Astrocyte-specific deletion of peroxisome-proliferator activated receptor-gamma (PPARγ) impairs glucose metabolism and estrous cycling in female mice.

Autores
Fernandez, Marina Olga; Hsueh, Katherine; Park, Hyun Tae; Sauceda, Consuelo; Hwang, Vicky; Kumar, Deepak; Kim, Sun; Rickert, Emily; Mahata, Sumana; Webster, Nicholas J. G.
Año de publicación
2017
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Mice lacking PPARγ in neurons do not become leptin resistant when placed on a high-fat diet (HFD). In males, this results in a decrease in food intake and an increase in energy expenditure causing reduced body weight, but this difference in body weight is not observed in female mice. In addition, estrous cycles are disturbed and the ovaries present with hemorrhagic follicles. We observed that PPARγ is more highly expressed in astrocytes than neurons, so we created an inducible, conditional knockout of PPARγ in astrocytes (AKO). The AKO mice showed impaired glucose tolerance and hepatic steatosis that did not worsen with HFD. Expression of gluconeogenic genes was elevated in the livers, as was expression of a number of genes involved in lipogenesis, lipid transport and storage. The AKO mice also showed a reproductive phenotype with reduced numbers of estrous cycles, elevated plasma testosterone, reduced corpora lutea formation, and alterations in hypothalamic and ovarian gene expression. Thus the phenotypes of the astrocyte knockout are very different from those seen in the neuronal knockout suggesting distinct roles for PPARγ in these two cell types.
Fil: Fernandez, Marina Olga. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina. University of California at San Diego; Estados Unidos
Fil: Hsueh, Katherine. University of California at San Diego; Estados Unidos
Fil: Park, Hyun Tae. University of California at San Diego; Estados Unidos. korea University Anam Hospital; Corea del Sur
Fil: Sauceda, Consuelo. University of California at San Diego; Estados Unidos
Fil: Hwang, Vicky. University of California at San Diego; Estados Unidos
Fil: Kumar, Deepak. University of California at San Diego; Estados Unidos
Fil: Kim, Sun. University of California at San Diego; Estados Unidos
Fil: Rickert, Emily. University of California at San Diego; Estados Unidos
Fil: Mahata, Sumana. University of California at San Diego; Estados Unidos
Fil: Webster, Nicholas J. G.. University of California at San Diego; Estados Unidos. VA San Diego Healthcare System; Estados Unidos
Materia
Astrocytes
Fertility
Glucose Intolerance
Obesity
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/36267

id CONICETDig_e5acce7aa494c15321644affdf9685f0
oai_identifier_str oai:ri.conicet.gov.ar:11336/36267
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Astrocyte-specific deletion of peroxisome-proliferator activated receptor-gamma (PPARγ) impairs glucose metabolism and estrous cycling in female mice.Fernandez, Marina OlgaHsueh, KatherinePark, Hyun TaeSauceda, ConsueloHwang, VickyKumar, DeepakKim, SunRickert, EmilyMahata, SumanaWebster, Nicholas J. G.AstrocytesFertilityGlucose IntoleranceObesityhttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3Mice lacking PPARγ in neurons do not become leptin resistant when placed on a high-fat diet (HFD). In males, this results in a decrease in food intake and an increase in energy expenditure causing reduced body weight, but this difference in body weight is not observed in female mice. In addition, estrous cycles are disturbed and the ovaries present with hemorrhagic follicles. We observed that PPARγ is more highly expressed in astrocytes than neurons, so we created an inducible, conditional knockout of PPARγ in astrocytes (AKO). The AKO mice showed impaired glucose tolerance and hepatic steatosis that did not worsen with HFD. Expression of gluconeogenic genes was elevated in the livers, as was expression of a number of genes involved in lipogenesis, lipid transport and storage. The AKO mice also showed a reproductive phenotype with reduced numbers of estrous cycles, elevated plasma testosterone, reduced corpora lutea formation, and alterations in hypothalamic and ovarian gene expression. Thus the phenotypes of the astrocyte knockout are very different from those seen in the neuronal knockout suggesting distinct roles for PPARγ in these two cell types.Fil: Fernandez, Marina Olga. