Cargando…
Proteolysis of Gingival Keratinocyte Cell Surface Proteins by Gingipains Secreted From Porphyromonas gingivalis – Proteomic Insights Into Mechanisms Behind Tissue Damage in the Diseased Gingiva
Porphyromonas gingivalis, the main etiologic agent of periodontitis, secretes cysteine proteases named gingipains. HRgpA and RgpB gingipains have Arg-specificity, while Kgp gingipain is Lys-specific. Together they can cleave an array of proteins and importantly contribute to the development of perio...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198712/ https://www.ncbi.nlm.nih.gov/pubmed/32411104 http://dx.doi.org/10.3389/fmicb.2020.00722 |
_version_ | 1783529039916433408 |
---|---|
author | Hočevar, Katarina Vizovišek, Matej Wong, Alicia Kozieł, Joanna Fonović, Marko Potempa, Barbara Lamont, Richard J. Potempa, Jan Turk, Boris |
author_facet | Hočevar, Katarina Vizovišek, Matej Wong, Alicia Kozieł, Joanna Fonović, Marko Potempa, Barbara Lamont, Richard J. Potempa, Jan Turk, Boris |
author_sort | Hočevar, Katarina |
collection | PubMed |
description | Porphyromonas gingivalis, the main etiologic agent of periodontitis, secretes cysteine proteases named gingipains. HRgpA and RgpB gingipains have Arg-specificity, while Kgp gingipain is Lys-specific. Together they can cleave an array of proteins and importantly contribute to the development of periodontitis. In this study we focused on gingipain-exerted proteolysis at the cell surface of human gingival epithelial cells [telomerase immortalized gingival keratinocytes (TIGK)] in order to better understand the molecular mechanisms behind tissue destruction in periodontitis. Using mass spectrometry, we investigated the whole sheddome/degradome of TIGK cell surface proteins by P. gingivalis strains differing in gingipain expression and by purified gingipains, and performed the first global proteomic analysis of gignpain proteolysis at the membrane. Incubation of TIGK cells with P. gingivalis resulted in massive degradation of proteins already at low multiplicity of infection, whereas incubating cells with purified gingipains resulted in more discrete patterns, indicative of a combination of complete degradation and shedding of membrane proteins. Most of the identified gingipain substrates were molecules involved in adhesion, suggesting that gingipains may cause tissue damage through cleavage of cell contacts, resulting in cell detachment and rounding, and consequently leading to anoikis. However, HRgpA and RgpB gingipains differ in their mechanism of action. While RgpB rapidly degraded the proteins, HRgpA exhibited a much slower proteolysis indicative of ectodomain shedding, as demonstrated for the transferrin receptor protein 1 (TFRC). These results reveal a molecular underpinning to P. gingivalis-induced tissue destruction and enhance our knowledge of the role of P. gingivalis proteases in the pathobiology of periodontitis. Proteomics data are available via ProteomeXchange with identifier PXD015679. |
format | Online Article Text |
id | pubmed-7198712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71987122020-05-14 Proteolysis of Gingival Keratinocyte Cell Surface Proteins by Gingipains Secreted From Porphyromonas gingivalis – Proteomic Insights Into Mechanisms Behind Tissue Damage in the Diseased Gingiva Hočevar, Katarina Vizovišek, Matej Wong, Alicia Kozieł, Joanna Fonović, Marko Potempa, Barbara Lamont, Richard J. Potempa, Jan Turk, Boris Front Microbiol Microbiology Porphyromonas gingivalis, the main etiologic agent of periodontitis, secretes cysteine proteases named gingipains. HRgpA and RgpB gingipains have Arg-specificity, while Kgp gingipain is Lys-specific. Together they can cleave an array of proteins and importantly contribute to the development of periodontitis. In this study we focused on gingipain-exerted proteolysis at the cell surface of human gingival epithelial cells [telomerase immortalized gingival keratinocytes (TIGK)] in order to better understand the molecular mechanisms behind tissue destruction in periodontitis. Using mass spectrometry, we investigated the whole sheddome/degradome of TIGK cell surface proteins by P. gingivalis strains differing in gingipain expression and by purified gingipains, and performed the first global proteomic analysis of gignpain proteolysis at the membrane. Incubation of TIGK cells with P. gingivalis resulted in massive degradation of proteins already at low multiplicity of infection, whereas incubating cells with purified gingipains resulted in more discrete patterns, indicative