Dolfini E, Elli L, Ferrero S, Braidotti P, Roncoroni L, Dasdia T, Falini M L, Forlani F, Bardella M T
Department of Biology and Genetics, University of Milan, Italy.
Scand J Clin Lab Invest. 2003;63(2):135-41.
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.
The three-dimensionally growing Lovo cell line was exposed to increasing concentrations of peptic-tryptic-digested bread wheat gliadin (from 125 to 1000 microg/mL) for 7 days in order to evaluate cell viability (colony-forming assay), and at the standard concentration of 500 microg/mL for 7 days in order to evaluate MCS diameters, volumes and cell morphology using light and electron microscopy.
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.
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.
为了阐明麦醇溶蛋白毒性在麸质不耐受(乳糜泻)发病机制中的作用,以往的体外研究基于二维人体细胞培养。然而,体内组织的特定形态和生化特性在三维细胞培养(多细胞球体,MCS)中能得到更好的维持。本研究的目的是建立一种三维体外模型,以研究麦醇溶蛋白对上皮细胞的影响,并加深我们对乳糜泻早期组织损伤的理解。
将三维生长的Lovo细胞系暴露于浓度递增的胃蛋白酶 - 胰蛋白酶消化的面包小麦麦醇溶蛋白(从125至1000微克/毫升)中7天,以评估细胞活力(集落形成试验),并在标准浓度500微克/毫升下暴露7天,以便使用光学和电子显微镜评估MCS的直径、体积和细胞形态。
与对照组相比,麦醇溶蛋白处理的MCS的细胞活力显著降低(20 - 80%),但大小没有差异。光学和电子显微镜均检测到不同程度的细胞损伤(自噬泡和胞浆内脂质样滴)。
这是第一项研究麦醇溶蛋白对MCS影响的研究。Lovo MCS似乎对麦醇溶蛋白暴露有反应,从而证实了先前使用二维细胞培养获得的结果。数据表明,三维细胞培养可能有助于拓宽我们对麦醇溶蛋白肽对上皮细胞一些早期影响的理解。