Department of Orofacial Sciences, School of Dentistry, University of California San Francisco, San Francisco, California, United States of America.
Department of Biological and Material Sciences & Prosthodontics, School of Dentistry, University of Michigan, Ann Arbor, Michigan, United States of America.
PLoS Pathog. 2021 Jul 13;17(7):e1009311. doi: 10.1371/journal.ppat.1009311. eCollection 2021 Jul.
Periodontal disease is driven by dysbiosis in the oral microbiome, resulting in over-representation of species that induce the release of pro-inflammatory cytokines, chemokines, and tissue-remodeling matrix metalloproteinases (MMPs) in the periodontium. These chronic tissue-destructive inflammatory responses result in gradual loss of tooth-supporting alveolar bone. The oral spirochete Treponema denticola, is consistently found at significantly elevated levels in periodontal lesions. Host-expressed Toll-Like Receptor 2 (TLR2) senses a variety of bacterial ligands, including acylated lipopolysaccharides and lipoproteins. T. denticola dentilisin, a surface-expressed protease complex comprised of three lipoproteins has been implicated as a virulence factor in periodontal disease, primarily due to its proteolytic activity. While the role of acylated bacterial components in induction of inflammation is well-studied, little attention has been given to the potential role of the acylated nature of dentilisin. The purpose of this study was to test the hypothesis that T. denticola dentilisin activates a TLR2-dependent mechanism, leading to upregulation of tissue-destructive genes in periodontal tissue. RNA-sequencing of periodontal ligament cells challenged with T. denticola bacteria revealed significant upregulation of genes associated with extracellular matrix organization and degradation including potentially tissue-specific inducible MMPs that may play novel roles in modulating host immune responses that have yet to be characterized within the context of oral disease. The Gram-negative oral commensal, Veillonella parvula, failed to upregulate these same MMPs. Dentilisin-induced upregulation of MMPs was mediated via TLR2 and MyD88 activation, since knockdown of expression of either abrogated these effects. Challenge with purified dentilisin upregulated the same MMPs while a dentilisin-deficient T. denticola mutant had no effect. Finally, T. denticola-mediated activation of TLR2/MyD88 lead to the nuclear translocation of the transcription factor Sp1, which was shown to be a critical regulator of all T. denticola-dependent MMP expression. Taken together, these data suggest that T. denticola dentilisin stimulates tissue-destructive cellular processes in a TLR2/MyD88/Sp1-dependent fashion.
牙周病是由口腔微生物组的失调引起的,导致诱导促炎细胞因子、趋化因子和组织重塑基质金属蛋白酶(MMPs)释放的物种过度表达,这些慢性组织破坏性炎症反应导致牙齿支持的牙槽骨逐渐丧失。口腔螺旋体Treponema denticola 始终在牙周病损中以显著升高的水平存在。宿主表达的 Toll 样受体 2(TLR2)感知多种细菌配体,包括酰化脂多糖和脂蛋白。T. denticola dentilisin 是一种由三种脂蛋白组成的表面表达蛋白酶复合物,被认为是牙周病的一种毒力因子,主要是由于其蛋白水解活性。虽然酰化细菌成分在诱导炎症中的作用得到了充分研究,但很少关注 dentilisin 的酰化性质的潜在作用。本研究旨在检验以下假设:T. denticola dentilisin 激活 TLR2 依赖性机制,导致牙周组织中组织破坏性基因的上调。用 T. denticola 细菌挑战牙周韧带细胞的 RNA 测序显示,与细胞外基质组织和降解相关的基因显著上调,包括可能具有组织特异性的诱导型 MMPs,它们可能在调节宿主免疫反应中发挥新的作用,这些作用尚未在口腔疾病背景下得到描述。革兰氏阴性口腔共生菌 Veillonella parvula 未能上调这些相同的 MMPs。Dentilisin 诱导的 MMPs 上调是通过 TLR2 和 MyD88 激活介导的,因为表达的敲低消除了这些效应。用纯化的 dentilisin 进行挑战可上调相同的 MMPs,而 dentilisin 缺陷型 T. denticola 突变体则没有影响。最后,T. denticola 介导的 TLR2/MyD88 激活导致转录因子 Sp1 的核易位,Sp1 被证明是所有 T. denticola 依赖性 MMP 表达的关键调节因子。总之,这些数据表明 T. denticola dentilisin 以 TLR2/MyD88/Sp1 依赖的方式刺激组织破坏性细胞过程。