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Porphyromonas gingivalis gingipains cause defective macrophage migration towards apoptotic cells and inhibit phagocytosis of primary apoptotic neutrophils:gingipains, apoptotic cell removal & inflammation

机译:牙龈卟啉单胞菌牙龈蛋白酶导致巨噬细胞向凋亡细胞的迁移缺陷并抑制原发性凋亡中性粒细胞的吞噬作用:牙龈蛋白酶,凋亡细胞清除和炎症

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摘要

Periodontal disease is a prevalent chronic inflammatory condition characterised by an aberrant host response to a pathogenic plaque biofilm resulting in local tissue damage and frustrated healing that can result in tooth loss. Cysteine proteases (gingipains) from the key periodontal pathogen Porphyromonas gingivalis have been implicated in periodontal disease pathogenesis by inhibiting inflammation resolution and are linked with systemic chronic inflammatory conditions such as rheumatoid arthritis. Efficient clearance of apoptotic cells is essential for the resolution of inflammation and tissue restoration. Here we sought to characterise the innate immune clearance of apoptotic cells and its modulation by gingipains. We examined the capacity of gingipain-treated macrophages to migrate towards and phagocytose apoptotic cells. Lysine gingipain treatment of macrophages impaired macrophage migration towards apoptotic neutrophils. Furthermore, lysine gingipain treatment reduced surface expression levels of CD14, a key macrophage receptor for apoptotic cells, which resulted in reduced macrophage interactions with apoptotic cells. Additionally, whilst apoptotic cells and their derived secretome were shown to inhibit TNF-α induced expression by P.gingivalis LPS, we demonstrated that gingipain preparations induced a rapid inflammatory response in macrophages that was resistant to the anti-inflammatory effects of apoptotic cells or their secretome. Taken together these data indicate that P.gingivalis may promote the chronic inflammation seen in periodontal disease patients by multiple mechanisms including rapid, potent gingipain-mediated inflammation coupled with receptor cleavage leading to defective clearance of apoptotic cells and reduced anti-inflammatory responses. Thus gingipains represent a potential therapeutic target for intervention in the management of chronic periodontal disease.
机译:牙周疾病是一种普遍存在的慢性炎症性疾病,其特征在于宿主对病原菌斑生物膜的异常反应导致局部组织损伤和愈合受挫,从而导致牙齿脱落。来自关键牙周病原体牙龈卟啉单胞菌的半胱氨酸蛋白酶(齿龈蛋白酶)已通过抑制炎症消退而与牙周疾病的发病机制有关,并与全身性慢性炎性疾病如类风湿性关节炎有关。有效清除凋亡细胞对于解决炎症和恢复组织至关重要。在这里,我们试图表征凋亡细胞的先天免疫清除及其对姜黄素的调节作用。我们检查了姜黄素处理的巨噬细胞向和吞噬凋亡细胞迁移的能力。赖氨酸姜黄素治疗巨噬细胞损害了巨噬细胞向凋亡中性粒细胞的迁移。此外,赖氨酸姜黄素处理降低了CD14的表面表达水平,CD14是凋亡细胞的关键巨噬细胞受体,导致巨噬细胞与凋亡细胞的相互作用降低。另外,尽管显示凋亡细胞及其衍生的分泌组抑制牙龈卟啉单胞菌LPS诱导的TNF-α表达,但我们证明了姜黄素制剂在巨噬细胞中诱导了快速的炎症反应,可抵抗凋亡细胞或它们的抗炎作用分泌组这些数据加在一起表明,牙龈卟啉单胞菌可通过多种机制促进牙周疾病患者中的慢性炎症,包括快速,有效的牙龈蛋白酶介导的炎症以及受体裂解,导致凋亡细胞清除不良和抗炎反应降低。因此,姜黄素代表了干预慢性牙周疾病的潜在治疗靶标。

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