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Astrocyte-Specific Deletion of Peroxisome-Proliferator Activated Receptor-gamma Impairs Glucose Metabolism and Estrous Cycling in Female Mice

Authors
Fernandez, Marina O.Hsueh, KatherinePark, Hyun TaeSauceda, ConsueloHwang, VickyKumar, DeepakKim, SunRickert, EmilyMahata, SumanaWebster, Nicholas J. G.
Issue Date
1-11월-2017
Publisher
ENDOCRINE SOC
Keywords
astrocytes; fertility; glucose intolerance; obesity; PPARgamma
Citation
JOURNAL OF THE ENDOCRINE SOCIETY, v.1, no.11, pp.1332 - 1350
Indexed
SCOPUS
Journal Title
JOURNAL OF THE ENDOCRINE SOCIETY
Volume
1
Number
11
Start Page
1332
End Page
1350
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/81593
DOI
10.1210/js.2017-00242
ISSN
2472-1972
Abstract
Mice lacking peroxisome-proliferator activated receptor-g (PPARg) in neurons do not become leptin resistant when placed on a high-fat diet (HFD). In male mice, this results in decreased food intake and increased 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 PPAR gamma was more highly expressed in astrocytes than neurons, so we created an inducible, conditional knockout of PPAR gamma in astrocytes (AKO). The AKO mice had impaired glucose tolerance and hepatic steatosis that did not worsen with HFD. Expression of gluconeogenic genes was elevated in the mouse livers, as was expression of several genes involved in lipogenesis, lipid transport, and storage. The AKO mice also had a reproductive phenotype with fewer estrous cycles, elevated plasma testosterone levels, reduced corpora lutea formation, and alterations in hypothalamic and ovarian gene expression. Thus, the phenotypes of the AKO mice were very different from those seen in the neuronal knockout mice, suggesting distinct roles for PPAR gamma in these two cell types. Copyright (c) 2017 Endocrine Society
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