A metabolic circadian clock controls rhythms in immortalized human glioblastoma T98G cells
- Autores
- Wagner, Paula Micaela; Sosa Alderete, Lucas Gastón; Gorne, Lucas Damián; Gaveglio, Virginia Lucía; Salvador, Gabriela Alejandra; Pasquaré, Susana Juana; Guido, Mario Eduardo
- Año de publicación
- 2016
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- Rat spermatogenic cell membranes contain sphingolipids with nonhydroxy and 2-hydroxy very long chain (C24-32) PUFA. The biosynthesis of such fatty acids requires the expression of very long chain fatty acid elongases (Elovl4 for > C24) and a fatty acid 2- hydroxylase (Fa2h). In this study, mRNA levels of Elovl4and Fa2h were measured by qPCR in rat testis at different postnatal ages and in cells isolated from the seminiferous epithelium of adults. At early prepuberal ages (P14), Elovl4 was highly expressed while Fa2h mRNA was absent. Fa2h started to be detected at P25-30 and increased thereafter, while Elovl4mRNA levels decreased. The expression of both genes, but mainly Fa2h, was markedly reduced in adult testes that had been depleted of germ cells by mild hyperthermia. In isolated spermatogenic cells, both genes were expressed at lower levels in pachytene spermatocytes than in post meiotic round and late spermatids. Interestingly, Sertoli cells had high Elovl4but lacked Fa2h mRNA. The Elovl4 protein was detected in spermatocytes from P21 to adulthood, when the protein was clearly observed in elongated spermatids. The Elovl4 enzyme was functional in germ cells, as these cells, in culture, were able to elongate [3H]20:4 to PUFA longer than C24. Our results underscore the presence of a well-timed, cell-specific regulation of Elovl4 and Fa2h in germ cells as differentiation proceeds.
Fil: Wagner, Paula Micaela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; Argentina
Fil: Sosa Alderete, Lucas Gastón. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; Argentina
Fil: Gorne, Lucas Damián. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; Argentina
Fil: Gaveglio, Virginia Lucía. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina
Fil: Salvador, Gabriela Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina
Fil: Pasquaré, Susana Juana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina
Fil: Guido, Mario Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; Argentina
52 th Annual Meeting Argentine Society for Biochemistry and Molecular Biology
Córdoba
Argentina
Universidad Nacional de Córdoba - Materia
-
GLIOBLASTOMA
CIRCADIAN CLOCK
LIPIDS
PHOSPHOLIPIDS - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/156379
Ver los metadatos del registro completo
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A metabolic circadian clock controls rhythms in immortalized human glioblastoma T98G cellsWagner, Paula MicaelaSosa Alderete, Lucas GastónGorne, Lucas DamiánGaveglio, Virginia LucíaSalvador, Gabriela AlejandraPasquaré, Susana JuanaGuido, Mario EduardoGLIOBLASTOMACIRCADIAN CLOCKLIPIDSPHOSPHOLIPIDShttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Rat spermatogenic cell membranes contain sphingolipids with nonhydroxy and 2-hydroxy very long chain (C24-32) PUFA. The biosynthesis of such fatty acids requires the expression of very long chain fatty acid elongases (Elovl4 for > C24) and a fatty acid 2- hydroxylase (Fa2h). In this study, mRNA levels of Elovl4and Fa2h were measured by qPCR in rat testis at different postnatal ages and in cells isolated from the seminiferous epithelium of adults. At early prepuberal ages (P14), Elovl4 was highly expressed while Fa2h mRNA was absent. Fa2h started to be detected at P25-30 and increased thereafter, while Elovl4mRNA levels decreased. The expression of both genes, but mainly Fa2h, was markedly reduced in adult testes that had been depleted of germ cells by mild hyperthermia. In isolated spermatogenic cells, both genes were expressed at lower levels in pachytene spermatocytes than in post meiotic round and late spermatids. Interestingly, Sertoli cells had high Elovl4but lacked Fa2h mRNA. The Elovl4 protein was detected in spermatocytes from P21 to adulthood, when the protein was clearly observed in elongated spermatids. The Elovl4 enzyme was functional in germ cells, as these cells, in culture, were able to elongate [3H]20:4 to PUFA longer than C24. Our results underscore the presence of a well-timed, cell-specific regulation of Elovl4 and Fa2h in germ cells as differentiation proceeds.Fil: Wagner, Paula Micaela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; ArgentinaFil: Sosa Alderete, Lucas Gastón. