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Comparative analysis of expression of microbial sensing molecules in mucosal tissues with periodontal disease

  • J. L. Ebersole
  • , S. Kirakodu
  • , M. J. Novak
  • , L. Orraca
  • , A. J. Stormberg
  • , J. Gonzalez-Martinez
  • , A. Burgos
  • , O. A. Gonzalez

Producción científica: Articlerevisión exhaustiva

9 Citas (Scopus)

Resumen

Host-derived pattern recognition receptors (PRRs) are necessary for effective innate immune engagement of pathogens that express microbial-associated molecular patterns (MAMP) ligands for these PRRs. This study used a nonhuman primate model to evaluate the expression of these sensing molecules in gingival tissues. Macaca mulatta aged 12–24 with a healthy periodontium (n = 13) or periodontitis (n = 11) provided gingival tissues for assessment of naturally-occurring periodontitis. An additional group of animals (12–23 years; n = 18) was subjected to a 5 month longitudinal study examining the initiation and progression of periodontitis, RNA was isolated and microarray analysis conducted for gene expression of the sensing PRRs. The results demonstrated increased expression of various PRRs in naturally-occurring established periodontitis. Selected PRRs also correlated with both bleeding on probing (BOP) and pocket depth (PD) in the animals. The longitudinal model demonstrated multiple TLRs, as well as selected other PRRs that were significantly increased by 2 weeks during initiation of the lesion. While gene expression levels of various PRRs correlated with BOP and PD at baseline and resolution of disease, few correlated with these clinical parameters during initiation and progression of the lesion. These findings suggest that the levels of various PRRs are affected in established periodontitis lesions, and that PRR expression increased most dramatically during the initiation of the disease process, presumably in response to the juxtaposed microbial challenge to the tissues and goal of reestablishing homeostasis.

Idioma originalEnglish
Páginas (desde-hasta)196-206
Número de páginas11
PublicaciónImmunobiology
Volumen224
N.º2
DOI
EstadoPublished - mar 2019

Nota bibliográfica

Publisher Copyright:
© 2018 Elsevier GmbH

Financiación

This project was supported by National Institute of Health grants P20GM103538 and UL1TR000117 . We express our gratitude to the Caribbean Primate Research Center (CPRC) supported by grant P40RR03640 , and the Microarray Core of University Kentucky for their invaluable technical assistance. We thank M. Kirakodu for data management support. The authors state no conflict of interest in the experimental design or data reported.

FinanciadoresNúmero del financiador
Caribbean Primate Research CenterP40RR03640
National Institutes of Health (NIH)UL1TR000117, P20GM103538
National Institutes of Health (NIH)
National Center for Research ResourcesP40RR003640
National Center for Research Resources

    ASJC Scopus subject areas

    • Immunology and Allergy
    • Immunology
    • Hematology

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