<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sachs L</submitter><funding>Bundesministerium für Bildung und Forschung (Federal Ministry of Education and Research)</funding><funding>Deutsche Forschungsgemeinschaft (German Research Foundation)</funding><pagination>86</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8782918</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(1)</volume><pubmed_abstract>Inherited platelet disorders affecting the human platelet cytoskeleton result in increased bleeding risk. However, deciphering their impact on cytoskeleton-dependent intrinsic biomechanics of platelets remains challenging and represents an unmet need from a diagnostic and prognostic perspective. It is currently unclear whether ex vivo anticoagulants used during collection of peripheral blood impact the mechanophenotype of cellular components of blood. Using unbiased, high-throughput functional mechanophenotyping of single human platelets by real-time deformability cytometry, we found that ex vivo anticoagulants are a critical pre-analytical variable that differentially influences platelet deformation, their size, and functional response to agonists by altering the cytoskeleton. We applied </pubmed_abstract><journal>Communications biology</journal><pubmed_title>Ex vivo anticoagulants affect human blood platelet biomechanics with implications for high-throughput functional mechanophenotyping.</pubmed_title><pmcid>PMC8782918</pmcid><funding_grant_id>03Z22CN11</funding_grant_id><funding_grant_id>374031971-CRC/TR 240</funding_grant_id><pubmed_authors>Sachs L</pubmed_authors><pubmed_authors>Palankar R</pubmed_authors><pubmed_authors>Otto O</pubmed_authors><pubmed_authors>Wesche J</pubmed_authors><pubmed_authors>Lenkeit L</pubmed_authors><pubmed_authors>Greinacher A</pubmed_authors><pubmed_authors>Bender M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ex vivo anticoagulants affect human blood platelet biomechanics with implications for high-throughput functional mechanophenotyping.</name><description>Inherited platelet disorders affecting the human platelet cytoskeleton result in increased bleeding risk. However, deciphering their impact on cytoskeleton-dependent intrinsic biomechanics of platelets remains challenging and represents an unmet need from a diagnostic and prognostic perspective. It is currently unclear whether ex vivo anticoagulants used during collection of peripheral blood impact the mechanophenotype of cellular components of blood. Using unbiased, high-throughput functional mechanophenotyping of single human platelets by real-time deformability cytometry, we found that ex vivo anticoagulants are a critical pre-analytical variable that differentially influences platelet deformation, their size, and functional response to agonists by altering the cytoskeleton. We applied </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2026-07-14T15:01:45.885Z</modification><creation>2025-04-06T04:01:59.433Z</creation></dates><accession>S-EPMC8782918</accession><cross_references><pubmed>35064207</pubmed><doi>10.1038/s42003-021-02982-6</doi></cross_references></HashMap>