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Altered expression of SARS-CoV-2 entry and processing genes by Porphyromonas gingivalis-derived lipopolysaccharide, inflammatory cytokines and prostaglandin E(2) in human gingival fibroblasts

OBJECTIVE: The aim of this in vitro study was to investigate the expression of SARS-CoV-2 entry and processing genes in human gingival fibroblasts (HGnF) following treatment with Porphyromonas gingivalis-derived lipopolysaccharide (PgLPS) or inflammatory cytokines/mediators. DESIGN: We assessed the...

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Autores principales: Sena, Kotaro, Furue, Kirara, Setoguchi, Fumiaki, Noguchi, Kazuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215882/
https://www.ncbi.nlm.nih.gov/pubmed/34174588
http://dx.doi.org/10.1016/j.archoralbio.2021.105201
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author Sena, Kotaro
Furue, Kirara
Setoguchi, Fumiaki
Noguchi, Kazuyuki
author_facet Sena, Kotaro
Furue, Kirara
Setoguchi, Fumiaki
Noguchi, Kazuyuki
author_sort Sena, Kotaro
collection PubMed
description OBJECTIVE: The aim of this in vitro study was to investigate the expression of SARS-CoV-2 entry and processing genes in human gingival fibroblasts (HGnF) following treatment with Porphyromonas gingivalis-derived lipopolysaccharide (PgLPS) or inflammatory cytokines/mediators. DESIGN: We assessed the expression of SARS-CoV-2 entry and processing genes; angiotensin-converting enzyme 2 (ACE2), cellular serine proteases transmembrane serine protease 2 (TMPRSS2), Furin, and basigin (BSG) in HGnF by real-time PCR. To further asses the contribution of PgLPS and inflammatory cytokines/mediators to proliferation and SARS-CoV-2 entry and processing gene expression, HGnF were treated with PgLPS, IL1β, TNFα, and PGE(2). RESULTS: The expression for ACE2 in HGnF was significantly elevated after PgLPS or IL1β, TNFα, PGE(2) treatment. The expression of TMPRSS2 was increased by PgLPS, IL1β, or PGE(2) while BSG was elevated by PgLPS and IL1β. The expression of BSG and FURIN decreased after TNFα treatment. CONCLUSION: SARS-CoV-2 entry and processing genes are expressed in human gingival fibroblasts and their expressions are altered by PgLPS, IL1β, TNFα and PGE(2) treatment.
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spelling pubmed-82158822021-06-21 Altered expression of SARS-CoV-2 entry and processing genes by Porphyromonas gingivalis-derived lipopolysaccharide, inflammatory cytokines and prostaglandin E(2) in human gingival fibroblasts Sena, Kotaro Furue, Kirara Setoguchi, Fumiaki Noguchi, Kazuyuki Arch Oral Biol Article OBJECTIVE: The aim of this in vitro study was to investigate the expression of SARS-CoV-2 entry and processing genes in human gingival fibroblasts (HGnF) following treatment with Porphyromonas gingivalis-derived lipopolysaccharide (PgLPS) or inflammatory cytokines/mediators. DESIGN: We assessed the expression of SARS-CoV-2 entry and processing genes; angiotensin-converting enzyme 2 (ACE2), cellular serine proteases transmembrane serine protease 2 (TMPRSS2), Furin, and basigin (BSG) in HGnF by real-time PCR. To further asses the contribution of PgLPS and inflammatory cytokines/mediators to proliferation and SARS-CoV-2 entry and processing gene expression, HGnF were treated with PgLPS, IL1β, TNFα, and PGE(2). RESULTS: The expression for ACE2 in HGnF was significantly elevated after PgLPS or IL1β, TNFα, PGE(2) treatment. The expression of TMPRSS2 was increased by PgLPS, IL1β, or PGE(2) while BSG was elevated by PgLPS and IL1β. The expression of BSG and FURIN decreased after TNFα treatment. CONCLUSION: SARS-CoV-2 entry and processing genes are expressed in human gingival fibroblasts and their expressions are altered by PgLPS, IL1β, TNFα and PGE(2) treatment. Elsevier Ltd. 2021-09 2021-06-21 /pmc/articles/PMC8215882/ /pubmed/34174588 http://dx.doi.org/10.1016/j.archoralbio.2021.105201 Text en © 2021 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Sena, Kotaro
Furue, Kirara
Setoguchi, Fumiaki
Noguchi, Kazuyuki
Altered expression of SARS-CoV-2 entry and processing genes by Porphyromonas gingivalis-derived lipopolysaccharide, inflammatory cytokines and prostaglandin E(2) in human gingival fibroblasts
title Altered expression of SARS-CoV-2 entry and processing genes by Porphyromonas gingivalis-derived lipopolysaccharide, inflammatory cytokines and prostaglandin E(2) in human gingival fibroblasts
title_full Altered expression of SARS-CoV-2 entry and processing genes by Porphyromonas gingivalis-derived lipopolysaccharide, inflammatory cytokines and prostaglandin E(2) in human gingival fibroblasts
title_fullStr Altered expression of SARS-CoV-2 entry and processing genes by Porphyromonas gingivalis-derived lipopolysaccharide, inflammatory cytokines and prostaglandin E(2) in human gingival fibroblasts
title_full_unstemmed Altered expression of SARS-CoV-2 entry and processing genes by Porphyromonas gingivalis-derived lipopolysaccharide, inflammatory cytokines and prostaglandin E(2) in human gingival fibroblasts
title_short Altered expression of SARS-CoV-2 entry and processing genes by Porphyromonas gingivalis-derived lipopolysaccharide, inflammatory cytokines and prostaglandin E(2) in human gingival fibroblasts
title_sort altered expression of sars-cov-2 entry and processing genes by porphyromonas gingivalis-derived lipopolysaccharide, inflammatory cytokines and prostaglandin e(2) in human gingival fibroblasts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215882/
https://www.ncbi.nlm.nih.gov/pubmed/34174588
http://dx.doi.org/10.1016/j.archoralbio.2021.105201
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