LncRNA HOTAIR is a novel endothelial mechanosensitive gene

Detalhes bibliográficos
Autor(a) principal: da Silva, Rodrigo A. [UNESP]
Data de Publicação: 2020
Outros Autores: Ferreira, Marcel Rodrigues [UNESP], Gomes, Anderson Moreira [UNESP], Zambuzzi, Willian F. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1002/jcp.29340
http://hdl.handle.net/11449/199589
Resumo: To better address whether the long noncoding RNAs (lncRNAs) HOTAIR and HOTTIP are mechanosensitive genes, they were investigated in differentially challenged endothelial cells with respect to a circuit of tensional forces, considering the performance of both arterial and venous endothelial cells. We subjected arterial- and venous-obtained endothelial cells to a circuit of tensional forces within a shear stress model in vitro. Real-time quantitative polymerase chain reaction analysis indicated that microRNA (miRNA)-related processing machinery is significantly required in shear stressed arterial endothelial cell metabolism, which orchestrates miRNA (small noncoding RNA) involvement, and their involvement suggests lncRNA involvement. Of lncRNAs HOTAIR and HOTTIP, only HOTAIR was mechanosensitive considering both arterial and venous endothelial cells, presenting a positive correlation between methylation signature and gene expression. Thereafter, using bioinformatics tools, lncRNA HOTAIR was predicted to modulate miRNA185, miRNA-21, and miRNA23b downregulation. We compared the values of gene expression with a Pearson's correlation test, and expected correlations were observed for miRNA185 (r = 0.8664), miRNA-21 (r = 0.8605), and miRNA23b (0.9128). Taken together, these findings clearly show that lncRNA HOTAIR responds to the shear stress and emerges as a novel mechanosensitive gene in endothelial cells. Altogether, this understanding of mechanosensitive transcriptional and posttranscriptional control involving HOTAIR can also lead to new forms of therapeutic intervention for various diseases, as well as new strategies for tissue engineering and regenerative medicine.
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spelling LncRNA HOTAIR is a novel endothelial mechanosensitive geneepigeneticsHOTAIRlncRNAmechanosensitivemiRNAshear stressTo better address whether the long noncoding RNAs (lncRNAs) HOTAIR and HOTTIP are mechanosensitive genes, they were investigated in differentially challenged endothelial cells with respect to a circuit of tensional forces, considering the performance of both arterial and venous endothelial cells. We subjected arterial- and venous-obtained endothelial cells to a circuit of tensional forces within a shear stress model in vitro. Real-time quantitative polymerase chain reaction analysis indicated that microRNA (miRNA)-related processing machinery is significantly required in shear stressed arterial endothelial cell metabolism, which orchestrates miRNA (small noncoding RNA) involvement, and their involvement suggests lncRNA involvement. Of lncRNAs HOTAIR and HOTTIP, only HOTAIR was mechanosensitive considering both arterial and venous endothelial cells, presenting a positive correlation between methylation signature and gene expression. Thereafter, using bioinformatics tools, lncRNA HOTAIR was predicted to modulate miRNA185, miRNA-21, and miRNA23b downregulation. We compared the values of gene expression with a Pearson's correlation test, and expected correlations were observed for miRNA185 (r = 0.8664), miRNA-21 (r = 0.8605), and miRNA23b (0.9128). Taken together, these findings clearly show that lncRNA HOTAIR responds to the shear stress and emerges as a novel mechanosensitive gene in endothelial cells. Altogether, this understanding of mechanosensitive transcriptional and posttranscriptional control involving HOTAIR can also lead to new forms of therapeutic intervention for various diseases, as well as new strategies for tissue engineering and regenerative medicine.