Dingle and H.B. Fell, eds.), p 395. Amsterdam, North Holland.

    Google Scholar 

  • KREAMER, B.L., STAECKER, J.L., SAWADA, N., SATTLER, G.L., HSIA, M.T.S. and PITOT, H.C. (1986). Use of a low-speed, iso-density percoll cnetrifugation method to increase the viability of isolated rat hepatocyte preparations. In Vitro Cell. Dev. Biol. 22:201–211.

    Google Scholar 

  • LAISHES, B.A., ROBERTS, E. and FARBER, E. (1978). In vitro measurement of carcinogen-resistant liver cells during hepatocarcinogenesis. Int. J. Cancer 21:186–193.

    Google Scholar 

  • LANGENBACH, R., FREED, H.J., RAVEH, D. and HUBERMAN, E. (1978). Cell specificity in metabolic activation of aflatoxin B1 and benzo(a)pyrene to mutagens for mammalian cells. Nature (lond.) 276:277–279.

    Google Scholar 

  • LECHNER, J. and LaVECK, M.A. (1985). A serum-free method for culturing normal human bronchial epithelial cells at clonal density. J. Tissue Cult. Methods 9:43–48.

    Google Scholar 

  • MAGEE, P.N. and BARNES, J.M. (1967). Carcinogenic nitroso compounds. Adv. Cancer Res. 10:163–246.

    Google Scholar 

  • MC QUEEN, C.A. and WILLIAMS, G.M. (1982). Cytotoxicity of xenobiotics in adult rat hepatocytes in primary culture. Fund Appl. Toxicol. 2:139–144.

    Google Scholar 

  • MICHALOPOULOS, G. and PITOT, H.C. (1975). Primary culture of parenchymal liver cells on collagen membranes. Exp. Cell Res. 94:70–78.

    Google Scholar 

  • MILLER, E.C. (1978). Some current perspectives on chemical carcinogenesis in humans and experimental animals: Presidential Address. Cancer Res. 38:1479–1496.

    Google Scholar 

  • ORRENIUS, S. and SIES, H. (1982). Compartmentation of detoxication reactions. In: Metabolic Compartmentation (H. Sies, ed.), pp 485–520. Academic Press, New York.

    Google Scholar 

  • PARISH, C.R. and ARNO, M. (1983). Automated colorimetric assay for T cell cytotoxicity. J. Immunol. Methods 58(1/2):225–238.

    Google Scholar 

  • PETERSON, G.L. (1977). A simplification of the protein assay method of Lowry et al. which is more generally applicable. Anal. Biochem. 83:346–356.

    Google Scholar 

  • POWIS, G., JARDINE, I., VAN DYKE, R., WEINSHILBOUM, R., MOORE, D., WILKE, T., RHODES, W., NELSON, R., BENSON, S. and SZUMLANSKI, C. (1988). Foreign compound metabolism studies with human liver obtained as surgical waste. Relation to donor characteristics and effects of tissue storage. Drug Metabolism and Disposition: The Biological Fate of Chemicals. 16(4):582–589.

    Google Scholar 

  • SALOCKS, C.B., HSIEH, D.P.H. and BYARD, J.L. (1981). Butylated hydroxytoluene pretreatment protects against cytotoxicity and reduces covalent binding of aflatoxin BI in primary hepatocyte cultures. Toxicol. Appl. Pharmacol. 59:331–345.

    Google Scholar 

  • SUOLINNA, E.M. (1982). Isolation and culture of liver cells and their use in the biochemical research of xenobiotics. Med. Biol. 60:237–254.

    Google Scholar 

  • TREUHAFT, M.W. (1983). A colorimetric assay for quantification of defective interfering particles of respiratory syncytial virus. J. Gen. Vitol. 64(6):1301–1310.

    Google Scholar 

  • WEISBURGER, E.K. (1981a). Species differences in response to aromatic amines. In: Symposium of Organ and Species Specificity in Chemical Carcinogenesis.

  • WEISBURGER, E.K. (1981b). N-substituted aryl compounds in carcinogenesis and mutagenesis. Natl. Cancer Inst. Monogr. 58:1–7.

    Google Scholar 

  • WILLIAMS, G.M., BERMUDEZ, E., SAN R.H.C., GOLDBLATT, P.J. and LASPIA, M.F. (1978). Rat hepatocyte primary cultures. IV. Maintenance in defmed medium and the role of production of plasminogen activator and other proteases. In Vitro 14:824–837.

    Google Scholar 

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Contribution No. 2816 from Laboratory of Genotoxicology.

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Zhang, SZ., Lipsky, M.M., Trump, B.F. et al. Neutral red (NR) assay for cell viability and xenobiotic-induced cytotoxicity in primary cultures of human and rat hepatocytes. Cell Biol Toxicol 6, 219–234 (1990). https://doi.org/10.1007/BF00249595

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