Acha-Orbea H, Scarpellino L, Hertig S, Dupuis M, Tschopp J
Ludwig Institute for Cancer Research, University of Lausanne, Epalinges, Switzerland.
EMBO J. 1990 Dec;9(12):3815-9. doi: 10.1002/j.1460-2075.1990.tb07599.x.
The granule/perforin exocytosis model of CTL mediated cytolysis proposes that CTL, upon recognition of the specific targets, release the cytolytic, pore-forming protein perforin into the intercellular space which then mediates the cytotoxic effect. However, direct evidence for the involvement of perforin is still lacking, and indeed, recent results even seem incompatible with the model. To determine directly the role of perforin in CTL cytotoxicity, perforin antisense oligonucleotides were exogenously added during the stimulation of mouse spleen derived T cells and human peripheral blood lymphocytes (PBL), respectively. Perforin protein expression in lymphocytes was reduced by up to 65%, and cytotoxicity of stimulated T cells by as much as 69% (5.7-fold). These results provide the first experimental evidence for a crucial role of perforin in lymphocyte mediated cytotoxicity.
细胞毒性T淋巴细胞(CTL)介导的细胞溶解的颗粒/穿孔素胞吐模型提出,CTL在识别特定靶标后,将具有细胞溶解作用的成孔蛋白穿孔素释放到细胞间空间,进而介导细胞毒性作用。然而,穿孔素参与其中的直接证据仍然缺乏,实际上,最近的结果甚至似乎与该模型不相符。为了直接确定穿孔素在CTL细胞毒性中的作用,分别在刺激小鼠脾脏来源的T细胞和人外周血淋巴细胞(PBL)的过程中,外源添加穿孔素反义寡核苷酸。淋巴细胞中穿孔素蛋白的表达降低了多达65%,刺激后的T细胞的细胞毒性降低了多达69%(5.7倍)。这些结果为穿孔素在淋巴细胞介导的细胞毒性中起关键作用提供了首个实验证据。