Chao Tzu-Chiao, Ros Alexandra
Department of Chemistry and Biochemistry, Arizona State University, Box 871604, Tempe, AZ 85287-1604, USA.
J R Soc Interface. 2008 Oct 6;5 Suppl 2(Suppl 2):S139-50. doi: 10.1098/rsif.2008.0233.focus.
Biological analyses traditionally probe cell ensembles in the range of 103-106 cells, thereby completely averaging over relevant individual cell responses, such as differences in cell proliferation, responses to external stimuli or disease onset. In past years, this fact has been realized and increasing interest has evolved for single-cell analytical methods, which could give exciting new insights into genomics, proteomics, transcriptomics and systems biology. Microfluidic or lab-on-a-chip devices are the method of choice for single-cell analytical tools as they allow the integration of a variety of necessary process steps involved in single-cell analysis, such as selection, navigation, positioning or lysis of single cells as well as separation and detection of cellular analytes. Along with this advantageous integration, microfluidic devices confine single cells in compartments near their intrinsic volume, thus minimizing dilution effects and increasing detection sensitivity. This review overviews the developments and achievements of microfluidic single-cell analysis of intracellular compounds in the past few years, from proof-of-principle devices to applications demonstrating a high biological relevance.
传统的生物学分析方法通常对10³至10⁶个细胞的群体进行检测,从而完全平均了相关的单个细胞反应,如细胞增殖差异、对外界刺激的反应或疾病发作情况。在过去几年里,人们已经认识到这一事实,并且对单细胞分析方法的兴趣与日俱增,这些方法可能会为基因组学、蛋白质组学、转录组学和系统生物学带来令人兴奋的新见解。微流控或芯片实验室设备是单细胞分析工具的首选方法,因为它们能够集成单细胞分析中涉及的各种必要处理步骤,例如单细胞的选择、导航、定位或裂解,以及细胞分析物的分离和检测。伴随着这种有利的集成,微流控设备将单个细胞限制在接近其固有体积的小室中,从而将稀释效应降至最低并提高检测灵敏度。本文综述了过去几年微流控单细胞分析细胞内化合物的发展和成就,从原理验证设备到具有高度生物学相关性的应用。