Key Laboratory of Bone Marrow Stem Cell, Jiangsu Province, Xuzhou 221002, China.
Department of Hematology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou 221002, China.
Biomed Res Int. 2018 Oct 2;2018:4953806. doi: 10.1155/2018/4953806. eCollection 2018.
Endothelial cells (ECs) could express some important cytokines and signal molecules which play a key role in normal hematopoiesis and repopulation. Busulfan-induced vascular endothelial injury is an important feature after hematopoietic stem cell transplantation (HSCT). But the molecular mechanism of how the injured ECs affect hematopoietic reconstruction is still unknown. It is possibly through modulation of the change of some gene expression. RT-qPCR is one of the most popular methods used to accurately determine gene expression levels, based on stable reference gene (RG) selection from housekeeping genes. So our aim is to select stable RGs for more accurate measures of mRNA levels during Busulfan-induced vascular endothelial injury. In this study, 14 RGs were selected to investigate their expression stability in ECs during 72 hours of EC injury treated with Busulfan. Our results revealed extreme variation in RG stability compared by five statistical algorithms. ywhaz and alas1 were recognized as the two idlest RGs on account of the final ranking, while the two most usually used RGs (gapdh and actb) were not the most stable RGs. Next, these data were verified by testing signalling pathway genes ctnnb1, robo4, and notch1 based on the above four genes ywha, alas1, gapdh, and actb. It shows that the normalization of mRNA expression data using unstable RGs greatly affects gene fold change, which means the reliability of the biological conclusions is questionable. Based on the best RGs used, we also found that robo4 is significantly overexpressed in Busulfan-impaired ECs. In conclusion, our data reaffirms the importance of RGs selection for the valid analysis of gene expression in Busulfan-impaired ECs. And it also provides very useful guidance and basis for more accurate differential expression gene screening and future expanding biomolecule study of different drugs such as cyclophosphamide and fludarabine-injured ECs.
内皮细胞 (ECs) 可以表达一些重要的细胞因子和信号分子,这些因子和信号分子在正常造血和再殖中起着关键作用。白消安诱导的血管内皮损伤是造血干细胞移植 (HSCT) 后的一个重要特征。但是,受损的 ECs 如何影响造血重建的分子机制尚不清楚。可能是通过调节某些基因表达的变化。实时荧光定量 PCR (RT-qPCR) 是基于管家基因选择稳定参考基因 (RG) 来准确确定基因表达水平的最常用方法之一。因此,我们的目的是选择稳定的 RG,以更准确地测量白消安诱导的血管内皮损伤过程中 mRNA 水平的变化。在这项研究中,选择了 14 个 RG 来研究它们在白消安处理的内皮细胞损伤后 72 小时内的表达稳定性。我们的结果通过五种统计算法揭示了 RG 稳定性的极端变化。ywhaz 和 alas1 被认为是最终排名中最不活跃的两个 RG,而最常用的两个 RG (gapdh 和 actb) 并不是最稳定的 RG。接下来,根据上述四个基因 ywha、alas1、gapdh 和 actb,通过测试信号通路基因 ctnnb1、robo4 和 notch1,对这些数据进行了验证。结果表明,使用不稳定 RG 归一化 mRNA 表达数据会极大地影响基因的倍数变化,这意味着生物结论的可靠性值得怀疑。基于最佳 RG 的使用,我们还发现 robo4 在白消安损伤的 ECs 中表达显著上调。总之,我们的数据再次证实了 RG 选择对于白消安损伤的 ECs 中基因表达有效分析的重要性。它还为更准确的差异表达基因筛选以及未来对不同药物(如环磷酰胺和氟达拉滨)损伤的 ECs 的扩展生物分子研究提供了非常有用的指导和依据。