<HashMap><database>biostudies-literature</database><scores/><additional><submitter>VandeKopple MJ</submitter><funding>NIDDK NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>27-38</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5567683</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>235(1)</volume><pubmed_abstract>Hypoxia-inducible lipid droplet-associated protein (HILPDA) has been shown to localize to lipid droplets in nutrient-responsive cell types such as hepatocytes and adipocytes. However, its role in the control of whole-body homeostasis is not known. We sought to measure cell-intrinsic and systemic stress responses in a mouse strain harboring whole-body Hilpda deficiency. We generated a genetically engineered mouse model of whole-body HILPDA deficiency by replacing the coding &lt;i>Hilpda&lt;/i> exon with luciferase. We subjected the knockout animals to environmental stresses and measured whole-animal metabolic and behavioral parameters. Brown adipocyte precursors were isolated and differentiated &lt;i>in vitro&lt;/i> to quantify the impact of HILPDA ablation in lipid storage and mobilization in these ce</pubmed_abstract><journal>The Journal of endocrinology</journal><pubmed_title>Stress-responsive HILPDA is necessary for thermoregulation during fasting.</pubmed_title><pmcid>PMC5567683</pmcid><funding_grant_id>P30 CA016058</funding_grant_id><funding_grant_id>R35 CA197713</funding_grant_id><funding_grant_id>R03 CA191653</funding_grant_id><funding_grant_id>K01 DK105109</funding_grant_id><funding_grant_id>P01 CA067166</funding_grant_id><pubmed_authors>Bal NC</pubmed_authors><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Maurya SK</pubmed_authors><pubmed_authors>Stanford KI</pubmed_authors><pubmed_authors>Denko NC</pubmed_authors><pubmed_authors>Periasamy M</pubmed_authors><pubmed_authors>Kalyanasundaram A</pubmed_authors><pubmed_authors>Giaccia AJ</pubmed_authors><pubmed_authors>Baer LA</pubmed_authors><pubmed_authors>Papandreou I</pubmed_authors><pubmed_authors>VandeKopple MJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Stress-responsive HILPDA is necessary for thermoregulation during fasting.</name><description>Hypoxia-inducible lipid droplet-associated protein (HILPDA) has been shown to localize to lipid droplets in nutrient-responsive cell types such as hepatocytes and adipocytes. However, its role in the control of whole-body homeostasis is not known. We sought to measure cell-intrinsic and systemic stress responses in a mouse strain harboring whole-body Hilpda deficiency. We generated a genetically engineered mouse model of whole-body HILPDA deficiency by replacing the coding &lt;i>Hilpda&lt;/i> exon with luciferase. We subjected the knockout animals to environmental stresses and measured whole-animal metabolic and behavioral parameters. Brown adipocyte precursors were isolated and differentiated &lt;i>in vitro&lt;/i> to quantify the impact of HILPDA ablation in lipid storage and mobilization in these ce</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Oct</publication><modification>2025-04-25T18:29:46.009Z</modification><creation>2019-06-06T17:58:53Z</creation></dates><accession>S-EPMC5567683</accession><cross_references><pubmed>28739822</pubmed><doi>10.1530/joe-17-0289</doi><doi>10.1530/JOE-17-0289</doi></cross_references></HashMap>