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Laboratory of Bioassays and Cellular Dynamics Department of Chemistry and Biochemistry Institute of Biosciences São Paulo State University - UNESPDivision of Dental Biology Department of Dentistry University of TaubatéLaboratory of Bioassays and Cellular Dynamics Department of Chemistry and Biochemistry Institute of Biosciences São Paulo State University - UNESPFAPESP: 2014/22689-3FAPESP: 2016/01139-0CNPq: PQ-2Universidade Estadual Paulista (Unesp)University of Taubatéda Silva, Rodrigo A. [UNESP]Ferreira, Marcel Rodrigues [UNESP]Gomes, Anderson Moreira [UNESP]Zambuzzi, Willian F. [UNESP]2020-12-12T01:44:02Z2020-12-12T01:44:02Z2020-05-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article4631-4642http://dx.doi.org/10.1002/jcp.29340Journal of Cellular Physiology, v. 235, n. 5, p. 4631-4642, 2020.1097-46520021-9541http://hdl.handle.net/11449/19958910.1002/jcp.293402-s2.0-85074337019Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Cellular Physiologyinfo:eu-repo/semantics/openAccess2021-10-23T08:25:02Zoai:repositorio.unesp.br:11449/199589Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-23T08:25:02Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv LncRNA HOTAIR is a novel endothelial mechanosensitive gene
title LncRNA HOTAIR is a novel endothelial mechanosensitive gene
spellingShingle LncRNA HOTAIR is a novel endothelial mechanosensitive gene
da Silva, Rodrigo A. [UNESP]
epigenetics
HOTAIR
lncRNA
mechanosensitive
miRNA
shear stress
title_short LncRNA HOTAIR is a novel endothelial mechanosensitive gene
title_full LncRNA HOTAIR is a novel endothelial mechanosensitive gene
title_fullStr LncRNA HOTAIR is a novel endothelial mechanosensitive gene
title_full_unstemmed LncRNA HOTAIR is a novel endothelial mechanosensitive gene
title_sort LncRNA HOTAIR is a novel endothelial mechanosensitive gene
author da Silva, Rodrigo A. [UNESP]
author_facet da Silva, Rodrigo A. [UNESP]
Ferreira, Marcel Rodrigues [UNESP]
Gomes, Anderson Moreira [UNESP]
Zambuzzi, Willian F. [UNESP]
author_role author
author2 Ferreira, Marcel Rodrigues [UNESP]
Gomes, Anderson Moreira [UNESP]
Zambuzzi, Willian F. [UNESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
University of Taubaté
dc.contributor.author.fl_str_mv da Silva, Rodrigo A. [UNESP]
Ferreira, Marcel Rodrigues [UNESP]
Gomes, Anderson Moreira [UNESP]
Zambuzzi, Willian F. [UNESP]
dc.subject.por.fl_str_mv epigenetics
HOTAIR
lncRNA
mechanosensitive
miRNA
shear stress
topic epigenetics
HOTAIR
lncRNA
mechanosensitive
miRNA
shear stress
description To better address whether the long noncoding RNAs (lncRNAs) HOTAIR and HOTTIP are mechanosensitive genes, they were investigated in differentially challenged endothelial cells with respect to a circuit of tensional forces, considering the performance of both arterial and venous endothelial cells. We subjected arterial- and venous-obtained endothelial cells to a circuit of tensional forces within a shear stress model in vitro. Real-time quantitative polymerase chain reaction analysis indicated that microRNA (miRNA)-related processing machinery is significantly required in shear stressed arterial endothelial cell metabolism, which orchestrates miRNA (small noncoding RNA) involvement, and their involvement suggests lncRNA involvement. Of lncRNAs HOTAIR and HOTTIP, only HOTAIR was mechanosensitive considering both arterial and venous endothelial cells, presenting a positive correlation between methylation signature and gene expression. Thereafter, using bioinformatics tools, lncRNA HOTAIR was predicted to modulate miRNA185, miRNA-21, and miRNA23b downregulation. We compared the values of gene expression with a Pearson's correlation test, and expected correlations were observed for miRNA185 (r = 0.8664), miRNA-21 (r = 0.8605), and miRNA23b (0.9128). Taken together, these findings clearly show that lncRNA HOTAIR responds to the shear stress and emerges as a novel mechanosensitive gene in endothelial cells. Altogether, this understanding of mechanosensitive transcriptional and posttranscriptional control involving HOTAIR can also lead to new forms of therapeutic intervention for various diseases, as well as new strategies for tissue engineering and regenerative medicine.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-12T01:44:02Z
2020-12-12T01:44:02Z
2020-05-01
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/10.1002/jcp.29340
Journal of Cellular Physiology, v. 235, n. 5, p. 4631-4642, 2020.
1097-4652
0021-9541
http://hdl.handle.net/11449/199589
10.1002/jcp.29340
2-s2.0-85074337019
url http://dx.doi.org/10.1002/jcp.29340
http://hdl.handle.net/11449/199589
identifier_str_mv Journal of Cellular Physiology, v. 235, n. 5, p. 4631-4642, 2020.
1097-4652
0021-9541
10.1002/jcp.29340
2-s2.0-85074337019
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Cellular Physiology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 4631-4642
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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