Salway F, Day P J R, Ollier W E R, Peakman T C
Manchester Interdisciplinary Biocentre (MIB), The University of Manchester, 131 Princess Street, Manchester, M1 7DN, UK.
Int J Epidemiol. 2008 Apr;37 Suppl 1:i11-5. doi: 10.1093/ije/dym279.
For biological sample banking it is important to precisely document sample treatment prior to extraction and storage. A major variable is the interval between blood sampling and subsequent processing and storage. We have determined the relationship between this time interval and frequency of 5' transcript tags. This study was designed to establish guidelines for collecting RNA from blood in prospective studies and ensure maximum availability of RNA analytes.
Venous blood was collected from 40 healthy volunteers. Samples were processed immediately, 12, 24 and 36 h post collection and buffy coat and/or plasma removed. Total RNA was extracted and reverse transcribed, assays were optimized and levels of 5' RNA tags quantified by qPCR.
Stably expressed reference genes were selected to examine 5' tags in plasma and buffy coat blood fractions. Whole blood was processed at various time points post collection to determine the affect on the presence and stability of 5' RNA tags. A significant increase (P < 0.05 to P < 0.001) in 5' RNA tags was observed at 12 h and up to 36 h in plasma and buffy coat samples isolated from EDTA blood which was maintained at 4 degrees C prior to processing when compared with plasma and buffy coat isolated from EDTA blood processed immediately.
Over time 5' RNA tags increase in both plasma and buffy coat samples. It has been previously shown that removing cells from their normal environment produces cellular activation and up-regulation of pathways resulting in increased transcript expression. Positive correlation was observed between the time interval from sample collection to storage and amount of 5' transcript tags present. This increase could be due to white blood cells undergoing necrosis and lysis, or from RNA protected within apoptotic bodies. As 5' RNA tags were targeted using random primers for reverse transcription, even RNA partly degraded by RNases would have been detected.
对于生物样本库而言,在提取和储存之前精确记录样本处理过程非常重要。一个主要变量是采血与后续处理及储存之间的时间间隔。我们已确定了该时间间隔与5'转录标签频率之间的关系。本研究旨在为前瞻性研究中从血液中收集RNA制定指导原则,并确保RNA分析物的最大可用性。
从40名健康志愿者采集静脉血。样本在采集后立即、12小时、24小时和36小时进行处理,并去除血沉棕黄层和/或血浆。提取总RNA并进行逆转录,优化检测方法,并通过qPCR定量5'RNA标签水平。
选择稳定表达的参考基因来检测血浆和血沉棕黄层血液组分中的5'标签。在采集后的不同时间点对全血进行处理,以确定对5'RNA标签的存在和稳定性的影响。与立即处理的EDTA血分离的血浆和血沉棕黄层相比,从4℃保存至处理前的EDTA血分离的血浆和血沉棕黄层样本在12小时至36小时时观察到5'RNA标签显著增加(P<0.05至P<0.001)。
随着时间推移,血浆和血沉棕黄层样本中的5'RNA标签均会增加。先前已表明,将细胞从其正常环境中移出会导致细胞活化和通路上调从而导致转录本表达增加。观察到从样本采集到储存的时间间隔与存在的5'转录标签数量之间呈正相关。这种增加可能是由于白细胞发生坏死和裂解,或者是由于凋亡小体中保护的RNA。由于使用随机引物靶向5'RNA标签进行逆转录,即使是被核糖核酸酶部分降解的RNA也会被检测到。