Initial periodontal treatment affects nucleotide-binding domain leucine-rich repeat-containing protein 3 inflammasome priming in peripheral blood mononuclear cells

被引:10
|
作者
Higuchi, Kanako [1 ]
Ziauddin, S. M. [1 ]
Yamashita, Yasunori [1 ]
Ozaki, Yukio [1 ]
Yoshimura, Atsutoshi [1 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Dept Periodontol & Endodontol, 1-7-1 Sakamoto, Nagasaki 8528588, Japan
基金
日本学术振兴会;
关键词
Chronic periodontitis; Inflammation; Inflammasome; Interleukin-1; beta; Mononuclear leukocyte; NALP3; INFLAMMASOME; NLRP3; DISEASE; ACTIVATION;
D O I
10.1016/j.archoralbio.2019.104625
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: Accumulating evidence suggests an association between periodontitis and several systemic diseases, such as atherosclerosis. In the lesions of these diseases, nucleotide-binding domain leucine-rich repeat-containing protein 3 (NLRP3), apoptosis-associated speck-like protein containing a caspase activation and recruitment domain (ASC) and caspase-1 form inflammasome complex, which leads to the functional maturation of interleukin (IL)-1 beta via cleavage of caspase-1 in macrophages. IL-1 beta plays a critical role in the etiology of these diseases; however, inflammasome priming-specifically, IL-1 beta and NLRP3 upregulation-is necessary for effective IL-1 beta production. We investigated the effect of initial periodontal treatment on the inflammasome priming of peripheral blood mononuclear cells (PBMCs). Methods: Twenty-two patients with chronic periodontitis were enrolled in this study and given initial periodontal treatment. Peripheral blood samples were collected at baseline and re-evaluation (41.1 +/- 29.1 d after the treatment), and the relative expression of IL-1 beta, and three inflammasome components, ASC, NLRP3 and Caspase1, mRNA was determined using quantitative reverse transcription PCR. PBMCs were stimulated with silica crystals, and the IL-1 beta secretion was measured via enzyme-linked immunosorbent assay. Results: Probing pocket depth and bleeding on probing (BOP) were significantly improved after the treatment. Expression of IL-1 beta and ASC in the PBMCs decreased after the treatment. PBMCs stimulated with silica crystals secreted IL-1 beta. The treatment attenuated IL-113 secretion by PBMCs in low BOP percentages group whereas IL-1 beta secretion was increased in high BOP percentages group. Conclusion: Periodontal treatment altered the inflammasome priming status of the PBMCs, however, the effects on systemic diseases need to be further investigated.
引用
收藏
页数:7
相关论文
共 50 条
  • [41] Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 (NLRP3) Gene
    Turunen, Joni A.
    Wedenoja, Juho
    Repo, Pauliina
    Jarvinen, Reetta-Stiina
    Jantti, Johannes E.
    Mortenhumer, Sanna
    Riikonen, Antti S.
    Lehesjoki, Anna-Elina
    Majander, Anna
    Kivela, Tero T.
    AMERICAN JOURNAL OF OPHTHALMOLOGY, 2018, 188 : 41 - 50
  • [42] Qingchi San(青赤散)treats ulcerative colitis in mice by inhibiting the nuclear factor-kappa B signaling pathway and Nucleotide-binding oligomerization domain,leucine-rich repeat and pyrin domain-containing 3 inflammasome formation
    ZHOU Zhenghua
    JI Jianbin
    WANG Hongxia
    YAN Lin
    KANG Hongchang
    JournalofTraditionalChineseMedicine, 2023, 43 (01) : 68 - 77
  • [43] Activation of nucleotide-binding domain-like receptor containing protein 3 inflammasome in dendritic cells and macrophages by Streptococcus sanguinis
    Saeki, Ayumi
    Suzuki, Toshihiko
    Hasebe, Akira
    Kamezaki, Ryousuke
    Fujita, Mari
    Nakazawa, Futoshi
    Shibata, Ken-Ichiro
    CELLULAR MICROBIOLOGY, 2017, 19 (03)
  • [44] Leucine-rich Repeat and Immunoglobulin Domain-containing Protein-1 (Lrigl) Negative Regulatory Action toward ErbB Receptor Tyrosine Kinases Is Opposed by Leucine-rich Repeat and Immunoglobulin Domain-containing Protein 3 (Lrig3)
    Rafidi, Hanine
    Mercado, Francisco, III
    Astudillo, Michael
    Fry, William H. D.
    Saldana, Matthew
    Carraway, Kermit L., III
    Sweeney, Colleen
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (30) : 21593 - 21605
  • [45] Leucine-rich repeat-containing protein 59 mediates nuclear import of cancerous inhibitor of PP2A in prostate cancer cells
    Pallai, Rajash
    Bhaskar, Aishwarya
    Barnett-Bernodat, Natalie
    Gallo-Ebert, Christina
    Pusey, Michelle
    Nickels, Joseph T., Jr.
    Rice, Lyndi M.
    TUMOR BIOLOGY, 2015, 36 (08) : 6383 - 6390
  • [46] Leucine-rich repeat-containing G-protein-coupled receptor 5-positive cells in the endometrial stem cell niche
    Cervello, Irene
    Gil-Sanchis, Claudia
    Santamaria, Xavier
    Faus, Amparo
    Vallve-Juanico, Julia
    Diaz-Gimeno, Patricia
    Genolet, Oriana
    Pellicer, Antonio
    Simon, Carlos
    FERTILITY AND STERILITY, 2017, 107 (02) : 510 - +
  • [47] THE A-THALIANA DISEASE RESISTANCE GENE RPS2 ENCODES A PROTEIN CONTAINING A NUCLEOTIDE-BINDING SITE AND LEUCINE-RICH REPEATS
    MINDRINOS, M
    KATAGIRI, F
    YU, GL
    AUSUBEL, FM
    CELL, 1994, 78 (06) : 1089 - 1099
  • [48] A Coiled-Coil Nucleotide-Binding Domain Leucine-Rich Repeat Receptor Gene MeRPPL1 Plays a Role in the Replication of a Geminivirus in Cassava
    Ramulifho, Elelwani
    Rey, Chrissie
    VIRUSES-BASEL, 2024, 16 (06):
  • [49] The Potato Nucleotide-binding Leucine-rich Repeat (NLR) Immune Receptor Rx1 Is a Pathogen-dependent DNA-deforming Protein
    Fenyk, Stepan
    Townsend, Philip D.
    Dixon, Christopher H.
    Spies, Gerhard B.
    Campillo, Alba de San Eustaquio
    Slootweg, Erik J.
    Westerhof, Lotte B.
    Gawehns, Fleur K. K.
    Knight, Marc R.
    Sharples, Gary J.
    Goverse, Aska
    Palsson, Lars-Olof
    Takken, Frank L. W.
    Cann, Martin J.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2015, 290 (41) : 24945 - 24960
  • [50] Leucine-rich repeat-containing G protein-coupled receptor 5 regulates epithelial cell phenotype and survival of hepatocellular carcinoma cells
    Fukuma, Mariko
    Tanese, Keiji
    Effendi, Kathryn
    Yamazaki, Ken
    Masugi, Yohei
    Suda, Mariko
    Sakamoto, Michiie
    EXPERIMENTAL CELL RESEARCH, 2013, 319 (03) : 113 - 121