The trophoblast clock controls transport across placenta in mice
- Autores
- Demarez, Cécile; Monteiro de Assis, Leonardo Vinícius; Krohn, Markus; Ramella, Nahuel Alberto; Schwaninger, Markus; Oster, Henrik; Astiz, Mariana
- Año de publicación
- 2021
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- In mammals, 24-h rhythms of physiology and behavior are organized by a body-wide network of clock genes and proteins. Despite the well-known function of the adult circadian system, the roles of maternal, fetal and placental clocks during pregnancy are poorly defined. In the mature mouse placenta, the labyrinth zone (LZ) is of fetal origin and key for selective nutrient and waste exchange. Recently, clock gene expression has been detected in LZ and other fetal tissues; however, there is no evidence of a placental function controlled by the LZ clock. Here, we demonstrate that specifically the trophoblast layer of the LZ harbors an already functional clock by late gestation, able to regulate in a circadian manner the expression and activity of the xenobiotic efflux pump, ATP-binding cassette sub-family B member 1 (ABCB1), likely gating the fetal exposure to drugs from the maternal circulation to certain times of the day. As more than 300 endogenous and exogenous compounds are substrates of ABCB1, our results might have implications in choosing the maternal treatment time when aiming either maximal/minimal drug availability to the fetus/mother.
Instituto de Investigaciones Bioquímicas de La Plata - Materia
-
Medicina
Biología
Circadian clock
Mice
Placenta
Trophoblast
Xenobiotic efflux transporter - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/142264
Ver los metadatos del registro completo
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The trophoblast clock controls transport across placenta in miceDemarez, CécileMonteiro de Assis, Leonardo ViníciusKrohn, MarkusRamella, Nahuel AlbertoSchwaninger, MarkusOster, HenrikAstiz, MarianaMedicinaBiologíaCircadian clockMicePlacentaTrophoblastXenobiotic efflux transporterIn mammals, 24-h rhythms of physiology and behavior are organized by a body-wide network of clock genes and proteins. Despite the well-known function of the adult circadian system, the roles of maternal, fetal and placental clocks during pregnancy are poorly defined. In the mature mouse placenta, the labyrinth zone (LZ) is of fetal origin and key for selective nutrient and waste exchange. Recently, clock gene expression has been detected in LZ and other fetal tissues; however, there is no evidence of a placental function controlled by the LZ clock. Here, we demonstrate that specifically the trophoblast layer of the LZ harbors an already functional clock by late gestation, able to regulate in a circadian manner the expression and activity of the xenobiotic efflux pump, ATP-binding cassette sub-family B member 1 (ABCB1), likely gating the fetal exposure to drugs from the maternal circulation to certain times of the day. As more than 300 endogenous and exogenous compounds are substrates of ABCB1, our results might have implications in choosing the maternal treatment time when aiming either maximal/minimal drug availability to the fetus/mother.Instituto de Investigaciones Bioquímicas de La Plata2021-04info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://sedici.unlp.edu.ar/handle/10915/142264enginfo:eu-repo/semantics/altIdentifier/issn/1477-9129info:eu-repo/semantics/altIdentifier/issn/0950-1991info:eu-repo/semantics/altIdentifier/doi/10.1242/dev.197673info:eu-repo/semantics/altIdentifier/pmid/33913482info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:32:27Zoai:sedici.unlp.edu.ar:10915/142264Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:32:28.19SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
The trophoblast clock controls transport across placenta in mice |
title |
The trophoblast clock controls transport across placenta in mice |
spellingShingle |
The trophoblast clock controls transport across placenta in mice Demarez, Cécile Medicina Biología Circadian clock Mice Placenta Trophoblast Xenobiotic efflux transporter |
title_short |
The trophoblast clock controls transport across placenta in mice |
title_full |
The trophoblast clock controls transport across placenta in mice |
title_fullStr |
The trophoblast clock controls transport across placenta in mice |
title_full_unstemmed |
The trophoblast clock controls transport across placenta in mice |
title_sort |
The trophoblast clock controls transport across placenta in mice |
dc.creator.none.fl_str_mv |
Demarez, Cécile Monteiro de Assis, Leonardo Vinícius Krohn, Markus Ramella, Nahuel Alberto Schwaninger, Markus Oster, Henrik Astiz, Mariana |
author |
Demarez, Cécile |
author_facet |
Demarez, Cécile Monteiro de Assis, Leonardo Vinícius Krohn, Markus Ramella, Nahuel Alberto Schwaninger, Markus Oster, Henrik Astiz, Mariana |
author_role |
author |
author2 |
Monteiro de Assis, Leonardo Vinícius Krohn, Markus Ramella, Nahuel Alberto Schwaninger, Markus Oster, Henrik Astiz, Mariana |
author2_role |
author author author author author author |
dc.subject.none.fl_str_mv |
Medicina Biología Circadian clock Mice Placenta Trophoblast Xenobiotic efflux transporter |
topic |
Medicina Biología Circadian clock Mice Placenta Trophoblast Xenobiotic efflux transporter |
dc.description.none.fl_txt_mv |
In mammals, 24-h rhythms of physiology and behavior are organized by a body-wide network of clock genes and proteins. Despite the well-known function of the adult circadian system, the roles of maternal, fetal and placental clocks during pregnancy are poorly defined. In the mature mouse placenta, the labyrinth zone (LZ) is of fetal origin and key for selective nutrient and waste exchange. Recently, clock gene expression has been detected in LZ and other fetal tissues; however, there is no evidence of a placental function controlled by the LZ clock. Here, we demonstrate that specifically the trophoblast layer of the LZ harbors an already functional clock by late gestation, able to regulate in a circadian manner the expression and activity of the xenobiotic efflux pump, ATP-binding cassette sub-family B member 1 (ABCB1), likely gating the fetal exposure to drugs from the maternal circulation to certain times of the day. As more than 300 endogenous and exogenous compounds are substrates of ABCB1, our results might have implications in choosing the maternal treatment time when aiming either maximal/minimal drug availability to the fetus/mother. Instituto de Investigaciones Bioquímicas de La Plata |
description |
In mammals, 24-h rhythms of physiology and behavior are organized by a body-wide network of clock genes and proteins. Despite the well-known function of the adult circadian system, the roles of maternal, fetal and placental clocks during pregnancy are poorly defined. In the mature mouse placenta, the labyrinth zone (LZ) is of fetal origin and key for selective nutrient and waste exchange. Recently, clock gene expression has been detected in LZ and other fetal tissues; however, there is no evidence of a placental function controlled by the LZ clock. Here, we demonstrate that specifically the trophoblast layer of the LZ harbors an already functional clock by late gestation, able to regulate in a circadian manner the expression and activity of the xenobiotic efflux pump, ATP-binding cassette sub-family B member 1 (ABCB1), likely gating the fetal exposure to drugs from the maternal circulation to certain times of the day. As more than 300 endogenous and exogenous compounds are substrates of ABCB1, our results might have implications in choosing the maternal treatment time when aiming either maximal/minimal drug availability to the fetus/mother. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-04 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://sedici.unlp.edu.ar/handle/10915/142264 |
url |
http://sedici.unlp.edu.ar/handle/10915/142264 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/issn/1477-9129 info:eu-repo/semantics/altIdentifier/issn/0950-1991 info:eu-repo/semantics/altIdentifier/doi/10.1242/dev.197673 info:eu-repo/semantics/altIdentifier/pmid/33913482 |
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info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International (CC BY 4.0) |
eu_rights_str_mv |
openAccess |
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http://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International (CC BY 4.0) |
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application/pdf |
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SEDICI (UNLP) - Universidad Nacional de La Plata |
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