<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Desai JV</submitter><funding>National Institute of Allergy and Infectious Diseases</funding><funding>National Institute of Allergy and Infectious Diseases Division of Intramural Research</funding><funding>New Jersey Health Foundation</funding><funding>NIAID NIH HHS</funding><funding>National Institutes of Health</funding><pagination>102781</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10770751</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(1)</volume><pubmed_abstract>Myeloid phagocytes are essential for antifungal host defense during systemic candidiasis. Here, we present a protocol for assessing phagocyte-fungal interactions in vivo in the kidney, the primary target organ of the murine systemic candidiasis model. We describe steps for intravital confocal microscopy and flow cytometry. We also detail a kidney tissue dissociation procedure to obtain highly pure functional phagocytes for utilization in downstream ex vivo fungal uptake and killing assays.</pubmed_abstract><journal>STAR protocols</journal><pubmed_title>Evaluation of murine renal phagocyte-fungal interactions using intravital confocal microscopy and flow cytometry.</pubmed_title><pmcid>PMC10770751</pmcid><funding_grant_id>R00AI141622</funding_grant_id><funding_grant_id>PC 177-23</funding_grant_id><funding_grant_id>R00 AI141622</funding_grant_id><pubmed_authors>Lionakis MS</pubmed_authors><pubmed_authors>Desai JV</pubmed_authors></additional><is_claimable>false</is_claimable><name>Evaluation of murine renal phagocyte-fungal interactions using intravital confocal microscopy and flow cytometry.</name><description>Myeloid phagocytes are essential for antifungal host defense during systemic candidiasis. Here, we present a protocol for assessing phagocyte-fungal interactions in vivo in the kidney, the primary target organ of the murine systemic candidiasis model. We describe steps for intravital confocal microscopy and flow cytometry. We also detail a kidney tissue dissociation procedure to obtain highly pure functional phagocytes for utilization in downstream ex vivo fungal uptake and killing assays.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-21T03:11:31.64Z</modification><creation>2025-04-04T21:55:13.605Z</creation></dates><accession>S-EPMC10770751</accession><cross_references><pubmed>38113143</pubmed><doi>10.1016/j.xpro.2023.102781</doi></cross_references></HashMap>