Korostoff J, Wang J F, Kieba I, Miller M, Shenker B J, Lally E T
Leon Levy Research Center for Oral Biology, University of Pennsylvania, Philadelphia, Pennsylvania, 19104-6002, USA.
Infect Immun. 1998 Sep;66(9):4474-83. doi: 10.1128/IAI.66.9.4474-4483.1998.
Actinobacillus actinomycetemcomitans leukotoxin (Ltx) is a member of the repeats-in-toxin (RTX) family of pore-forming toxins and kills human immune cells. Currently, it remains unclear whether toxin-mediated killing of target cells involves the induction of necrosis or apoptosis. Therefore, the goal of this investigation was to determine whether Ltx is capable of causing apoptotic cell death in toxin-sensitive promyelocytic HL-60 cells. Multiparameter flow cytometric analysis of toxin-treated cells stained with Hoechst 33258 (or 33342) and 7-aminoactinomycin D allowed us to identify four populations: viable cells, early apoptotic cells, late apoptotic and/or secondarily necrotic cells, and a final population that was composed of cellular debris. Compared with control cells, HL-60 cells treated with Ltx exhibited a gradual decrease in forward light scatter with a coincident increase in side light scatter, indicative of a decrease in cell size and organelle condensation, respectively. Additional experiments demonstrated that Ltx-treated cells showed evidence of internucleosomal DNA fragmentation and phosphatidylserine translocation. The results of our studies clearly demonstrate that Ltx can kill HL-60 cells by inducing apoptosis. We hypothesize that elimination of acute inflammatory cells via this mechanism plays a critical role in the pathogenesis of diseases caused by A. actinomycetemeomitans.
伴放线放线杆菌白细胞毒素(Ltx)是形成孔道毒素的重复毒素(RTX)家族成员,可杀死人类免疫细胞。目前,毒素介导的靶细胞杀伤是否涉及坏死或凋亡的诱导尚不清楚。因此,本研究的目的是确定Ltx是否能够在毒素敏感的早幼粒细胞HL-60细胞中引起凋亡性细胞死亡。用Hoechst 33258(或33342)和7-氨基放线菌素D对毒素处理的细胞进行多参数流式细胞术分析,使我们能够识别四个群体:活细胞、早期凋亡细胞、晚期凋亡和/或继发性坏死细胞,以及由细胞碎片组成的最终群体。与对照细胞相比,用Ltx处理的HL-60细胞前向光散射逐渐降低,同时侧向光散射增加,分别表明细胞大小减小和细胞器浓缩。额外的实验表明,Ltx处理的细胞显示出核小体间DNA片段化和磷脂酰丝氨酸易位的证据。我们的研究结果清楚地表明,Ltx可通过诱导凋亡杀死HL-60细胞。我们推测,通过这种机制消除急性炎症细胞在伴放线放线杆菌引起的疾病发病机制中起关键作用。