<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ren P</submitter><funding>NHLBI NIH HHS</funding><pagination>260-276</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12053597</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>45(2)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Smooth muscle cells (SMCs) of cardiac and neural crest origin contribute to the developing proximal aorta and are linked to disease propensity in adults.&lt;h4>Methods&lt;/h4>We analyzed single-cell transcriptomes of aortic SMCs from adult mice to determine basal states and changes after disrupting TGFβ (transforming growth factor-β) signaling necessary for aortic homeostasis.&lt;h4>Results&lt;/h4>A minority of Myh11 lineage-marked SMCs differentially expressed genes suggestive of embryological origin. Additional analyses in Nkx2-5 and Wnt1 lineage-marked SMCs derived from cardiac and neural crest progenitors, respectively, showed both lineages contributed to a major common cluster and each lineage to a minor distinct cluster. Common cluster SMCs extended from root to arch, cardiac </pubmed_abstract><journal>Arteriosclerosis, thrombosis, and vascular biology</journal><pubmed_title>Heterogeneous Cardiac-Derived and Neural Crest-Derived Aortic Smooth Muscle Cells Exhibit Similar Transcriptional Changes After TGFβ Signaling Disruption.</pubmed_title><pmcid>PMC12053597</pmcid><funding_grant_id>R01 HL146723</funding_grant_id><funding_grant_id>R01 HL152197</funding_grant_id><funding_grant_id>P01 HL107205</funding_grant_id><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Hassab AHM</pubmed_authors><pubmed_authors>Tellides G</pubmed_authors><pubmed_authors>Ren P</pubmed_authors><pubmed_authors>Jiang B</pubmed_authors><pubmed_authors>Assi R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Heterogeneous Cardiac-Derived and Neural Crest-Derived Aortic Smooth Muscle Cells Exhibit Similar Transcriptional Changes After TGFβ Signaling Disruption.</name><description>&lt;h4>Background&lt;/h4>Smooth muscle cells (SMCs) of cardiac and neural crest origin contribute to the developing proximal aorta and are linked to disease propensity in adults.&lt;h4>Methods&lt;/h4>We analyzed single-cell transcriptomes of aortic SMCs from adult mice to determine basal states and changes after disrupting TGFβ (transforming growth factor-β) signaling necessary for aortic homeostasis.&lt;h4>Results&lt;/h4>A minority of Myh11 lineage-marked SMCs differentially expressed genes suggestive of embryological origin. Additional analyses in Nkx2-5 and Wnt1 lineage-marked SMCs derived from cardiac and neural crest progenitors, respectively, showed both lineages contributed to a major common cluster and each lineage to a minor distinct cluster. Common cluster SMCs extended from root to arch, cardiac </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2026-06-11T05:37:50.027Z</modification><creation>2026-06-11T03:08:26.238Z</creation></dates><accession>S-EPMC12053597</accession><cross_references><pubmed>39697172</pubmed><doi>10.1161/atvbaha.124.321706</doi><doi>10.1161/ATVBAHA.124.321706</doi></cross_references></HashMap>