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Induction of β-Defensin Expression by Porphyromonas gingivalis-Infected Human Gingival Graft Transplanted in nu/nu Mouse Subdermis

It is important to understand the onset of periodontal disease in terms of bacterial infection and host factors. Host-bacteria interactions can be elicited in human cultured cells and animal models, but these models provide only limited biological information about human host reactions against bacte...

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Autores principales: To, Masahiro, Kamata, Yohei, Saruta, Juri, Shimizu, Tomoko, Sato, Takenori, Kondo, Yusuke, Hayashi, Takashi, Hamada, Nobushiro, Tsukinoki, Keiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Society of Histochemistry and Cytochemistry 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596604/
https://www.ncbi.nlm.nih.gov/pubmed/23554537
http://dx.doi.org/10.1267/ahc.12033
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author To, Masahiro
Kamata, Yohei
Saruta, Juri
Shimizu, Tomoko
Sato, Takenori
Kondo, Yusuke
Hayashi, Takashi
Hamada, Nobushiro
Tsukinoki, Keiichi
author_facet To, Masahiro
Kamata, Yohei
Saruta, Juri
Shimizu, Tomoko
Sato, Takenori
Kondo, Yusuke
Hayashi, Takashi
Hamada, Nobushiro
Tsukinoki, Keiichi
author_sort To, Masahiro
collection PubMed
description It is important to understand the onset of periodontal disease in terms of bacterial infection and host factors. Host-bacteria interactions can be elicited in human cultured cells and animal models, but these models provide only limited biological information about human host reactions against bacterial attacks. Development of an in vivo model using human gingival tissue is needed. We established an in vivo model using nu/nu mice and evaluated host defense following bacterial infection in human gingiva. Human gingival samples were collected from periodontitis patients and transplanted in nu/nu mouse subdermis. After 2 weeks, human characteristics were confirmed by positive immunohistochemical reactions for human-specific markers. We used this model to investigate human β-defensin-2 (hBD-2), an antimicrobial peptide that contributes to initial defense against bacterial invasion. Using real-time polymerase chain reaction, in situ hybridization, and immunohistochemistry, we investigated whether hBD-2 expression was induced in human gingiva as a response to Porphyromonas gingivalis as a periodontal pathogen. Two hours after infection with bacteria, we detected increased expression of hBD-2 mRNA, which was localized in the epithelium of human gingiva. Using our in vivo model, we concluded that increased hBD-2 may play an important role in early defense from bacterial infection in human gingival epithelium.
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spelling pubmed-35966042013-04-01 Induction of β-Defensin Expression by Porphyromonas gingivalis-Infected Human Gingival Graft Transplanted in nu/nu Mouse Subdermis To, Masahiro Kamata, Yohei Saruta, Juri Shimizu, Tomoko Sato, Takenori Kondo, Yusuke Hayashi, Takashi Hamada, Nobushiro Tsukinoki, Keiichi Acta Histochem Cytochem Regular Article It is important to understand the onset of periodontal disease in terms of bacterial infection and host factors. Host-bacteria interactions can be elicited in human cultured cells and animal models, but these models provide only limited biological information about human host reactions against bacterial attacks. Development of an in vivo model using human gingival tissue is needed. We established an in vivo model using nu/nu mice and evaluated host defense following bacterial infection in human gingiva. Human gingival samples were collected from periodontitis patients and transplanted in nu/nu mouse subdermis. After 2 weeks, human characteristics were confirmed by positive immunohistochemical reactions for human-specific markers. We used this model to investigate human β-defensin-2 (hBD-2), an antimicrobial peptide that contributes to initial defense against bacterial invasion. Using real-time polymerase chain reaction, in situ hybridization, and immunohistochemistry, we investigated whether hBD-2 expression was induced in human gingiva as a response to Porphyromonas gingivalis as a periodontal pathogen. Two hours after infection with bacteria, we detected increased expression of hBD-2 mRNA, which was localized in the epithelium of human gingiva. Using our in vivo model, we concluded that increased hBD-2 may play an important role in early defense from bacterial infection in human gingival epithelium. Japan Society of Histochemistry and Cytochemistry 2013-02-28 2013-01-11 /pmc/articles/PMC3596604/ /pubmed/23554537 http://dx.doi.org/10.1267/ahc.12033 Text en © 2013 The Japan Society of Histochemistry and Cytochemistry This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Article
To, Masahiro
Kamata, Yohei
Saruta, Juri
Shimizu, Tomoko
Sato, Takenori
Kondo, Yusuke
Hayashi, Takashi
Hamada, Nobushiro
Tsukinoki, Keiichi
Induction of β-Defensin Expression by Porphyromonas gingivalis-Infected Human Gingival Graft Transplanted in nu/nu Mouse Subdermis
title Induction of β-Defensin Expression by Porphyromonas gingivalis-Infected Human Gingival Graft Transplanted in nu/nu Mouse Subdermis
title_full Induction of β-Defensin Expression by Porphyromonas gingivalis-Infected Human Gingival Graft Transplanted in nu/nu Mouse Subdermis
title_fullStr Induction of β-Defensin Expression by Porphyromonas gingivalis-Infected Human Gingival Graft Transplanted in nu/nu Mouse Subdermis
title_full_unstemmed Induction of β-Defensin Expression by Porphyromonas gingivalis-Infected Human Gingival Graft Transplanted in nu/nu Mouse Subdermis
title_short Induction of β-Defensin Expression by Porphyromonas gingivalis-Infected Human Gingival Graft Transplanted in nu/nu Mouse Subdermis
title_sort induction of β-defensin expression by porphyromonas gingivalis-infected human gingival graft transplanted in nu/nu mouse subdermis
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596604/
https://www.ncbi.nlm.nih.gov/pubmed/23554537
http://dx.doi.org/10.1267/ahc.12033
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