<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Foks AC</submitter><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><pagination>456-65</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4853762</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>36(3)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>T cell immunoglobulin and mucin domain (Tim) proteins are expressed by numerous immune cells, recognize phosphatidylserine on apoptotic cells, and function as costimulators or coinhibitors. Tim-1 is expressed by activated T cells but is also found on dendritic cells and B cells. Tim-4, present on macrophages and dendritic cells, plays a critical role in apoptotic cell clearance, regulates the number of phosphatidylserine-expressing activated T cells, and is genetically associated with low low-density lipoprotein and triglyceride levels. Because these functions of Tim-1 and Tim-4 could affect atherosclerosis, their modulation has potential therapeutic value in cardiovascular disease.&lt;h4>Approach and results&lt;/h4>ldlr(-/-) mice were fed a high-fat diet for 4 weeks while bein</pubmed_abstract><journal>Arteriosclerosis, thrombosis, and vascular biology</journal><pubmed_title>Blockade of Tim-1 and Tim-4 Enhances Atherosclerosis in Low-Density Lipoprotein Receptor-Deficient Mice.</pubmed_title><pmcid>PMC4853762</pmcid><funding_grant_id>HL087282</funding_grant_id><funding_grant_id>P50 HL056985</funding_grant_id><funding_grant_id>R01 HL087282</funding_grant_id><funding_grant_id>R01AI089955</funding_grant_id><funding_grant_id>R01 HL121363</funding_grant_id><funding_grant_id>P01AI054456</funding_grant_id><funding_grant_id>R01 AI089955</funding_grant_id><funding_grant_id>P01 AI054456</funding_grant_id><pubmed_authors>Kuperwaser F</pubmed_authors><pubmed_authors>Gonen A</pubmed_authors><pubmed_authors>Jarolim P</pubmed_authors><pubmed_authors>DeKruyff RH</pubmed_authors><pubmed_authors>Freeman GJ</pubmed_authors><pubmed_authors>Witztum JL</pubmed_authors><pubmed_authors>Alberts-Grill N</pubmed_authors><pubmed_authors>Foks AC</pubmed_authors><pubmed_authors>Lederer J</pubmed_authors><pubmed_authors>Lichtman AH</pubmed_authors><pubmed_authors>Engelbertsen D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Blockade of Tim-1 and Tim-4 Enhances Atherosclerosis in Low-Density Lipoprotein Receptor-Deficient Mice.</name><description>&lt;h4>Objective&lt;/h4>T cell immunoglobulin and mucin domain (Tim) proteins are expressed by numerous immune cells, recognize phosphatidylserine on apoptotic cells, and function as costimulators or coinhibitors. Tim-1 is expressed by activated T cells but is also found on dendritic cells and B cells. Tim-4, present on macrophages and dendritic cells, plays a critical role in apoptotic cell clearance, regulates the number of phosphatidylserine-expressing activated T cells, and is genetically associated with low low-density lipoprotein and triglyceride levels. Because these functions of Tim-1 and Tim-4 could affect atherosclerosis, their modulation has potential therapeutic value in cardiovascular disease.&lt;h4>Approach and results&lt;/h4>ldlr(-/-) mice were fed a high-fat diet for 4 weeks while bein</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Mar</publication><modification>2026-05-05T08:28:38.595Z</modification><creation>2019-03-27T02:12:53Z</creation></dates><accession>S-EPMC4853762</accession><cross_references><pubmed>26821944</pubmed><doi>10.1161/ATVBAHA.115.306860</doi><doi>10.1161/atvbaha.115.306860</doi></cross_references></HashMap>