Effects of fetal calf serum on cGMP pathway and oocyte lipid metabolism in vitro
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , |
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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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 |
|
_version_ |
1808128348879060992 |