<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jeong HW</submitter><funding>University of Münster and the German Research Foundation</funding><funding>Cluster of Excellence &amp;apos;Cells in Motion&amp;apos;</funding><funding>Max-Planck-Gesellschaft</funding><pagination>e57520</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9566870</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11</volume><pubmed_abstract>The blood-brain barrier (BBB) limits the entry of leukocytes and potentially harmful substances from the circulation into the central nervous system (CNS). While BBB defects are a hallmark of many neurological disorders, the cellular heterogeneity at the neurovascular interface, and the mechanisms governing neuroinflammation are not fully understood.Through single-cell RNA sequencing of non-neuronal cell populations of the murine cerebral cortex during development, adulthood, ageing, and neuroinflammation, we identify reactive endothelial venules, a compartment of specialized postcapillary endothelial cells that are characterized by consistent expression of cell adhesion molecules, preferential leukocyte transmigration, association with perivascular macrophage populations, and endothelial </pubmed_abstract><journal>eLife</journal><pubmed_title>Single-cell transcriptomics reveals functionally specialized vascular endothelium in brain.</pubmed_title><pmcid>PMC9566870</pmcid><funding_grant_id>CRC1366A01</funding_grant_id><funding_grant_id>SO285/11-1</funding_grant_id><funding_grant_id>CRC1009A02</funding_grant_id><funding_grant_id>EXC1003</funding_grant_id><pubmed_authors>Dieguez-Hurtado R</pubmed_authors><pubmed_authors>Jeong HW</pubmed_authors><pubmed_authors>Park H</pubmed_authors><pubmed_authors>Arf H</pubmed_authors><pubmed_authors>Sorokin L</pubmed_authors><pubmed_authors>Adams RH</pubmed_authors><pubmed_authors>Kruse K</pubmed_authors><pubmed_authors>Song J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-cell transcriptomics reveals functionally specialized vascular endothelium in brain.</name><description>The blood-brain barrier (BBB) limits the entry of leukocytes and potentially harmful substances from the circulation into the central nervous system (CNS). While BBB defects are a hallmark of many neurological disorders, the cellular heterogeneity at the neurovascular interface, and the mechanisms governing neuroinflammation are not fully understood.Through single-cell RNA sequencing of non-neuronal cell populations of the murine cerebral cortex during development, adulthood, ageing, and neuroinflammation, we identify reactive endothelial venules, a compartment of specialized postcapillary endothelial cells that are characterized by consistent expression of cell adhesion molecules, preferential leukocyte transmigration, association with perivascular macrophage populations, and endothelial </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2026-06-20T03:24:20.496Z</modification><creation>2025-04-06T00:14:34.264Z</creation></dates><accession>S-EPMC9566870</accession><cross_references><pubmed>36197007</pubmed><doi>10.7554/eLife.57520</doi></cross_references></HashMap>