Kataoka T, Yamada A, Bando M, Honma T, Mizoue K, Nagai K
Department of Bioengineering, Tokyo Institute of Technology, Midori-ku, Yokohama, Taisho Pharmaceutical Co. Ltd, Ohmiya-shi, Saitama, Japan.
Immunology. 2000 Jun;100(2):170-7. doi: 10.1046/j.1365-2567.2000.00039.x.
FD-891 belongs to a group of 18-membered macrolides, and is a structural analogue of a specific inhibitor of vacuolar type H+-ATPase, concanamycin A (CMA). In our previous work, we have shown that CMA specifically inhibits perforin-dependent cytotoxic T lymphocyte (CTL)-mediated cytotoxicity through the degradation and inactivation of perforin, although CMA does not affect Fas ligand (FasL)-dependent cytotoxicity. Here, we show that FD-891 potently prevents not only perforin-dependent but also FasL-dependent CTL-mediated killing pathways by blocking CTL-target conjugate formation. In contrast to CMA, FD-891 was unable to inhibit vacuolar acidification and only slightly decreased the perforin activity in lytic granules. FD-891 blocked granule exocytosis in response to anti-CD3, mainly owing to the lack of CTL binding to immobilized anti-CD3. The conjugate formation was markedly inhibited only when effector cells were pretreated with FD-891. Consistent with these observations, fluorescence-activated cell sorter (FACS) analysis for cell surface receptors revealed that FD-891 significantly reduced the expression of the T-cell receptor (TCR)/CD3 complex. These data suggest that the blockage of conjugate formation and subsequent target cell killing might be at least partly owing to FD-891-induced down-regulation of the TCR/CD3 complex.
FD - 891属于一组18元大环内酯类化合物,是液泡型H⁺ - ATP酶特异性抑制剂 concanamycin A(CMA)的结构类似物。在我们之前的研究中,我们已经表明,CMA通过降解和失活穿孔素特异性抑制穿孔素依赖性细胞毒性T淋巴细胞(CTL)介导的细胞毒性,尽管CMA不影响Fas配体(FasL)依赖性细胞毒性。在此,我们表明,FD - 891不仅能有效阻止穿孔素依赖性,还能阻止FasL依赖性CTL介导的杀伤途径,通过阻断CTL - 靶细胞共轭物的形成。与CMA不同,FD - 891不能抑制液泡酸化,仅略微降低溶细胞颗粒中的穿孔素活性。FD - 891可阻断抗CD3诱导的颗粒胞吐作用,主要是由于CTL与固定化抗CD3缺乏结合。仅当效应细胞用FD - 891预处理时,共轭物的形成才会受到显著抑制。与这些观察结果一致,细胞表面受体的荧光激活细胞分选(FACS)分析表明,FD - 891显著降低了T细胞受体(TCR)/CD3复合物的表达。这些数据表明,共轭物形成的阻断以及随后靶细胞的杀伤可能至少部分归因于FD - 891诱导的TCR/CD3复合物下调。