<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xiao Z</submitter><funding>NHLBI NIH HHS</funding><pagination>2221-34</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC1386801</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>90(6)</volume><pubmed_abstract>Platelet-leukocyte adhesion may contribute to thrombosis and inflammation. We examined the heterotypic interaction between unactivated neutrophils and either thrombin receptor activating peptide (TRAP)-stimulated platelets or P-selectin-bearing beads (Ps-beads) in suspension. Cone-plate viscometers were used to apply controlled shear rates from 14 to 3000/s. Platelet-neutrophil and bead-neutrophil adhesion analysis was performed using both flow cytometry and high-speed videomicroscopy. We observed that although blocking antibodies against either P-selectin or P-selectin glycoprotein ligand-1 (PSGL-1) alone inhibited platelet-neutrophil adhesion by approximately 60% at 140/s, these reagents completely blocked adhesion at 3000/s. Anti-Mac-1 alone did not alter platelet-neutrophil adhesion ra</pubmed_abstract><journal>Biophysical journal</journal><pubmed_title>Biomechanics of P-selectin PSGL-1 bonds: shear threshold and integrin-independent cell adhesion.</pubmed_title><pmcid>PMC1386801</pmcid><funding_grant_id>K02 HL076211</funding_grant_id><funding_grant_id>HL63014</funding_grant_id><funding_grant_id>R01 HL063014</funding_grant_id><funding_grant_id>HL76211</funding_grant_id><pubmed_authors>Goldsmith HL</pubmed_authors><pubmed_authors>Xiao Z</pubmed_authors><pubmed_authors>McIntosh FA</pubmed_authors><pubmed_authors>Neelamegham S</pubmed_authors><pubmed_authors>Shankaran H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Biomechanics of P-selectin PSGL-1 bonds: shear threshold and integrin-independent cell adhesion.</name><description>Platelet-leukocyte adhesion may contribute to thrombosis and inflammation. We examined the heterotypic interaction between unactivated neutrophils and either thrombin receptor activating peptide (TRAP)-stimulated platelets or P-selectin-bearing beads (Ps-beads) in suspension. Cone-plate viscometers were used to apply controlled shear rates from 14 to 3000/s. Platelet-neutrophil and bead-neutrophil adhesion analysis was performed using both flow cytometry and high-speed videomicroscopy. We observed that although blocking antibodies against either P-selectin or P-selectin glycoprotein ligand-1 (PSGL-1) alone inhibited platelet-neutrophil adhesion by approximately 60% at 140/s, these reagents completely blocked adhesion at 3000/s. Anti-Mac-1 alone did not alter platelet-neutrophil adhesion ra</description><dates><release>2006-01-01T00:00:00Z</release><publication>2006 Mar</publication><modification>2025-04-04T13:41:42.492Z</modification><creation>2019-03-27T01:26:04Z</creation></dates><accession>S-EPMC1386801</accession><cross_references><pubmed>16387772</pubmed><doi>10.1529/biophysj.105.065789</doi></cross_references></HashMap>