Bread wheat gliadin cytotoxicity: a new three-dimensional cell model

• Published in: Scandinavian journal of clinical and laboratory investigation 2003, Vol.63 (2), p.135-142
• Main Authors: DOLFINI, E., ELLI, L., FERRERO, S., BRAIDOTTI, P., RONCORONI, L., DASDIA, T., FALINI, M. L., FORLANI, F., BARDELLA, M. T.
• Format: Article
• Language: English
• Subjects: Adenocarcinoma - pathology; Biological and medical sciences; Celiac disease; Celiac Disease - etiology; Celiac Disease - pathology; cell culture; Cell Line, Tumor - drug effects; Cell Size - drug effects; Cell Survival - drug effects; Colonic Neoplasms - pathology; Dose-Response Relationship, Drug; Food toxicology; Gliadin - toxicity; gluten intolerance; Humans; Medical sciences; multicellular spheroids; Neoplastic Stem Cells; Spheroids, Cellular - drug effects; Spheroids, Cellular - pathology; Spheroids, Cellular - ultrastructure; Toxicology
• ISSN: 0036-5513; 1502-7686
• DOI: 10.1080/00365510310000088

Background: In an attempt to clarify the role of gliadin toxicity in the pathogenesis of gluten intolerance (celiac disease), previous in vitro studies have been based on two-dimensional human cell cultures. However, the specific morphological and biochemical properties of in vivo tissue are better maintained in three-dimensional cell cultures (multicellular spheroids, MCS). The aim of this study was to develop a three-dimensional in vitro model to investigate the effects of gliadin on epithelial cells and broaden our understanding of the early tissue damage occurring in celiac disease. Methods: The three-dimensionally growing Lovo cell line was exposed to increasing concentrations of peptic-tryptic-digested bread wheat gliadin (from 125 to 1000 g mL) for 7 days in order to evaluate cell viability (colony-forming assay), and at the standard concentration of 500 g mL for 7 days in order to evaluate MCS diameters, volumes and cell morphology using light and electron microscopy. Results: In comparison with the controls, the cell viability of the gliadin-treated MCS was significantly reduced (20-80%), but there was no difference in size. Various degrees of cell damage (autophagic vacuoles and intra-cytoplasmic lipid-like droplets) were detected by both light and electron microscopy. Conclusion: This is the first study investigating the effects of gliadin on MCS. Lovo MCS seem to be responsive to gliadin exposure, thus confirming previous results obtained using two-dimensional cell cultures. The data suggest that three-dimensional cell cultures may be useful in broadening our understanding of some of the early effects of gliadin peptides on epithelial cells.