Role of Cathepsin S in Periodontal Inflammation and Infection

Cathepsin S is a cysteine protease and regulator of autophagy with possible involvement in periodontitis. The objective of this study was to investigate whether cathepsin S is involved in the pathogenesis of periodontal diseases. Human periodontal fibroblasts were cultured under inflammatory and inf...

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Main Authors: S. Memmert, A. Damanaki, A. V. B. Nogueira, S. Eick, M. Nokhbehsaim, A. K. Papadopoulou, A. Till, B. Rath, S. Jepsen, W. Götz, C. Piperi, E. K. Basdra, J. A. Cirelli, A. Jäger, J. Deschner
Format: Article
Language:English
Published: Hindawi Limited 2017-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2017/4786170
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spelling doaj-25f310afe6034165a67654f1277949682020-11-24T21:42:03ZengHindawi LimitedMediators of Inflammation0962-93511466-18612017-01-01201710.1155/2017/47861704786170Role of Cathepsin S in Periodontal Inflammation and InfectionS. Memmert0A. Damanaki1A. V. B. Nogueira2S. Eick3M. Nokhbehsaim4A. K. Papadopoulou5A. Till6B. Rath7S. Jepsen8W. Götz9C. Piperi10E. K. Basdra11J. A. Cirelli12A. Jäger13J. Deschner14Section of Experimental Dento-Maxillo-Facial Medicine, Center of Dento-Maxillo-Facial Medicine, University of Bonn, Bonn, GermanySection of Experimental Dento-Maxillo-Facial Medicine, Center of Dento-Maxillo-Facial Medicine, University of Bonn, Bonn, GermanyDepartment of Diagnosis and Surgery, School of Dentistry at Araraquara, Sao Paulo State University (UNESP), Araraquara, SP, BrazilDepartment of Periodontology, Laboratory for Oral Microbiology, School of Dental Medicine, University of Bern, Bern, SwitzerlandSection of Experimental Dento-Maxillo-Facial Medicine, Center of Dento-Maxillo-Facial Medicine, University of Bonn, Bonn, GermanyDiscipline of Orthodontics, Faculty of Dentistry, University of Sydney, Sydney, NSW, AustraliaInstitute of Reconstructive Neurobiology, Life & Brain Center, University of Bonn, Bonn, GermanyDepartment of Orthodontics, Center of Dento-Maxillo-Facial Medicine, University of Bonn, Bonn, GermanyDepartment of Periodontology, Operative and Preventive Dentistry, University of Bonn, Bonn, GermanyDepartment of Orthodontics, Center of Dento-Maxillo-Facial Medicine, University of Bonn, Bonn, GermanyDepartment of Biological Chemistry, Medical School, National and Kapodistrian University of Athens, Athens, GreeceDepartment of Biological Chemistry, Medical School, National and Kapodistrian University of Athens, Athens, GreeceDepartment of Diagnosis and Surgery, School of Dentistry at Araraquara, Sao Paulo State University (UNESP), Araraquara, SP, BrazilDepartment of Orthodontics, Center of Dento-Maxillo-Facial Medicine, University of Bonn, Bonn, GermanySection of Experimental Dento-Maxillo-Facial Medicine, Center of Dento-Maxillo-Facial Medicine, University of Bonn, Bonn, GermanyCathepsin S is a cysteine protease and regulator of autophagy with possible involvement in periodontitis. The objective of this study was to investigate whether cathepsin S is involved in the pathogenesis of periodontal diseases. Human periodontal fibroblasts were cultured under inflammatory and infectious conditions elicited by interleukin-1β and Fusobacterium nucleatum, respectively. An array-based approach was used to analyze differential expression of autophagy-associated genes. Cathepsin S was upregulated most strongly and thus further studied in vitro at gene and protein levels. In vivo, gingival tissue biopsies from rats with ligature-induced periodontitis and from periodontitis patients were also analyzed at transcriptional and protein levels. Multiple gene expression changes due to interleukin-1β and F. nucleatum were observed in vitro. Both stimulants caused a significant cathepsin S upregulation. A significantly elevated cathepsin S expression in gingival biopsies from rats with experimental periodontitis was found in vivo, as compared to that from control. Gingival biopsies from periodontitis patients showed a significantly higher cathepsin S expression than those from healthy gingiva. Our findings provide original evidence that cathepsin S is increased in periodontal cells and tissues under inflammatory and infectious conditions, suggesting a critical role of this autophagy-associated molecule in the pathogenesis of periodontitis.http://dx.doi.org/10.1155/2017/4786170
collection DOAJ
language English
format Article
sources DOAJ
author S. Memmert
A. Damanaki
A. V. B. Nogueira
S. Eick
M. Nokhbehsaim
A. K. Papadopoulou
A. Till
B. Rath
S. Jepsen
W. Götz
C. Piperi
E. K. Basdra
J. A. Cirelli
A. Jäger
J. Deschner
spellingShingle S. Memmert
A. Damanaki
A. V. B. Nogueira
S. Eick
M. Nokhbehsaim
A. K. Papadopoulou
A. Till
B. Rath
S. Jepsen
W. Götz
C. Piperi
E. K. Basdra
J. A. Cirelli
A. Jäger
J. Deschner
Role of Cathepsin S in Periodontal Inflammation and Infection
Mediators of Inflammation
author_facet S. Memmert
A. Damanaki
A. V. B. Nogueira
S. Eick
M. Nokhbehsaim
A. K. Papadopoulou
A. Till
B. Rath
S. Jepsen
W. Götz
C. Piperi
E. K. Basdra
J. A. Cirelli
A. Jäger
J. Deschner
author_sort S. Memmert
title Role of Cathepsin S in Periodontal Inflammation and Infection
title_short Role of Cathepsin S in Periodontal Inflammation and Infection
title_full Role of Cathepsin S in Periodontal Inflammation and Infection
title_fullStr Role of Cathepsin S in Periodontal Inflammation and Infection
title_full_unstemmed Role of Cathepsin S in Periodontal Inflammation and Infection
title_sort role of cathepsin s in periodontal inflammation and infection
publisher Hindawi Limited
series Mediators of Inflammation
issn 0962-9351
1466-1861
publishDate 2017-01-01
description Cathepsin S is a cysteine protease and regulator of autophagy with possible involvement in periodontitis. The objective of this study was to investigate whether cathepsin S is involved in the pathogenesis of periodontal diseases. Human periodontal fibroblasts were cultured under inflammatory and infectious conditions elicited by interleukin-1β and Fusobacterium nucleatum, respectively. An array-based approach was used to analyze differential expression of autophagy-associated genes. Cathepsin S was upregulated most strongly and thus further studied in vitro at gene and protein levels. In vivo, gingival tissue biopsies from rats with ligature-induced periodontitis and from periodontitis patients were also analyzed at transcriptional and protein levels. Multiple gene expression changes due to interleukin-1β and F. nucleatum were observed in vitro. Both stimulants caused a significant cathepsin S upregulation. A significantly elevated cathepsin S expression in gingival biopsies from rats with experimental periodontitis was found in vivo, as compared to that from control. Gingival biopsies from periodontitis patients showed a significantly higher cathepsin S expression than those from healthy gingiva. Our findings provide original evidence that cathepsin S is increased in periodontal cells and tissues under inflammatory and infectious conditions, suggesting a critical role of this autophagy-associated molecule in the pathogenesis of periodontitis.
url http://dx.doi.org/10.1155/2017/4786170
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