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Interactions of periodontal pathogens with megakaryocytic cells and platelets

机译:牙周病原体与巨核细胞和血小板的相互作用

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摘要

Introduction: Cardiovascular disease (CVD) is a leading cause of morbidity, accounting for around 17.3 million deaths worldwide. Recent studies have linked periodontitis to CVD with the periodonto-pathogens Porphyromonas gingivalis and Tannerella forsythia thought to contribute and exacerbate atherosclerosis through interactions with platelets. To date, while platelet activation following challenge with periodonto-pathogens has been reported, the underlying mechanisms of these interactions are yet to be elucidated. The aim of this study is to determine how periodonto-pathogens interact with platelets using both megakaryocytic cells and isolated platelets.ududMethods: To characterise expression levels of surface markers including ubiquitously expressed platelet-specific markers (CD41, CD42b) and platelet activation markers (CD62P, PAC-1), a multi-colour flow cytometry panel was developed using undifferentiated megakaryocytic cells CHRF-288-11 before validation using platelets isolated from healthy donors. Changes in levels of surface markers following bacterial challenge both with megakaryocytic cells and isolated platelets were determined using flow cytometry. Interaction with pathogens was visualised by platelet aggregometry and fluorescence microscopy using pathogen-specific antibodies.ududResults and conclusions: Both pathogens invaded megakaryocytic cells as visualised by immunofluorescence microscopy. The pathogens also bound platelets causing increased levels of aggregation and upregulated expression of activation markers including in CD62P in flow cytometric assays.
机译:简介:心血管疾病(CVD)是发病的主要原因,在世界范围内,约有1730万人死亡。最近的研究已将牙周炎与CVD与牙周病原体牙龈卟啉单胞菌和连翘坦索菌联系起来,认为它们通过与血小板的相互作用来促进和加剧动脉粥样硬化。迄今为止,尽管已经报道了用牙周病原体攻击后血小板活化,但是这些相互作用的潜在机制尚待阐明。这项研究的目的是使用巨核细胞和分离的血小板来确定牙周病原体如何与血小板相互作用。 ud ud方法:表征表面标志物的表达水平,包括普遍表达的血小板特异性标志物(CD41,CD42b)和血小板活化标记(CD62P,PAC-1),使用未分化的巨核细胞CHRF-288-11开发了一种多色流式细胞仪,然后使用从健康供体中分离的血小板进行验证。使用流式细胞仪测定巨核细胞和分离的血小板对细菌的攻击后表面标志物水平的变化。通过病原体特异性抗体的血小板凝集和荧光显微镜观察与病原体的相互作用。 ud ud结果与结论:免疫荧光显微镜观察,两种病原体均侵入巨核细胞。病原体还与血小板结合,导致流式细胞术检测中包括CD62P中的聚集标志物增加和活化标志物表达上调。

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