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Evaluation of techniques for performing cellular isolation and preservation during microgravity conditions

机译:在微重力条件下进行细胞分离和保存的技术评估

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摘要

Genomic and epigenomic studies require the precise transfer of microliter volumes among different types of tubes in order to purify DNA, RNA, or protein from biological samples and subsequently perform analyses of DNA methylation, RNA expression, and chromatin modifications on a genome-wide scale. Epigenomic and transcriptional analyses of human blood cells, for example, require separation of purified cell types to avoid confounding contributions of altered cellular proportions, and long-term preservation of these cells requires their isolation and transfer into appropriate freezing media. There are currently no protocols for these cellular isolation procedures on the International Space Station (ISS). Currently human blood samples are either frozen as mixed cell populations (within the CPT collection tubes) with poor yield of viable cells required for cell-type isolations, or returned under ambient conditions, which requires timing with Soyuz missions. Here we evaluate the feasibility of translating terrestrial cell purification techniques to the ISS. Our evaluations were performed in microgravity conditions during parabolic atmospheric flight. The pipetting of open liquids in microgravity was evaluated using analog-blood fluids and several types of pipette hardware. The best-performing pipettors were used to evaluate the pipetting steps required for peripheral blood mononuclear cell (PBMC) isolation following terrestrial density-gradient centrifugation. Evaluation of actual blood products was performed for both the overlay of diluted blood, and the transfer of isolated PBMCs. We also validated magnetic purification of cells. We found that positive-displacement pipettors avoided air bubbles, and the tips allowed the strong surface tension of water, glycerol, and blood to maintain a patent meniscus and withstand robust pipetting in microgravity. These procedures will greatly increase the breadth of research that can be performed on board the ISS, and allow improvised experimentation by astronauts on extraterrestrial missions.
机译:基因组学和表观基因组学研究要求在不同类型的试管之间精确转移微升体积,以从生物样品中纯化DNA,RNA或蛋白质,然后在全基因组范围内进行DNA甲基化,RNA表达和染色质修饰的分析。例如,人类血细胞的表观基因组学和转录分析需要分离纯化的细胞类型,以避免混淆改变的细胞比例的贡献,而这些细胞的长期保存需要将其分离并转移到适当的冷冻培养基中。目前国际空间站(ISS)上没有用于这些蜂窝隔离程序的协议。目前,人类血液样本要么作为混合细胞群体(在CPT收集管内)冷冻,而细胞类型分离所需的活细胞产量却很低,或者在环境条件下返回,这需要与Soyuz任务同步进行。在这里,我们评估了将陆地细胞纯化技术转化为国际空间站的可行性。我们的评估是在抛物线大气飞行过程中的微重力条件下进行的。使用模拟血液流体和几种类型的移液器硬件对微重力下开放液体的移液进行了评估。表现最佳的移液器用于评估地面密度梯度离心后分离外周血单核细胞(PBMC)所需的移液步骤。对稀释血液的覆盖和分离的PBMC的转移都进行了实际血液制品的评估。我们还验证了细胞的磁性纯化。我们发现,正排量的移液器避免了气泡,并且吸头使水,甘油和血液的强大表面张力保持半月板,并且可以承受微重力下的强力移液。这些程序将极大地增加可在国际空间站上进行的研究的广度,并允许宇航员对外星任务进行即兴实验。

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