<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2</volume><submitter>Itano MS</submitter><pubmed_abstract>Dendritic cells express DC-SIGN and CD206, C-type lectins (CTLs) that bind a variety of pathogens and may facilitate pathogen uptake for subsequent antigen presentation. Both proteins form punctate membrane nanodomains (∼80 nm) on naïve cells. We analyzed the spatiotemporal distribution of CTLs following host-fungal particle contact using confocal microscopy and three distinct methods of cluster identification and measurement of receptor clusters in super-resolution datasets: DBSCAN, Pair Correlation and a custom implementation of the Getis spatial statistic. Quantitative analysis of confocal and super-resolution images demonstrated that CTL nanodomains become concentrated in the contact site relative to non-contact membrane after the first hour of exposure and established that this recrui</pubmed_abstract><journal>Frontiers in physics</journal><pagination>46</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4262399</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Super-resolution imaging of C-type lectin spatial rearrangement within the dendritic cell plasma membrane at fungal microbe contact sites.</pubmed_title><pmcid>PMC4262399</pmcid><pubmed_authors>Itano MS</pubmed_authors><pubmed_authors>Graus MS</pubmed_authors><pubmed_authors>Liu P</pubmed_authors><pubmed_authors>Thompson NL</pubmed_authors><pubmed_authors>Pehlke C</pubmed_authors><pubmed_authors>Jacobson K</pubmed_authors><pubmed_authors>Wester MJ</pubmed_authors><pubmed_authors>Lidke KA</pubmed_authors><pubmed_authors>Neumann AK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Super-resolution imaging of C-type lectin spatial rearrangement within the dendritic cell plasma membrane at fungal microbe contact sites.</name><description>Dendritic cells express DC-SIGN and CD206, C-type lectins (CTLs) that bind a variety of pathogens and may facilitate pathogen uptake for subsequent antigen presentation. Both proteins form punctate membrane nanodomains (∼80 nm) on naïve cells. We analyzed the spatiotemporal distribution of CTLs following host-fungal particle contact using confocal microscopy and three distinct methods of cluster identification and measurement of receptor clusters in super-resolution datasets: DBSCAN, Pair Correlation and a custom implementation of the Getis spatial statistic. Quantitative analysis of confocal and super-resolution images demonstrated that CTL nanodomains become concentrated in the contact site relative to non-contact membrane after the first hour of exposure and established that this recrui</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Aug</publication><modification>2025-05-29T20:28:02.938Z</modification><creation>2019-03-27T01:41:28Z</creation></dates><accession>S-EPMC4262399</accession><cross_references><pubmed>25506589</pubmed><doi>10.3389/fphy.2014.00046</doi></cross_references></HashMap>