<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(2)</volume><submitter>Wang C</submitter><pubmed_abstract>Thoracic aortic aneurysm (TAA) is progressive fatal aortic pathological dilation. However, the underlying molecular mechanisms are still largely unknown. Evidences suggest that endothelial cells and renin-angiotensin system may participate in the pathogenesis of TAA. This study aimed to investigate whether angiotensin II type 2 receptor (AT2) positive cells are involved in TAA formation. The mRNA level of AT2 is dramatically elevated in TAA compared with in controls. CD4(+)AT2(+) cells increased in both aortic wall and circulation of TAA patients. The levels of IL-1β and IL-17B in CD4(+)AT2(+) cells were lower than those in CD4(+)AT2(-) cells. When compared with endothelial cells (ECs) cultured alone, CD4(+)AT2(+) cells showed an inhibitory effect on proliferation and MMP2 expression in EC</pubmed_abstract><journal>American journal of translational research</journal><pagination>232-41</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4399088</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Identification and characterization of CD4(+)AT2(+) T lymphocyte population in human thoracic aortic aneurysm.</pubmed_title><pmcid>PMC4399088</pmcid><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Hu Z</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Hu X</pubmed_authors><pubmed_authors>Feng Y</pubmed_authors><pubmed_authors>Huang R</pubmed_authors><pubmed_authors>Lian F</pubmed_authors><pubmed_authors>Zhai X</pubmed_authors><pubmed_authors>Xue S</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Gu J</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Wu T</pubmed_authors><pubmed_authors>Xie B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification and characterization of CD4(+)AT2(+) T lymphocyte population in human thoracic aortic aneurysm.</name><description>Thoracic aortic aneurysm (TAA) is progressive fatal aortic pathological dilation. However, the underlying molecular mechanisms are still largely unknown. Evidences suggest that endothelial cells and renin-angiotensin system may participate in the pathogenesis of TAA. This study aimed to investigate whether angiotensin II type 2 receptor (AT2) positive cells are involved in TAA formation. The mRNA level of AT2 is dramatically elevated in TAA compared with in controls. CD4(+)AT2(+) cells increased in both aortic wall and circulation of TAA patients. The levels of IL-1β and IL-17B in CD4(+)AT2(+) cells were lower than those in CD4(+)AT2(-) cells. When compared with endothelial cells (ECs) cultured alone, CD4(+)AT2(+) cells showed an inhibitory effect on proliferation and MMP2 expression in EC</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015</publication><modification>2025-04-04T23:24:11.163Z</modification><creation>2019-03-27T01:50:00Z</creation></dates><accession>S-EPMC4399088</accession><cross_references><pubmed>25901193</pubmed></cross_references></HashMap>