PMID- 28379411 OWN - NLM STAT- MEDLINE DCOM- 20180223 LR - 20190816 IS - 2049-632X (Electronic) IS - 2049-632X (Linking) VI - 75 IP - 5 DP - 2017 Jul 31 TI - Comparison of the inflammatory response of brain microvascular and peripheral endothelial cells following infection with Neisseria meningitidis. LID - 10.1093/femspd/ftx038 [doi] AB - The interaction of Neisseria meningitidis with both peripheral and brain endothelial cells is a critical event in the development of invasive meningococcal disease. In this study, we used in vitro models based on human brain microvascular endothelial cells (HBMEC), and peripheral endothelial EA.hy926 cells, to investigate their roles in the inflammatory response towards meningococcal infection. Both cell lines were infected with two pathogenic N. meningitidis isolates and secretion of the cytokine interleukin-6 (IL-6), the CXC chemokine IL-8 and the monocyte chemoattractant protein-1 (MCP-1) were estimated by ELISA. Neisseria meningitidis was able to stimulate the production of IL-6 and IL-8 by HBMEC and EA.hy926 cells in a time- and concentration-dependent manner. Interestingly, HBMEC released significant higher amounts of IL-6 and IL-8. Moreover, we observed that heat-killed bacteria stimulated high levels of IL-8. In addition, capsule expression had an inhibitory effect on IL-8 release. We extended our study and included serogroup C strains belonging to sequence type 11 clonal complex (cc) from a recent outbreak in France, as well as isolates belonging to the hypervirulent clonal complexes cc8, cc18, cc32 and cc269 and analyzed their ability to induce the secretion of IL-8 from both cell lines. Although individual variations were observed among different isolates, no clear correlations were observed between strain origin, clinical presentation and IL-8 levels. CI - (c) FEMS 2017. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. FAU - Dick, Julia AU - Dick J AD - Institute of Hygiene and Microbiology, Julius-Maximilians University, 97080 Wurzburg, Germany. FAU - Hebling, Sabrina AU - Hebling S AD - Institute of Hygiene and Microbiology, Julius-Maximilians University, 97080 Wurzburg, Germany. FAU - Becam, Jerome AU - Becam J AD - Institute of Hygiene and Microbiology, Julius-Maximilians University, 97080 Wurzburg, Germany. FAU - Taha, Muhamed-Kheir AU - Taha MK AD - Institut Pasteur, Unit of Invasive Bacterial Infections, Paris 75015, France. FAU - Schubert-Unkmeir, Alexandra AU - Schubert-Unkmeir A AD - Institute of Hygiene and Microbiology, Julius-Maximilians University, 97080 Wurzburg, Germany. LA - eng PT - Comparative Study PT - Journal Article PL - United States TA - Pathog Dis JT - Pathogens and disease JID - 101595366 RN - 0 (CCL2 protein, human) RN - 0 (CXCL8 protein, human) RN - 0 (Chemokine CCL2) RN - 0 (IL6 protein, human) RN - 0 (Interleukin-6) RN - 0 (Interleukin-8) SB - IM MH - Cells, Cultured MH - Chemokine CCL2/analysis/*metabolism MH - Disease Outbreaks MH - Endothelial Cells/*immunology MH - Enzyme-Linked Immunosorbent Assay MH - France/epidemiology MH - *Host-Pathogen Interactions MH - Humans MH - Interleukin-6/analysis/*metabolism MH - Interleukin-8/analysis/*metabolism MH - Meningitis, Meningococcal/epidemiology/microbiology MH - Neisseria meningitidis/*immunology/isolation & purification OTO - NOTNLM OT - IL-6 OT - IL-8 OT - MCP-1 OT - Neisseria meningitidis OT - brain and peripheral endothelial cells OT - hypervirulent clonal complexes EDAT- 2017/04/06 06:00 MHDA- 2018/02/24 06:00 CRDT- 2017/04/06 06:00 PHST- 2016/12/09 00:00 [received] PHST- 2017/03/29 00:00 [accepted] PHST- 2017/04/06 06:00 [pubmed] PHST- 2018/02/24 06:00 [medline] PHST- 2017/04/06 06:00 [entrez] AID - 3098218 [pii] AID - 10.1093/femspd/ftx038 [doi] PST - ppublish SO - Pathog Dis. 2017 Jul 31;75(5). doi: 10.1093/femspd/ftx038.