Stopford C R, Wolberg G, Prus K L, Reynolds-Vaughn R, Zimmerman T P
Proc Natl Acad Sci U S A. 1985 Jun;82(12):4060-4. doi: 10.1073/pnas.82.12.4060.
3-Deazaadenosine (c3Ado) has been reported to inhibit a number of cellular functions. These biological effects of c3Ado have generally been attributed to its ability to act as inhibitor and substrate of S-adenosylhomocysteine hydrolase. In this report, it is revealed by fluorescence microscopy that c3Ado caused disorganization of the microfilament system of mouse macrophages at concentrations (greater than or equal to 5 microM) similar to those that inhibited antibody-dependent phagocytosis and zymosan-stimulated H2O2 production by these cells. Inhibition of phagocytosis and perturbation of microfilaments by c3Ado were completely abrogated by washing the macrophages free of this agent and allowing the cells a 30-min recovery period. Furthermore, these effects of c3Ado on phagocytosis and microfilaments appeared to be independent of the increase in S-adenosylhomocysteine and S-3-deazaadenosylhomocysteine that occurred in these macrophages. First, periodate-oxidized adenosine and 3-deaza(+/-)aristeromycin, two other inhibitors of S-adenosylhomocysteine hydrolase that caused greater increases in macrophage S-adenosylhomocysteine than did c3Ado, had no effect on either phagocytosis or microfilaments. Second, pretreatment of macrophages with periodate-oxidized adenosine (to inhibit S-adenosylhomocysteine hydrolase) prevented the subsequent metabolism of c3Ado to S-3-deazaadenosylhomocysteine but did not diminish the effects of c3Ado on phagocytosis or microfilaments. These results demonstrate that c3Ado can perturb the microfilament system of cells and provide an alternative mechanism for the biological effects of c3Ado.
据报道,3 - 去氮腺苷(c3Ado)可抑制多种细胞功能。c3Ado的这些生物学效应通常归因于其作为S - 腺苷同型半胱氨酸水解酶抑制剂和底物的能力。在本报告中,通过荧光显微镜观察发现,c3Ado在与抑制这些细胞的抗体依赖性吞噬作用和酵母聚糖刺激的H2O2产生相似的浓度(大于或等于5 microM)下,会导致小鼠巨噬细胞微丝系统紊乱。通过洗涤巨噬细胞以去除该试剂并使细胞有30分钟的恢复期,c3Ado对吞噬作用的抑制和对微丝的扰动被完全消除。此外,c3Ado对吞噬作用和微丝的这些影响似乎与这些巨噬细胞中S - 腺苷同型半胱氨酸和S - 3 - 去氮腺苷同型半胱氨酸的增加无关。首先,高碘酸盐氧化腺苷和3 - 去氮(±)阿瑞霉素是另外两种S - 腺苷同型半胱氨酸水解酶抑制剂,它们导致巨噬细胞中S - 腺苷同型半胱氨酸的增加比c3Ado更大,但对吞噬作用或微丝均无影响。其次,用高碘酸盐氧化腺苷预处理巨噬细胞(以抑制S - 腺苷同型半胱氨酸水解酶)可阻止c3Ado随后代谢为S - 3 - 去氮腺苷同型半胱氨酸,但并未减弱c3Ado对吞噬作用或微丝的影响。这些结果表明,c3Ado可扰乱细胞的微丝系统,并为c3Ado的生物学效应提供了一种替代机制。