<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang SH</submitter><funding>Ministry of Science and Technology, Taiwan</funding><funding>Chang Gung Memorial Hospital, Linkou</funding><pagination>105</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9753400</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>In endothelial cells, phospholipase C (PLC) β1-activated Ca&lt;sup>2+&lt;/sup> is a crucial second messenger for the signaling pathways governing angiogenesis. PLCβ1 is inactivated by complexing with an intracellular protein called translin-associated factor X (TRAX). This study demonstrates specific interactions between Globo H ceramide (GHCer) and TRAX, which highlight a new angiogenic control through PLCβ1 activation.&lt;h4>Methods&lt;/h4>Globo-series glycosphingolipids (GSLs), including GHCer and stage-specific embryonic antigen-3 ceramide (SSEA3Cer), were analyzed using enzyme-linked immunosorbent assay (ELISA) and Biacore for their binding with TRAX. Angiogenic activities of GSLs in human umbilical vein endothelial cells (HUVECs) were evaluated. Molecular dynamics (MD) simulat</pubmed_abstract><journal>Journal of biomedical science</journal><pubmed_title>Conformational alteration in glycan induces phospholipase Cβ1 activation and angiogenesis.</pubmed_title><pmcid>PMC9753400</pmcid><funding_grant_id>CIRPG3L0011</funding_grant_id><funding_grant_id>MOST 111-2321-B-182A-002</funding_grant_id><funding_grant_id>OMRPG3C0047</funding_grant_id><funding_grant_id>MOST 108-2321-B-182A-004</funding_grant_id><funding_grant_id>MOST 109-2321-B-182A-005</funding_grant_id><pubmed_authors>Hung JT</pubmed_authors><pubmed_authors>Ho YH</pubmed_authors><pubmed_authors>Wang SH</pubmed_authors><pubmed_authors>Kuo HH</pubmed_authors><pubmed_authors>Yu AL</pubmed_authors><pubmed_authors>Lin CC</pubmed_authors><pubmed_authors>Lee CW</pubmed_authors><pubmed_authors>Tsai HH</pubmed_authors><pubmed_authors>Cheng JY</pubmed_authors><pubmed_authors>Yu J</pubmed_authors><pubmed_authors>Lo TC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Conformational alteration in glycan induces phospholipase Cβ1 activation and angiogenesis.</name><description>&lt;h4>Background&lt;/h4>In endothelial cells, phospholipase C (PLC) β1-activated Ca&lt;sup>2+&lt;/sup> is a crucial second messenger for the signaling pathways governing angiogenesis. PLCβ1 is inactivated by complexing with an intracellular protein called translin-associated factor X (TRAX). This study demonstrates specific interactions between Globo H ceramide (GHCer) and TRAX, which highlight a new angiogenic control through PLCβ1 activation.&lt;h4>Methods&lt;/h4>Globo-series glycosphingolipids (GSLs), including GHCer and stage-specific embryonic antigen-3 ceramide (SSEA3Cer), were analyzed using enzyme-linked immunosorbent assay (ELISA) and Biacore for their binding with TRAX. Angiogenic activities of GSLs in human umbilical vein endothelial cells (HUVECs) were evaluated. Molecular dynamics (MD) simulat</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2026-05-28T05:37:00.419Z</modification><creation>2025-04-05T15:42:58.392Z</creation></dates><accession>S-EPMC9753400</accession><cross_references><pubmed>36517806</pubmed><doi>10.1186/s12929-022-00889-w</doi></cross_references></HashMap>