Abstract

BackgroundThree-dimensional (3D) spheroids are frequently used in toxicological study because their morphology and function closely resemble those of tissue. As these properties are maintained over a long term, repeated treatment of the spheroids with a test object is possible. Generally, in the repeated treatment test to assess cytotoxicity in the spheroids, ATP assay, colorimetric measurement using pigments or high-content imaging analysis is performed. However, continuous assessment of cytotoxicity in the same spheroids using the above assays or analysis is impossible because the spheroids must be disrupted or killed. To overcome this technical limitation, we constructed a simple monitoring system in which cytotoxicity in the spheroids can be continuously monitored by nondestructive bioluminescence measurement.ResultsMouse primary hepatocytes were isolated from transchromosomic (Tc) mice harboring a mouse artificial chromosome (MAC) vector expressing beetle luciferase Emerald Luc (ELuc) under the control of cytomegalovirus immediate early enhancer/chicken β-actin promoter/rabbit β-globin intron II (CAG) promoter, and used in 3D cultures. We confirmed that both luminescence and albumin secretion from the spheroids seeded in the 96-well format Cell-ableTM were maintained for approximately 1 month. Finally, we repetitively treated the luminescent 3D spheroids with representative hepatotoxicants for approximately 1 month, and continuously and nondestructively measured bioluminescence every day. We successfully obtained daily changes of the dose-response bioluminescence curves for the respective toxicants.ConclusionsIn this study, we constructed a monitoring system in which cytotoxicity in the same 3D spheroids was continuously and sensitively monitored over a long term. Because this system can be easily applied to other cells, such as human primary cells or stem cells, it is expected to serve as the preferred platform for simple and cost-effective long-term monitoring of cellular events, including cytotoxicity.

Highlights

  • Three-dimensional (3D) spheroids are frequently used in toxicological study because their morphology and function closely resemble those of tissue

  • Verification of reporter construction and correlation between bioluminescence intensity and cytotoxicity In this study, we chose Emerald Luc (ELuc) [18], a greenemitting beetle luciferase from P. termitilluminans [19], to continuously monitor cytotoxicity in primary hepatocytes induced by repeated toxicant treatment for two reasons: (i) light output of ELuc from living cells is higher than that of firefly luciferase, the most widely used luciferase reporter gene, and high light output could be expected from hepatocytes; and (ii) D-luciferin, a luminescent substrate of ELuc, is highly stable in the culture medium and penetrates cells and tissues; these physicochemical properties are preferred for longitudinal and nondestructive bioluminescence measurement

  • The A9 stable cell line was generated by the specific insertion of expression plasmid carrying the chicken β-actin promoter/rabbit β-globin intron II (CAG) promoter and ELuc, into a multi-integrase mouse artificial chromosome (MI-MAC) vector (Additional file 1: Figure S1) [20]

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Summary

Introduction

Three-dimensional (3D) spheroids are frequently used in toxicological study because their morphology and function closely resemble those of tissue. As these properties are maintained over a long term, repeated treatment of the spheroids with a test object is possible. In the repeated treatment test to assess cytotoxicity in the spheroids, ATP assay, colorimetric measurement using pigments or high-content imaging analysis is performed. Among the possible luciferin-luciferase reactions, the beetle luciferase and D-luciferin (benzothiazole) pair is the best probe for long-term noninvasive monitoring of cellular events, because the luminescence generated by the reaction is highly quantitative and has an extremely low background, and D-luciferin is very stable in culture medium and permeates cells [7,8,9]. The inherent properties of the beetle luciferin-luciferase reaction enable the longitudinal and quantitative monitoring of cellular events

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