<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(16)</volume><submitter>Hirano Y</submitter><pubmed_abstract>We previously demonstrated that neural stem/progenitor cells (NSPCs) were induced within and around the ischemic areas in a mouse model of ischemic stroke. These injury/ischemia-induced NSPCs (iNSPCs) differentiated to electrophysiologically functional neurons in vitro, indicating the presence of a self-repair system following injury. However, during the healing process after stroke, ischemic areas were gradually occupied by inflammatory cells, mainly microglial cells/macrophages (MGs/MΦs), and neurogenesis rarely occurred within and around the ischemic areas. Therefore, to achieve neural regeneration by utilizing endogenous iNSPCs, regulation of MGs/MΦs after an ischemic stroke might be necessary. To test this hypothesis, we used iNSPCs isolated from the ischemic areas after a stroke in o</pubmed_abstract><journal>Cells</journal><pagination>2040</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10453473</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Microglia Negatively Regulate the Proliferation and Neuronal Differentiation of Neural Stem/Progenitor Cells Isolated from Poststroke Mouse Brains.</pubmed_title><pmcid>PMC10453473</pmcid><pubmed_authors>Kubo S</pubmed_authors><pubmed_authors>Sakagami M</pubmed_authors><pubmed_authors>Sawano T</pubmed_authors><pubmed_authors>Nakano-Doi A</pubmed_authors><pubmed_authors>Minato Y</pubmed_authors><pubmed_authors>Nakagomi T</pubmed_authors><pubmed_authors>Tsuzuki K</pubmed_authors><pubmed_authors>Hirano Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Microglia Negatively Regulate the Proliferation and Neuronal Differentiation of Neural Stem/Progenitor Cells Isolated from Poststroke Mouse Brains.</name><description>We previously demonstrated that neural stem/progenitor cells (NSPCs) were induced within and around the ischemic areas in a mouse model of ischemic stroke. These injury/ischemia-induced NSPCs (iNSPCs) differentiated to electrophysiologically functional neurons in vitro, indicating the presence of a self-repair system following injury. However, during the healing process after stroke, ischemic areas were gradually occupied by inflammatory cells, mainly microglial cells/macrophages (MGs/MΦs), and neurogenesis rarely occurred within and around the ischemic areas. Therefore, to achieve neural regeneration by utilizing endogenous iNSPCs, regulation of MGs/MΦs after an ischemic stroke might be necessary. To test this hypothesis, we used iNSPCs isolated from the ischemic areas after a stroke in o</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Aug</publication><modification>2025-04-26T23:41:45.212Z</modification><creation>2025-04-06T17:34:53.577Z</creation></dates><accession>S-EPMC10453473</accession><cross_references><pubmed>37626850</pubmed><doi>10.3390/cells12162040</doi></cross_references></HashMap>