Non-coding RNAs repressive role in post-transcriptional processing of RUNX2 during the acquisition of the osteogenic phenotype of periodontal ligament mesenchymal stem cells

Detalhes bibliográficos
Autor(a) principal: Assis, Rahyza I.F.
Data de Publicação: 2021
Outros Autores: Feltran, Geórgia da S. [UNESP], Silva, Maria Eduarda Salomão, Palma, Iasmin Caroline do Rosário, Rovai, Emanuel Silva, Miranda, Taís Browne de, Ferreira, Marcel Rodrigues [UNESP], Zambuzzi, Willian F. [UNESP], Birbrair, Alexander, Andia, Denise C., da Silva, Rodrigo A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.ydbio.2020.10.012
http://hdl.handle.net/11449/205528
Resumo: Mesenchymal stem cells are candidates for therapeutic strategies in periodontal repair due to their osteogenic potential. In this study, we identified epigenetic markers during osteogenic differentiation, taking advantage of the individual pattern of mesenchymal cells of the periodontal ligament with high (h-PDLCs) and low (l-PDLCs) osteogenic capacity. We found that the involvement of non-coding RNAs in the regulation of the RUNX2 gene is strongly associated with high osteogenic potential. Moreover, we evaluated miRs and genes that encode enzymes to process miRs and their biogenesis. Our data show the high expression of the XPO5 gene, and miRs 7 and 22 observed in the l-PDLCs might be involved in acquiring osteogenic potential, suppressing RUNX2 gene expression. Further, an inversely proportional correlation between lncRNAs (HOTAIR and HOTTIP) and RUNX2 gene expression was observed in both l- and h-PDLCs, and it was also related to the distinct osteogenic phenotypes. Thus, our results indicate the low expression of XPO5 in h-PDLC might be the limiting point for blocking the miRs biogenesis, allowing the high gene expression of RUNX2. In accordance, the low expression of miRs, HOTAIR, and HOTTIP could be a prerequisite for increased osteogenic potential in h-PDLCs. These results will help us to better understand the underlying mechanisms of osteogenesis, considering the heterogeneity in the osteogenic potential of PDLCs that might be related to a distinct transcriptional profile of lncRNAs and the biogenesis machinery.
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spelling Non-coding RNAs repressive role in post-transcriptional processing of RUNX2 during the acquisition of the osteogenic phenotype of periodontal ligament mesenchymal stem cellsEpigenetic backgroundOsteogenic potentialPeriodontal regenerationStem cellsTissue engineeringMesenchymal stem cells are candidates for therapeutic strategies in periodontal repair due to their osteogenic potential. In this study, we identified epigenetic markers during osteogenic differentiation, taking advantage of the individual pattern of mesenchymal cells of the periodontal ligament with high (h-PDLCs) and low (l-PDLCs) osteogenic capacity. We found that the involvement of non-coding RNAs in the regulation of the RUNX2 gene is strongly associated with high osteogenic potential. Moreover, we evaluated miRs and genes that encode enzymes to process miRs and their biogenesis. Our data show the high expression of the XPO5 gene, and miRs 7 and 22 observed in the l-PDLCs might be involved in acquiring osteogenic potential, suppressing RUNX2 gene expression. Further, an inversely proportional correlation between lncRNAs (HOTAIR and HOTTIP) and RUNX2 gene expression was observed in both l- and h-PDLCs, and it was also related to the distinct osteogenic phenotypes. Thus, our results indicate the low expression of XPO5 in h-PDLC might be the limiting point for blocking the miRs biogenesis, allowing the high gene expression of RUNX2. In accordance, the low expression of miRs, HOTAIR, and HOTTIP could be a prerequisite for increased osteogenic potential in h-PDLCs. These results will help us to better understand the underlying mechanisms of osteogenesis, considering the heterogeneity in the osteogenic potential of PDLCs that might be related to a distinct transcriptional profile of lncRNAs and the biogenesis machinery.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Faculty of Dentistry University of TaubatéProgram in Environmental and Experimental Pathology Paulista University São PauloLab. of Bioassays and Cellular Dynamics Department of Chemical and Biological Sciences Institute of Biosciences UNESP – São Paulo State University, São PauloDepartment of Pathology Federal University of Minas GeraisDepartment of Radiology Columbia University Medical CenterSchool of Dentistry Health Science Institute Paulista UniversityDepartment of Prosthodontics and Periodontics Piracicaba Dental School University of CampinasLab. of Bioassays and Cellular Dynamics Department of Chemical and Biological Sciences Institute of Biosciences UNESP – São Paulo State University, São PauloCNPq: ODO 154/2019University of TaubatéSão PauloUniversidade Estadual Paulista (Unesp)Universidade Federal de Minas Gerais (UFMG)Columbia University Medical CenterPaulista UniversityUniversidade Estadual de Campinas (UNICAMP)Assis, Rahyza I.F.Feltran, Geórgia da S. [UNESP]Silva, Maria Eduarda SalomãoPalma, Iasmin Caroline do RosárioRovai, Emanuel SilvaMiranda, Taís Browne deFerreira, Marcel Rodrigues [UNESP]Zambuzzi, Willian F. [UNESP]Birbrair, AlexanderAndia, Denise C.da Silva, Rodrigo A.2021-06-25T10:16:56Z2021-06-25T10:16:56Z2021-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article37-48http://dx.doi.org/10.1016/j.ydbio.2020.10.012Developmental Biology, v. 470, p. 37-48.1095-564X0012-1606http://hdl.handle.net/11449/20552810.1016/j.ydbio.2020.10.0122-s2.0-85096697889Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengDevelopmental Biologyinfo:eu-repo/semantics/openAccess2021-10-23T14:48:15Zoai:repositorio.unesp.br:11449/205528Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:21:05.669731Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Non-coding RNAs repressive role in post-transcriptional processing of RUNX2 during the acquisition of the osteogenic phenotype of periodontal ligament mesenchymal stem cells
title Non-coding RNAs repressive role in post-transcriptional processing of RUNX2 during the acquisition of the osteogenic phenotype of periodontal ligament mesenchymal stem cells
spellingShingle Non-coding RNAs repressive role in post-transcriptional processing of RUNX2 during the acquisition of the osteogenic phenotype of periodontal ligament mesenchymal stem cells
Assis, Rahyza I.F.
