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The importance of cellular and exosomal miRNAs in mesenchymal stem cell osteoblastic differentiation
The differentiation of osteoblasts is under complex regulation that includes autocrine and paracrine signaling from MSCs. Exosomes are important components of the MSC secretome and their cargo contains numerous miRNAs. In this study, the importance of MSC miRNAs in modulation of osteoblastic differe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7960990/ https://www.ncbi.nlm.nih.gov/pubmed/33723364 http://dx.doi.org/10.1038/s41598-021-85306-2 |
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author | Shirazi, Sajjad Huang, Chun-Chieh Kang, Miya Lu, Yu Ravindran, Sriram Cooper, Lyndon F. |
author_facet | Shirazi, Sajjad Huang, Chun-Chieh Kang, Miya Lu, Yu Ravindran, Sriram Cooper, Lyndon F. |
author_sort | Shirazi, Sajjad |
collection | PubMed |
description | The differentiation of osteoblasts is under complex regulation that includes autocrine and paracrine signaling from MSCs. Exosomes are important components of the MSC secretome and their cargo contains numerous miRNAs. In this study, the importance of MSC miRNAs in modulation of osteoblastic differentiation was examined by global reduction of miRNA biosynthesis in Dicer knock down hMSCs. We additionally impaired hMSC responses to miRNAs by knockdown of Argonaute 2 expression. Knockdown of Dicer and Argonaute 2 both reduced osteoblastic differentiation of hMSCs. This was observed at the levels of hMSC culture mineralization and osteoblastic gene expression. The treatment of Dicer deficient hMSCs with wild type hMSC exosomes effectively recovered the impaired osteoblastic differentiation. Dicer knockdown reduced the quantity and diversity of miRNAs present in hMSC exosomes. miRSeq data and KEGG analysis implicated the miRNA-dependent effects on multiple osteoinductive pathways in Dicer deficient cells, including the Hippo signaling and TGF-beta signaling pathways. Treatment of hMSCs with mimics of miRNAs significantly downregulated in Dicer knockdown cells recovered functions of exosome-mediated signaling in hMSCs. These results indicate that hMSC exosomes exert miRNA-dependent control that contributes to osteoblastic differentiation. |
format | Online Article Text |
id | pubmed-7960990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79609902021-03-19 The importance of cellular and exosomal miRNAs in mesenchymal stem cell osteoblastic differentiation Shirazi, Sajjad Huang, Chun-Chieh Kang, Miya Lu, Yu Ravindran, Sriram Cooper, Lyndon F. Sci Rep Article The differentiation of osteoblasts is under complex regulation that includes autocrine and paracrine signaling from MSCs. Exosomes are important components of the MSC secretome and their cargo contains numerous miRNAs. In this study, the importance of MSC miRNAs in modulation of osteoblastic differentiation was examined by global reduction of miRNA biosynthesis in Dicer knock down hMSCs. We additionally impaired hMSC responses to miRNAs by knockdown of Argonaute 2 expression. Knockdown of Dicer and Argonaute 2 both reduced osteoblastic differentiation of hMSCs. This was observed at the levels of hMSC culture mineralization and osteoblastic gene expression. The treatment of Dicer deficient hMSCs with wild type hMSC exosomes effectively recovered the impaired osteoblastic differentiation. Dicer knockdown reduced the quantity and diversity of miRNAs present in hMSC exosomes. miRSeq data and KEGG analysis implicated the miRNA-dependent effects on multiple osteoinductive pathways in Dicer deficient cells, including the Hippo signaling and TGF-beta signaling pathways. Treatment of hMSCs with mimics of miRNAs significantly downregulated in Dicer knockdown cells recovered functions of exosome-mediated signaling in hMSCs. These results indicate that hMSC exosomes exert miRNA-dependent control that contributes to osteoblastic differentiation. Nature Publishing Group UK 2021-03-15 /pmc/articles/PMC7960990/ /pubmed/33723364 http://dx.doi.org/10.1038/s41598-021-85306-2 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Shirazi, Sajjad Huang, Chun-Chieh Kang, Miya Lu, Yu Ravindran, Sriram Cooper, Lyndon F. The importance of cellular and exosomal miRNAs in mesenchymal stem cell osteoblastic differentiation |
title | The importance of cellular and exosomal miRNAs in mesenchymal stem cell osteoblastic differentiation |
title_full | The importance of cellular and exosomal miRNAs in mesenchymal stem cell osteoblastic differentiation |
title_fullStr | The importance of cellular and exosomal miRNAs in mesenchymal stem cell osteoblastic differentiation |
title_full_unstemmed | The importance of cellular and exosomal miRNAs in mesenchymal stem cell osteoblastic differentiation |
title_short | The importance of cellular and exosomal miRNAs in mesenchymal stem cell osteoblastic differentiation |
title_sort | importance of cellular and exosomal mirnas in mesenchymal stem cell osteoblastic differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7960990/ https://www.ncbi.nlm.nih.gov/pubmed/33723364 http://dx.doi.org/10.1038/s41598-021-85306-2 |
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