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; ArgentinaFil: Gorne, Lucas Damián. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; ArgentinaFil: Gaveglio, Virginia Lucía. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; ArgentinaFil: Salvador, Gabriela Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; ArgentinaFil: Pasquaré, Susana Juana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; ArgentinaFil: Guido, Mario Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; Argentina52 th Annual Meeting Argentine Society for Biochemistry and Molecular BiologyCórdobaArgentinaUniversidad Nacional de CórdobaTech Science Press2016info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectReuniónJournalhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/156379A metabolic circadian clock controls rhythms in immortalized human glioblastoma T98G cells; 52 th Annual Meeting Argentine Society for Biochemistry and Molecular Biology; Córdoba; Argentina; 2016; 37-371667-5746CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://www.saib.org.ar/index.php?q=node/562info:eu-repo/semantics/altIdentifier/url/http://www.saib.org.ar/sites/default/files/BIOCELL-SAIB-2016.pdfNacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:56:18Zoai:ri.conicet.gov.ar:11336/156379instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:56:19.002CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
A metabolic circadian clock controls rhythms in immortalized human glioblastoma T98G cells |
title |
A metabolic circadian clock controls rhythms in immortalized human glioblastoma T98G cells |
spellingShingle |
A metabolic circadian clock controls rhythms in immortalized human glioblastoma T98G cells Wagner, Paula Micaela GLIOBLASTOMA CIRCADIAN CLOCK LIPIDS PHOSPHOLIPIDS |
title_short |
A metabolic circadian clock controls rhythms in immortalized human glioblastoma T98G cells |
title_full |
A metabolic circadian clock controls rhythms in immortalized human glioblastoma T98G cells |
title_fullStr |
A metabolic circadian clock controls rhythms in immortalized human glioblastoma T98G cells |
title_full_unstemmed |
A metabolic circadian clock controls rhythms in immortalized human glioblastoma T98G cells |
title_sort |
A metabolic circadian clock controls rhythms in immortalized human glioblastoma T98G cells |
dc.creator.none.fl_str_mv |
Wagner, Paula Micaela Sosa Alderete, Lucas Gastón Gorne, Lucas Damián Gaveglio, Virginia Lucía Salvador, Gabriela Alejandra Pasquaré, Susana Juana Guido, Mario Eduardo |
author |
Wagner, Paula Micaela |
author_facet |
Wagner, Paula Micaela Sosa Alderete, Lucas Gastón Gorne, Lucas Damián Gaveglio, Virginia Lucía Salvador, Gabriela Alejandra Pasquaré, Susana Juana Guido, Mario Eduardo |
author_role |
author |
author2 |
Sosa Alderete, Lucas Gastón Gorne, Lucas Damián Gaveglio, Virginia Lucía Salvador, Gabriela Alejandra Pasquaré, Susana Juana Guido, Mario Eduardo |
author2_role |
author author author author author author |
dc.subject.none.fl_str_mv |
GLIOBLASTOMA CIRCADIAN CLOCK LIPIDS PHOSPHOLIPIDS |
topic |
GLIOBLASTOMA CIRCADIAN CLOCK LIPIDS PHOSPHOLIPIDS |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Rat spermatogenic cell membranes contain sphingolipids with nonhydroxy and 2-hydroxy very long chain (C24-32) PUFA. The biosynthesis of such fatty acids requires the expression of very long chain fatty acid elongases (Elovl4 for > C24) and a fatty acid 2- hydroxylase (Fa2h). In this study, mRNA levels of Elovl4and Fa2h were measured by qPCR in rat testis at different postnatal ages and in cells isolated from the seminiferous epithelium of adults. At early prepuberal ages (P14), Elovl4 was highly expressed while Fa2h mRNA was absent. Fa2h started to be detected at P25-30 and