<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang S</submitter><funding>The National Natural Science Foundation of China/Research Grants Council Joint Research Scheme</funding><funding>Shenzhen Knowledge Innovation Programme of the Shenzhen Science and Technology Innovation Commission</funding><funding>The Hong Kong University Shenzhen Hospital Scientific Research Training Plan</funding><pagination>4613</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9104239</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(9)</volume><pubmed_abstract>Human endometrium is an incredibly dynamic tissue undergoing cyclic regeneration and shedding during a woman's reproductive life. Endometrial mesenchymal stromal/stem-like cells (eMSC) contribute to this process. A hypoxic niche with low oxygen levels has been reported in multiple somatic stem cell types. However, the knowledge of hypoxia on eMSC remains limited. In mice, stromal stem/progenitor cells can be identified by the label-retaining technique. We examined the relationship between the label-retaining stromal cells (LRSC) and hypoxia during tissue breakdown in a mouse model of simulated menses. Our results demonstrated that LRSC resided in a hypoxic microenvironment during endometrial breakdown and early repair. Immunofluorescence staining revealed that the hypoxic-located LRSC unde</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Hypoxia Regulates the Self-Renewal of Endometrial Mesenchymal Stromal/Stem-like Cells via Notch Signaling.</pubmed_title><pmcid>PMC9104239</pmcid><funding_grant_id>HKUSZH20192003</funding_grant_id><funding_grant_id>JCYJ20180508153031952</funding_grant_id><funding_grant_id>N_HKU 732/20</funding_grant_id><pubmed_authors>Yeung WSB</pubmed_authors><pubmed_authors>Chan RWS</pubmed_authors><pubmed_authors>Ng EHY</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hypoxia Regulates the Self-Renewal of Endometrial Mesenchymal Stromal/Stem-like Cells via Notch Signaling.</name><description>Human endometrium is an incredibly dynamic tissue undergoing cyclic regeneration and shedding during a woman's reproductive life. Endometrial mesenchymal stromal/stem-like cells (eMSC) contribute to this process. A hypoxic niche with low oxygen levels has been reported in multiple somatic stem cell types. However, the knowledge of hypoxia on eMSC remains limited. In mice, stromal stem/progenitor cells can be identified by the label-retaining technique. We examined the relationship between the label-retaining stromal cells (LRSC) and hypoxia during tissue breakdown in a mouse model of simulated menses. Our results demonstrated that LRSC resided in a hypoxic microenvironment during endometrial breakdown and early repair. Immunofluorescence staining revealed that the hypoxic-located LRSC unde</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-04T20:35:59.909Z</modification><creation>2025-04-04T20:35:59.909Z</creation></dates><accession>S-EPMC9104239</accession><cross_references><pubmed>35563003</pubmed><doi>10.3390/ijms23094613</doi></cross_references></HashMap>