Glass A, Walsh C M, Lynch D H, Clark W R
Department of Biology, University of California, Los Angeles 90095, USA.
J Immunol. 1996 May 15;156(10):3638-44.
Cloned murine CTL activated via the TCR or by PMA and ionomycin up-regulate surface Fas ligand and show an increased ability to kill non-Ag-specific Fas+ target cells. This up-regulation starts after 45 to 60 min and has a t1/2 for reversal of about 90 min. Up-regulation of lytic function is accompanied by up-regulation of Fas ligand on the CTL surface, which can be blocked by protein synthesis inhibitors. When up-regulation of Fas lytic function was induced by PMA and ionomycin, EGTA blocked both activation of lytic function and expression of Fas ligand detected by FACS analysis. However, when up-regulation was induced by specific Ag, EGTA blocked activation of lytic function, but not up-regulation of Fas ligand. Moreover, EL-4 cells have very high levels of surface Fas ligand, although they are not cytotoxic. Thus, expression of surface Fas ligand may be required, but not sufficient, for Fas-mediated lysis.
通过TCR或经佛波酯(PMA)和离子霉素激活的克隆化小鼠细胞毒性T淋巴细胞(CTL)可上调表面Fas配体,并显示出更强的杀伤非抗原特异性Fas⁺靶细胞的能力。这种上调在45至60分钟后开始,其逆转的半衰期约为90分钟。裂解功能的上调伴随着CTL表面Fas配体的上调,这可被蛋白质合成抑制剂阻断。当通过PMA和离子霉素诱导Fas裂解功能上调时,乙二醇双四乙酸(EGTA)可阻断裂解功能的激活以及通过荧光激活细胞分选(FACS)分析检测到的Fas配体的表达。然而,当通过特异性抗原诱导上调时,EGTA可阻断裂解功能的激活,但不能阻断Fas配体的上调。此外,EL-4细胞具有非常高的表面Fas配体水平,尽管它们没有细胞毒性。因此,表面Fas配体的表达对于Fas介导的裂解可能是必需的,但并不充分。