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina. University of California at San Diego; Estados UnidosFil: Hsueh, Katherine. University of California at San Diego; Estados UnidosFil: Park, Hyun Tae. University of California at San Diego; Estados Unidos. korea University Anam Hospital; Corea del SurFil: Sauceda, Consuelo. University of California at San Diego; Estados UnidosFil: Hwang, Vicky. University of California at San Diego; Estados UnidosFil: Kumar, Deepak. University of California at San Diego; Estados UnidosFil: Kim, Sun. University of California at San Diego; Estados UnidosFil: Rickert, Emily. University of California at San Diego; Estados UnidosFil: Mahata, Sumana. University of California at San Diego; Estados UnidosFil: Webster, Nicholas J. G.. University of California at San Diego; Estados Unidos. VA San Diego Healthcare System; Estados UnidosEndocrine Society2017-09-27info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/36267Fernandez, Marina Olga; Hsueh, Katherine; Park, Hyun Tae; Sauceda, Consuelo; Hwang, Vicky; et al.; Astrocyte-specific deletion of peroxisome-proliferator activated receptor-gamma (PPARγ) impairs glucose metabolism and estrous cycling in female mice.; Endocrine Society; The Journal of the Endocrine Society; 1; 11; 27-9-2017; 1332-13502472-19722472-1972CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://academic.oup.com/jes/article/doi/10.1210/js.2017-00242/4201666/Astrocytespecific-deletion-ofinfo:eu-repo/semantics/altIdentifier/doi/10.1210/js.2017-00242info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:09:53Zoai:ri.conicet.gov.ar:11336/36267instacron: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 10:09:54.193CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Astrocyte-specific deletion of peroxisome-proliferator activated receptor-gamma (PPARγ) impairs glucose metabolism and estrous cycling in female mice.
title Astrocyte-specific deletion of peroxisome-proliferator activated receptor-gamma (PPARγ) impairs glucose metabolism and estrous cycling in female mice.
spellingShingle Astrocyte-specific deletion of peroxisome-proliferator activated receptor-gamma (PPARγ) impairs glucose metabolism and estrous cycling in female mice.
Fernandez, Marina Olga
Astrocytes
Fertility
Glucose Intolerance
Obesity
title_short Astrocyte-specific deletion of peroxisome-proliferator activated receptor-gamma (PPARγ) impairs glucose metabolism and estrous cycling in female mice.
title_full Astrocyte-specific deletion of peroxisome-proliferator activated receptor-gamma (PPARγ) impairs glucose metabolism and estrous cycling in female mice.
title_fullStr Astrocyte-specific deletion of peroxisome-proliferator activated receptor-gamma (PPARγ) impairs glucose metabolism and estrous cycling in female mice.
title_full_unstemmed Astrocyte-specific deletion of peroxisome-proliferator activated receptor-gamma (PPARγ) impairs glucose metabolism and estrous cycling in female mice.
title_sort Astrocyte-specific deletion of peroxisome-proliferator activated receptor-gamma (PPARγ) impairs glucose metabolism and estrous cycling in female mice.
dc.creator.none.fl_str_mv Fernandez, Marina Olga
Hsueh, Katherine
Park, Hyun Tae
Sauceda, Consuelo
Hwang, Vicky
Kumar, Deepak
Kim, Sun
Rickert, Emily
Mahata, Sumana
Webster, Nicholas J. G.
author Fernandez, Marina Olga
author_facet Fernandez, Marina Olga
Hsueh, Katherine
Park, Hyun Tae
Sauceda, Consuelo
Hwang, Vicky
Kumar, Deepak
Kim, Sun
Rickert, Emily
Mahata, Sumana
Webster, Nicholas J. G.
author_role author
author2 Hsueh, Katherine
Park, Hyun Tae
Sauceda, Consuelo
Hwang, Vicky
Kumar, Deepak
Kim, Sun
Rickert, Emily
Mahata, Sumana
Webster, Nicholas J. G.
