Pena Jose, Fu Zhu, Schwarzer Christian, Machen Terry E
Department of Molecular and Cell Biology, University of California, Berkeley, California 94720-3200, USA.
Infect Immun. 2009 Jul;77(7):2857-65. doi: 10.1128/IAI.01355-08. Epub 2009 May 18.
Pseudomonas aeruginosa-induced activation of NF-kappaB and secretion of proinflammatory cytokines by airway epithelial cells require that the bacteria express flagellin. We tested whether P. aeruginosa and human airway epithelial cells secrete factors that modulated this response. Experiments were performed with both the Calu-3 cell line and primary cultures of tracheal epithelial cells. P. aeruginosa strain PAK DeltafliC (flagellin knockout) did not activate NF-kappaB or interleukin-8 (IL-8) but inhibited flagellin-activated NF-kappaB by 40 to 50% and IL-8 secretion by 20 to 25%. PAK DeltafliC also inhibited NF-kappaB induced by IL-1beta and Toll-like receptor 2 agonist Pam3CSK4. Similar inhibitions were observed with strains PAK, PAO1, and PA14. The inhibitory factor was present in conditioned medium isolated from PAK DeltafliC or Calu-3 plus PAK DeltafliC, but it was not present in conditioned medium isolated from Calu-3 cells alone or from PAK DeltafliC that had been heat treated. Inhibition by PAK DeltafliC-conditioned medium was exerted from either the apical or the basolateral side of the epithelium, was enhanced in simple Ringer's solution over that in tissue culture medium, and did not result from altered pH or depletion of glucose. The inhibitory effect of conditioned medium was abolished by boiling and appeared from filtration studies to result from effects of a factor with a molecular mass of <3 kDa. These and further studies with isogenic mutants led to the conclusion that the NF-kappaB and IL-8 response of airway epithelial cells to P. aeruginosa results from a balance of proinflammatory effects of flagellin and antiinflammatory effects of a small (<3-kDa), heat-sensitive factor(s) that is not lipopolysaccharide, C12 homoserine lactone, alginate, CIF, or exotoxin A, S, T, U, or Y.
铜绿假单胞菌诱导气道上皮细胞激活核因子κB(NF-κB)并分泌促炎细胞因子需要细菌表达鞭毛蛋白。我们测试了铜绿假单胞菌和人气道上皮细胞是否分泌调节这种反应的因子。使用Calu-3细胞系和气管上皮细胞原代培养物进行了实验。铜绿假单胞菌PAK ΔfliC菌株(鞭毛蛋白敲除株)未激活NF-κB或白细胞介素-8(IL-8),但能将鞭毛蛋白激活的NF-κB抑制40%至50%,并将IL-8分泌抑制20%至25%。PAK ΔfliC还抑制了IL-1β和Toll样受体2激动剂Pam3CSK4诱导的NF-κB。在PAK、PAO1和PA14菌株中也观察到了类似的抑制作用。抑制因子存在于从PAK ΔfliC或Calu-3加PAK ΔfliC分离的条件培养基中,但不存在于仅从Calu-3细胞或经过热处理的PAK ΔfliC分离的条件培养基中。PAK ΔfliC条件培养基的抑制作用是从上皮细胞的顶端或基底外侧施加的,在单纯林格氏液中比在组织培养基中增强,并且不是由pH改变或葡萄糖耗尽引起的。条件培养基的抑制作用通过煮沸被消除,并且从过滤研究来看似乎是由分子量<3 kDa的因子的作用导致的。这些以及对同基因突变体的进一步研究得出结论,气道上皮细胞对铜绿假单胞菌的NF-κB和IL-8反应是由鞭毛蛋白的促炎作用与一种非脂多糖、C12高丝氨酸内酯、藻酸盐、CIF或外毒素A、S、T、U或Y的小(<3 kDa)、热敏感因子的抗炎作用之间的平衡所导致的。