<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rueter J</submitter><funding>Deutsche Forschungsgemeinschaft</funding><funding>Christian-Albrechts-Universität zu Kiel</funding><pagination>59</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9905200</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>80(3)</volume><pubmed_abstract>&lt;h4>Background and aims&lt;/h4>Apolipoprotein E (APOE) is known for its role in lipid metabolism and its association with age-related disease pathology. The aim of the present work was to identify previously unknown functions of APOE based on the detection of novel APOE protein-protein interaction candidates.&lt;h4>Approach and results&lt;/h4>APOE targeted replacement mice and transfected cultured hepatocytes expressing the human isoforms APOE3 and APOE4 were used. For 7 months, APOE3 and APOE4 mice were fed a high-fat and high-sugar diet to induce obesity, while a subgroup was subjected to 30% dietary restriction. Proteomic analysis of coimmunoprecipitation products from APOE mouse liver extracts revealed 28 APOE-interacting candidate proteins, including branched-chain alpha-keto acid dehydrogenas</pubmed_abstract><journal>Cellular and molecular life sciences : CMLS</journal><pubmed_title>The mitochondrial BCKD complex interacts with hepatic apolipoprotein E in cultured cells in vitro and mouse livers in vivo.</pubmed_title><pmcid>PMC9905200</pmcid><funding_grant_id>HU 1702/6-1</funding_grant_id><funding_grant_id>TH 872/13-1</funding_grant_id><pubmed_authors>Tholey A</pubmed_authors><pubmed_authors>Huebbe P</pubmed_authors><pubmed_authors>Treitz C</pubmed_authors><pubmed_authors>Rueter J</pubmed_authors><pubmed_authors>Luersen K</pubmed_authors><pubmed_authors>Rimbach G</pubmed_authors><pubmed_authors>Schloesser A</pubmed_authors></additional><is_claimable>false</is_claimable><name>The mitochondrial BCKD complex interacts with hepatic apolipoprotein E in cultured cells in vitro and mouse livers in vivo.</name><description>&lt;h4>Background and aims&lt;/h4>Apolipoprotein E (APOE) is known for its role in lipid metabolism and its association with age-related disease pathology. The aim of the present work was to identify previously unknown functions of APOE based on the detection of novel APOE protein-protein interaction candidates.&lt;h4>Approach and results&lt;/h4>APOE targeted replacement mice and transfected cultured hepatocytes expressing the human isoforms APOE3 and APOE4 were used. For 7 months, APOE3 and APOE4 mice were fed a high-fat and high-sugar diet to induce obesity, while a subgroup was subjected to 30% dietary restriction. Proteomic analysis of coimmunoprecipitation products from APOE mouse liver extracts revealed 28 APOE-interacting candidate proteins, including branched-chain alpha-keto acid dehydrogenas</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-07-14T19:06:05.688Z</modification><creation>2024-11-20T01:39:21.053Z</creation></dates><accession>S-EPMC9905200</accession><cross_references><pubmed>36749362</pubmed><doi>10.1007/s00018-023-04706-x</doi></cross_references></HashMap>