Duke R C, Persechini P M, Chang S, Liu C C, Cohen J J, Young J D
Department of Microbiology and Immunology, University of Colorado School of Medicine, Denver 80262.
J Exp Med. 1989 Oct 1;170(4):1451-6. doi: 10.1084/jem.170.4.1451.
Rapid and extensive target cell DNA fragmentation is a unique characteristic of CTL-mediated killing. We studied the role of the granule pore-forming protein (PFP/perforin/cytolysin) of CTL in mediating lysis and DNA fragmentation of target cells. Perforin was isolated from murine CTL by sequential application of perforin-enriched granule fractions to four chromatographic columns: DEAE-Sepharose, Q-Sepharose, Polyanion SI, and Superose 12. Purified perforin was eluted as a single band of 70 kD in SDS-PAGE. While purified perforin produced potent lysis of a variety of target cells tested, it did not induce any measurable amount of DNA fragmentation. In parallel experiments, intact CTL produced marked DNA fragmentation of the same target cell populations. Our results suggest that perforin alone is not responsible for the DNA fragmentation observed during CTL-mediated killing and that other, as yet unknown, mediators or mechanisms are likely to be involved in the induction of target cell nuclear damage.
快速且广泛的靶细胞DNA片段化是CTL介导杀伤的独特特征。我们研究了CTL的颗粒孔形成蛋白(PFP/穿孔素/溶细胞素)在介导靶细胞裂解和DNA片段化中的作用。通过将富含穿孔素的颗粒级分依次应用于四个色谱柱:DEAE-琼脂糖、Q-琼脂糖、聚阴离子SI和Superose 12,从小鼠CTL中分离出穿孔素。纯化的穿孔素在SDS-PAGE中以70 kD的单一条带洗脱。虽然纯化的穿孔素对所测试的多种靶细胞产生了有效的裂解作用,但它并未诱导任何可测量的DNA片段化。在平行实验中,完整的CTL对相同的靶细胞群体产生了明显的DNA片段化。我们的结果表明,单独的穿孔素并不负责CTL介导杀伤过程中观察到的DNA片段化,并且其他尚未知的介质或机制可能参与了靶细胞核损伤的诱导。