Epigenetic background
Osteogenic potential
Periodontal regeneration
Stem cells
Tissue engineering
title_short Non-coding RNAs repressive role in post-transcriptional processing of RUNX2 during the acquisition of the osteogenic phenotype of periodontal ligament mesenchymal stem cells
title_full Non-coding RNAs repressive role in post-transcriptional processing of RUNX2 during the acquisition of the osteogenic phenotype of periodontal ligament mesenchymal stem cells
title_fullStr Non-coding RNAs repressive role in post-transcriptional processing of RUNX2 during the acquisition of the osteogenic phenotype of periodontal ligament mesenchymal stem cells
title_full_unstemmed Non-coding RNAs repressive role in post-transcriptional processing of RUNX2 during the acquisition of the osteogenic phenotype of periodontal ligament mesenchymal stem cells
title_sort Non-coding RNAs repressive role in post-transcriptional processing of RUNX2 during the acquisition of the osteogenic phenotype of periodontal ligament mesenchymal stem cells
author Assis, Rahyza I.F.
author_facet Assis, Rahyza I.F.
Feltran, Geórgia da S. [UNESP]
Silva, Maria Eduarda Salomão
Palma, Iasmin Caroline do Rosário
Rovai, Emanuel Silva
Miranda, Taís Browne de
Ferreira, Marcel Rodrigues [UNESP]
Zambuzzi, Willian F. [UNESP]
Birbrair, Alexander
Andia, Denise C.
da Silva, Rodrigo A.
author_role author
author2 Feltran, Geórgia da S. [UNESP]
Silva, Maria Eduarda Salomão
Palma, Iasmin Caroline do Rosário
Rovai, Emanuel Silva
Miranda, Taís Browne de
Ferreira, Marcel Rodrigues [UNESP]
Zambuzzi, Willian F. [UNESP]
Birbrair, Alexander
Andia, Denise C.
da Silva, Rodrigo A.
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv University of Taubaté
São Paulo
Universidade Estadual Paulista (Unesp)
Universidade Federal de Minas Gerais (UFMG)
Columbia University Medical Center
Paulista University
Universidade Estadual de Campinas (UNICAMP)
dc.contributor.author.fl_str_mv Assis, Rahyza I.F.
Feltran, Geórgia da S. [UNESP]
Silva, Maria Eduarda Salomão
Palma, Iasmin Caroline do Rosário
Rovai, Emanuel Silva
Miranda, Taís Browne de
Ferreira, Marcel Rodrigues [UNESP]
Zambuzzi, Willian F. [UNESP]
Birbrair, Alexander
Andia, Denise C.
da Silva, Rodrigo A.
dc.subject.por.fl_str_mv Epigenetic background
Osteogenic potential
Periodontal regeneration
Stem cells
Tissue engineering
topic Epigenetic background
Osteogenic potential
Periodontal regeneration
Stem cells
Tissue engineering
description Mesenchymal stem cells are candidates for therapeutic strategies in periodontal repair due to their osteogenic potential. In this study, we identified epigenetic markers during osteogenic differentiation, taking advantage of the individual pattern of mesenchymal cells of the periodontal ligament with high (h-PDLCs) and low (l-PDLCs) osteogenic capacity. We found that the involvement of non-coding RNAs in the regulation of the RUNX2 gene is strongly associated with high osteogenic potential. Moreover, we evaluated miRs and genes that encode enzymes to process miRs and their biogenesis. Our data show the high expression of the XPO5 gene, and miRs 7 and 22 observed in the l-PDLCs might be involved in acquiring osteogenic potential, suppressing RUNX2 gene expression. Further, an inversely proportional correlation between lncRNAs (HOTAIR and HOTTIP) and RUNX2 gene expression was observed in both l- and h-PDLCs, and it was also related to the distinct osteogenic phenotypes. Thus, our results indicate the low expression of XPO5 in h-PDLC might be the limiting point for blocking the miRs biogenesis, allowing the high gene expression of RUNX2. In accordance, the low expression of miRs, HOTAIR, and HOTTIP could be a prerequisite for increased osteogenic potential in h-PDLCs. These results will help us to better understand the underlying mechanisms of osteogenesis, considering the heterogeneity in the osteogenic potential of PDLCs that might be related to a distinct transcriptional profile of lncRNAs and the biogenesis machinery.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T10:16:56Z
2021-06-25T10:16:56Z
2021-02-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.ydbio.2020.10.012
Developmental Biology, v. 470, p. 37-48.
1095-564X
0012-1606
http://hdl.handle.net/11449/205528
10.1016/j.ydbio.2020.10.012
2-s2.0-85096697889
url http://dx.doi.org/10.1016/j.ydbio.2020.10.012
http://hdl.handle.net/11449/205528
identifier_str_mv Developmental Biology, v. 470, p. 37-48.
1095-564X
0012-1606
10.1016/j.ydbio.2020.10.012
2-s2.0-85096697889
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Developmental Biology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 37-48
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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