Ojcius D M, Jiang S B, Persechini P M, Storch J, Young J D
Laboratory of Cellular Physiology and Immunology, Rockefeller University, New York, NY 10021.
Mol Immunol. 1990 Sep;27(9):839-45. doi: 10.1016/0161-5890(90)90149-t.
Cytotoxic T lymphocytes (CTL) release from their granules a 70 kDa protein, called PFP, perforin or cytolysin, which inserts into the target cell plasma membrane in its monomeric form. Here it polymerizes into a macromolecular complex forming pores as large as 20 nm. Although purified PFP/perforin can effectively lyze all target cells tested. CTL are refractory to lysis. The mechanism underlying the resistance of CTL is currently unknown. This study represents a search for membrane structural properties that could confer resistance to CTL against PFP/perforin-mediated lysis. The fluorescent dye merocyanine 540 was used to measure the lipid head group packing of CTL and several target cells, and 1-[4-(trimethylamine)phenyl]-6-phenylhexa-1,3,5-triene was used to estimate the fluidity of the membrane hydrocarbon region. The resistance against PFP/perforin-mediated lysis was determined by the 51Cr release assay. A comparison of the membrane rigidity with cell resistance led to the conclusion that the membrane lipid structure cannot account for the unusually high resistance of CTL. In particular, the resistant CTL line CTLL-2 has a lipid head group packing that is looser than that of Yac-1, and the sensitive target cells Jy-25 and EL-4 have membrane acyl chains that are less fluid than those of the effector CTLL-R8.
细胞毒性T淋巴细胞(CTL)从其颗粒中释放出一种70 kDa的蛋白质,称为穿孔素、成孔蛋白或细胞溶素,它以单体形式插入靶细胞质膜。在此,它聚合成一个大分子复合物,形成直径达20 nm的孔。尽管纯化的穿孔素/成孔蛋白能有效裂解所有测试的靶细胞,但CTL对裂解具有抗性。CTL抗性的潜在机制目前尚不清楚。本研究旨在寻找可能赋予CTL对穿孔素/成孔蛋白介导的裂解具有抗性的膜结构特性。使用荧光染料部花青540来测量CTL和几种靶细胞的脂质头部基团堆积情况,并使用1-[4-(三甲胺基)苯基]-6-苯基己-1,3,5-三烯来估计膜烃区域的流动性。通过51Cr释放试验确定对穿孔素/成孔蛋白介导的裂解的抗性。将膜刚性与细胞抗性进行比较得出结论,膜脂质结构不能解释CTL异常高的抗性。特别是,抗性CTL系CTLL-2的脂质头部基团堆积比Yac-1的更松散,而敏感靶细胞Jy-25和EL-4的膜酰基链流动性比效应细胞CTL-R8的更低。