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α2-HS Glycoprotein in Plasma Extracellular Vesicles Inhibits the Osteogenic Differentiation of Human Mesenchymal Stromal Cells In Vitro

Extracellular vesicles (Evs) contain diverse functional proteins, mRNAs, miRNAs, and DNA fragments, are secreted by various types of cells, and play important roles in cellular communication. Here, we show for the first time that plasma Evs inhibited the osteogenic differentiation of mesenchymal str...

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Autores principales: Wu, Xiaohua, Ma, Mengjun, Wang, Peng, Xie, Zhongyu, Wang, Shan, Su, Hongjun, Deng, Wen, Feng, Pei, Su, Chunyan, Yang, Jiewen, Li, Jinteng, Tang, Su'an, Wu, Yanfeng, Shen, Huiyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383392/
https://www.ncbi.nlm.nih.gov/pubmed/30881463
http://dx.doi.org/10.1155/2019/7246479
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author Wu, Xiaohua
Ma, Mengjun
Wang, Peng
Xie, Zhongyu
Wang, Shan
Su, Hongjun
Deng, Wen
Feng, Pei
Su, Chunyan
Yang, Jiewen
Li, Jinteng
Tang, Su'an
Wu, Yanfeng
Shen, Huiyong
author_facet Wu, Xiaohua
Ma, Mengjun
Wang, Peng
Xie, Zhongyu
Wang, Shan
Su, Hongjun
Deng, Wen
Feng, Pei
Su, Chunyan
Yang, Jiewen
Li, Jinteng
Tang, Su'an
Wu, Yanfeng
Shen, Huiyong
author_sort Wu, Xiaohua
collection PubMed
description Extracellular vesicles (Evs) contain diverse functional proteins, mRNAs, miRNAs, and DNA fragments, are secreted by various types of cells, and play important roles in cellular communication. Here, we show for the first time that plasma Evs inhibited the osteogenic differentiation of mesenchymal stromal cells (MSCs) in vitro and the level of inhibition was positively correlated with the plasma Evs concentration. Plasma Evs downregulated the expression of markers such as osteocalcin (OCN), Runt-related transcription factor 2 (Runx2), and Osterix at mRNA levels required for osteogenic differentiation and reduced pSmad1/5/8 levels in MSCs. Furthermore, pSmad1/5/8 levels increased and MSCs underwent normal osteogenic differentiation after Evs-derived α2-HS glycoprotein (AHSG) function was inhibited with an anti-AHSG neutralizing antibody. However, the levels of pERK1/2, active β-catenin, and HES1 were not significantly altered. Therefore, we propose that as essential components of the extracellular microenvironment of MSCs, plasma Evs are taken up by MSCs and subsequently repress osteogenic differentiation through an AHSG-mediated decrease in pSmad1/5/8 levels. Our work identifies plasma Evs as novel regulators of MSC osteogenic differentiation.
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spelling pubmed-63833922019-03-17 α2-HS Glycoprotein in Plasma Extracellular Vesicles Inhibits the Osteogenic Differentiation of Human Mesenchymal Stromal Cells In Vitro Wu, Xiaohua Ma, Mengjun Wang, Peng Xie, Zhongyu Wang, Shan Su, Hongjun Deng, Wen Feng, Pei Su, Chunyan Yang, Jiewen Li, Jinteng Tang, Su'an Wu, Yanfeng Shen, Huiyong Stem Cells Int Research Article Extracellular vesicles (Evs) contain diverse functional proteins, mRNAs, miRNAs, and DNA fragments, are secreted by various types of cells, and play important roles in cellular communication. Here, we show for the first time that plasma Evs inhibited the osteogenic differentiation of mesenchymal stromal cells (MSCs) in vitro and the level of inhibition was positively correlated with the plasma Evs concentration. Plasma Evs downregulated the expression of markers such as osteocalcin (OCN), Runt-related transcription factor 2 (Runx2), and Osterix at mRNA levels required for osteogenic differentiation and reduced pSmad1/5/8 levels in MSCs. Furthermore, pSmad1/5/8 levels increased and MSCs underwent normal osteogenic differentiation after Evs-derived α2-HS glycoprotein (AHSG) function was inhibited with an anti-AHSG neutralizing antibody. However, the levels of pERK1/2, active β-catenin, and HES1 were not significantly altered. Therefore, we propose that as essential components of the extracellular microenvironment of MSCs, plasma Evs are taken up by MSCs and subsequently repress osteogenic differentiation through an AHSG-mediated decrease in pSmad1/5/8 levels. Our work identifies plasma Evs as novel regulators of MSC osteogenic differentiation. Hindawi 2019-02-07 /pmc/articles/PMC6383392/ /pubmed/30881463 http://dx.doi.org/10.1155/2019/7246479 Text en Copyright © 2019 Xiaohua Wu et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wu, Xiaohua
Ma, Mengjun
Wang, Peng
Xie, Zhongyu
Wang, Shan
Su, Hongjun
Deng, Wen
Feng, Pei
Su, Chunyan
Yang, Jiewen
Li, Jinteng
Tang, Su'an
Wu, Yanfeng
Shen, Huiyong
α2-HS Glycoprotein in Plasma Extracellular Vesicles Inhibits the Osteogenic Differentiation of Human Mesenchymal Stromal Cells In Vitro
title α2-HS Glycoprotein in Plasma Extracellular Vesicles Inhibits the Osteogenic Differentiation of Human Mesenchymal Stromal Cells In Vitro
title_full α2-HS Glycoprotein in Plasma Extracellular Vesicles Inhibits the Osteogenic Differentiation of Human Mesenchymal Stromal Cells In Vitro
title_fullStr α2-HS Glycoprotein in Plasma Extracellular Vesicles Inhibits the Osteogenic Differentiation of Human Mesenchymal Stromal Cells In Vitro
title_full_unstemmed α2-HS Glycoprotein in Plasma Extracellular Vesicles Inhibits the Osteogenic Differentiation of Human Mesenchymal Stromal Cells In Vitro
title_short α2-HS Glycoprotein in Plasma Extracellular Vesicles Inhibits the Osteogenic Differentiation of Human Mesenchymal Stromal Cells In Vitro
title_sort α2-hs glycoprotein in plasma extracellular vesicles inhibits the osteogenic differentiation of human mesenchymal stromal cells in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383392/
https://www.ncbi.nlm.nih.gov/pubmed/30881463
http://dx.doi.org/10.1155/2019/7246479
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