<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5</volume><submitter>Rai A</submitter><pubmed_abstract>The peroxisome proliferator-activated receptor gamma (PPARγ), a group of ligand-activated transcriptional factors, is expressed in glial fibrillary acidic protein (GFAP)-immunoreactive astrocytes. Here, we investigated the role of PPARγ in regulating GFAP using a mixture of As, Cd and Pb (metal mixture, MM) that induces apoptosis and aberrant morphology in rat brain astrocytes. We observed a phospho PPARγ (serine 112 (S112)) (p-PPARγ (S112))-mediated downregulation of GFAP in the MM-exposed astrocytes. We validated this using pure PPARγ agonist, troglitazone (TZ). As reported with MM, TZ induced astrocyte damage owing to reduced GFAP. In silico analysis in the non-coding region of GFAP gene revealed two PPARγ response elements (PPREs); inverted repeat 10 and direct repeat 1 sequences. Gel </pubmed_abstract><journal>Cell death &amp; disease</journal><pagination>e1033</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4040704</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>CDK5-induced p-PPARγ(Ser 112) downregulates GFAP via PPREs in developing rat brain: effect of metal mixture and troglitazone in astrocytes.</pubmed_title><pmcid>PMC4040704</pmcid><pubmed_authors>Kushwaha R</pubmed_authors><pubmed_authors>Singh P</pubmed_authors><pubmed_authors>Bandyopadhyay S</pubmed_authors><pubmed_authors>Rai A</pubmed_authors><pubmed_authors>Tripathi S</pubmed_authors><pubmed_authors>Sanyal S</pubmed_authors><pubmed_authors>Srivastava P</pubmed_authors></additional><is_claimable>false</is_claimable><name>CDK5-induced p-PPARγ(Ser 112) downregulates GFAP via PPREs in developing rat brain: effect of metal mixture and troglitazone in astrocytes.</name><description>The peroxisome proliferator-activated receptor gamma (PPARγ), a group of ligand-activated transcriptional factors, is expressed in glial fibrillary acidic protein (GFAP)-immunoreactive astrocytes. Here, we investigated the role of PPARγ in regulating GFAP using a mixture of As, Cd and Pb (metal mixture, MM) that induces apoptosis and aberrant morphology in rat brain astrocytes. We observed a phospho PPARγ (serine 112 (S112)) (p-PPARγ (S112))-mediated downregulation of GFAP in the MM-exposed astrocytes. We validated this using pure PPARγ agonist, troglitazone (TZ). As reported with MM, TZ induced astrocyte damage owing to reduced GFAP. In silico analysis in the non-coding region of GFAP gene revealed two PPARγ response elements (PPREs); inverted repeat 10 and direct repeat 1 sequences. Gel </description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Jan</publication><modification>2026-04-29T10:31:09.35Z</modification><creation>2019-03-27T01:29:16Z</creation></dates><accession>S-EPMC4040704</accession><cross_references><pubmed>24481447</pubmed><doi>10.1038/cddis.2013.514</doi></cross_references></HashMap>