<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nguyen LP</submitter><funding>NOVO Nordisk Foundation</funding><funding>NHLBI</funding><funding>NHLBI NIH HHS</funding><funding>Knut and Alice Wallenberg Foundation</funding><funding>Swedish Cancer Society</funding><funding>Leducq Foundation</funding><funding>Swedish Research Council</funding><funding>Novo Nordisk Fonden</funding><pagination>e184940</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11529983</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(20)</volume><pubmed_abstract>Lipoprotein lipase (LPL) and multiple regulators of LPL activity (e.g., APOC2 and ANGPTL4) are present in all vertebrates, but GPIHBP1-the endothelial cell (EC) protein that captures LPL within the subendothelial spaces and transports it to its site of action in the capillary lumen-is present in mammals but in not chickens or other lower vertebrates. In mammals, GPIHBP1 deficiency causes severe hypertriglyceridemia, but chickens maintain low triglyceride levels despite the absence of GPIHBP1. To understand intravascular lipolysis in lower vertebrates, we examined LPL expression in mouse and chicken hearts. In both species, LPL was abundant on capillaries, but the distribution of Lpl transcripts was strikingly different. In mouse hearts, Lpl transcripts were extremely abundant in cardiomyoc</pubmed_abstract><journal>JCI insight</journal><pubmed_title>Distinct strategies for intravascular triglyceride metabolism in hearts of mammals and lower vertebrate species.</pubmed_title><pmcid>PMC11529983</pmcid><funding_grant_id>R01 HL087228</funding_grant_id><funding_grant_id>2020.0057</funding_grant_id><funding_grant_id>150735</funding_grant_id><funding_grant_id>2015–00550</funding_grant_id><funding_grant_id>HL171737,HL146358,HL087228,HL139725</funding_grant_id><funding_grant_id>P01 HL146358</funding_grant_id><funding_grant_id>NNF20OC0063444</funding_grant_id><funding_grant_id>2023-02655</funding_grant_id><funding_grant_id>R35 HL139725</funding_grant_id><funding_grant_id>12CVD04,22CVD01,23CVD02</funding_grant_id><funding_grant_id>R01 HL171737</funding_grant_id><pubmed_authors>Birrane G</pubmed_authors><pubmed_authors>Yu RG</pubmed_authors><pubmed_authors>Ploug M</pubmed_authors><pubmed_authors>Fong LG</pubmed_authors><pubmed_authors>Scheithauer J</pubmed_authors><pubmed_authors>Arnold H</pubmed_authors><pubmed_authors>Goodwin JL</pubmed_authors><pubmed_authors>Jung H</pubmed_authors><pubmed_authors>Mae MA</pubmed_authors><pubmed_authors>Koltowska K</pubmed_authors><pubmed_authors>He L</pubmed_authors><pubmed_authors>Kim JR</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Nguyen LP</pubmed_authors><pubmed_authors>Xie K</pubmed_authors><pubmed_authors>Presnell AM</pubmed_authors><pubmed_authors>Tran AP</pubmed_authors><pubmed_authors>Weston TA</pubmed_authors><pubmed_authors>Kim PH</pubmed_authors><pubmed_authors>Young SG</pubmed_authors><pubmed_authors>Song W</pubmed_authors><pubmed_authors>Tu Y</pubmed_authors><pubmed_authors>Beigneux AP</pubmed_authors><pubmed_authors>Betsholtz C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Distinct strategies for intravascular triglyceride metabolism in hearts of mammals and lower vertebrate species.</name><description>Lipoprotein lipase (LPL) and multiple regulators of LPL activity (e.g., APOC2 and ANGPTL4) are present in all vertebrates, but GPIHBP1-the endothelial cell (EC) protein that captures LPL within the subendothelial spaces and transports it to its site of action in the capillary lumen-is present in mammals but in not chickens or other lower vertebrates. In mammals, GPIHBP1 deficiency causes severe hypertriglyceridemia, but chickens maintain low triglyceride levels despite the absence of GPIHBP1. To understand intravascular lipolysis in lower vertebrates, we examined LPL expression in mouse and chicken hearts. In both species, LPL was abundant on capillaries, but the distribution of Lpl transcripts was strikingly different. In mouse hearts, Lpl transcripts were extremely abundant in cardiomyoc</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Sep</publication><modification>2026-05-04T06:39:29.835Z</modification><creation>2025-04-06T09:32:19.025Z</creation></dates><accession>S-EPMC11529983</accession><cross_references><pubmed>39435661</pubmed><doi>10.1172/jci.insight.184940</doi></cross_references></HashMap>