Molecular markers distinguishing T Cell subtypes with TSDR strand-bias methylation

Detalhes bibliográficos
Autor(a) principal: Minskaia, Ekaterina
Data de Publicação: 2018
Outros Autores: Saraiva, Bárbara C., Soares, Maria Vieira, Azevedo, Rita I., Ribeiro, Ruy M., Kumar, Saumya, Vieira, Ana I. S., Lacerda, João
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10451/45068
Resumo: Copyright © 2018 Minskaia, Saraiva, Soares, Azevedo, Ribeiro, Kumar, Vieira and Lacerda. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
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spelling Molecular markers distinguishing T Cell subtypes with TSDR strand-bias methylationStrand-bias methylationCAMTAFOXP3FUT7EpigeneticsRegulatory T lymphocytesCopyright © 2018 Minskaia, Saraiva, Soares, Azevedo, Ribeiro, Kumar, Vieira and Lacerda. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.Human regulatory CD4+CD25+FOXP3+ T cells (Treg) play important roles in the maintenance of self-tolerance and immune homeostasis in various disease settings and are also involved in the suppression of effective immune responses. These cells are heterogeneous in phenotype and function, and the ability to reliably distinguish between various FOXP3-expressing subpopulations can affect the development of successful therapies. This study demonstrates that hypomethylated CpG sites, present in four regions of the FOXP3 locus, CAMTA1 and FUT7 gene regions, can be used to distinguish several subsets of Treg from conventional CD4+ T lymphocytes (Tcon) in donors of both genders. We describe a previously unreported strand-bias hemimethylation pattern in FOXP3 promoter and TSDR in donors of both genders, with the coding strand being demethylated within promoter and methylated within TSDR in all CD4+ lymphocyte subtypes, whereas the template strand follows the previously described pattern of methylation with both regions being more demethylated in Treg subtypes and mostly methylated in Tcon. This strand-specific approach within the TSDR may prove to be instrumental in correctly defining Treg subsets in health and in disease.This research was funded by: Fundação para a Ciência e Tecnologia, Portugal under the Harvard Medical School–Portugal Program project Induction of Immune Tolerance in Human Allogeneic Hematopoietic Stem Cell Transplantation (HMSP-ICT/0001/2011), Gabinete de Apoio à Investigação Científica, Tecnológica e Inovação, GAPIC (Faculdade de Medicina ULisboa, GAPIC-04-2016 Project 20160011), LISBOA-01-0145-FEDER-007391 (project co-funded by FEDER through POR Lisboa 2020—Programa Operacional Regional de Lisboa, PORTUGAL 2020 and Fundação para a Ciência e a Tecnologia) and ENLIGHT-TEN project (European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement 675395).FrontiersRepositório da Universidade de LisboaMinskaia, EkaterinaSaraiva, Bárbara C.Soares, Maria VieiraAzevedo, Rita I.Ribeiro, Ruy M.Kumar, SaumyaVieira, Ana I. S.Lacerda, João2020-12-02T13:59:54Z20182018-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10451/45068engFront Immunol. 2018 Nov 5; 9: 2540.10.3389/fimmu.2018.025401664-3224info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-08T16:46:32Zoai:repositorio.ul.pt:10451/45068Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:57:33.122108Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Molecular markers distinguishing T Cell subtypes with TSDR strand-bias methylation
title Molecular markers distinguishing T Cell subtypes with TSDR strand-bias methylation
spellingShingle Molecular markers distinguishing T Cell subtypes with TSDR strand-bias methylation
Minskaia, Ekaterina
Strand-bias methylation
CAMTA
FOXP3
FUT7
Epigenetics
Regulatory T lymphocytes
title_short Molecular markers distinguishing T Cell subtypes with TSDR strand-bias methylation
title_full Molecular markers distinguishing T Cell subtypes with TSDR strand-bias methylation
title_fullStr Molecular markers distinguishing T Cell subtypes with TSDR strand-bias methylation
title_full_unstemmed Molecular markers distinguishing T Cell subtypes with TSDR strand-bias methylation
title_sort Molecular markers distinguishing T Cell subtypes with TSDR strand-bias methylation
author Minskaia, Ekaterina
author_facet Minskaia, Ekaterina
Saraiva, Bárbara C.
Soares, Maria Vieira
Azevedo, Rita I.
Ribeiro, Ruy M.
Kumar, Saumya
Vieira, Ana I. S.
Lacerda, João
author_role author
author2 Saraiva, Bárbara C.
Soares, Maria Vieira
Azevedo, Rita I.
Ribeiro, Ruy M.
Kumar, Saumya
Vieira, Ana I. S.
Lacerda, João
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório da Universidade de Lisboa
dc.contributor.author.fl_str_mv Minskaia, Ekaterina
Saraiva, Bárbara C.
Soares, Maria Vieira
Azevedo, Rita I.
Ribeiro, Ruy M.
Kumar, Saumya
Vieira, Ana I. S.
Lacerda, João
dc.subject.por.fl_str_mv Strand-bias methylation
CAMTA
FOXP3
FUT7
Epigenetics
Regulatory T lymphocytes
topic Strand-bias methylation
CAMTA
FOXP3
FUT7
Epigenetics
Regulatory T lymphocytes
description Copyright © 2018 Minskaia, Saraiva, Soares, Azevedo, Ribeiro, Kumar, Vieira and Lacerda. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
publishDate 2018
dc.date.none.fl_str_mv 2018
2018-01-01T00:00:00Z
2020-12-02T13:59:54Z
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://hdl.handle.net/10451/45068
url http://hdl.handle.net/10451/45068
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Front Immunol. 2018 Nov 5; 9: 2540.
10.3389/fimmu.2018.02540
1664-3224
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Frontiers
publisher.none.fl_str_mv Frontiers
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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