<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Li OQ</submitter><funding>NCATS NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Thrombosis is a major cause of myocardial infarction and ischemic stroke. The sodium/potassium ATPase (NKA), comprising α and β subunits, is crucial in maintaining intracellular sodium and potassium gradients. However, the role of NKA in platelet function and thrombosis remains unclear.&lt;h4>Methods&lt;/h4>We utilized wild-type (WT, α&lt;i>1&lt;/i> &lt;sup>+/+&lt;/sup>) and NKA α1 heterozygous (α&lt;i>1&lt;/i> &lt;sup>+/-&lt;/sup>) mice, aged 8 to 16 weeks, of both sexes. An intravital microscopy-based, FeCl&lt;sub>3&lt;/sub>-induced carotid artery injury thrombosis model was employed for in vivo thrombosis assessment. Platelet transfusion assays were used to evaluate platelet NKA α1 function on thrombosis. Human platelets isolated from healthy donors and heart failure patients treated with/without digoxi</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2024.05.13.593923</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11118499</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Sodium/Potassium ATPase Alpha 1 Subunit Fine-tunes Platelet GPCR Signaling Function and is Essential for Thrombosis.</pubmed_title><pmcid>PMC11118499</pmcid><funding_grant_id>R15 HL145666</funding_grant_id><funding_grant_id>UL1 TR003017</funding_grant_id><funding_grant_id>R15 HL164682</funding_grant_id><funding_grant_id>P20 GM103434</funding_grant_id><funding_grant_id>R01 DK129937</funding_grant_id><funding_grant_id>R15 HL145573</funding_grant_id><funding_grant_id>U54 GM104942</funding_grant_id><pubmed_authors>Kennedy D</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Roytenberg R</pubmed_authors><pubmed_authors>Aguilar R</pubmed_authors><pubmed_authors>Yue H</pubmed_authors><pubmed_authors>Olanipekun O</pubmed_authors><pubmed_authors>Thompson E</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>DeHart AR</pubmed_authors><pubmed_authors>Fedorova O</pubmed_authors><pubmed_authors>Li OQ</pubmed_authors><pubmed_authors>Pierre SV</pubmed_authors><pubmed_authors>Bai F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sodium/Potassium ATPase Alpha 1 Subunit Fine-tunes Platelet GPCR Signaling Function and is Essential for Thrombosis.</name><description>&lt;h4>Background&lt;/h4>Thrombosis is a major cause of myocardial infarction and ischemic stroke. The sodium/potassium ATPase (NKA), comprising α and β subunits, is crucial in maintaining intracellular sodium and potassium gradients. However, the role of NKA in platelet function and thrombosis remains unclear.&lt;h4>Methods&lt;/h4>We utilized wild-type (WT, α&lt;i>1&lt;/i> &lt;sup>+/+&lt;/sup>) and NKA α1 heterozygous (α&lt;i>1&lt;/i> &lt;sup>+/-&lt;/sup>) mice, aged 8 to 16 weeks, of both sexes. An intravital microscopy-based, FeCl&lt;sub>3&lt;/sub>-induced carotid artery injury thrombosis model was employed for in vivo thrombosis assessment. Platelet transfusion assays were used to evaluate platelet NKA α1 function on thrombosis. Human platelets isolated from healthy donors and heart failure patients treated with/without digoxi</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-06-26T03:18:17.322Z</modification><creation>2026-06-26T03:09:28.807Z</creation></dates><accession>S-EPMC11118499</accession><cross_references><pubmed>38798556</pubmed><doi>10.1101/2024.05.13.593923</doi></cross_references></HashMap>