Literature DB >> 33661916

Mast cells contribute to alveolar bone loss in Spontaneously Hypertensive Rats with periodontal disease regulating cytokines production.

Victor Gustavo Balera Brito1,2, Mariana Sousa Patrocinio2, Maria Carolina Linjardi Sousa2, Ayná Emanuelli Alves Barreto1,2, Sabrina Cruz Tfaile Frasnelli2, Vanessa Soares Lara3, Carlos Ferreira Santos4, Sandra Helena Penha Oliveira1,2.   

Abstract

Mast cells (MCs) play a pivotal role in inflammatory responses and had been studied in inflammatory bone disorders, however, their role in alveolar bone loss induced by periodontal disease (PD) is not yet fully understood. We, therefore, aimed to evaluate the effects of MCs depletion in the PD-induced alveolar bone loss in Wistar (W) and Spontaneously Hypertensive Rats (SHRs). PD was induced by ligating the lower first molars with silk thread one day after the MCs depletion, by the pre-treatment with compound 48/80 for 4 days. After 15 days of PD induction, the hemi-mandibles were surgically collected for qRT-PCR, histological analyses, immunostaining, and ELISA. Systolic blood pressure (SBP) was verified by tail plethysmography to confirm the hypertensive status, and SHR presented SBP >150 mmHg, and previous MC depletion alone or associated with PD did not alter this parameter. SHRs showed a more severe alveolar bone loss compared to W, and MC depletion significantly inhibited this response in both strains, with a more significant response in SHRs. MCs were less abundant in 48/80+PD groups, thus validating the previous MCs depletion in our model. PD increased the number of MC in the gingival tissue of SHR. Cytokine production (TNF-α, IL-6, IL-1β, and CXCL3) was constitutively higher in SHR and increased further after PD, which was also significantly reduced in the MCs-depleted animals. PD led to an increased expression of Opn, Rankl, Rank, Vtn, Itga5, Itgb5, Trap, and Ctsk in the mandible of W and SHRs, which was reversed in MCs-depleted animals. These results suggest that MCs significantly contributes to the PD-induced alveolar bone resorption, especially in the SHR, which is associated with a more severe PD progression compared to Wistar, partly explained by these cells contribution to the inflammatory status and mediator production, stimulating osteoclast-related response markers, which were reduced after MC depletion in our experimental model.

Entities:  

Year:  2021        PMID: 33661916      PMCID: PMC7932174          DOI: 10.1371/journal.pone.0247372

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


  68 in total

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Journal:  Inflamm Res       Date:  2020-07-06       Impact factor: 4.575

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6.  Serum and alveolar bone phosphatase changes reflect bone turnover during orthodontic tooth movement.

Authors:  S D Keeling; G J King; E A McCoy; M Valdez
Journal:  Am J Orthod Dentofacial Orthop       Date:  1993-04       Impact factor: 2.650

7.  Histamine promotes osteoclastogenesis through the differential expression of histamine receptors on osteoclasts and osteoblasts.

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8.  Mast Cells Contribute to Porphyromonas gingivalis-induced Bone Loss.

Authors:  J Malcolm; O Millington; E Millhouse; L Campbell; A Adrados Planell; J P Butcher; C Lawrence; K Ross; G Ramage; I B McInnes; S Culshaw
Journal:  J Dent Res       Date:  2016-03-01       Impact factor: 6.116

9.  Osteogenic markers are reduced in bone-marrow mesenchymal cells and femoral bone of young spontaneously hypertensive rats.

Authors:  Thamine Landim de Barros; Victor Gustavo Balera Brito; Caril Constante Ferreira do Amaral; Antonio Hernandes Chaves-Neto; Ana Paula Campanelli; Sandra Helena Penha Oliveira
Journal:  Life Sci       Date:  2016-01-13       Impact factor: 5.037

10.  Impairment of bone microstructure and upregulation of osteoclastogenic markers in spontaneously hypertensive rats.

Authors:  Wacharaporn Tiyasatkulkovit; Worachet Promruk; Catleya Rojviriya; Phakkhananan Pakawanit; Khuanjit Chaimongkolnukul; Kanchana Kengkoom; Jarinthorn Teerapornpuntakit; Nattapon Panupinthu; Narattaphol Charoenphandhu
Journal:  Sci Rep       Date:  2019-08-23       Impact factor: 4.379

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