of a combination of complete degradation and shedding of membrane proteins. Most of the identified gingipain substrates were molecules involved in adhesion, suggesting that gingipains may cause tissue damage through cleavage of cell contacts, resulting in cell detachment and rounding, and consequently leading to anoikis. However, HRgpA and RgpB gingipains differ in their mechanism of action. While RgpB rapidly degraded the proteins, HRgpA exhibited a much slower proteolysis indicative of ectodomain shedding, as demonstrated for the transferrin receptor protein 1 (TFRC). These results reveal a molecular underpinning to P. gingivalis-induced tissue destruction and enhance our knowledge of the role of P. gingivalis proteases in the pathobiology of periodontitis. Proteomics data are available via ProteomeXchange with identifier PXD015679. Frontiers Media S.A. 2020-04-28 /pmc/articles/PMC7198712/ /pubmed/32411104 http://dx.doi.org/10.3389/fmicb.2020.00722 Text en Copyright © 2020 Hočevar, Vizovišek, Wong, Kozieł, Fonović, Potempa, Lamont, Potempa and Turk. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Hočevar, Katarina Vizovišek, Matej Wong, Alicia Kozieł, Joanna Fonović, Marko Potempa, Barbara Lamont, Richard J. Potempa, Jan Turk, Boris Proteolysis of Gingival Keratinocyte Cell Surface Proteins by Gingipains Secreted From Porphyromonas gingivalis – Proteomic Insights Into Mechanisms Behind Tissue Damage in the Diseased Gingiva |
title | Proteolysis of Gingival Keratinocyte Cell Surface Proteins by Gingipains Secreted From Porphyromonas gingivalis – Proteomic Insights Into Mechanisms Behind Tissue Damage in the Diseased Gingiva |
title_full | Proteolysis of Gingival Keratinocyte Cell Surface Proteins by Gingipains Secreted From Porphyromonas gingivalis – Proteomic Insights Into Mechanisms Behind Tissue Damage in the Diseased Gingiva |
title_fullStr | Proteolysis of Gingival Keratinocyte Cell Surface Proteins by Gingipains Secreted From Porphyromonas gingivalis – Proteomic Insights Into Mechanisms Behind Tissue Damage in the Diseased Gingiva |
title_full_unstemmed | Proteolysis of Gingival Keratinocyte Cell Surface Proteins by Gingipains Secreted From Porphyromonas gingivalis – Proteomic Insights Into Mechanisms Behind Tissue Damage in the Diseased Gingiva |
title_short | Proteolysis of Gingival Keratinocyte Cell Surface Proteins by Gingipains Secreted From Porphyromonas gingivalis – Proteomic Insights Into Mechanisms Behind Tissue Damage in the Diseased Gingiva |
title_sort | proteolysis of gingival keratinocyte cell surface proteins by gingipains secreted from porphyromonas gingivalis – proteomic insights into mechanisms behind tissue damage in the diseased gingiva |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198712/ https://www.ncbi.nlm.nih.gov/pubmed/32411104 http://dx.doi.org/10.3389/fmicb.2020.00722 |
work_keys_str_mv | AT hocevarkatarina proteolysisofgingivalkeratinocytecellsurfaceproteinsbygingipainssecretedfromporphyromonasgingivalisproteomicinsightsintomechanismsbehindtissuedamageinthediseasedgingiva AT vizovisekmatej proteolysisofgingivalkeratinocytecellsurfaceproteinsbygingipainssecretedfromporphyromonasgingivalisproteomicinsightsintomechanismsbehindtissuedamageinthediseasedgingiva AT wongalicia proteolysisofgingivalkeratinocytecellsurfaceproteinsbygingipainssecretedfromporphyromonasgingivalisproteomicinsightsintomechanismsbehindtissuedamageinthediseasedgingiva AT koziełjoanna proteolysisofgingivalkeratinocytecellsurfaceproteinsbygingipainssecretedfromporphyromonasgingivalisproteomicinsightsintomechanismsbehindtissuedamageinthediseasedgingiva AT fonovicmarko proteolysisofgingivalkeratinocytecellsurfaceproteinsbygingipainssecretedfromporphyromonasgingivalisproteomicinsightsintomechanismsbehindtissuedamageinthediseasedgingiva AT potempabarbara proteolysisofgingivalkeratinocytecellsurfaceproteinsbygingipainssecretedfromporphyromonasgingivalisproteomicinsightsintomechanismsbehindtissuedamageinthediseasedgingiva AT lamontrichardj proteolysisofgingivalkeratinocytecellsurfaceproteinsbygingipainssecretedfromporphyromonasgingivalisproteomicinsightsintomechanismsbehindtissuedamageinthediseasedgingiva AT potempajan proteolysisofgingivalkeratinocytecellsurfaceproteinsbygingipainssecretedfromporphyromonasgingivalisproteomicinsightsintomechanismsbehindtissuedamageinthediseasedgingiva AT turkboris proteolysisofgingivalkeratinocytecellsurfaceproteinsbygingipainssecretedfromporphyromonasgingivalisproteomicinsightsintomechanismsbehindtissuedamageinthediseasedgingiva |