Hidore M R, Nabavi N, Sonleitner F, Murphy J W
Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City 73190.
Infect Immun. 1991 May;59(5):1747-54. doi: 10.1128/iai.59.5.1747-1754.1991.
Murine natural killer (NK) cells have been shown to bind to and inhibit the growth of Cryptococcus neoformans in vitro and to contribute to clearance of the organism in vivo. However, it is unclear whether NK cells actually kill cryptococci or simply inhibit proliferation of the fungal target. Therefore, the studies presented here were designed to determine whether NK cells are fungicidal to C. neoformans targets. C. neoformans viability was determined on the basis of the metabolic function of two different enzyme systems, as measured by the two vital stains MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] and fluorescein diacetate. Cryptococcal viability, as determined by vital stains, was compared with cryptococcal proliferation, as measured by microcolony formation in agarose at the individual cell level and by CFU counts or extinction dilution analysis in the total cell suspension. Initial comparisons of the vital stains and proliferation assays indicated that these methods effectively distinguished between live and heat-killed cryptococci at the individual cell level and in the total cell suspensions. After cryptococci were incubated with murine NK cells for 18 h, vital stains demonstrated that at the single conjugate level and in the total cell suspension, NK cells kill bound C. neoformans target cells. In addition, the numbers of dead cryptococci in the NK cell-C. neoformans suspensions as determined by the vital stains were comparable to the numbers of cryptococci that were unable to proliferate. Kinetics of NK cell-mediated C. neoformans binding and killing at the single conjugate level and in the total cell suspension were assessed by MTT staining at 2-h intervals after mixing effector and target cells, and the data support the concept that NK cell-C. neoformans binding precedes cryptococcal death. Furthermore, unbound, dead fungal cells were observed in the NK cell-C. neoformans suspensions after 18 h, suggesting that NK cell-C. neoformans interactions may involve both effector cell recycling and killing of unbound cryptococci by soluble cytotoxic factors. In conclusion, the results of these studies firmly establish that NK cells kill C. neoformans.
小鼠自然杀伤(NK)细胞已被证明在体外可与新型隐球菌结合并抑制其生长,且在体内有助于清除该病原体。然而,尚不清楚NK细胞是真正杀死隐球菌,还是仅仅抑制真菌靶标的增殖。因此,本文开展的研究旨在确定NK细胞对新型隐球菌靶标是否具有杀真菌作用。基于两种不同酶系统的代谢功能来确定新型隐球菌的活力,这通过两种活细胞染色剂MTT [3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐]和荧光素二乙酸酯来测定。通过活细胞染色剂确定的隐球菌活力,与通过在个体细胞水平上在琼脂糖中形成微菌落以及在总细胞悬液中通过菌落形成单位(CFU)计数或倍比稀释分析测定的隐球菌增殖情况进行比较。活细胞染色剂和增殖试验的初步比较表明,这些方法能够在个体细胞水平和总细胞悬液中有效区分活的和热杀死的隐球菌。将隐球菌与小鼠NK细胞孵育18小时后,活细胞染色剂显示,在单个共轭体水平和总细胞悬液中,NK细胞杀死结合的新型隐球菌靶细胞。此外,通过活细胞染色剂确定的NK细胞-新型隐球菌悬液中死亡隐球菌的数量与无法增殖的隐球菌数量相当。在效应细胞和靶细胞混合后,每隔2小时通过MTT染色评估单个共轭体水平和总细胞悬液中NK细胞介导的新型隐球菌结合和杀伤的动力学,数据支持NK细胞-新型隐球菌结合先于隐球菌死亡这一概念。此外,在18小时后,在NK细胞-新型隐球菌悬液中观察到未结合的死亡真菌细胞,这表明NK细胞-新型隐球菌相互作用可能涉及效应细胞的再循环以及通过可溶性细胞毒性因子杀死未结合的隐球菌。总之,这些研究结果确凿地证实NK细胞可杀死新型隐球菌。