<script type="text/javascript">
<!--
document.write('<div id="oa_widget"></div>');
document.write('<script type="text/javascript" src="https://www.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=undefined&type=result"></script>');
-->
</script>Placental PPARγ regulates spatiotemporally diverse genes and a unique metabolic network
Placental PPARγ regulates spatiotemporally diverse genes and a unique metabolic network
The nuclear receptor peroxisome proliferator-activated receptor γ (PPARγ) is essential for placental development. For insights into its functions in the placenta, we screened for PPARγ-regulated genes by integrating expression profiles of Pparg-null and Rxra-null placentas with those of WT and Pparg-null trophoblast stem cells differentiated in the presence or absence of a PPARγ agonist. Intersection of these paradigms identified high-probability PPARγ target genes. A few of these genes were previously reported as PPARγ targets in other tissues, but most are new in the context of either PPARγ or placental biology. Transcriptional profiling demonstrated a widespread role for the coactivator NCOA6/AIB3, but not MED1/PBP, in PPARγ-dependent placental gene expression. Spatial and temporal expression analyses revealed that PPARγ impacts genes in diverse trophoblast lineages and during different stages of differentiation. We further validated the Ldhb gene, which encodes the H isoform of lactate dehydrogenase, as a robust PPARγ target in trophoblasts, and propose a hypothetical model that integrates it with a network of PPARγ-regulated genes into a novel pathway of placental fuel metabolism. These findings offer insights not only into the placental functions of PPARγ, but also into unique, previously unsuspected biosynthetic functions of trophoblasts.
- Baylor College of Medicine United States
- Washington University in St. Louis School of Medicine United States
- University of Mary United States
- Washington State University United States
- University of Pittsburgh United States
Male, Chromatin Immunoprecipitation, PPARγ, L-Lactate Dehydrogenase, Placenta, Stem Cells, Trophoblast, Gene Expression Regulation, Developmental, Mice, Transgenic, Cell Biology, LDHB, Placentation, Trophoblasts, PPAR gamma, Mice, Pregnancy, Animals, Female, Molecular Biology, NCOA6, Metabolic Networks and Pathways, Developmental Biology
Male, Chromatin Immunoprecipitation, PPARγ, L-Lactate Dehydrogenase, Placenta, Stem Cells, Trophoblast, Gene Expression Regulation, Developmental, Mice, Transgenic, Cell Biology, LDHB, Placentation, Trophoblasts, PPAR gamma, Mice, Pregnancy, Animals, Female, Molecular Biology, NCOA6, Metabolic Networks and Pathways, Developmental Biology
199 Research products, page 1 of 20
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
chevron_left - 1
- 2
- 3
- 4
- 5
chevron_right
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).24 popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.Top 10% influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Average impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Top 10%
