Effects of fetal calf serum on cGMP pathway and oocyte lipid metabolism in vitro

Detalhes bibliográficos
Autor(a) principal: Schwarz, Katia R. L.
Data de Publicação: 2017
Outros Autores: Botigelli, Ramon Cesar [UNESP], Del Collado, Maite, Castro, Fernanda Cavallari de, Fernandes, Hugo, Paschoal, Daniela M., Verde Leal, Claudia Lima
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1071/RD15512
http://hdl.handle.net/11449/159624
Resumo: Intracellular levels of cyclic nucleotides, such as cGMP, are involved in the regulation of adipocyte lipolysis. Cumulus-oocyte complexes (COCs) express enzymes that both synthesise (guanylate cyclase) and degrade (phosphodiesterase (PDE) 5A) cGMP. Because serum interferes with lipid metabolism, its effects on the cGMP pathway and lipid content in bovine COCs were examined. COCs were matured in medium containing fetal calf serum (FCS; 2% or 10%) or 0.4% bovine serum albumin (BSA; control). At both 2% and 10%, FCS decreased cGMP levels in COCs compared with BSA (0.64 and 1.04 vs 9.46 fmol per COC respectively; P < 0.05) and decreased transcript levels of guanylate cyclase 1, soluble, beta 3 (GUCY1B3), whereas PDE5A levels were increased. FCS also affected the expression of genes related to lipolysis, increasing relative expression of perilipin 2 (PLIN2) and carnitine palmitoyltransferase 1B (CPT1B) in cumulus cells. Effects of FCS and cGMP on the lipid content of oocytes and embryos were evaluated by Nile red staining. COCs were matured with 10% FCS, FCS + 10(-5) M sildenafil (SDF), a PDE5 inhibitor, or 0.4% BSA. The lipid content was increased in oocytes matured in FCS compared with BSA (fluorescence intensity 20.1 vs 17.61 respectively; P < 0.05), whereas the lipid content in oocytes matured in FCS+SDF (fluorescence intensity 16.33) was similar to that in the BSA-treated group (P > 0.05). In addition, lipid content was higher in embryos from oocytes matured with FCS than BSA (fluorescence intensity 31.12 vs 22.31 respectively; P < 0.05), but was increased even further in the FCS+SDF-treated group (fluorescence intensity 40.35; P < 0.05), possibly due to a compensatory mechanism during embryo culture without SDF for the reduction in lipid content during IVM. The present study provides, for the first time, evidence that the cGMP pathway may be involved in lipid metabolism in bovine COCs and that this pathway is affected by FCS.
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spelling Effects of fetal calf serum on cGMP pathway and oocyte lipid metabolism in vitroblastocystcumulus cellgene expressionin vitro maturationIntracellular levels of cyclic nucleotides, such as cGMP, are involved in the regulation of adipocyte lipolysis. Cumulus-oocyte complexes (COCs) express enzymes that both synthesise (guanylate cyclase) and degrade (phosphodiesterase (PDE) 5A) cGMP. Because serum interferes with lipid metabolism, its effects on the cGMP pathway and lipid content in bovine COCs were examined. COCs were matured in medium containing fetal calf serum (FCS; 2% or 10%) or 0.4% bovine serum albumin (BSA; control). At both 2% and 10%, FCS decreased cGMP levels in COCs compared with BSA (0.64 and 1.04 vs 9.46 fmol per COC respectively; P < 0.05) and decreased transcript levels of guanylate cyclase 1, soluble, beta 3 (GUCY1B3), whereas PDE5A levels were increased. FCS also affected the expression of genes related to lipolysis, increasing relative expression of perilipin 2 (PLIN2) and carnitine palmitoyltransferase 1B (CPT1B) in cumulus cells. Effects of FCS and cGMP on the lipid content of oocytes and embryos were evaluated by Nile red staining. COCs were matured with 10% FCS, FCS + 10(-5) M sildenafil (SDF), a PDE5 inhibitor, or 0.4% BSA. The lipid content was increased in oocytes matured in FCS compared with BSA (fluorescence intensity 20.1 vs 17.61 respectively; P < 0.05), whereas the lipid content in oocytes matured in FCS+SDF (fluorescence intensity 16.33) was similar to that in the BSA-treated group (P > 0.05). In addition, lipid content was higher in embryos from oocytes matured with FCS than BSA (fluorescence intensity 31.12 vs 22.31 respectively; P < 0.05), but was increased even further in the FCS+SDF-treated group (fluorescence intensity 40.35; P < 0.05), possibly due to a compensatory mechanism during embryo culture without SDF for the reduction in lipid content during IVM. The present study provides, for the first time, evidence that the cGMP pathway may be involved in lipid metabolism in bovine COCs and that this pathway is affected by FCS.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Univ Sao Paulo, Fac Zootecnia & Engn Alimentos, Dept Med Vet, Av Duque Caxias Norte 225, BR-13635900 Pirassununga, SP, BrazilUniv Estadual Paulista, Inst Biociencias Botucatu, Road Domingos Sartori 21500, BR-18618689 Botucatu, SP, BrazilUniv Estadual Paulista, Inst Biociencias Botucatu, Road Domingos Sartori 21500, BR-18618689 Botucatu, SP, BrazilFAPESP: 2010/18023-9Csiro PublishingUniversidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Schwarz, Katia R. L.Botigelli, Ramon Cesar [UNESP]Del Collado, MaiteCastro, Fernanda Cavallari deFernandes, HugoPaschoal, Daniela M.Verde Leal, Claudia Lima2018-11-26T15:44:41Z2018-11-26T15:44:41Z2017-07-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1593-1601http://dx.doi.org/10.1071/RD15512Reproduction Fertility And Development. Clayton: Csiro Publishing, v. 29, n. 8, p. 1593-1601, 2017.1031-3613http://hdl.handle.net/11449/15962410.1071/RD15512WOS:000405782100014Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengReproduction Fertility And Development0,681info:eu-repo/semantics/openAccess2021-10-23T15:17:14Zoai:repositorio.unesp.br:11449/159624Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:20:10.137228Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Effects of fetal calf serum on cGMP pathway and oocyte lipid metabolism in vitro
title Effects of fetal calf serum on cGMP pathway and oocyte lipid metabolism in vitro
spellingShingle Effects of fetal calf serum on cGMP pathway and oocyte lipid metabolism in vitro
Schwarz, Katia R. L.
