INSERM, UMR-S 996, Cytokines, Chemokines and Immunopathology, Châtenay-Malabry, France.
Infect Immun. 2012 May;80(5):1891-9. doi: 10.1128/IAI.00050-12. Epub 2012 Feb 27.
We recently documented the neutrophil response to enterovirulent diffusely adherent Escherichia coli expressing Afa/Dr fimbriae (Afa/Dr DAEC), using the human myeloid cell line PLB-985 differentiated into fully mature neutrophils. Upon activation, particularly during infections, neutrophils release neutrophil extracellular traps (NETs), composed of a nuclear DNA backbone associated with antimicrobial peptides, histones, and proteases, which entrap and kill pathogens. Here, using fluorescence microscopy and field emission scanning electron microscopy, we observed NET production by PLB-985 cells infected with the Afa/Dr wild-type (WT) E. coli strain C1845. We found that these NETs were able to capture, immobilize, and kill WT C1845 bacteria. We also developed a coculture model of human enterocyte-like Caco-2/TC7 cells and PLB-985 cells previously treated with WT C1845 and found, for the first time, that the F-actin cytoskeleton of enterocyte-like cells is damaged in the presence of bacterium-induced NETs and that this deleterious effect is prevented by inhibition of protease release. These findings provide new insights into the neutrophil response to bacterial infection via the production of bactericidal NETs and suggest that NETs may damage the intestinal epithelium, particularly in situations such as inflammatory bowel diseases.
我们最近使用分化为完全成熟中性粒细胞的人髓样细胞系 PLB-985 记录了表达 Afa/Dr 菌毛的肠侵袭性弥漫性粘附性大肠杆菌(Afa/Dr DAEC)对中性粒细胞的反应。在激活过程中,特别是在感染期间,中性粒细胞会释放中性粒细胞细胞外陷阱(NETs),由与抗菌肽、组蛋白和蛋白酶相关的核 DNA 骨架组成,这些 NETs可以捕获和杀死病原体。在这里,我们使用荧光显微镜和场发射扫描电子显微镜观察了 Afa/Dr 野生型(WT)大肠杆菌菌株 C1845 感染 PLB-985 细胞产生的 NET。我们发现这些 NET 能够捕获、固定和杀死 WT C1845 细菌。我们还开发了一种人肠上皮样 Caco-2/TC7 细胞和 PLB-985 细胞的共培养模型,这些细胞先前用 WT C1845 处理过,我们首次发现,在细菌诱导的 NET 存在下,肠上皮样细胞的 F-肌动蛋白细胞骨架受损,而蛋白酶释放的抑制可防止这种有害影响。这些发现为中性粒细胞通过产生杀菌 NET 对细菌感染的反应提供了新的见解,并表明 NET 可能会损害肠道上皮,特别是在炎症性肠病等情况下。