<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Meng S</submitter><funding>NEI NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><pagination>1647-1662</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7987209</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>142(17)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The angiogenic response to ischemia restores perfusion so as to preserve tissue. A role for mesenchymal-to-endothelial transition in the angiogenic response is controversial. This study is to determine if resident fibroblasts contribute to angiogenesis.&lt;h4>Methods&lt;/h4>We utilized the murine model of hindlimb ischemia, and in vivo Matrigel plug assay together with lineage tracing studies and single cell RNA-sequencing to examine the transcriptional and functional changes in fibroblasts in response to ischemia.&lt;h4>Results&lt;/h4>Lineage tracing using Fsp1-Cre: R26R-EYFP mice revealed the emergence within the ischemic hindlimb of a small subset of YFP&lt;sup>+&lt;/sup> CD144&lt;sup>+&lt;/sup> CD11b&lt;sup>-&lt;/sup> fibroblasts (E* cells) that expressed endothelial cell (EC) genes. Subcutaneous</pubmed_abstract><journal>Circulation</journal><pubmed_title>Reservoir of Fibroblasts Promotes Recovery From Limb Ischemia.</pubmed_title><pmcid>PMC7987209</pmcid><funding_grant_id>R01 HL148338</funding_grant_id><funding_grant_id>R01 HL133254</funding_grant_id><funding_grant_id>S10 OD018033</funding_grant_id><funding_grant_id>R01 GM125632</funding_grant_id><funding_grant_id>P30 EY002520</funding_grant_id><funding_grant_id>S10 OD023469</funding_grant_id><pubmed_authors>Lv J</pubmed_authors><pubmed_authors>Meng S</pubmed_authors><pubmed_authors>Chen K</pubmed_authors><pubmed_authors>Cooke JP</pubmed_authors><pubmed_authors>Owusu I</pubmed_authors><pubmed_authors>Chanda PK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Reservoir of Fibroblasts Promotes Recovery From Limb Ischemia.</name><description>&lt;h4>Background&lt;/h4>The angiogenic response to ischemia restores perfusion so as to preserve tissue. A role for mesenchymal-to-endothelial transition in the angiogenic response is controversial. This study is to determine if resident fibroblasts contribute to angiogenesis.&lt;h4>Methods&lt;/h4>We utilized the murine model of hindlimb ischemia, and in vivo Matrigel plug assay together with lineage tracing studies and single cell RNA-sequencing to examine the transcriptional and functional changes in fibroblasts in response to ischemia.&lt;h4>Results&lt;/h4>Lineage tracing using Fsp1-Cre: R26R-EYFP mice revealed the emergence within the ischemic hindlimb of a small subset of YFP&lt;sup>+&lt;/sup> CD144&lt;sup>+&lt;/sup> CD11b&lt;sup>-&lt;/sup> fibroblasts (E* cells) that expressed endothelial cell (EC) genes. Subcutaneous</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Oct</publication><modification>2025-04-04T18:41:58.864Z</modification><creation>2025-04-04T18:41:58.864Z</creation></dates><accession>S-EPMC7987209</accession><cross_references><pubmed>32820662</pubmed><doi>10.1161/CIRCULATIONAHA.120.046872</doi><doi>10.1161/circulationaha.120.046872</doi></cross_references></HashMap>