<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chaitanya GV</submitter><funding>NINDS NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>125</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3854084</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Multiple sclerosis (MS) is associated with ectopic lymphoid follicle formation. Podoplanin+ (lymphatic marker) T helper17 (Th17) cells and B cell aggregates have been implicated in the formation of tertiary lymphoid organs (TLOs) in MS and experimental autoimmune encephalitis (EAE). Since podoplanin expressed by Th17 cells in MS brains is also expressed by lymphatic endothelium, we investigated whether the pathophysiology of MS involves inductions of lymphatic proteins in the inflamed neurovasculature.&lt;h4>Methods&lt;/h4>We assessed the protein levels of lymphatic vessel endothelial hyaluronan receptor and podoplanin, which are specific to the lymphatic system and prospero-homeobox protein-1, angiopoietin-2, vascular endothelial growth factor-D, vascular endothelial growth f</pubmed_abstract><journal>Journal of neuroinflammation</journal><pubmed_title>Inflammation induces neuro-lymphatic protein expression in multiple sclerosis brain neurovasculature.</pubmed_title><pmcid>PMC3854084</pmcid><funding_grant_id>R21 NS059724</funding_grant_id><funding_grant_id>P20 GM103433</funding_grant_id><pubmed_authors>Sato F</pubmed_authors><pubmed_authors>Guttman BW</pubmed_authors><pubmed_authors>Minagar A</pubmed_authors><pubmed_authors>Chaitanya GV</pubmed_authors><pubmed_authors>Alexander JS</pubmed_authors><pubmed_authors>Zivadinov R</pubmed_authors><pubmed_authors>Tsunoda I</pubmed_authors><pubmed_authors>Omura S</pubmed_authors><pubmed_authors>Martinez NE</pubmed_authors><pubmed_authors>Ramanathan M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Inflammation induces neuro-lymphatic protein expression in multiple sclerosis brain neurovasculature.</name><description>&lt;h4>Background&lt;/h4>Multiple sclerosis (MS) is associated with ectopic lymphoid follicle formation. Podoplanin+ (lymphatic marker) T helper17 (Th17) cells and B cell aggregates have been implicated in the formation of tertiary lymphoid organs (TLOs) in MS and experimental autoimmune encephalitis (EAE). Since podoplanin expressed by Th17 cells in MS brains is also expressed by lymphatic endothelium, we investigated whether the pathophysiology of MS involves inductions of lymphatic proteins in the inflamed neurovasculature.&lt;h4>Methods&lt;/h4>We assessed the protein levels of lymphatic vessel endothelial hyaluronan receptor and podoplanin, which are specific to the lymphatic system and prospero-homeobox protein-1, angiopoietin-2, vascular endothelial growth factor-D, vascular endothelial growth f</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Oct</publication><modification>2026-05-06T22:54:43.473Z</modification><creation>2026-04-07T22:25:51.72Z</creation></dates><accession>S-EPMC3854084</accession><cross_references><pubmed>24124909</pubmed><doi>10.1186/1742-2094-10-125</doi></cross_references></HashMap>