author2_role author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Astrocytes
Fertility
Glucose Intolerance
Obesity
topic Astrocytes
Fertility
Glucose Intolerance
Obesity
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.1
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv Mice lacking PPARγ in neurons do not become leptin resistant when placed on a high-fat diet (HFD). In males, this results in a decrease in food intake and an increase in energy expenditure causing reduced body weight, but this difference in body weight is not observed in female mice. In addition, estrous cycles are disturbed and the ovaries present with hemorrhagic follicles. We observed that PPARγ is more highly expressed in astrocytes than neurons, so we created an inducible, conditional knockout of PPARγ in astrocytes (AKO). The AKO mice showed impaired glucose tolerance and hepatic steatosis that did not worsen with HFD. Expression of gluconeogenic genes was elevated in the livers, as was expression of a number of genes involved in lipogenesis, lipid transport and storage. The AKO mice also showed a reproductive phenotype with reduced numbers of estrous cycles, elevated plasma testosterone, reduced corpora lutea formation, and alterations in hypothalamic and ovarian gene expression. Thus the phenotypes of the astrocyte knockout are very different from those seen in the neuronal knockout suggesting distinct roles for PPARγ in these two cell types.
Fil: Fernandez, Marina Olga. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina. University of California at San Diego; Estados Unidos
Fil: Hsueh, Katherine. University of California at San Diego; Estados Unidos
Fil: Park, Hyun Tae. University of California at San Diego; Estados Unidos. korea University Anam Hospital; Corea del Sur
Fil: Sauceda, Consuelo. University of California at San Diego; Estados Unidos
Fil: Hwang, Vicky. University of California at San Diego; Estados Unidos
Fil: Kumar, Deepak. University of California at San Diego; Estados Unidos
Fil: Kim, Sun. University of California at San Diego; Estados Unidos
Fil: Rickert, Emily. University of California at San Diego; Estados Unidos
Fil: Mahata, Sumana. University of California at San Diego; Estados Unidos
Fil: Webster, Nicholas J. G.. University of California at San Diego; Estados Unidos. VA San Diego Healthcare System; Estados Unidos
description Mice lacking PPARγ in neurons do not become leptin resistant when placed on a high-fat diet (HFD). In males, this results in a decrease in food intake and an increase in energy expenditure causing reduced body weight, but this difference in body weight is not observed in female mice. In addition, estrous cycles are disturbed and the ovaries present with hemorrhagic follicles. We observed that PPARγ is more highly expressed in astrocytes than neurons, so we created an inducible, conditional knockout of PPARγ in astrocytes (AKO). The AKO mice showed impaired glucose tolerance and hepatic steatosis that did not worsen with HFD. Expression of gluconeogenic genes was elevated in the livers, as was expression of a number of genes involved in lipogenesis, lipid transport and storage. The AKO mice also showed a reproductive phenotype with reduced numbers of estrous cycles, elevated plasma testosterone, reduced corpora lutea formation, and alterations in hypothalamic and ovarian gene expression. Thus the phenotypes of the astrocyte knockout are very different from those seen in the neuronal knockout suggesting distinct roles for PPARγ in these two cell types.
publishDate 2017
dc.date.none.fl_str_mv 2017-09-27
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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://hdl.handle.net/11336/36267
Fernandez, Marina Olga; Hsueh, Katherine; Park, Hyun Tae; Sauceda, Consuelo; Hwang, Vicky; et al.; Astrocyte-specific deletion of peroxisome-proliferator activated receptor-gamma (PPARγ) impairs glucose metabolism and estrous cycling in female mice.; Endocrine Society; The Journal of the Endocrine Society; 1; 11; 27-9-2017; 1332-1350
2472-1972
2472-1972
CONICET Digital
CONICET
url http://hdl.handle.net/11336/36267
identifier_str_mv Fernandez, Marina Olga; Hsueh, Katherine; Park, Hyun Tae; Sauceda, Consuelo; Hwang, Vicky; et al.; Astrocyte-specific deletion of peroxisome-proliferator activated receptor-gamma (PPARγ) impairs glucose metabolism and estrous cycling in female mice.; Endocrine Society; The Journal of the Endocrine Society; 1; 11; 27-9-2017; 1332-1350
2472-1972
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://academic.oup.com/jes/article/doi/10.1210/js.2017-00242/4201666/Astrocytespecific-deletion-of
info:eu-repo/semantics/altIdentifier/doi/10.1210/js.2017-00242
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Endocrine Society
publisher.none.fl_str_mv Endocrine Society
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
_version_ 1842270098494062592
score 13.13397