LncRNA HOTAIR is a novel endothelial mechanosensitive gene
Autor(a) principal: | |
---|---|
Data de Publicação: | 2020 |
Outros Autores: | , , |
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. |
id |
UNSP_b3393a6e04504187815fdb67ceb5f869 |
---|---|
oai_identifier_str |
oai:repositorio.unesp.br:11449/199589 |
network_acronym_str |
UNSP |
network_name_str |
Repositório Institucional da UNESP |
repository_id_str |
2946 |
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:29462024-08-05T14:50:12.467833Repositório 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 |
|
_version_ |
1808128422997655552 |