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Protein deubiquitinase USP7 is required for osteogenic differentiation of human adipose-derived stem cells
BACKGROUND: Human adipose-derived stem cells (hASCs) are multipotent progenitor cells with self-renewal capabilities and multilineage differentiation potential, including osteogenesis. Although protein deubiquitinases have been linked to stem cell fate determination, whether protein deubiquitination...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557518/ https://www.ncbi.nlm.nih.gov/pubmed/28807012 http://dx.doi.org/10.1186/s13287-017-0637-8 |
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author | Tang, Yiman Lv, Longwei Li, Wenyue Zhang, Xiao Jiang, Yong Ge, Wenshu Zhou, Yongsheng |
author_facet | Tang, Yiman Lv, Longwei Li, Wenyue Zhang, Xiao Jiang, Yong Ge, Wenshu Zhou, Yongsheng |
author_sort | Tang, Yiman |
collection | PubMed |
description | BACKGROUND: Human adipose-derived stem cells (hASCs) are multipotent progenitor cells with self-renewal capabilities and multilineage differentiation potential, including osteogenesis. Although protein deubiquitinases have been linked to stem cell fate determination, whether protein deubiquitination contributes to lineage commitment during osteogenic differentiation of hASCs remains to be investigated. The objective of this study was to evaluate the effects of the ubiquitin specific protease 7 (USP7) on osteogenic differentiation of hASCs. METHODS: An osteocalcin promoter driven luciferase reporter system was established to initially discover the potential association between USP7 and hASC osteogenesis. To further characterize the function of USP7 in osteogenic differentiation of hASCs, a combination of in vitro and in vivo experiments were carried out through genetic depletion or overexpression of USP7 using a lentiviral strategy. Moreover, HBX 41,108, a cyanoindenopyrazine-derived deubiquitinase inhibitor of USP7, was utilized at different doses to further examine whether USP7 regulated osteogenic differentiation of hASCs through its enzymatic activity. RESULTS: We demonstrated that USP7 depletion was associated with remarkable downregulation of the reporter gene activity. Genetic depletion of USP7 by lentiviral RNAi markedly suppressed hASC osteogenesis both in vitro and in vivo, while overexpression of USP7 enhanced the osteogenic differentiation of hASCs. Notably, chemical blockade via the small molecular inhibitor HBX 41,108 could efficiently mimic the effects of USP7 genetic depletion in a dose-dependent manner. CONCLUSIONS: Taken together, our study revealed that protein deubiquitinase USP7 is an essential player in osteogenic differentiation of hASCs through its catalytic activity, and supported the pursuit of USP7 as a potential target for modulation of hASC-based stem cell therapy and bone tissue engineering. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-017-0637-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5557518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55575182017-08-16 Protein deubiquitinase USP7 is required for osteogenic differentiation of human adipose-derived stem cells Tang, Yiman Lv, Longwei Li, Wenyue Zhang, Xiao Jiang, Yong Ge, Wenshu Zhou, Yongsheng Stem Cell Res Ther Research BACKGROUND: Human adipose-derived stem cells (hASCs) are multipotent progenitor cells with self-renewal capabilities and multilineage differentiation potential, including osteogenesis. Although protein deubiquitinases have been linked to stem cell fate determination, whether protein deubiquitination contributes to lineage commitment during osteogenic differentiation of hASCs remains to be investigated. The objective of this study was to evaluate the effects of the ubiquitin specific protease 7 (USP7) on osteogenic differentiation of hASCs. METHODS: An osteocalcin promoter driven luciferase reporter system was established to initially discover the potential association between USP7 and hASC osteogenesis. To further characterize the function of USP7 in osteogenic differentiation of hASCs, a combination of in vitro and in vivo experiments were carried out through genetic depletion or overexpression of USP7 using a lentiviral strategy. Moreover, HBX 41,108, a cyanoindenopyrazine-derived deubiquitinase inhibitor of USP7, was utilized at different doses to further examine whether USP7 regulated osteogenic differentiation of hASCs through its enzymatic activity. RESULTS: We demonstrated that USP7 depletion was associated with remarkable downregulation of the reporter gene activity. Genetic depletion of USP7 by lentiviral RNAi markedly suppressed hASC osteogenesis both in vitro and in vivo, while overexpression of USP7 enhanced the osteogenic differentiation of hASCs. Notably, chemical blockade via the small molecular inhibitor HBX 41,108 could efficiently mimic the effects of USP7 genetic depletion in a dose-dependent manner. CONCLUSIONS: Taken together, our study revealed that protein deubiquitinase USP7 is an essential player in osteogenic differentiation of hASCs through its catalytic activity, and supported the pursuit of USP7 as a potential target for modulation of hASC-based stem cell therapy and bone tissue engineering. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-017-0637-8) contains supplementary material, which is available to authorized users. BioMed Central 2017-08-14 /pmc/articles/PMC5557518/ /pubmed/28807012 http://dx.doi.org/10.1186/s13287-017-0637-8 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Tang, Yiman Lv, Longwei Li, Wenyue Zhang, Xiao Jiang, Yong Ge, Wenshu Zhou, Yongsheng Protein deubiquitinase USP7 is required for osteogenic differentiation of human adipose-derived stem cells |
title | Protein deubiquitinase USP7 is required for osteogenic differentiation of human adipose-derived stem cells |
title_full | Protein deubiquitinase USP7 is required for osteogenic differentiation of human adipose-derived stem cells |
title_fullStr | Protein deubiquitinase USP7 is required for osteogenic differentiation of human adipose-derived stem cells |
title_full_unstemmed | Protein deubiquitinase USP7 is required for osteogenic differentiation of human adipose-derived stem cells |
title_short | Protein deubiquitinase USP7 is required for osteogenic differentiation of human adipose-derived stem cells |
title_sort | protein deubiquitinase usp7 is required for osteogenic differentiation of human adipose-derived stem cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557518/ https://www.ncbi.nlm.nih.gov/pubmed/28807012 http://dx.doi.org/10.1186/s13287-017-0637-8 |
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