Laboratory of Molecular Diagnostics, Department of Laboratory Medicine & Advanced Biotechnologies, IRCCS San Raffaele Pisana, Rome - Italy.
Int J Biol Markers. 2012 Jul 19;27(2):e90-8. doi: 10.5301/JBM.2012.9235.
Multicenter studies and biobanking projects require blood transportation from the participating center to a central collection or diagnostic laboratory. The impact of time delays between venous blood collection and peripheral blood mononuclear cells (PBMC) isolation prior to RNA extraction may affect the quality and quantity of isolated nucleic acids for genomic applications. Thus, standard operating procedure (SOP) optimization for the treatment of biological samples before RNA extraction is crucial in a biological repository. In order to define SOPs for whole blood preservation prior to RNA extraction, we sought to determine whether different blood storage times (0, 3, 6, 10, 24, and 30 hours) prior to PBMCs isolation and storage at -80°C, could affect the quality and quantity of extracted RNA. After spectrophotometric quantification, the quality and integrity of RNA were assessed by agarose gel electrophoresis, RNA integrity number and real time-PCR (RT-PCR). Across the different time points we did not observe significant differences within the first 24 hours of blood storage at room temperature, while a significant loss in RNA yield and integrity was detected between 24 and 30 hours. We conclude that time delays before PBMCs isolation prior to RNA extraction may have a significant impact on downstream molecular biological applications.
多中心研究和生物库项目需要将血液从参与中心运送到中央采集或诊断实验室。在提取 RNA 之前,静脉采血与外周血单核细胞 (PBMC) 分离之间的时间延迟可能会影响用于基因组应用的分离核酸的质量和数量。因此,在生物存储库中,在提取 RNA 之前对生物样本进行标准操作程序 (SOP) 优化至关重要。为了定义 RNA 提取前全血保存的 SOP,我们试图确定在 -80°C 下分离和储存 PBMC 之前,不同的血液储存时间(0、3、6、10、24 和 30 小时)是否会影响提取 RNA 的质量和数量。在分光光度定量后,通过琼脂糖凝胶电泳、RNA 完整性数和实时 PCR (RT-PCR) 评估 RNA 的质量和完整性。在不同的时间点,我们没有观察到在室温下血液储存的前 24 小时内有显著差异,而在 24 至 30 小时之间,RNA 产量和完整性显著下降。我们得出结论,在提取 RNA 之前进行 PBMC 分离之前的时间延迟可能会对下游分子生物学应用产生重大影响。