Russell J H, Dobos C B
J Immunol. 1983 Sep;131(3):1138-41.
Cloned CTL have been loaded with the K+ analogue 86Rb+. When mixed with unlabeled target cells, accelerated 86Rb+ release occurs from the CTL. The magnitude of accelerated 86Rb+ release is proportional to the efficacy of the target in standard 51Cr release assays. The signal responsible for accelerated 86Rb+ release has been localized to a postbinding event and has the physiologic requirements of delivery of the lethal hit. Thus, accelerated 86Rb+ release from the CTL represents the first direct observation of a physiologic event within the CTL related to a functional CTL-target interaction.
克隆的细胞毒性T淋巴细胞(CTL)已被加载钾离子类似物86Rb+。当与未标记的靶细胞混合时,CTL会加速释放86Rb+。加速释放86Rb+的程度与标准51Cr释放试验中靶细胞的杀伤效力成正比。导致加速释放86Rb+的信号已定位到结合后事件,并且具有传递致死性打击的生理要求。因此,CTL加速释放86Rb+代表了首次直接观察到CTL内与功能性CTL-靶细胞相互作用相关的生理事件。