Dragavon Joe, Molter Tim, Young Cody, Strovas Tim, McQuaide Sarah, Holl Mark, Zhang Meng, Cookson Brad, Jen Alex, Lidstrom Mary, Meldrum Deirdre, Burgess Lloyd
Department of Chemistry, University of Washington, Seattle, WA 98195-2180, USA.
J R Soc Interface. 2008 Oct 6;5 Suppl 2(Suppl 2):S151-9. doi: 10.1098/rsif.2008.0106.focus.
The development of a cellular isolation system (CIS) that enables the monitoring of single-cell oxygen consumption rates in real time is presented. The CIS was developed through a multidisciplinary effort within the Microscale Life Sciences Center (MLSC) at the University of Washington. The system comprises arrays of microwells containing Pt-porphyrin-embedded polystyrene microspheres as the reporter chemistry, a lid actuator system and a gated intensified imaging camera, all mounted on a temperature-stabilized confocal microscope platform. Oxygen consumption determination experiments were performed on RAW264.7 mouse macrophage cells as proof of principle. Repeatable and consistent measurements indicate that the oxygen measurements did not adversely affect the physiological state of the cells measured. The observation of physiological rates in real time allows studies of cell-to-cell heterogeneity in oxygen consumption rate to be performed. Such studies have implications in understanding the role of mitochondrial function in the progression of inflammatory-based diseases, and in diagnosing and treating such diseases.
本文介绍了一种细胞隔离系统(CIS)的开发,该系统能够实时监测单细胞耗氧率。CIS是通过华盛顿大学微尺度生命科学中心(MLSC)内的多学科合作开发的。该系统包括装有嵌入铂卟啉的聚苯乙烯微球作为报告化学物质的微孔阵列、一个盖子驱动系统和一个门控增强成像相机,所有这些都安装在温度稳定的共聚焦显微镜平台上。作为原理验证,对RAW264.7小鼠巨噬细胞进行了耗氧量测定实验。可重复且一致的测量表明,氧气测量对所测细胞的生理状态没有不利影响。实时观察生理速率使得能够对细胞间耗氧率的异质性进行研究。此类研究对于理解线粒体功能在炎症性疾病进展中的作用以及诊断和治疗此类疾病具有重要意义。