Blankenstein G, Scampavia L D, Ruzicka J, Christian G D
Department of Chemistry, University of Washington, Seattle 98195-1700, USA.
Cytometry. 1996 Oct 1;25(2):200-4. doi: 10.1002/(SICI)1097-0320(19961001)25:2<200::AID-CYTO9>3.0.CO;2-K.
Improved time resolution of kinetic cellular events in flow cytometry is demonstrated by using a coaxial flow-mixing device integrated within a flow-injection (FI) system. The instrument is used in combination with a Becton Dickinson FACS Analyzer for on-line reagent addition, rapid sample mixing, and temperature control of cell suspensions. The coaxial flow device can instantaneously (< 60 ms) mix reagent and sample streams, allowing cytometric analysis of subsecond events to be performed. Kinetic measurements can be performed on the FACS analyzer in a variable time range of from 100 ms to 3 min. The system also allows the collection of unlimited cellular events at a specific incubation time point. Because the system operates continuously and no boost in core flow is required, disturbances of flow conditions are avoided. The capabilities of the flow injection cytometer have been demonstrated by the determination of internal [Ca2+]i mobilization in Jurkat T lymphocytes perfused internally with INDO-1 and stimulated by ionomycin.
通过使用集成在流动注射(FI)系统中的同轴流动混合装置,证明了流式细胞术中细胞动力学事件的时间分辨率得到了提高。该仪器与贝克曼库尔特公司的FACS分析仪结合使用,用于在线添加试剂、快速混合样品以及控制细胞悬液的温度。同轴流动装置能够在瞬间(<60毫秒)混合试剂流和样品流,从而可以进行亚秒级事件的细胞计数分析。动力学测量可以在FACS分析仪上在100毫秒至3分钟的可变时间范围内进行。该系统还允许在特定孵育时间点收集无限数量的细胞事件。由于该系统连续运行且无需增加核心流速,因此避免了流动条件的干扰。通过测定用indo-1内部灌注并受离子霉素刺激的Jurkat T淋巴细胞中的内部[Ca2+]i动员,证明了流动注射细胞仪的功能。