<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lu Y</submitter><funding>NIAID NIH HHS</funding><pagination>858256</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8934864</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13</volume><pubmed_abstract>To determine whether aorta becomes immune organ in pathologies, we performed transcriptomic analyses of six types of secretomic genes (SGs) in aorta and vascular cells and made the following findings: 1) 53.7% out of 21,306 human protein genes are classified into six secretomes, namely, canonical, caspase 1, caspase 4, exosome, Weibel-Palade body, and autophagy; 2) Atherosclerosis (AS), chronic kidney disease (CKD) and abdominal aortic aneurysm (AAA) modulate six secretomes in aortas; and Middle East Respiratory Syndrome Coronavirus (MERS-CoV, COVID-19 homologous) infected endothelial cells (ECs) and angiotensin-II (Ang-II) treated vascular smooth muscle cells (VSMCs) modulate six secretomes; 3) AS aortas upregulate T and B cell immune SGs; CKD aortas upregulate SGs for cardiac hypertrophy</pubmed_abstract><journal>Frontiers in immunology</journal><pubmed_title>Aorta in Pathologies May Function as an Immune Organ by Upregulating Secretomes for Immune and Vascular Cell Activation, Differentiation and Trans-Differentiation-Early Secretomes may Serve as Drivers for Trained Immunity.</pubmed_title><pmcid>PMC8934864</pmcid><funding_grant_id>R01 AI145034</funding_grant_id><pubmed_authors>Xu K</pubmed_authors><pubmed_authors>Lu Y</pubmed_authors><pubmed_authors>Hu W</pubmed_authors><pubmed_authors>Saaoud F</pubmed_authors><pubmed_authors>Drummer C</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Yu J</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Vazquez-Padron RI</pubmed_authors><pubmed_authors>Kunapuli SP</pubmed_authors><pubmed_authors>Shao Y</pubmed_authors><pubmed_authors>Bethea JR</pubmed_authors><pubmed_authors>Jiang X</pubmed_authors><pubmed_authors>Wu S</pubmed_authors><pubmed_authors>Sun J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Aorta in Pathologies May Function as an Immune Organ by Upregulating Secretomes for Immune and Vascular Cell Activation, Differentiation and Trans-Differentiation-Early Secretomes may Serve as Drivers for Trained Immunity.</name><description>To determine whether aorta becomes immune organ in pathologies, we performed transcriptomic analyses of six types of secretomic genes (SGs) in aorta and vascular cells and made the following findings: 1) 53.7% out of 21,306 human protein genes are classified into six secretomes, namely, canonical, caspase 1, caspase 4, exosome, Weibel-Palade body, and autophagy; 2) Atherosclerosis (AS), chronic kidney disease (CKD) and abdominal aortic aneurysm (AAA) modulate six secretomes in aortas; and Middle East Respiratory Syndrome Coronavirus (MERS-CoV, COVID-19 homologous) infected endothelial cells (ECs) and angiotensin-II (Ang-II) treated vascular smooth muscle cells (VSMCs) modulate six secretomes; 3) AS aortas upregulate T and B cell immune SGs; CKD aortas upregulate SGs for cardiac hypertrophy</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-18T12:10:14.522Z</modification><creation>2025-04-06T21:48:50.151Z</creation></dates><accession>S-EPMC8934864</accession><cross_references><pubmed>35320939</pubmed><doi>10.3389/fimmu.2022.858256</doi></cross_references></HashMap>