Institute of Experimental Hematology and Transfusion Medicine, University of Bonn, Venusberg-Campus 1, 53127 Bonn, Germany.
Qiagen GmbH, 40724 Hilden, Germany.
Int J Mol Sci. 2020 Oct 21;21(20):7776. doi: 10.3390/ijms21207776.
In humans, Factor VIII (F8) deficiency leads to hemophilia A and F8 is largely synthesized and secreted by the liver sinusoidal endothelial cells (LSECs). However, the specificity and characteristics of these cells in comparison to other endothelial cells is not well known. In this study, we performed genome wide expression and CpG methylation profiling of fetal and adult human primary LSECs together with other fetal primary endothelial cells from lung (micro-vascular and arterial), and heart (micro-vascular). Our results reveal expression and methylation markers distinguishing LSECs at both fetal and adult stages. Differential gene expression of fetal LSECs in comparison to other fetal endothelial cells pointed to several differentially regulated pathways and biofunctions in fetal LSECs. We used targeted bisulfite resequencing to confirm selected top differentially methylated regions. We further designed an assay where we used the selected methylation markers to test the degree of similarity of in-house iPS generated vascular endothelial cells to primary LSECs; a higher similarity was found to fetal than to adult LSECs. In this study, we provide a detailed molecular profile of LSECs and a guide to testing the effectiveness of production of in vitro differentiated LSECs.
在人类中,因子 VIII(F8)缺乏导致血友病 A,而 F8 主要由肝窦内皮细胞(LSEC)合成和分泌。然而,这些细胞与其他内皮细胞相比的特异性和特征尚不清楚。在这项研究中,我们对胎儿和成人原代 LSEC 以及来自肺(微血管和动脉)和心脏(微血管)的其他胎儿原代内皮细胞进行了全基因组表达和 CpG 甲基化谱分析。我们的结果揭示了在胎儿和成人阶段区分 LSEC 的表达和甲基化标志物。与其他胎儿内皮细胞相比,胎儿 LSEC 的差异基因表达表明在胎儿 LSEC 中存在几个差异调控的途径和生物功能。我们使用靶向亚硫酸氢盐重测序来验证选定的 top 差异甲基化区域。我们进一步设计了一种检测方法,使用选定的甲基化标志物来测试内部产生的 iPS 血管内皮细胞与原代 LSEC 的相似程度;发现与成人 LSEC 相比,与胎儿 LSEC 的相似程度更高。在这项研究中,我们提供了 LSEC 的详细分子图谱,并为测试体外分化的 LSEC 产生的有效性提供了指导。