Department of Agricultural and Environmental Sciences, University of Milan, 20133 Milan, Italy.
Department of Veterinary Medicine and Animal Sciences, University of Milan, 26900 Lodi, Italy.
Cells. 2023 Jul 13;12(14):1843. doi: 10.3390/cells12141843.
In vitro organotypic cell-based intestinal platforms, able to faithfully recapitulate the complex functions of the organ in vivo, would be a great support to search for more sustainable feed ingredients in aquaculture. We previously demonstrated that proliferation or differentiation of rainbow trout intestinal cell lines is dictated by the culture environment. The aim of the present work was to develop a culture platform that can efficiently promote cell differentiation into mature enterocytes. We compared four options, seeding the RTpiMI cell line derived from the proximal intestine on (1) polyethylene terephthalate (PET) culture inserts ThinCert™ (TC), (2) TC coated with the solubilized basement membrane matrix Matrigel (MM), (3) TC with the rainbow trout fibroblast cell line RTskin01 embedded within the Matrigel matrix (MMfb), or (4) the highly porous polystyrene scaffold Alvetex populated with the abovementioned fibroblast cell line (AV). We evaluated the presence of columnar cells with a clear polarization of brush border enzymes, the formation of an efficient barrier with a significant increase in transepithelial electrical resistance (TEER), and its ability to prevent the paracellular flux of large molecules but allow the transit of small compounds (proline and glucose) from the apical to the basolateral compartment. All parameters improved moving from the simplest (TC) through the more complex platforms. The presence of fibroblasts was particularly effective in enhancing epithelial cell differentiation within the AV platform recreating more closely the complexity of the intestinal mucosa, including the presence of extracellular vesicles between fibroblasts and epithelial cells.
在体外器官型细胞培养平台上,能够真实地再现体内器官的复杂功能,将极大地支持水产养殖中寻找更可持续的饲料成分。我们之前已经证明,虹鳟肠道细胞系的增殖或分化取决于培养环境。本研究的目的是开发一种能够有效促进细胞分化为成熟肠细胞的培养平台。我们比较了四种选择,将源自近端肠道的 RTpiMI 细胞系接种在(1)聚对苯二甲酸乙二醇酯(PET)培养插入物 ThinCert™(TC)上,(2)涂有可溶基底膜基质 Matrigel(MM)的 TC,(3)含有虹鳟成纤维细胞系 RTskin01 的 MM 基质中的 TC(MMfb),或(4)用上述成纤维细胞系填充的高度多孔聚苯乙烯支架 Alvetex(AV)。我们评估了存在具有明显刷状边界酶极化的柱状细胞、形成有效的屏障,显著增加跨上皮电阻(TEER),以及其阻止大分子量物质的旁细胞通量但允许小化合物(脯氨酸和葡萄糖)从顶侧向基底侧腔室转运的能力。所有参数都通过从最简单的(TC)到更复杂的平台的改进而得到提高。成纤维细胞的存在特别有效地增强了 AV 平台中上皮细胞的分化,更紧密地再现了肠道黏膜的复杂性,包括成纤维细胞和上皮细胞之间存在细胞外囊泡。