Mork T, Hancock R E
Department of Microbiology, University of British Columbia, Vancouver, Canada.
Infect Immun. 1993 Aug;61(8):3287-93. doi: 10.1128/iai.61.8.3287-3293.1993.
The interaction of the macrophage cell line P388D1 with Pseudomonas aeruginosa in the absence of stimulators or opsonins led to substantial association of bacteria, as judged by visual counting and FACScan assays. This association was observable within 5 min of addition of bacteria, could not be disturbed by exhaustive washing, and occurred with pilus- or flagellum-deficient mutants but not with rpoN mutants, which have been proposed to lack a secondary adhesin. In contrast, specific antibody was capable of causing similar enhancement of bacterial uptake regardless of the rpoN phenotype. Fibronectin stimulated uptake of bacteria with the pilus as an adhesin, and stimulation was observable within 5 min. Both fibronectin-enhanced and antibody-opsonized uptake were susceptible to inhibition by pertussis toxin but not by cholera toxin. The influence of fibronectin on P388D1 cells was distinguishable from that of lipopolysaccharide, which caused substantial morphological changes in cells. Although lipopolysaccharide stimulated bacterial uptake, it actually suppressed fibronectin-mediated enhancement of uptake at high concentrations.
在没有刺激物或调理素的情况下,巨噬细胞系P388D1与铜绿假单胞菌的相互作用导致细菌大量聚集,这通过视觉计数和流式细胞仪分析得以判断。在加入细菌后5分钟内即可观察到这种聚集,彻底洗涤也无法使其受到干扰,并且在缺乏菌毛或鞭毛的突变体中也会发生,但在已被提出缺乏二级粘附素的rpoN突变体中则不会发生。相比之下,无论rpoN表型如何,特异性抗体都能够引起类似的细菌摄取增强。纤连蛋白以菌毛作为粘附素刺激细菌摄取,并且在5分钟内即可观察到刺激作用。纤连蛋白增强的摄取和抗体调理的摄取均易受百日咳毒素抑制,但不受霍乱毒素抑制。纤连蛋白对P388D1细胞的影响与脂多糖不同,脂多糖会导致细胞发生显著的形态变化。尽管脂多糖刺激细菌摄取,但在高浓度下它实际上会抑制纤连蛋白介导的摄取增强。