Luo Kathy Q, Yu Vivian C, Pu Yongmei, Chang Donald C
Department of Biology, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong, China.
Biochem Biophys Res Commun. 2003 May 2;304(2):217-22. doi: 10.1016/s0006-291x(03)00559-x.
In this study, we reported the first measurement of the dynamics of activation of caspase-8 in a single living cell. This measurement was conducted using a specially developed molecular sensor based on the FRET (fluorescence resonance energy transfer) technique. This sensor was constructed by fusing a CFP (cyan fluorescent protein) and a YFP (yellow fluorescent protein) with a linker containing a tandem caspase-8-specific cleavage site. The change of the FRET ratio upon cleavage was larger than 4-fold. Using this sensor, we found that during TNFalpha-induced apoptosis, the activation of caspase-8 was a slower process than that of caspase-3, and it was initiated much earlier than the caspase-3 activation. Inhibition of caspase-9 delayed the full activation of caspase-3 but did not affect the dynamics of caspase-8. Results of these single-cell measurements suggested that caspase-3 was activated by caspase-8 through two parallel pathways during TNFalpha-induced apoptosis in HeLa cells.
在本研究中,我们报告了首次在单个活细胞中对caspase-8激活动力学的测量。该测量使用了基于荧光共振能量转移(FRET)技术专门开发的分子传感器进行。该传感器通过将青色荧光蛋白(CFP)和黄色荧光蛋白(YFP)与含有串联caspase-8特异性切割位点的接头融合构建而成。切割时FRET比率的变化大于4倍。使用该传感器,我们发现,在肿瘤坏死因子α(TNFα)诱导的细胞凋亡过程中,caspase-8的激活比caspase-3的激活过程更慢,并且它比caspase-3激活更早开始。caspase-9的抑制延迟了caspase-3的完全激活,但不影响caspase-8的动力学。这些单细胞测量结果表明,在HeLa细胞中TNFα诱导的细胞凋亡过程中,caspase-3通过两条平行途径被caspase-8激活。