Taylor James A G E, Benwell Christopher J, Robinson Stephen D
Gut Microbes and Health Programme, Quadram Institute Bioscience, Norwich Research Park, Norwich, UK.
School of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, UK.
Methods Mol Biol. 2022;2475:133-141. doi: 10.1007/978-1-0716-2217-9_9.
The ability to study the role of specific genes in endothelial cell biology is made possible by our ability to modulate their expression through siRNA or knockout technologies. However, many in vitro protocols, particularly those of a biochemical nature, require large numbers of endothelial cells. These types of analyses are encumbered by the need to repeatedly produce and characterize primary endothelial cell cultures and can be greatly facilitated by the use of immortalized microvascular endothelial cells. However, we have found that the manipulation of gene expression in these cells is not always straight forward. Here we describe how we alter gene expression in polyoma middle T antigen immortalized microvascular endothelial cells isolated from wild-type and genetically modified mice to study the role of cell adhesion molecules in downstream assays.
通过利用小干扰RNA(siRNA)或基因敲除技术调节特定基因的表达,我们得以研究这些基因在内皮细胞生物学中的作用。然而,许多体外实验方案,尤其是那些具有生化性质的方案,需要大量的内皮细胞。这类分析因需要反复培养和鉴定原代内皮细胞而受到阻碍,而使用永生化微血管内皮细胞则可极大地促进此类分析。然而,我们发现,在这些细胞中操纵基因表达并非总是一帆风顺。在此,我们描述了我们如何改变从野生型和转基因小鼠分离的多瘤病毒中T抗原永生化微血管内皮细胞中的基因表达,以研究细胞粘附分子在下游实验中的作用。