Jones J, Morgan B P
Department of Medical Biochemistry, University of Wales College of Medicine, Cardiff, U.K.
Biochem J. 1991 Nov 15;280 ( Pt 1)(Pt 1):199-204. doi: 10.1042/bj2800199.
Different cell types vary widely in their susceptibility to killing by the pore-forming cytolytic molecule perforin. In particular, the cells responsible for synthesis of perforin, i.e. cytotoxic T lymphocytes (CTL) and natural killer (NK) cells, are very resistant to cytolysis by this molecule. It has previously been suggested that resistance is due, at least in part, to diminished binding of perforin to these cells. The purpose of the present study was to compare binding of perforin to sensitive and resistant cell types. To this end, perforin was biosynthetically labelled prior to purification. The purified labelled protein was then utilized to obtain a direct measure of the amount of perforin bound to cells during attack. Resistant cells (CTL, neutrophils) bound at least as much perforin as did sensitive cells (K562, HL60 etc.), indicating that resistance to perforin involves mechanisms operating after binding of the lytic molecule.
不同细胞类型对成孔溶细胞分子穿孔素杀伤作用的敏感性差异很大。特别是,负责合成穿孔素的细胞,即细胞毒性T淋巴细胞(CTL)和自然杀伤(NK)细胞,对该分子的细胞溶解作用具有很强的抗性。此前曾有人提出,这种抗性至少部分是由于穿孔素与这些细胞的结合减少所致。本研究的目的是比较穿孔素与敏感和抗性细胞类型的结合情况。为此,在纯化之前对穿孔素进行生物合成标记。然后利用纯化的标记蛋白直接测量攻击过程中与细胞结合的穿孔素量。抗性细胞(CTL、中性粒细胞)与敏感细胞(K562、HL60等)结合的穿孔素量至少相同,这表明对穿孔素的抗性涉及在裂解分子结合后起作用的机制。