blastocyst
cumulus cell
gene expression
in vitro maturation
title_short Effects of fetal calf serum on cGMP pathway and oocyte lipid metabolism in vitro
title_full Effects of fetal calf serum on cGMP pathway and oocyte lipid metabolism in vitro
title_fullStr Effects of fetal calf serum on cGMP pathway and oocyte lipid metabolism in vitro
title_full_unstemmed Effects of fetal calf serum on cGMP pathway and oocyte lipid metabolism in vitro
title_sort Effects of fetal calf serum on cGMP pathway and oocyte lipid metabolism in vitro
author Schwarz, Katia R. L.
author_facet Schwarz, Katia R. L.
Botigelli, Ramon Cesar [UNESP]
Del Collado, Maite
Castro, Fernanda Cavallari de
Fernandes, Hugo
Paschoal, Daniela M.
Verde Leal, Claudia Lima
author_role author
author2 Botigelli, Ramon Cesar [UNESP]
Del Collado, Maite
Castro, Fernanda Cavallari de
Fernandes, Hugo
Paschoal, Daniela M.
Verde Leal, Claudia Lima
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Schwarz, Katia R. L.
Botigelli, Ramon Cesar [UNESP]
Del Collado, Maite
Castro, Fernanda Cavallari de
Fernandes, Hugo
Paschoal, Daniela M.
Verde Leal, Claudia Lima
dc.subject.por.fl_str_mv blastocyst
cumulus cell
gene expression
in vitro maturation
topic blastocyst
cumulus cell
gene expression
in vitro maturation
description Intracellular levels of cyclic nucleotides, such as cGMP, are involved in the regulation of adipocyte lipolysis. Cumulus-oocyte complexes (COCs) express enzymes that both synthesise (guanylate cyclase) and degrade (phosphodiesterase (PDE) 5A) cGMP. Because serum interferes with lipid metabolism, its effects on the cGMP pathway and lipid content in bovine COCs were examined. COCs were matured in medium containing fetal calf serum (FCS; 2% or 10%) or 0.4% bovine serum albumin (BSA; control). At both 2% and 10%, FCS decreased cGMP levels in COCs compared with BSA (0.64 and 1.04 vs 9.46 fmol per COC respectively; P < 0.05) and decreased transcript levels of guanylate cyclase 1, soluble, beta 3 (GUCY1B3), whereas PDE5A levels were increased. FCS also affected the expression of genes related to lipolysis, increasing relative expression of perilipin 2 (PLIN2) and carnitine palmitoyltransferase 1B (CPT1B) in cumulus cells. Effects of FCS and cGMP on the lipid content of oocytes and embryos were evaluated by Nile red staining. COCs were matured with 10% FCS, FCS + 10(-5) M sildenafil (SDF), a PDE5 inhibitor, or 0.4% BSA. The lipid content was increased in oocytes matured in FCS compared with BSA (fluorescence intensity 20.1 vs 17.61 respectively; P < 0.05), whereas the lipid content in oocytes matured in FCS+SDF (fluorescence intensity 16.33) was similar to that in the BSA-treated group (P > 0.05). In addition, lipid content was higher in embryos from oocytes matured with FCS than BSA (fluorescence intensity 31.12 vs 22.31 respectively; P < 0.05), but was increased even further in the FCS+SDF-treated group (fluorescence intensity 40.35; P < 0.05), possibly due to a compensatory mechanism during embryo culture without SDF for the reduction in lipid content during IVM. The present study provides, for the first time, evidence that the cGMP pathway may be involved in lipid metabolism in bovine COCs and that this pathway is affected by FCS.
publishDate 2017
dc.date.none.fl_str_mv 2017-07-01
2018-11-26T15:44:41Z
2018-11-26T15:44:41Z
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/10.1071/RD15512
Reproduction Fertility And Development. Clayton: Csiro Publishing, v. 29, n. 8, p. 1593-1601, 2017.
1031-3613
http://hdl.handle.net/11449/159624
10.1071/RD15512
WOS:000405782100014
url http://dx.doi.org/10.1071/RD15512
http://hdl.handle.net/11449/159624
identifier_str_mv Reproduction Fertility And Development. Clayton: Csiro Publishing, v. 29, n. 8, p. 1593-1601, 2017.
1031-3613
10.1071/RD15512
WOS:000405782100014
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Reproduction Fertility And Development
0,681
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1593-1601
dc.publisher.none.fl_str_mv Csiro Publishing
publisher.none.fl_str_mv Csiro Publishing
dc.source.none.fl_str_mv Web of Science
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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