Transforming growth factor-beta family members are regulated during induced luteolysis in cattle

Detalhes bibliográficos
Autor(a) principal: Haas, Cristina Sangoi
Data de Publicação: 2019
Outros Autores: Rovani, Monique Tomazele, Ilha, Gustavo Freitas, Bertolin, Kalyne, Ferst, Juliana Germano, Bridi, Alessandra, Bordignon, Vilceu, Duggavathi, Raj, Antoniazzi, Alfredo Quites, Goncalves, Paulo Bayard Dias, Gasperin, Bernardo Garziera
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/224311
Resumo: The transforming growth factors beta (TGFβ) are local factors produced by ovarian cells which, after binding to their receptors, regulate follicular deviation and ovulation. However, their regulation and function during corpus luteum (CL) regression has been poorly investigated. The present study evaluated the mRNA regulation of some TGFβ family ligands and their receptors in the bovine CL during induced luteolysis in vivo. On day 10 of the estrous cycle, cows received an injection of prostaglandin F2α (PGF) and luteal samples were obtained from separate groups of cows (n= 4-5 cows per time-point) at 0, 2, 12, 24 or 48 h after treatment. Since TGF beta family comprises more than 30 ligands, we focused in some candidates genes such as activin receptors (ACVR-1A, -1B, -2A, -2B) AMH, AMHR2, BMPs (BMP-1, -2, -3, -4, -6 and -7), BMP receptors (BMPR 1A, -1B and -2), inhibin subunits (INH-A, -BA, -BB) and betaglycan (TGFBR3). The mRNA levels of BMP4, BMP6 and INHBA were higher at 2 h after PGF administration (P<0.05) in comparison to 0 h. The relative mRNA abundance of BMP1, BMP2, BMP3, BMP4, BMP6, ACVR1B, INHBA and INHBB was upregulated up to 12 h post PGF (P<0.05). On the other hand, TGFBR3 mRNA that codes for a reservoir of ligands that bind to TGF-beta receptors, was lower at 48 h. In conclusion, findings from this study demonstrated that genes encoding several TGFβ family members are expressed in a time-specific manner after PGF administration.
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spelling Haas, Cristina SangoiRovani, Monique TomazeleIlha, Gustavo FreitasBertolin, KalyneFerst, Juliana GermanoBridi, AlessandraBordignon, VilceuDuggavathi, RajAntoniazzi, Alfredo QuitesGoncalves, Paulo Bayard DiasGasperin, Bernardo Garziera2021-07-21T04:24:42Z20191806-9614http://hdl.handle.net/10183/224311001127449The transforming growth factors beta (TGFβ) are local factors produced by ovarian cells which, after binding to their receptors, regulate follicular deviation and ovulation. However, their regulation and function during corpus luteum (CL) regression has been poorly investigated. The present study evaluated the mRNA regulation of some TGFβ family ligands and their receptors in the bovine CL during induced luteolysis in vivo. On day 10 of the estrous cycle, cows received an injection of prostaglandin F2α (PGF) and luteal samples were obtained from separate groups of cows (n= 4-5 cows per time-point) at 0, 2, 12, 24 or 48 h after treatment. Since TGF beta family comprises more than 30 ligands, we focused in some candidates genes such as activin receptors (ACVR-1A, -1B, -2A, -2B) AMH, AMHR2, BMPs (BMP-1, -2, -3, -4, -6 and -7), BMP receptors (BMPR 1A, -1B and -2), inhibin subunits (INH-A, -BA, -BB) and betaglycan (TGFBR3). The mRNA levels of BMP4, BMP6 and INHBA were higher at 2 h after PGF administration (P<0.05) in comparison to 0 h. The relative mRNA abundance of BMP1, BMP2, BMP3, BMP4, BMP6, ACVR1B, INHBA and INHBB was upregulated up to 12 h post PGF (P<0.05). On the other hand, TGFBR3 mRNA that codes for a reservoir of ligands that bind to TGF-beta receptors, was lower at 48 h. In conclusion, findings from this study demonstrated that genes encoding several TGFβ family members are expressed in a time-specific manner after PGF administration.application/pdfengAnimal reproduction. Belo Horizonte. Vol. 16, n. 4 (2019), p. 829-837Fator de crescimento transformador BetaReceptores de fatores de crescimento transformadores betaCorpo lúteoLuteóliseBovinosCorpus luteumLuteolysisCattleTransforming growth factor-beta family members are regulated during induced luteolysis in cattleinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001127449.pdf.txt001127449.pdf.txtExtracted Texttext/plain40378http://www.lume.ufrgs.br/bitstream/10183/224311/2/001127449.pdf.txtec2b80c4bc1aabe5f6d04f81a5ede170MD52ORIGINAL001127449.pdfTexto completo (inglês)application/pdf4983180http://www.lume.ufrgs.br/bitstream/10183/224311/1/001127449.pdf0980394b5550b6bd2f5a957a7095ac12MD5110183/2243112021-08-18 04:50:51.145568oai:www.lume.ufrgs.br:10183/224311Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2021-08-18T07:50:51Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Transforming growth factor-beta family members are regulated during induced luteolysis in cattle
