<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Khan M</submitter><funding>National Basic Research Program of China</funding><funding>National Natural Science Foundation of China</funding><pagination>1900778</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6794618</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(20)</volume><pubmed_abstract>Tumor cells exhibit prominent metabolic alterations through which they acclimatize to their stressful microenvironment. These cells have a high rate of glutaminolysis and release ammonia (NH&lt;sub>3&lt;/sub>) as a byproduct, which may function as a diffusible signal among cancer cells and can reveal cellular heterogeneity. E7, a nematic liquid crystal (LC), is doped with 4-pentyl-4'-biphenyl carboxylic acid (PBA) and encapsulated in polymeric microcapsules (P-E7&lt;sub>PBA&lt;/sub>), which are then immobilized on cells in a microfluidic channel. Normal human umbilical vein endothelial cells (HUVECs) and myeloma, human primary glioblastoma (U87), human colon carcinoma (Caco-2), and human breast adenocarcinoma (MCF-7) cells are investigated for the release of NH&lt;sub>3&lt;/sub>. The P-E7&lt;sub>PBA&lt;/sub> is able to visualize NH&lt;sub>3&lt;/sub> release from the cell via a radial-to-bipolar (R-B) orientation change, observed through a polarized optical microscope. The various cell lines significantly differ in their response time required for an R-B change. The mean response times for Caco-2, U87, and MCF-7 cells are 277, 155, and 121 s, respectively. NH&lt;sub>3&lt;/sub> release from a single cell captured in a microwell flow chip shows a similar R-B change. The P-E7&lt;sub>PBA&lt;/sub> droplets technology could be applied to other multiple targets by functionalizing LCs with different probes.</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Real-Time Imaging of Ammonia Release from Single Live Cells via Liquid Crystal Droplets Immobilized on the Cell Membrane.</pubmed_title><pmcid>PMC6794618</pmcid><funding_grant_id>21435002</funding_grant_id><funding_grant_id>21621003</funding_grant_id><funding_grant_id>2017YFC0906800</funding_grant_id><funding_grant_id>21727814</funding_grant_id><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Mao S</pubmed_authors><pubmed_authors>Khan M</pubmed_authors><pubmed_authors>Lin JM</pubmed_authors><pubmed_authors>Shah SNA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Real-Time Imaging of Ammonia Release from Single Live Cells via Liquid Crystal Droplets Immobilized on the Cell Membrane.</name><description>Tumor cells exhibit prominent metabolic alterations through which they acclimatize to their stressful microenvironment. These cells have a high rate of glutaminolysis and release ammonia (NH&lt;sub>3&lt;/sub>) as a byproduct, which may function as a diffusible signal among cancer cells and can reveal cellular heterogeneity. E7, a nematic liquid crystal (LC), is doped with 4-pentyl-4'-biphenyl carboxylic acid (PBA) and encapsulated in polymeric microcapsules (P-E7&lt;sub>PBA&lt;/sub>), which are then immobilized on cells in a microfluidic channel. Normal human umbilical vein endothelial cells (HUVECs) and myeloma, human primary glioblastoma (U87), human colon carcinoma (Caco-2), and human breast adenocarcinoma (MCF-7) cells are investigated for the release of NH&lt;sub>3&lt;/sub>. The P-E7&lt;sub>PBA&lt;/sub> is able to visualize NH&lt;sub>3&lt;/sub> release from the cell via a radial-to-bipolar (R-B) orientation change, observed through a polarized optical microscope. The various cell lines significantly differ in their response time required for an R-B change. The mean response times for Caco-2, U87, and MCF-7 cells are 277, 155, and 121 s, respectively. NH&lt;sub>3&lt;/sub> release from a single cell captured in a microwell flow chip shows a similar R-B change. The P-E7&lt;sub>PBA&lt;/sub> droplets technology could be applied to other multiple targets by functionalizing LCs with different probes.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Oct</publication><modification>2024-11-12T12:09:27.786Z</modification><creation>2019-11-05T08:06:19Z</creation></dates><accession>S-EPMC6794618</accession><cross_references><pubmed>31637159</pubmed><doi>10.1002/advs.201900778</doi></cross_references></HashMap>