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...

Descripción completa

Detalles Bibliográficos
Autores principales: Arfat, Yasir, Basra, Muhammad Asim R., Shahzad, Muhammad, Majeed, Kashif, Mahmood, Nasir, Munir, Hina
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