Division of Animal Physiology and Immunology, TUM School of Life Sciences, Technical University of Munich, Weihenstephaner Berg 3, 85354, Freising, Germany.
BMC Res Notes. 2024 Jun 5;17(1):154. doi: 10.1186/s13104-024-06812-w.
The IPEC-J2 cell line is used as an in vitro small intestine model for swine, but it is also used as a model for the human intestine, presenting a relatively unique setting. By combining electric cell-substrate impedance sensing, with next-generation-sequencing technology, we showed that mRNA gene expression profiles and related pathways can depend on the growth phase of IPEC-J2 cells. Our investigative approach welcomes scientists to reproduce or modify our protocols and endorses putting their gene expression data in the context of the respective growth phase of the cells.
Three time points are presented: (TP1) 1 h after medium change (= 6 h after seeding of cells), (TP2) the time point of the first derivative maximum of the cell growth curve, and a third point at the beginning of the plateau phase (TP3). Significantly outstanding at TP1 compared to TP2 was upregulated PLEKHN1, further FOSB and DEGS2 were significantly downregulated at TP2 compared to TP3. Any provided data can be used to improve next-generation experiments with IPEC-J2 cells.
IPEC-J2 细胞系被用作猪的体外小肠模型,但也被用作人类肠道的模型,呈现出相对独特的设置。通过将电细胞-底物阻抗感应与下一代测序技术相结合,我们表明 mRNA 基因表达谱和相关途径可能取决于 IPEC-J2 细胞的生长阶段。我们的研究方法欢迎科学家复制或修改我们的方案,并赞成将他们的基因表达数据置于细胞相应的生长阶段的背景下。
呈现了三个时间点:(TP1)换液后 1 小时(=细胞接种后 6 小时),(TP2)细胞生长曲线的一阶导数最大值的时间点,以及平台期开始时的第三个时间点(TP3)。与 TP2 相比,TP1 时 PLEKHN1 上调显著,进一步与 TP3 相比,TP2 时 FOSB 和 DEGS2 下调显著。提供的任何数据都可用于改进 IPEC-J2 细胞的下一代实验。