<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nakayama Y</submitter><funding>NHLBI NIH HHS</funding><pagination>510-527</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9444972</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>131(6)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>An ancient family of arrestin-fold proteins, termed alpha-arrestins, may have conserved roles in regulating nutrient transporter trafficking and cellular metabolism as adaptor proteins. One alpha-arrestin, TXNIP (thioredoxin-interacting protein), is known to regulate myocardial glucose uptake. However, the in vivo role of the related alpha-arrestin, ARRDC4 (arrestin domain-containing protein 4), is unknown.&lt;h4>Methods&lt;/h4>We first tested whether interaction with GLUTs (glucose transporters) is a conserved function of the mammalian alpha-arrestins. To define the in vivo function of ARRDC4, we generated and characterized a novel &lt;i>Arrdc4&lt;/i> knockout (KO) mouse model. We then analyzed the molecular interaction between arrestin domains and the basal GLUT1.&lt;h4>Results&lt;/h4>A</pubmed_abstract><journal>Circulation research</journal><pubmed_title>Interaction of ARRDC4 With GLUT1 Mediates Metabolic Stress in the Ischemic Heart.</pubmed_title><pmcid>PMC9444972</pmcid><funding_grant_id>R01 HL130861</funding_grant_id><funding_grant_id>R01 HL166620</funding_grant_id><pubmed_authors>Patwari P</pubmed_authors><pubmed_authors>Mukai N</pubmed_authors><pubmed_authors>Nakayama Y</pubmed_authors><pubmed_authors>Kreitzer G</pubmed_authors><pubmed_authors>Yoshioka J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Interaction of ARRDC4 With GLUT1 Mediates Metabolic Stress in the Ischemic Heart.</name><description>&lt;h4>Background&lt;/h4>An ancient family of arrestin-fold proteins, termed alpha-arrestins, may have conserved roles in regulating nutrient transporter trafficking and cellular metabolism as adaptor proteins. One alpha-arrestin, TXNIP (thioredoxin-interacting protein), is known to regulate myocardial glucose uptake. However, the in vivo role of the related alpha-arrestin, ARRDC4 (arrestin domain-containing protein 4), is unknown.&lt;h4>Methods&lt;/h4>We first tested whether interaction with GLUTs (glucose transporters) is a conserved function of the mammalian alpha-arrestins. To define the in vivo function of ARRDC4, we generated and characterized a novel &lt;i>Arrdc4&lt;/i> knockout (KO) mouse model. We then analyzed the molecular interaction between arrestin domains and the basal GLUT1.&lt;h4>Results&lt;/h4>A</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2026-05-28T14:15:45.443Z</modification><creation>2024-11-20T03:03:38.407Z</creation></dates><accession>S-EPMC9444972</accession><cross_references><pubmed>35950500</pubmed><doi>10.1161/CIRCRESAHA.122.321351</doi><doi>10.1161/circresaha.122.321351</doi></cross_references></HashMap>