Chen Yan, Zhong Jiang F
Bioengineering, California Institute of Technology, Pasadena, CA, USA.
Methods Mol Biol. 2008;438:293-303. doi: 10.1007/978-1-59745-133-8_22.
Isolating pure stem cell populations is one of the major obstacles in stem cell gene expression profiling due to the lack of stem cell markers. Many results of gene expression profiling studies are difficult to interpret because of the heterogeneous cell populations used in these studies. Single-cell gene expression profiling is perhaps the most attractive gene expression profiling method for studying stem cell gene regulation, because isolating pure stem cell population is not needed. However, current single-cell gene expression profiling methods such as laser capture microdissection (LCM) and patch-clamp analysis lack the high-throughput ability in sample processing. For better understanding of the gene regulation networks during cellular events, a large number of gene expression profiles are required. Therefore, we developed inexpensive microfluidic devices for high-throughput single-cell gene expression profiling. With our devices, cDNA could be obtained from 50 individual cells within 3 hours. This approach can be applied to neural stem cells, and other cell types.
由于缺乏干细胞标志物,分离纯干细胞群体是干细胞基因表达谱分析中的主要障碍之一。由于这些研究中使用的细胞群体异质性,许多基因表达谱分析研究的结果难以解释。单细胞基因表达谱分析可能是研究干细胞基因调控最具吸引力的基因表达谱分析方法,因为不需要分离纯干细胞群体。然而,当前的单细胞基因表达谱分析方法,如激光捕获显微切割(LCM)和膜片钳分析,在样品处理方面缺乏高通量能力。为了更好地理解细胞事件中的基因调控网络,需要大量的基因表达谱。因此,我们开发了用于高通量单细胞基因表达谱分析的廉价微流控装置。使用我们的装置,可在3小时内从50个单个细胞中获得cDNA。这种方法可应用于神经干细胞和其他细胞类型。