<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hesketh EE</submitter><funding>Kidney Research UK</funding><pagination>e0131849</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4488261</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(6)</volume><pubmed_abstract>Autoimmunity is associated with defective phagocytic clearance of apoptotic cells. IgM deficient mice exhibit an autoimmune phenotype consistent with a role for circulating IgM antibodies in apoptotic cell clearance. We have extensively characterised IgM binding to non-apoptotic and apoptotic mouse thymocytes and human Jurkat cells using flow cytometry, confocal imaging and electron microscopy. We demonstrate strong specific IgM binding to a subset of Annexin-V (AnnV)+PI (Propidium Iodide)+ apoptotic cells with disrupted cell membranes. Electron microscopy studies indicated that IgM+AnnV+PI+ apoptotic cells exhibited morphologically advanced apoptosis with marked plasma membrane disruption compared to IgM-AnnV+PI+ apoptotic cells, suggesting that access to intracellular epitopes is require</pubmed_abstract><journal>PloS one</journal><pubmed_title>Circulating IgM Requires Plasma Membrane Disruption to Bind Apoptotic and Non-Apoptotic Nucleated Cells and Erythrocytes.</pubmed_title><pmcid>PMC4488261</pmcid><funding_grant_id>ST4/2011</funding_grant_id><pubmed_authors>Kluth DC</pubmed_authors><pubmed_authors>Hesketh EE</pubmed_authors><pubmed_authors>Hughes J</pubmed_authors><pubmed_authors>Dransfield I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Circulating IgM Requires Plasma Membrane Disruption to Bind Apoptotic and Non-Apoptotic Nucleated Cells and Erythrocytes.</name><description>Autoimmunity is associated with defective phagocytic clearance of apoptotic cells. IgM deficient mice exhibit an autoimmune phenotype consistent with a role for circulating IgM antibodies in apoptotic cell clearance. We have extensively characterised IgM binding to non-apoptotic and apoptotic mouse thymocytes and human Jurkat cells using flow cytometry, confocal imaging and electron microscopy. We demonstrate strong specific IgM binding to a subset of Annexin-V (AnnV)+PI (Propidium Iodide)+ apoptotic cells with disrupted cell membranes. Electron microscopy studies indicated that IgM+AnnV+PI+ apoptotic cells exhibited morphologically advanced apoptosis with marked plasma membrane disruption compared to IgM-AnnV+PI+ apoptotic cells, suggesting that access to intracellular epitopes is require</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015</publication><modification>2025-06-01T01:35:39.42Z</modification><creation>2019-03-26T23:33:30Z</creation></dates><accession>S-EPMC4488261</accession><cross_references><pubmed>26121639</pubmed><doi>10.1371/journal.pone.0131849</doi></cross_references></HashMap>