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Induction of migration of periodontal ligament cells by selective regulation of integrin subunits

The recruitment of tissue‐resident stem cells is important for wound regeneration. Periodontal ligament cells (PDL cells) are heterogeneous cell populations with stemness features that migrate into wound sites to regenerate periodontal fibres and neighbouring hard tissues. Cell migration is regulate...

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Autores principales: Kawamura, Mari, Yamamoto, Tadashi, Yamashiro, Keisuke, Kochi, Shinsuke, Yoshihara‐Hirata, Chiaki, Ideguchi, Hidetaka, Aoyagi, Hiroaki, Omori, Kazuhiro, Takashiba, Shogo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349235/
https://www.ncbi.nlm.nih.gov/pubmed/30511442
http://dx.doi.org/10.1111/jcmm.14023
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author Kawamura, Mari
Yamamoto, Tadashi
Yamashiro, Keisuke
Kochi, Shinsuke
Yoshihara‐Hirata, Chiaki
Ideguchi, Hidetaka
Aoyagi, Hiroaki
Omori, Kazuhiro
Takashiba, Shogo
author_facet Kawamura, Mari
Yamamoto, Tadashi
Yamashiro, Keisuke
Kochi, Shinsuke
Yoshihara‐Hirata, Chiaki
Ideguchi, Hidetaka
Aoyagi, Hiroaki
Omori, Kazuhiro
Takashiba, Shogo
author_sort Kawamura, Mari
collection PubMed
description The recruitment of tissue‐resident stem cells is important for wound regeneration. Periodontal ligament cells (PDL cells) are heterogeneous cell populations with stemness features that migrate into wound sites to regenerate periodontal fibres and neighbouring hard tissues. Cell migration is regulated by the local microenvironment, coordinated by growth factors and the extracellular matrix (ECM). Integrin‐mediated cell adhesion to the ECM provides essential signals for migration. We hypothesized that PDL cell migration could be enhanced by selective expression of integrins. The migration of primary cultured PDL cells was induced by platelet‐derived growth factor‐BB (PDGF‐BB). The effects of blocking specific integrins on migration and ECM adhesion were investigated based on the integrin expression profiles observed during migration. Up‐regulation of integrins α3, α5, and fibronectin was identified at distinct localizations in migrating PDL cells. Treatment with anti‐integrin α5 antibodies inhibited PDL cell migration. Treatment with anti‐integrin α3, α3‐blocking peptide, and α3 siRNA significantly enhanced cell migration, comparable to treatment with PDGF‐BB. Furthermore, integrin α3 inhibition preferentially enhanced adhesion to fibronectin via integrin α5. These findings indicate that PDL cell migration is reciprocally regulated by integrin α3‐mediated inhibition and α5‐mediated promotion. Thus, targeting integrin expression is a possible therapeutic strategy for periodontal regeneration.
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spelling pubmed-63492352019-02-01 Induction of migration of periodontal ligament cells by selective regulation of integrin subunits Kawamura, Mari Yamamoto, Tadashi Yamashiro, Keisuke Kochi, Shinsuke Yoshihara‐Hirata, Chiaki Ideguchi, Hidetaka Aoyagi, Hiroaki Omori, Kazuhiro Takashiba, Shogo J Cell Mol Med Original Articles The recruitment of tissue‐resident stem cells is important for wound regeneration. Periodontal ligament cells (PDL cells) are heterogeneous cell populations with stemness features that migrate into wound sites to regenerate periodontal fibres and neighbouring hard tissues. Cell migration is regulated by the local microenvironment, coordinated by growth factors and the extracellular matrix (ECM). Integrin‐mediated cell adhesion to the ECM provides essential signals for migration. We hypothesized that PDL cell migration could be enhanced by selective expression of integrins. The migration of primary cultured PDL cells was induced by platelet‐derived growth factor‐BB (PDGF‐BB). The effects of blocking specific integrins on migration and ECM adhesion were investigated based on the integrin expression profiles observed during migration. Up‐regulation of integrins α3, α5, and fibronectin was identified at distinct localizations in migrating PDL cells. Treatment with anti‐integrin α5 antibodies inhibited PDL cell migration. Treatment with anti‐integrin α3, α3‐blocking peptide, and α3 siRNA significantly enhanced cell migration, comparable to treatment with PDGF‐BB. Furthermore, integrin α3 inhibition preferentially enhanced adhesion to fibronectin via integrin α5. These findings indicate that PDL cell migration is reciprocally regulated by integrin α3‐mediated inhibition and α5‐mediated promotion. Thus, targeting integrin expression is a possible therapeutic strategy for periodontal regeneration. John Wiley and Sons Inc. 2018-12-03 2019-02 /pmc/articles/PMC6349235/ /pubmed/30511442 http://dx.doi.org/10.1111/jcmm.14023 Text en © 2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Kawamura, Mari
Yamamoto, Tadashi
Yamashiro, Keisuke
Kochi, Shinsuke
Yoshihara‐Hirata, Chiaki
Ideguchi, Hidetaka
Aoyagi, Hiroaki
Omori, Kazuhiro
Takashiba, Shogo
Induction of migration of periodontal ligament cells by selective regulation of integrin subunits
title Induction of migration of periodontal ligament cells by selective regulation of integrin subunits
title_full Induction of migration of periodontal ligament cells by selective regulation of integrin subunits
title_fullStr Induction of migration of periodontal ligament cells by selective regulation of integrin subunits
title_full_unstemmed Induction of migration of periodontal ligament cells by selective regulation of integrin subunits
title_short Induction of migration of periodontal ligament cells by selective regulation of integrin subunits
title_sort induction of migration of periodontal ligament cells by selective regulation of integrin subunits
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6349235/
https://www.ncbi.nlm.nih.gov/pubmed/30511442
http://dx.doi.org/10.1111/jcmm.14023
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