title Transforming growth factor-beta family members are regulated during induced luteolysis in cattle
spellingShingle Transforming growth factor-beta family members are regulated during induced luteolysis in cattle
Haas, Cristina Sangoi
Fator de crescimento transformador Beta
Receptores de fatores de crescimento transformadores beta
Corpo lúteo
Luteólise
Bovinos
Corpus luteum
Luteolysis
Cattle
title_short Transforming growth factor-beta family members are regulated during induced luteolysis in cattle
title_full Transforming growth factor-beta family members are regulated during induced luteolysis in cattle
title_fullStr Transforming growth factor-beta family members are regulated during induced luteolysis in cattle
title_full_unstemmed Transforming growth factor-beta family members are regulated during induced luteolysis in cattle
title_sort Transforming growth factor-beta family members are regulated during induced luteolysis in cattle
author Haas, Cristina Sangoi
author_facet Haas, Cristina Sangoi
Rovani, Monique Tomazele
Ilha, Gustavo Freitas
Bertolin, Kalyne
Ferst, Juliana Germano
Bridi, Alessandra
Bordignon, Vilceu
Duggavathi, Raj
Antoniazzi, Alfredo Quites
Goncalves, Paulo Bayard Dias
Gasperin, Bernardo Garziera
author_role author
author2 Rovani, Monique Tomazele
Ilha, Gustavo Freitas
Bertolin, Kalyne
Ferst, Juliana Germano
Bridi, Alessandra
Bordignon, Vilceu
Duggavathi, Raj
Antoniazzi, Alfredo Quites
Goncalves, Paulo Bayard Dias
Gasperin, Bernardo Garziera
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Haas, Cristina Sangoi
Rovani, Monique Tomazele
Ilha, Gustavo Freitas
Bertolin, Kalyne
Ferst, Juliana Germano
Bridi, Alessandra
Bordignon, Vilceu
Duggavathi, Raj
Antoniazzi, Alfredo Quites
Goncalves, Paulo Bayard Dias
Gasperin, Bernardo Garziera
dc.subject.por.fl_str_mv Fator de crescimento transformador Beta
Receptores de fatores de crescimento transformadores beta
Corpo lúteo
Luteólise
Bovinos
topic Fator de crescimento transformador Beta
Receptores de fatores de crescimento transformadores beta
Corpo lúteo
Luteólise
Bovinos
Corpus luteum
Luteolysis
Cattle
dc.subject.eng.fl_str_mv Corpus luteum
Luteolysis
Cattle
description The transforming growth factors beta (TGFβ) are local factors produced by ovarian cells which, after binding to their receptors, regulate follicular deviation and ovulation. However, their regulation and function during corpus luteum (CL) regression has been poorly investigated. The present study evaluated the mRNA regulation of some TGFβ family ligands and their receptors in the bovine CL during induced luteolysis in vivo. On day 10 of the estrous cycle, cows received an injection of prostaglandin F2α (PGF) and luteal samples were obtained from separate groups of cows (n= 4-5 cows per time-point) at 0, 2, 12, 24 or 48 h after treatment. Since TGF beta family comprises more than 30 ligands, we focused in some candidates genes such as activin receptors (ACVR-1A, -1B, -2A, -2B) AMH, AMHR2, BMPs (BMP-1, -2, -3, -4, -6 and -7), BMP receptors (BMPR 1A, -1B and -2), inhibin subunits (INH-A, -BA, -BB) and betaglycan (TGFBR3). The mRNA levels of BMP4, BMP6 and INHBA were higher at 2 h after PGF administration (P<0.05) in comparison to 0 h. The relative mRNA abundance of BMP1, BMP2, BMP3, BMP4, BMP6, ACVR1B, INHBA and INHBB was upregulated up to 12 h post PGF (P<0.05). On the other hand, TGFBR3 mRNA that codes for a reservoir of ligands that bind to TGF-beta receptors, was lower at 48 h. In conclusion, findings from this study demonstrated that genes encoding several TGFβ family members are expressed in a time-specific manner after PGF administration.
publishDate 2019
dc.date.issued.fl_str_mv 2019
dc.date.accessioned.fl_str_mv 2021-07-21T04:24:42Z
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/224311
dc.identifier.issn.pt_BR.fl_str_mv 1806-9614
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url http://hdl.handle.net/10183/224311
dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Animal reproduction. Belo Horizonte. Vol. 16, n. 4 (2019), p. 829-837
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