Improving a fish intestinal barrier model by combining two rainbow trout cell lines: epithelial RTgutGC and fibroblastic RTgutF

被引:0
作者
Carolin Drieschner
Nguyen T. K. Vo
Hannah Schug
Michael Burkard
Niels C. Bols
Philippe Renaud
Kristin Schirmer
机构
[1] Eawag (Swiss Federal Institute of Aquatic Science and Technology),Department of Environmental Toxicology
[2] EPFL (École Polytechnique Fédérale de Lausanne),Microsystems Laboratory 4, School of Engineering
[3] McMaster University,Department of Biology
[4] University of Waterloo,Department of Biology
[5] EPFL (École Polytechnique Fédérale de Lausanne),Laboratory of Environmental Toxicology, School of Architecture, Civil and Environmental Engineering
[6] ETHZ (Swiss Federal Institute of Technology in Zurich),Department of Environmental Systems Science
来源
Cytotechnology | 2019年 / 71卷
关键词
Fish-gut-on-chip; Rainbow trout (; ); Epithelial barrier model; Anodized aluminum; Impedance spectroscopy; TEER;
D O I
暂无
中图分类号
学科分类号
摘要
An in vitro model of the fish intestine is of interest for research and application in diverse fields such as fish physiology, aquaculture and chemical risk assessment. The recently developed epithelial barrier model of the fish intestine relies on the RTgutGC cell line from rainbow trout (Oncorhynchus mykiss), cultured in inserts on permeable membranes. Our aim was to extend the current system by introducing intestinal fibroblasts as supportive layer in order to reconstruct the epithelial–mesenchymal interface as found in vivo. We therefore initiated and characterized the first fibroblast cell line from the intestine of rainbow trout, which has been termed RTgutF. Co-culture studies of RTgutGC and RTgutF were performed on commercially available electric cell substrate for impedance sensing (ECIS) and on newly developed ultrathin, highly porous alumina membranes to imitate the cellular interaction with the basement membrane. Cellular events were examined with non-invasive impedance spectroscopy to distinguish between barrier tightness and cell density in the ECIS system and to determine transepithelial electrical resistance for cells cultured on the alumina membranes. We highlight the relevance of the piscine intestinal fibroblasts for an advanced intestinal barrier model, particularly on ultrathin alumina membranes. These membranes enable rapid crosstalk of cells cultured on opposite sides, which led to increased barrier tightening in the fish cell line-based epithelial–mesenchymal model.
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页码:835 / 848
页数:13
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