Cargando…
miR-208a-3p Suppresses Osteoblast Differentiation and Inhibits Bone Formation by Targeting ACVR1
Emerging evidence indicates that many microRNAs (miRNAs) are indispensable regulators of osteoblast differentiation and bone formation. However, the role of miRNAs in mechanotransduction of osteoblasts remains to be elucidated. This study aimed to identify a mechanosensitive miRNA that regulates Act...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992884/ https://www.ncbi.nlm.nih.gov/pubmed/29858067 http://dx.doi.org/10.1016/j.omtn.2017.11.009 |
_version_ | 1783330127243902976 |
---|---|
author | Arfat, Yasir Basra, Muhammad Asim R. Shahzad, Muhammad Majeed, Kashif Mahmood, Nasir Munir, Hina |
author_facet | Arfat, Yasir Basra, Muhammad Asim R. Shahzad, Muhammad Majeed, Kashif Mahmood, Nasir Munir, Hina |
author_sort | Arfat, Yasir |
collection | PubMed |
description | Emerging evidence indicates that many microRNAs (miRNAs) are indispensable regulators of osteoblast differentiation and bone formation. However, the role of miRNAs in mechanotransduction of osteoblasts remains to be elucidated. This study aimed to identify a mechanosensitive miRNA that regulates Activin A receptor type I (ACVR1)-induced osteogenic differentiation. After 4 weeks of hindlimb unloading (HLU) suspension of 6-month-old male C57BL/6J mice, femurs and tibias were harvested to extract total bone RNAs. Elevated levels of miR-208a-3p correlated with a lower degree of bone formation in whole-bone samples of HLU mice. However, in vitro overexpression of miR-208a-3p inhibited osteoblast differentiation, whereas silencing of miR-208a-3p by antagomiR-208a-3p promoted expression of osteoblast activity, bone formation marker genes, and matrix mineralization under mechanical unloading condition. Bioinformatics analysis and a luciferase assay revealed that ACVR1 is a target gene of miR-208a-3p that negatively regulates osteoblast differentiation under mechanical unloading environment. Further, this study also demonstrates that in vivo pre-treatment with antagomiR-208a-3p led to an increase in bone formation and trabecular microarchitecture and partly rescued the bone loss caused by mechanical unloading. Collectively, these results suggest that in vivo, inhibition of miRNA-208a-3p by antagomiR-208a-3p may be a potential therapeutic strategy for ameliorating bone loss. |
format | Online Article Text |
id | pubmed-5992884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-59928842018-06-11 miR-208a-3p Suppresses Osteoblast Differentiation and Inhibits Bone Formation by Targeting ACVR1 Arfat, Yasir Basra, Muhammad Asim R. Shahzad, Muhammad Majeed, Kashif Mahmood, Nasir Munir, Hina Mol Ther Nucleic Acids Article Emerging evidence indicates that many microRNAs (miRNAs) are indispensable regulators of osteoblast differentiation and bone formation. However, the role of miRNAs in mechanotransduction of osteoblasts remains to be elucidated. This study aimed to identify a mechanosensitive miRNA that regulates Activin A receptor type I (ACVR1)-induced osteogenic differentiation. After 4 weeks of hindlimb unloading (HLU) suspension of 6-month-old male C57BL/6J mice, femurs and tibias were harvested to extract total bone RNAs. Elevated levels of miR-208a-3p correlated with a lower degree of bone formation in whole-bone samples of HLU mice. However, in vitro overexpression of miR-208a-3p inhibited osteoblast differentiation, whereas silencing of miR-208a-3p by antagomiR-208a-3p promoted expression of osteoblast activity, bone formation marker genes, and matrix mineralization under mechanical unloading condition. Bioinformatics analysis and a luciferase assay revealed that ACVR1 is a target gene of miR-208a-3p that negatively regulates osteoblast differentiation under mechanical unloading environment. Further, this study also demonstrates that in vivo pre-treatment with antagomiR-208a-3p led to an increase in bone formation and trabecular microarchitecture and partly rescued the bone loss caused by mechanical unloading. Collectively, these results suggest that in vivo, inhibition of miRNA-208a-3p by antagomiR-208a-3p may be a potential therapeutic strategy for ameliorating bone loss. American Society of Gene & Cell Therapy 2017-11-24 /pmc/articles/PMC5992884/ /pubmed/29858067 http://dx.doi.org/10.1016/j.omtn.2017.11.009 Text en © 2017. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Arfat, Yasir Basra, Muhammad Asim R. Shahzad, Muhammad Majeed, Kashif Mahmood, Nasir Munir, Hina miR-208a-3p Suppresses Osteoblast Differentiation and Inhibits Bone Formation by Targeting ACVR1 |
title | miR-208a-3p Suppresses Osteoblast Differentiation and Inhibits Bone Formation by Targeting ACVR1 |
title_full | miR-208a-3p Suppresses Osteoblast Differentiation and Inhibits Bone Formation by Targeting ACVR1 |
title_fullStr | miR-208a-3p Suppresses Osteoblast Differentiation and Inhibits Bone Formation by Targeting ACVR1 |
title_full_unstemmed | miR-208a-3p Suppresses Osteoblast Differentiation and Inhibits Bone Formation by Targeting ACVR1 |
title_short | miR-208a-3p Suppresses Osteoblast Differentiation and Inhibits Bone Formation by Targeting ACVR1 |
title_sort | mir-208a-3p suppresses osteoblast differentiation and inhibits bone formation by targeting acvr1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992884/ https://www.ncbi.nlm.nih.gov/pubmed/29858067 http://dx.doi.org/10.1016/j.omtn.2017.11.009 |
work_keys_str_mv | AT arfatyasir mir208a3psuppressesosteoblastdifferentiationandinhibitsboneformationbytargetingacvr1 AT basramuhammadasimr mir208a3psuppressesosteoblastdifferentiationandinhibitsboneformationbytargetingacvr1 AT shahzadmuhammad mir208a3psuppressesosteoblastdifferentiationandinhibitsboneformationbytargetingacvr1 AT majeedkashif mir208a3psuppressesosteoblastdifferentiationandinhibitsboneformationbytargetingacvr1 AT mahmoodnasir mir208a3psuppressesosteoblastdifferentiationandinhibitsboneformationbytargetingacvr1 AT munirhina mir208a3psuppressesosteoblastdifferentiationandinhibitsboneformationbytargetingacvr1 |