<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sathe K</submitter><funding>Wellcome Trust</funding><pagination>3336-47</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3501971</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>135(Pt 11)</volume><pubmed_abstract>Parkinson's disease is a neurodegenerative disorder that can, at least partly, be mimicked by the neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine. S100B is a calcium-binding protein expressed in, and secreted by, astrocytes. There is increasing evidence that S100B acts as a cytokine or damage-associated molecular pattern protein not only in inflammatory but also in neurodegenerative diseases. In this study, we show that S100B protein levels were higher in post-mortem substantia nigra of patients with Parkinson's disease compared with control tissue, and cerebrospinal fluid S100B levels were higher in a large cohort of patients with Parkinson's disease compared with controls. Correspondingly, mice treated with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine showed upregulated S100B mes</pubmed_abstract><journal>Brain : a journal of neurology</journal><pubmed_title>S100B is increased in Parkinson's disease and ablation protects against MPTP-induced toxicity through the RAGE and TNF-α pathway.</pubmed_title><pmcid>PMC3501971</pmcid><funding_grant_id>WT080782MF</funding_grant_id><pubmed_authors>Mustafa S</pubmed_authors><pubmed_authors>Maetzler W</pubmed_authors><pubmed_authors>Sathe K</pubmed_authors><pubmed_authors>Lang JD</pubmed_authors><pubmed_authors>Martin HL</pubmed_authors><pubmed_authors>Teismann P</pubmed_authors><pubmed_authors>Schulte C</pubmed_authors><pubmed_authors>Berg D</pubmed_authors><pubmed_authors>Synofzik M</pubmed_authors><pubmed_authors>Mounsey RB</pubmed_authors><pubmed_authors>Fleckenstein C</pubmed_authors><pubmed_authors>Vukovic Z</pubmed_authors><pubmed_authors>Itohara S</pubmed_authors></additional><is_claimable>false</is_claimable><name>S100B is increased in Parkinson's disease and ablation protects against MPTP-induced toxicity through the RAGE and TNF-α pathway.</name><description>Parkinson's disease is a neurodegenerative disorder that can, at least partly, be mimicked by the neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine. S100B is a calcium-binding protein expressed in, and secreted by, astrocytes. There is increasing evidence that S100B acts as a cytokine or damage-associated molecular pattern protein not only in inflammatory but also in neurodegenerative diseases. In this study, we show that S100B protein levels were higher in post-mortem substantia nigra of patients with Parkinson's disease compared with control tissue, and cerebrospinal fluid S100B levels were higher in a large cohort of patients with Parkinson's disease compared with controls. Correspondingly, mice treated with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine showed upregulated S100B mes</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Nov</publication><modification>2026-05-02T09:21:47.625Z</modification><creation>2025-07-09T03:05:13.908Z</creation></dates><accession>S-EPMC3501971</accession><cross_references><pubmed>23169921</pubmed><doi>10.1093/brain/aws250</doi></cross_references></HashMap>