Cargando…
CCN3 Facilitates Runx2 and Osterix Expression by Inhibiting miR-608 through PI3K/Akt Signaling in Osteoblasts
CCN3, otherwise known as the nephroblastoma overexpressed (NOV) protein, is a cysteine-rich protein that belongs to the CCN family and regulates several cellular functions. Osteoblasts are major bone-forming cells that undergo proliferation, mineralization, renewal, and repair during the bone format...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6651805/ https://www.ncbi.nlm.nih.gov/pubmed/31284378 http://dx.doi.org/10.3390/ijms20133300 |
_version_ | 1783438429601660928 |
---|---|
author | Chen, Po-Chun Liu, Ju-Fang Fong, Yi-Chin Huang, Yuan-Lin Chao, Chia-Chia Tang, Chih-Hsin |
author_facet | Chen, Po-Chun Liu, Ju-Fang Fong, Yi-Chin Huang, Yuan-Lin Chao, Chia-Chia Tang, Chih-Hsin |
author_sort | Chen, Po-Chun |
collection | PubMed |
description | CCN3, otherwise known as the nephroblastoma overexpressed (NOV) protein, is a cysteine-rich protein that belongs to the CCN family and regulates several cellular functions. Osteoblasts are major bone-forming cells that undergo proliferation, mineralization, renewal, and repair during the bone formation process. We have previously reported that CCN3 increases bone morphogenetic protein 4 (BMP-4) production and bone mineralization in osteoblasts, although the role of CCN3 remains unclear with regard to osteogenic transcription factors (runt-related transcription factor 2 (Runx2) and osterix). Here, we used alizarin red-S and alkaline phosphatase staining to show that CCN3 enhances osteoblast differentiation. Stimulation of osteoblasts with CCN3 increases expression of osteogenic factors such as BMPs, Runx2, and osterix. Moreover, we found that the inhibition of miR-608 expression is involved in the effects of CCN3 and that incubation of osteoblasts with CCN3 promotes focal adhesion kinase (FAK) and Akt phosphorylation. Our results indicate that CCN3 promotes the expression of Runx2 and osterix in osteoblasts by inhibiting miR-608 expression via the FAK and Akt signaling pathways. |
format | Online Article Text |
id | pubmed-6651805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66518052019-08-08 CCN3 Facilitates Runx2 and Osterix Expression by Inhibiting miR-608 through PI3K/Akt Signaling in Osteoblasts Chen, Po-Chun Liu, Ju-Fang Fong, Yi-Chin Huang, Yuan-Lin Chao, Chia-Chia Tang, Chih-Hsin Int J Mol Sci Article CCN3, otherwise known as the nephroblastoma overexpressed (NOV) protein, is a cysteine-rich protein that belongs to the CCN family and regulates several cellular functions. Osteoblasts are major bone-forming cells that undergo proliferation, mineralization, renewal, and repair during the bone formation process. We have previously reported that CCN3 increases bone morphogenetic protein 4 (BMP-4) production and bone mineralization in osteoblasts, although the role of CCN3 remains unclear with regard to osteogenic transcription factors (runt-related transcription factor 2 (Runx2) and osterix). Here, we used alizarin red-S and alkaline phosphatase staining to show that CCN3 enhances osteoblast differentiation. Stimulation of osteoblasts with CCN3 increases expression of osteogenic factors such as BMPs, Runx2, and osterix. Moreover, we found that the inhibition of miR-608 expression is involved in the effects of CCN3 and that incubation of osteoblasts with CCN3 promotes focal adhesion kinase (FAK) and Akt phosphorylation. Our results indicate that CCN3 promotes the expression of Runx2 and osterix in osteoblasts by inhibiting miR-608 expression via the FAK and Akt signaling pathways. MDPI 2019-07-05 /pmc/articles/PMC6651805/ /pubmed/31284378 http://dx.doi.org/10.3390/ijms20133300 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chen, Po-Chun Liu, Ju-Fang Fong, Yi-Chin Huang, Yuan-Lin Chao, Chia-Chia Tang, Chih-Hsin CCN3 Facilitates Runx2 and Osterix Expression by Inhibiting miR-608 through PI3K/Akt Signaling in Osteoblasts |
title | CCN3 Facilitates Runx2 and Osterix Expression by Inhibiting miR-608 through PI3K/Akt Signaling in Osteoblasts |
title_full | CCN3 Facilitates Runx2 and Osterix Expression by Inhibiting miR-608 through PI3K/Akt Signaling in Osteoblasts |
title_fullStr | CCN3 Facilitates Runx2 and Osterix Expression by Inhibiting miR-608 through PI3K/Akt Signaling in Osteoblasts |
title_full_unstemmed | CCN3 Facilitates Runx2 and Osterix Expression by Inhibiting miR-608 through PI3K/Akt Signaling in Osteoblasts |
title_short | CCN3 Facilitates Runx2 and Osterix Expression by Inhibiting miR-608 through PI3K/Akt Signaling in Osteoblasts |
title_sort | ccn3 facilitates runx2 and osterix expression by inhibiting mir-608 through pi3k/akt signaling in osteoblasts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6651805/ https://www.ncbi.nlm.nih.gov/pubmed/31284378 http://dx.doi.org/10.3390/ijms20133300 |
work_keys_str_mv | AT chenpochun ccn3facilitatesrunx2andosterixexpressionbyinhibitingmir608throughpi3kaktsignalinginosteoblasts AT liujufang ccn3facilitatesrunx2andosterixexpressionbyinhibitingmir608throughpi3kaktsignalinginosteoblasts AT fongyichin ccn3facilitatesrunx2andosterixexpressionbyinhibitingmir608throughpi3kaktsignalinginosteoblasts AT huangyuanlin ccn3facilitatesrunx2andosterixexpressionbyinhibitingmir608throughpi3kaktsignalinginosteoblasts AT chaochiachia ccn3facilitatesrunx2andosterixexpressionbyinhibitingmir608throughpi3kaktsignalinginosteoblasts AT tangchihhsin ccn3facilitatesrunx2andosterixexpressionbyinhibitingmir608throughpi3kaktsignalinginosteoblasts |