Biochemical Mapping of the Inflamed Human Dental Pulp

Dental pulp inflammation, caused by the evolution of caries, involves numerous interrelated activities at a cellular and molecular level. Cytokines, proteases, growth factors, and other biomarkers of the host response may take part in dental pulp’s immune defense. The aim of this pilot study was to...

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Autores principales: Konstantina Kritikou, Marina Imre, Mihaela Tanase, Arina Vinereanu, Alexandra Ripszky Totan, Tudor-Claudiu Spinu, Radu Ilinca, Daniela Miricescu, Iulia-Ioana Stanescu-Spinu, Maria Greabu
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:24d93aa20fff436290be673a3c5a23b32021-11-11T15:23:58ZBiochemical Mapping of the Inflamed Human Dental Pulp10.3390/app1121103952076-3417https://doaj.org/article/24d93aa20fff436290be673a3c5a23b32021-11-01T00:00:00Zhttps://www.mdpi.com/2076-3417/11/21/10395https://doaj.org/toc/2076-3417Dental pulp inflammation, caused by the evolution of caries, involves numerous interrelated activities at a cellular and molecular level. Cytokines, proteases, growth factors, and other biomarkers of the host response may take part in dental pulp’s immune defense. The aim of this pilot study was to determine the levels of inflammation, oxidative stress, and extracellular matrix degradation biomarkers in healthy and symptomatic irreversibly inflamed dental pulp samples from children and adolescents. Twenty-three dental pulp samples were collected from permanent teeth with irreversible inflammation, while nineteen healthy dental pulp samples were obtained from teeth extracted for orthodontic reasons. Pulp lysates were obtained and the levels of IL-2, IL-17, TNF-α, SOD3, TGF-<i>β</i>1, catalase, osteocalcin, MMP-7, and MMP-9 were determined using the enzyme-linked immunosorbent assay (ELISA) technique. We detected significantly higher levels (<i>p</i> < 0.001) of IL-2, IL-17, TNF-α, SOD3, osteocalcin, and TGF-<i>β</i>1 in pulp samples with irreversible inflammation than in controls. Catalase and MMP-7 showed higher levels in the experimental group, while MMP-9 showed slightly increased levels in the control group, but none of these differences were statistically significant (<i>p</i> = 0.064/<i>p</i> = 0.061/<i>p</i> = 0.625). Inflamed dental pulp samples showed an up-regulation of IL-2, IL-17, TNF-α, SOD3, osteocalcin, and TGF-<i>β</i>1. These biomarkers appear to have a powerful role in the inflammation process of human dental pulp.Konstantina KritikouMarina ImreMihaela TanaseArina VinereanuAlexandra Ripszky TotanTudor-Claudiu SpinuRadu IlincaDaniela MiricescuIulia-Ioana Stanescu-SpinuMaria GreabuMDPI AGarticledental pulpinflammationbiomarkersenzyme-linked immunosorbent assayoxidative stressextracellular matrix degradationTechnologyTEngineering (General). Civil engineering (General)TA1-2040Biology (General)QH301-705.5PhysicsQC1-999ChemistryQD1-999ENApplied Sciences, Vol 11, Iss 10395, p 10395 (2021)
institution DOAJ
collection DOAJ
language EN
topic dental pulp
inflammation
biomarkers
enzyme-linked immunosorbent assay
oxidative stress
extracellular matrix degradation
Technology
T
Engineering (General). Civil engineering (General)
TA1-2040
Biology (General)
QH301-705.5
Physics
QC1-999
Chemistry
QD1-999
spellingShingle dental pulp
inflammation
biomarkers
enzyme-linked immunosorbent assay
oxidative stress
extracellular matrix degradation
Technology
T
Engineering (General). Civil engineering (General)
TA1-2040
Biology (General)
QH301-705.5
Physics
QC1-999
Chemistry
QD1-999
Konstantina Kritikou
Marina Imre
Mihaela Tanase
Arina Vinereanu
Alexandra Ripszky Totan
Tudor-Claudiu Spinu
Radu Ilinca
Daniela Miricescu
Iulia-Ioana Stanescu-Spinu
Maria Greabu
Biochemical Mapping of the Inflamed Human Dental Pulp
description Dental pulp inflammation, caused by the evolution of caries, involves numerous interrelated activities at a cellular and molecular level. Cytokines, proteases, growth factors, and other biomarkers of the host response may take part in dental pulp’s immune defense. The aim of this pilot study was to determine the levels of inflammation, oxidative stress, and extracellular matrix degradation biomarkers in healthy and symptomatic irreversibly inflamed dental pulp samples from children and adolescents. Twenty-three dental pulp samples were collected from permanent teeth with irreversible inflammation, while nineteen healthy dental pulp samples were obtained from teeth extracted for orthodontic reasons. Pulp lysates were obtained and the levels of IL-2, IL-17, TNF-α, SOD3, TGF-<i>β</i>1, catalase, osteocalcin, MMP-7, and MMP-9 were determined using the enzyme-linked immunosorbent assay (ELISA) technique. We detected significantly higher levels (<i>p</i> < 0.001) of IL-2, IL-17, TNF-α, SOD3, osteocalcin, and TGF-<i>β</i>1 in pulp samples with irreversible inflammation than in controls. Catalase and MMP-7 showed higher levels in the experimental group, while MMP-9 showed slightly increased levels in the control group, but none of these differences were statistically significant (<i>p</i> = 0.064/<i>p</i> = 0.061/<i>p</i> = 0.625). Inflamed dental pulp samples showed an up-regulation of IL-2, IL-17, TNF-α, SOD3, osteocalcin, and TGF-<i>β</i>1. These biomarkers appear to have a powerful role in the inflammation process of human dental pulp.
format article
author Konstantina Kritikou
Marina Imre
Mihaela Tanase
Arina Vinereanu
Alexandra Ripszky Totan
Tudor-Claudiu Spinu
Radu Ilinca
Daniela Miricescu
Iulia-Ioana Stanescu-Spinu
Maria Greabu
author_facet Konstantina Kritikou
Marina Imre
Mihaela Tanase
Arina Vinereanu
Alexandra Ripszky Totan
Tudor-Claudiu Spinu
Radu Ilinca
Daniela Miricescu
Iulia-Ioana Stanescu-Spinu
Maria Greabu
author_sort Konstantina Kritikou
title Biochemical Mapping of the Inflamed Human Dental Pulp
title_short Biochemical Mapping of the Inflamed Human Dental Pulp
title_full Biochemical Mapping of the Inflamed Human Dental Pulp
title_fullStr Biochemical Mapping of the Inflamed Human Dental Pulp
title_full_unstemmed Biochemical Mapping of the Inflamed Human Dental Pulp
title_sort biochemical mapping of the inflamed human dental pulp
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/24d93aa20fff436290be673a3c5a23b3
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