Yamaba S, Yamada S, Kajikawa T, Awata T, Sakashita H, Tsushima K, Fujihara C, Yanagita M, Murakami S
Department of Periodontology, Osaka University Graduate School, Suita, Osaka, Japan.
Department of Periodontology, Osaka University Graduate School, Suita, Osaka, Japan
J Dent Res. 2015 Dec;94(12):1706-14. doi: 10.1177/0022034515606859. Epub 2015 Sep 23.
Periodontal ligament-associated protein 1 (PLAP-1)/asporin is an extracellular matrix protein preferentially expressed in periodontal ligaments. PLAP-1/asporin inhibits the cytodifferentiation and mineralization of periodontal ligament cells and has important roles in the maintenance of periodontal tissue homeostasis. However, the involvement of PLAP-1/asporin in inflammatory responses during periodontitis is poorly understood. This study hypothesized that PLAP-1/asporin might affect the pathogenesis of periodontitis by regulating periodontopathic bacteria-induced inflammatory responses. Proinflammatory cytokine expression induced by Toll-like receptor 2 (TLR2) and TLR4 was significantly downregulated when PLAP-1/asporin was overexpressed in periodontal ligament cells. Similarly, recombinant PLAP-1/asporin inhibited TLR2- and TLR4-induced proinflammatory cytokine expression in macrophages. We also confirmed that NF-κB activity induced by TLR2 and TLR4 signaling was suppressed by the addition of recombinant PLAP-1/asporin. Furthermore, IκB kinase α degradation induced by TLR4 was reduced by PLAP-1/asporin. Immunoprecipitation assays demonstrated the binding abilities of PLAP-1/asporin to both TLR2 and TLR4. Taken together, PLAP-1/asporin negatively regulates TLR2- and TLR4-induced inflammatory responses through direct molecular interactions. These findings indicate that PLAP-1/asporin has a defensive role in periodontitis lesions by suppressing pathophysiologic TLR signaling and that the modulating effects of PLAP-1/asporin might be useful for periodontal treatments.
牙周膜相关蛋白1(PLAP - 1)/阿spor蛋白是一种优先在牙周膜中表达的细胞外基质蛋白。PLAP - 1/阿spor蛋白抑制牙周膜细胞的细胞分化和矿化,并在维持牙周组织稳态中发挥重要作用。然而,人们对PLAP - 1/阿spor蛋白在牙周炎炎症反应中的作用了解甚少。本研究假设PLAP - 1/阿spor蛋白可能通过调节牙周病原菌诱导的炎症反应来影响牙周炎的发病机制。当PLAP - 1/阿spor蛋白在牙周膜细胞中过表达时,由Toll样受体2(TLR2)和TLR4诱导的促炎细胞因子表达显著下调。同样,重组PLAP - 1/阿spor蛋白抑制巨噬细胞中TLR2和TLR4诱导的促炎细胞因子表达。我们还证实,添加重组PLAP - 1/阿spor蛋白可抑制TLR2和TLR4信号诱导的NF - κB活性。此外,PLAP - 1/阿spor蛋白可减少TLR4诱导的IκB激酶α降解。免疫沉淀试验证明PLAP - 1/阿spor蛋白与TLR2和TLR4均具有结合能力。综上所述,PLAP - 1/阿spor蛋白通过直接分子相互作用负向调节TLR2和TLR4诱导的炎症反应。这些发现表明,PLAP - 1/阿spor蛋白通过抑制病理生理TLR信号在牙周炎病变中发挥防御作用,并且PLAP - 1/阿spor蛋白的调节作用可能对牙周治疗有用。