Motta C, Salmeri M, Anfuso C D, Amodeo A, Scalia M, Toscano M A, Giurdanella G, Alberghina M, Lupo G
Department of Clinical and Molecular Biomedicine, University of Catania, Catania, Italy.
Infect Immun. 2014 Feb;82(2):851-63. doi: 10.1128/IAI.00843-13. Epub 2013 Dec 9.
Klebsiella pneumoniae has become an important pathogen in recent years. Although most cases of K. pneumoniae endogenous endophthalmitis occur via hematogenous spread, it is not yet clear which microbial and host factors are responsible for the ability of K. pneumoniae to cross the blood-retinal barrier (BRB). In the present study, we show that in an in vitro model of BRB based on coculturing primary bovine retinal endothelial cells (BREC) and primary bovine retinal pericytes (BRPC), K. pneumoniae infection determines changes of transendothelial electrical resistance (TEER) and permeability to sodium fluorescein. In the coculture model, bacteria are able to stimulate the enzyme activities of endothelial cytosolic and Ca(2+)-independent phospholipase A2s (cPLA2 and iPLA2). These results were confirmed by the incremental expression of cPLA2, iPLA2, cyclo-oxygenase-1 (COX1), and COX2 in BREC, as well as by cPLA2 phosphorylation. In supernatants of K. pneumoniae-stimulated cocultures, increases in prostaglandin E2 (PGE2), interleukin-6 (IL-6), IL-8, and vascular endothelial growth factor (VEGF) production were found. Incubation with K. pneumoniae in the presence of arachidonoyl trifluoromethyl ketone (AACOCF3) or bromoenol lactone (BEL) caused decreased PGE2 and VEGF release. Scanning electron microscopy and transmission electron microscopy images of BREC and BRPC showed adhesion of K. pneumoniae to the cells, but no invasion occurred. K. pneumoniae infection also produced reductions in pericyte numbers; transfection of BREC cocultured with BRPC and of human retinal endothelial cells (HREC) cocultured with human retinal pericytes (HRPC) with small interfering RNAs (siRNAs) targeted to cPLA2 and iPLA2 restored the pericyte numbers and the TEER and permeability values. Our results show the proinflammatory effect of K. pneumoniae on BREC, suggest a possible mechanism by which BREC and BRPC react to the K. pneumoniae infection, and may provide physicians and patients with new ways of fighting blinding diseases.
肺炎克雷伯菌近年来已成为一种重要的病原体。尽管大多数肺炎克雷伯菌内源性眼内炎病例是通过血行传播发生的,但目前尚不清楚哪些微生物和宿主因素导致肺炎克雷伯菌能够穿过血视网膜屏障(BRB)。在本研究中,我们表明,在基于原代牛视网膜内皮细胞(BREC)和原代牛视网膜周细胞(BRPC)共培养的BRB体外模型中,肺炎克雷伯菌感染可导致跨内皮电阻(TEER)和对荧光素钠通透性的变化。在共培养模型中,细菌能够刺激内皮细胞胞质和Ca(2+)非依赖性磷脂酶A2(cPLA2和iPLA2)的酶活性。这些结果通过BREC中cPLA2、iPLA2、环氧化酶-1(COX1)和COX2的表达增加以及cPLA2磷酸化得到证实。在肺炎克雷伯菌刺激的共培养物上清液中,发现前列腺素E2(PGE2)、白细胞介素-6(IL-6)、IL-8和血管内皮生长因子(VEGF)的产生增加。在花生四烯酰三氟甲基酮(AACOCF3)或溴烯醇内酯(BEL)存在下与肺炎克雷伯菌孵育导致PGE2和VEGF释放减少。BREC和BRPC的扫描电子显微镜和透射电子显微镜图像显示肺炎克雷伯菌与细胞粘附,但未发生侵袭。肺炎克雷伯菌感染还导致周细胞数量减少;用靶向cPLA2和iPLA2的小干扰RNA(siRNA)转染与BRPC共培养的BREC以及与人类视网膜周细胞(HRPC)共培养的人类视网膜内皮细胞(HREC)可恢复周细胞数量以及TEER和通透性值。我们的结果显示了肺炎克雷伯菌对BREC的促炎作用,提示了BREC和BRPC对肺炎克雷伯菌感染作出反应的一种可能机制,并可能为医生和患者提供对抗致盲疾病的新方法。