Literature DB >> 26464397

Can Pulp Fibroblasts Kill Cariogenic Bacteria? Role of Complement Activation.

C Jeanneau1, P Rufas1, C Rombouts1, T Giraud2, J Dejou2, I About3.   

Abstract

Complement system activation has been shown to be involved in inflammation and regeneration processes that can be observed within the dental pulp after moderate carious decay. Studies simulating carious injuries in vitro have shown that when human pulp fibroblasts are stimulated by lipoteichoic acid (LTA), they synthetize all complement components. Complement activation leads to the formation of the membrane attack complex (MAC), which is known for its bacterial lytic effect. This work was designed to find out whether human pulp fibroblasts can kill Streptococcus mutans and Streptococcus sanguinis via complement activation. First, histological staining of carious tooth sections showed that the presence of S. mutans correlated with an intense MAC staining. Next, to simulate bacterial infection in vitro, human pulp fibroblasts were incubated in serum-free medium with LTA. Quantification by an enzymatic assay showed a significant increase of MAC formation on bacteria grown in this LTA-conditioned medium. To determine whether the MAC produced by pulp fibroblasts was functional, bacteria sensitivity to LTA-conditioned medium was evaluated using agar well diffusion assay and succinyl dehydrogenase (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide [MTT]) assay. Both assays showed that S. mutans and S. sanguinis were sensitive to LTA-conditioned medium. Finally, to evaluate whether MAC formation on cariogenic bacteria, by pulp fibroblasts, can be directly induced by the presence of these bacteria, a specific coculture model of human pulp fibroblasts and bacteria was developed. Immunofluorescence revealed an intense MAC labeling on bacteria after direct contact with pulp fibroblasts. The observed MAC formation and its lethal effects were significantly reduced when CD59, an inhibitor of MAC formation, was added. Our findings demonstrate that the MAC produced by LTA-stimulated pulp fibroblasts is functional and can kill S. mutans and S. sanguinis. Taken together, these data clearly highlight the function of pulp fibroblasts in destroying cariogenic bacteria. © International & American Associations for Dental Research 2015.

Entities:  

Keywords:  Streptococcus mutans; carious decay; dental pulp; inflammation; membrane attack complex; microbial viability

Mesh:

Substances:

Year:  2015        PMID: 26464397     DOI: 10.1177/0022034515611074

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  6 in total

1.  C5L2 Regulates DMP1 Expression during Odontoblastic Differentiation.

Authors:  F Chmilewsky; R Liang; M Kanazawa; I About; L F Cooper; A George
Journal:  J Dent Res       Date:  2019-01-31       Impact factor: 6.116

2.  Novel Two-Component System of Streptococcus sanguinis Affecting Functions Associated with Viability in Saliva and Biofilm Formation.

Authors:  Tarsila M Camargo; Rafael N Stipp; Lívia A Alves; Erika N Harth-Chu; José F Höfling; Renata O Mattos-Graner
Journal:  Infect Immun       Date:  2018-03-22       Impact factor: 3.441

3.  Ultrashort Peptide Hydrogels Display Antimicrobial Activity and Enhance Angiogenic Growth Factor Release by Dental Pulp Stem/Stromal Cells.

Authors:  Marina E Afami; Ikhlas El Karim; Imad About; Sophie M Coulter; Garry Laverty; Fionnuala T Lundy
Journal:  Materials (Basel)       Date:  2021-04-27       Impact factor: 3.623

Review 4.  Stem Cells of Dental Origin: Current Research Trends and Key Milestones towards Clinical Application.

Authors:  Athina Bakopoulou; Imad About
Journal:  Stem Cells Int       Date:  2016-10-13       Impact factor: 5.443

Review 5.  Inflammatory Response Mechanisms of the Dentine-Pulp Complex and the Periapical Tissues.

Authors:  Kerstin M Galler; Manuel Weber; Yüksel Korkmaz; Matthias Widbiller; Markus Feuerer
Journal:  Int J Mol Sci       Date:  2021-02-02       Impact factor: 5.923

6.  Complementing the pulp proteome via sampling with a picosecond infrared laser (PIRL).

Authors:  Yaghoup Feridouni Khamaneh; Parnian Kiani; R J Dwayne Miller; Hartmut Schlüter; Reinhard E Friedrich
Journal:  Clin Oral Investig       Date:  2021-05-12       Impact factor: 3.573

  6 in total

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