<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lovelace MD</submitter><funding>NIDDK NIH HHS</funding><pagination>1066-1078</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5391183</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(8)</volume><pubmed_abstract>RhoGTPases are important regulators of the cell cytoskeleton, controlling cell shape, migration and proliferation. Previously we showed that ARHGAP18 in endothelial cells is important in cell junctions. Here we show, using structured illumination microscopy (SIM), ground-state depletion (GSD), and total internal reflection fluorescence microscopy (TIRF) that a proportion of ARHGAP18 localizes to microtubules in endothelial cells, as well as in nonendothelial cells, an association confirmed biochemically. In endothelial cells, some ARHGAP18 puncta also colocalized to Weibel-Palade bodies on the microtubules. Depletion of ARHGAP18 by small interfering RNA or analysis of endothelial cells isolated from ARHGAP18-knockout mice showed microtubule destabilization, as evidenced by altered morpholo</pubmed_abstract><journal>Molecular biology of the cell</journal><pubmed_title>The RhoGAP protein ARHGAP18/SENEX localizes to microtubules and regulates their stability in endothelial cells.</pubmed_title><pmcid>PMC5391183</pmcid><funding_grant_id>R01 DK107309</funding_grant_id><pubmed_authors>Lovelace MD</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Parker A</pubmed_authors><pubmed_authors>Coleman PR</pubmed_authors><pubmed_authors>Gamble JR</pubmed_authors><pubmed_authors>Kavallaris M</pubmed_authors><pubmed_authors>Bertolino P</pubmed_authors><pubmed_authors>Chang GH</pubmed_authors><pubmed_authors>Powter EE</pubmed_authors><pubmed_authors>Vadas MA</pubmed_authors><pubmed_authors>McCaughan G</pubmed_authors><pubmed_authors>Lay AJ</pubmed_authors><pubmed_authors>McGrath AP</pubmed_authors><pubmed_authors>Jormakka M</pubmed_authors><pubmed_authors>Hunter J</pubmed_authors></additional><is_claimable>false</is_claimable><name>The RhoGAP protein ARHGAP18/SENEX localizes to microtubules and regulates their stability in endothelial cells.</name><description>RhoGTPases are important regulators of the cell cytoskeleton, controlling cell shape, migration and proliferation. Previously we showed that ARHGAP18 in endothelial cells is important in cell junctions. Here we show, using structured illumination microscopy (SIM), ground-state depletion (GSD), and total internal reflection fluorescence microscopy (TIRF) that a proportion of ARHGAP18 localizes to microtubules in endothelial cells, as well as in nonendothelial cells, an association confirmed biochemically. In endothelial cells, some ARHGAP18 puncta also colocalized to Weibel-Palade bodies on the microtubules. Depletion of ARHGAP18 by small interfering RNA or analysis of endothelial cells isolated from ARHGAP18-knockout mice showed microtubule destabilization, as evidenced by altered morpholo</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Apr</publication><modification>2025-04-04T12:39:07.969Z</modification><creation>2019-03-27T02:41:18Z</creation></dates><accession>S-EPMC5391183</accession><cross_references><pubmed>28251925</pubmed><doi>10.1091/mbc.E16-05-0285</doi></cross_references></HashMap>