<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu LY</submitter><funding>AHA Grant-in-Aid</funding><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NIH</funding><pagination>805-12</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9875669</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>70(7)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Priming with cytokines such as granulocyte-macrophage colony-stimulating factor (GM-CSF) enhances eosinophil migration and exacerbates the excessive accumulation of eosinophils within the bronchial mucosa of asthmatics. However, mechanisms that drive GM-CSF priming are incompletely understood. Notch signaling is an evolutionarily conserved pathway that regulates cellular processes, including migration, by integrating exogenous and cell-intrinsic cues. This study investigates the hypothesis that the priming-induced enhanced migration of human eosinophils requires the Notch signaling pathway.&lt;h4>Methods&lt;/h4>Using pan Notch inhibitors and newly developed human antibodies that specifically neutralize Notch receptor 1 activation, we investigated a role for Notch signaling in </pubmed_abstract><journal>Allergy</journal><pubmed_title>Notch signaling mediates granulocyte-macrophage colony-stimulating factor priming-induced transendothelial migration of human eosinophils.</pubmed_title><pmcid>PMC9875669</pmcid><funding_grant_id>R01 HL095699</funding_grant_id><funding_grant_id>R37 AI020241</funding_grant_id><pubmed_authors>Xenakis JJ</pubmed_authors><pubmed_authors>Liu LY</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Spencer LA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Notch signaling mediates granulocyte-macrophage colony-stimulating factor priming-induced transendothelial migration of human eosinophils.</name><description>&lt;h4>Background&lt;/h4>Priming with cytokines such as granulocyte-macrophage colony-stimulating factor (GM-CSF) enhances eosinophil migration and exacerbates the excessive accumulation of eosinophils within the bronchial mucosa of asthmatics. However, mechanisms that drive GM-CSF priming are incompletely understood. Notch signaling is an evolutionarily conserved pathway that regulates cellular processes, including migration, by integrating exogenous and cell-intrinsic cues. This study investigates the hypothesis that the priming-induced enhanced migration of human eosinophils requires the Notch signaling pathway.&lt;h4>Methods&lt;/h4>Using pan Notch inhibitors and newly developed human antibodies that specifically neutralize Notch receptor 1 activation, we investigated a role for Notch signaling in </description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jul</publication><modification>2025-04-04T00:02:57.226Z</modification><creation>2025-04-04T00:02:57.226Z</creation></dates><accession>S-EPMC9875669</accession><cross_references><pubmed>25846339</pubmed><doi>10.1111/all.12624</doi></cross_references></HashMap>