Hiebl Verena, Schachner Daniel, Ladurner Angela, Heiss Elke H, Stangl Herbert, Dirsch Verena M
1Department of Pharmacognosy, University of Vienna, Althanstrasse 14, 1090 Vienna, Austria.
2Institute of Medical Chemistry, Center for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Biol Proced Online. 2020 Apr 11;22:7. doi: 10.1186/s12575-020-00120-w. eCollection 2020.
The human Caco-2 cell line is a common in vitro model of the intestinal epithelial barrier. As the intestine is a major interface in cholesterol turnover and represents a non-biliary pathway for cholesterol excretion, Caco-2 cells are also a valuable model for studying cholesterol homeostasis, including cholesterol uptake and efflux. Currently available protocols are, however, either sketchy or not consistent among different laboratories. Our aim was therefore to generate a collection of optimized protocols, considering the different approaches of the different laboratories and to highlight possibilities and limitations of measuring cholesterol transport with this cell line.
We developed comprehensive and quality-controlled protocols for the cultivation of Caco-2 cells on filter inserts in a single tight monolayer. A cholesterol uptake as well as a cholesterol efflux assay is described in detail, including suitable positive controls. We further show that Caco-2 cells can be efficiently transfected for luciferase reporter gene assays in order to determine nuclear receptor activation, main transcriptional regulators of cholesterol transporters (ABCA1, ABCB1, ABCG5/8, NPC1L1). Detection of protein and mRNA levels of cholesterol transporters in cells grown on filter inserts can pose challenges for which we highlight essential steps and alternative approaches for consideration. A protocol for viability assays with cells differentiated on filter inserts is provided for the first time.
The Caco-2 cell line is widely used in the scientific community as model for the intestinal epithelium, although with highly divergent protocols. The herein provided information and protocols can be a common basis for researchers intending to use Caco-2 cells in the context of cellular cholesterol homeostasis.
人Caco-2细胞系是肠上皮屏障常用的体外模型。由于肠道是胆固醇代谢的主要界面,代表了胆固醇排泄的非胆汁途径,Caco-2细胞也是研究胆固醇稳态(包括胆固醇摄取和流出)的重要模型。然而,目前可用的方案要么粗略,要么在不同实验室之间不一致。因此,我们的目标是收集一系列优化方案,考虑不同实验室的不同方法,并强调使用该细胞系测量胆固醇转运的可能性和局限性。
我们制定了全面且质量可控的方案,用于在滤膜上以紧密单层培养Caco-2细胞。详细描述了胆固醇摄取和胆固醇流出测定法,包括合适的阳性对照。我们还表明,可以有效地转染Caco-2细胞用于荧光素酶报告基因测定,以确定核受体激活,这是胆固醇转运蛋白(ABCA1、ABCB1、ABCG5/8、NPC1L1)的主要转录调节因子。检测滤膜上生长的细胞中胆固醇转运蛋白的蛋白质和mRNA水平可能具有挑战性,对此我们强调了需要考虑的关键步骤和替代方法。首次提供了在滤膜上分化的细胞进行活力测定的方案。
Caco-2细胞系在科学界被广泛用作肠上皮模型,尽管方案差异很大。本文提供的信息和方案可为打算在细胞胆固醇稳态背景下使用Caco-2细胞的研究人员提供共同基础。