increased thereafter, while Elovl4mRNA levels decreased. The expression of both genes, but mainly Fa2h, was markedly reduced in adult testes that had been depleted of germ cells by mild hyperthermia. In isolated spermatogenic cells, both genes were expressed at lower levels in pachytene spermatocytes than in post meiotic round and late spermatids. Interestingly, Sertoli cells had high Elovl4but lacked Fa2h mRNA. The Elovl4 protein was detected in spermatocytes from P21 to adulthood, when the protein was clearly observed in elongated spermatids. The Elovl4 enzyme was functional in germ cells, as these cells, in culture, were able to elongate [3H]20:4 to PUFA longer than C24. Our results underscore the presence of a well-timed, cell-specific regulation of Elovl4 and Fa2h in germ cells as differentiation proceeds. Fil: Wagner, Paula Micaela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; Argentina Fil: Sosa Alderete, Lucas Gastón. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; Argentina Fil: Gorne, Lucas Damián. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; Argentina Fil: Gaveglio, Virginia Lucía. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina Fil: Salvador, Gabriela Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina Fil: Pasquaré, Susana Juana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina Fil: Guido, Mario Eduardo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; Argentina 52 th Annual Meeting Argentine Society for Biochemistry and Molecular Biology Córdoba Argentina Universidad Nacional de Córdoba |
description |
Rat spermatogenic cell membranes contain sphingolipids with nonhydroxy and 2-hydroxy very long chain (C24-32) PUFA. The biosynthesis of such fatty acids requires the expression of very long chain fatty acid elongases (Elovl4 for > C24) and a fatty acid 2- hydroxylase (Fa2h). In this study, mRNA levels of Elovl4and Fa2h were measured by qPCR in rat testis at different postnatal ages and in cells isolated from the seminiferous epithelium of adults. At early prepuberal ages (P14), Elovl4 was highly expressed while Fa2h mRNA was absent. Fa2h started to be detected at P25-30 and increased thereafter, while Elovl4mRNA levels decreased. The expression of both genes, but mainly Fa2h, was markedly reduced in adult testes that had been depleted of germ cells by mild hyperthermia. In isolated spermatogenic cells, both genes were expressed at lower levels in pachytene spermatocytes than in post meiotic round and late spermatids. Interestingly, Sertoli cells had high Elovl4but lacked Fa2h mRNA. The Elovl4 protein was detected in spermatocytes from P21 to adulthood, when the protein was clearly observed in elongated spermatids. The Elovl4 enzyme was functional in germ cells, as these cells, in culture, were able to elongate [3H]20:4 to PUFA longer than C24. Our results underscore the presence of a well-timed, cell-specific regulation of Elovl4 and Fa2h in germ cells as differentiation proceeds. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/conferenceObject Reunión Journal http://purl.org/coar/resource_type/c_5794 info:ar-repo/semantics/documentoDeConferencia |
status_str |
publishedVersion |
format |
conferenceObject |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/156379 A metabolic circadian clock controls rhythms in immortalized human glioblastoma T98G cells; 52 th Annual Meeting Argentine Society for Biochemistry and Molecular Biology; Córdoba; Argentina; 2016; 37-37 1667-5746 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/156379 |
identifier_str_mv |
A metabolic circadian clock controls rhythms in immortalized human glioblastoma T98G cells; 52 th Annual Meeting Argentine Society for Biochemistry and Molecular Biology; Córdoba; Argentina; 2016; 37-37 1667-5746 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
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https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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Tech Science Press |
publisher.none.fl_str_mv |
Tech Science Press |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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