<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE341nnn/GSE341505/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE341505</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transplantation of endothelial progenitor cells attenuates pulmonary fibrosis via IFITM3-containing exosomes</name><description>Pulmonary endothelial progenitor cells contribute to vascular regeneration, but their molecular characteristics in the adult lung remain incompletely defined. In this study, single-cell RNA sequencing was performed on endothelial cells isolated from adult wild-type mouse lungs. KIT-positive endothelial cells were stratified into Foxf1-positive capillary endothelial progenitor cells (capEPCs) and Foxf1-negative endothelial cells. Differential gene expression analysis identified Ifitm3 as highly enriched in capEPCs, supporting a role for the FOXF1–IFITM3 pathway in endothelial regeneration and pulmonary fibrosis.</description><dates><publication>2026/08/13</publication></dates><accession>GSE341505</accession><cross_references><GSM>GSM9907912</GSM><GPL>24247</GPL><GSE>341505</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>