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Activin A Promotes Osteoblastic Differentiation of Human Preosteoblasts through the ALK1-Smad1/5/9 Pathway
Activin A, a member of transforming growth factor-β superfamily, is involved in the regulation of cellular differentiation and promotes tissue healing. Previously, we reported that expression of activin A was upregulated around the damaged periodontal tissue including periodontal ligament (PDL) tiss...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704413/ https://www.ncbi.nlm.nih.gov/pubmed/34948289 http://dx.doi.org/10.3390/ijms222413491 |
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author | Sugii, Hideki Albougha, Mhd Safwan Adachi, Orie Tomita, Hiroka Tomokiyo, Atsushi Hamano, Sayuri Hasegawa, Daigaku Yoshida, Shinichiro Itoyama, Tomohiro Maeda, Hidefumi |
author_facet | Sugii, Hideki Albougha, Mhd Safwan Adachi, Orie Tomita, Hiroka Tomokiyo, Atsushi Hamano, Sayuri Hasegawa, Daigaku Yoshida, Shinichiro Itoyama, Tomohiro Maeda, Hidefumi |
author_sort | Sugii, Hideki |
collection | PubMed |
description | Activin A, a member of transforming growth factor-β superfamily, is involved in the regulation of cellular differentiation and promotes tissue healing. Previously, we reported that expression of activin A was upregulated around the damaged periodontal tissue including periodontal ligament (PDL) tissue and alveolar bone, and activin A promoted PDL-related gene expression of human PDL cells (HPDLCs). However, little is known about the biological function of activin A in alveolar bone. Thus, this study analyzed activin A-induced biological functions in preosteoblasts (Saos2 cells). Activin A promoted osteoblastic differentiation of Saos2 cells. Activin receptor-like kinase (ALK) 1, an activin type I receptor, was more strongly expressed in Saos2 cells than in HPDLCs, and knockdown of ALK1 inhibited activin A-induced osteoblastic differentiation of Saos2 cells. Expression of ALK1 was upregulated in alveolar bone around damaged periodontal tissue when compared with a nondamaged site. Furthermore, activin A promoted phosphorylation of Smad1/5/9 during osteoblastic differentiation of Saos2 cells and knockdown of ALK1 inhibited activin A-induced phosphorylation of Smad1/5/9 in Saos2 cells. Collectively, these findings suggest that activin A promotes osteoblastic differentiation of preosteoblasts through the ALK1-Smad1/5/9 pathway and could be used as a therapeutic product for the healing of alveolar bone as well as PDL tissue. |
format | Online Article Text |
id | pubmed-8704413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87044132021-12-25 Activin A Promotes Osteoblastic Differentiation of Human Preosteoblasts through the ALK1-Smad1/5/9 Pathway Sugii, Hideki Albougha, Mhd Safwan Adachi, Orie Tomita, Hiroka Tomokiyo, Atsushi Hamano, Sayuri Hasegawa, Daigaku Yoshida, Shinichiro Itoyama, Tomohiro Maeda, Hidefumi Int J Mol Sci Article Activin A, a member of transforming growth factor-β superfamily, is involved in the regulation of cellular differentiation and promotes tissue healing. Previously, we reported that expression of activin A was upregulated around the damaged periodontal tissue including periodontal ligament (PDL) tissue and alveolar bone, and activin A promoted PDL-related gene expression of human PDL cells (HPDLCs). However, little is known about the biological function of activin A in alveolar bone. Thus, this study analyzed activin A-induced biological functions in preosteoblasts (Saos2 cells). Activin A promoted osteoblastic differentiation of Saos2 cells. Activin receptor-like kinase (ALK) 1, an activin type I receptor, was more strongly expressed in Saos2 cells than in HPDLCs, and knockdown of ALK1 inhibited activin A-induced osteoblastic differentiation of Saos2 cells. Expression of ALK1 was upregulated in alveolar bone around damaged periodontal tissue when compared with a nondamaged site. Furthermore, activin A promoted phosphorylation of Smad1/5/9 during osteoblastic differentiation of Saos2 cells and knockdown of ALK1 inhibited activin A-induced phosphorylation of Smad1/5/9 in Saos2 cells. Collectively, these findings suggest that activin A promotes osteoblastic differentiation of preosteoblasts through the ALK1-Smad1/5/9 pathway and could be used as a therapeutic product for the healing of alveolar bone as well as PDL tissue. MDPI 2021-12-16 /pmc/articles/PMC8704413/ /pubmed/34948289 http://dx.doi.org/10.3390/ijms222413491 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sugii, Hideki Albougha, Mhd Safwan Adachi, Orie Tomita, Hiroka Tomokiyo, Atsushi Hamano, Sayuri Hasegawa, Daigaku Yoshida, Shinichiro Itoyama, Tomohiro Maeda, Hidefumi Activin A Promotes Osteoblastic Differentiation of Human Preosteoblasts through the ALK1-Smad1/5/9 Pathway |
title | Activin A Promotes Osteoblastic Differentiation of Human Preosteoblasts through the ALK1-Smad1/5/9 Pathway |
title_full | Activin A Promotes Osteoblastic Differentiation of Human Preosteoblasts through the ALK1-Smad1/5/9 Pathway |
title_fullStr | Activin A Promotes Osteoblastic Differentiation of Human Preosteoblasts through the ALK1-Smad1/5/9 Pathway |
title_full_unstemmed | Activin A Promotes Osteoblastic Differentiation of Human Preosteoblasts through the ALK1-Smad1/5/9 Pathway |
title_short | Activin A Promotes Osteoblastic Differentiation of Human Preosteoblasts through the ALK1-Smad1/5/9 Pathway |
title_sort | activin a promotes osteoblastic differentiation of human preosteoblasts through the alk1-smad1/5/9 pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704413/ https://www.ncbi.nlm.nih.gov/pubmed/34948289 http://dx.doi.org/10.3390/ijms222413491 |
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