<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hong YM</submitter><funding>National Research Foundation of Korea</funding><pagination>7982389</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5322441</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2017</volume><pubmed_abstract>In a previous study, we found that the short isoform of DNAJB6 (DNAJB6(S)) had been decreased in the striatum of a mouse model of Parkinson's disease (PD) induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). DNAJB6, one of the heat shock proteins, has been implicated in the pathogenesis of PD. In this study, we explored the cytoprotective effect of DNAJB6(S) against 1-methyl-4-phenylpyridinium ion- (MPP&lt;sup>+&lt;/sup>-) induced apoptosis and the underlying molecular mechanisms in cultured LN18 cells from astrocytic tumors. We observed that MPP&lt;sup>+&lt;/sup> significantly reduced the cell viability and induced apoptosis in LN18 glioblastoma cells. DNAJB6(S) protected LN18 cells against MPP&lt;sup>+&lt;/sup>-induced apoptosis not only by suppressing Bax cleavage but also by inhibiting a seri</pubmed_abstract><journal>Oxidative medicine and cellular longevity</journal><pubmed_title>The Short Isoform of DNAJB6 Protects against 1-Methyl-4-phenylpridinium Ion-Induced Apoptosis in LN18 Cells via Inhibiting Both ROS Formation and Mitochondrial Membrane Potential Loss.</pubmed_title><pmcid>PMC5322441</pmcid><funding_grant_id>NRF-2014R1A2A1A11052795</funding_grant_id><pubmed_authors>Yeo S</pubmed_authors><pubmed_authors>Lim S</pubmed_authors><pubmed_authors>Hong Y</pubmed_authors><pubmed_authors>Jin SH</pubmed_authors><pubmed_authors>Lee SW</pubmed_authors><pubmed_authors>Jung H</pubmed_authors><pubmed_authors>Lee SH</pubmed_authors><pubmed_authors>Choi YG</pubmed_authors><pubmed_authors>Sung B</pubmed_authors><pubmed_authors>Hong YM</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Short Isoform of DNAJB6 Protects against 1-Methyl-4-phenylpridinium Ion-Induced Apoptosis in LN18 Cells via Inhibiting Both ROS Formation and Mitochondrial Membrane Potential Loss.</name><description>In a previous study, we found that the short isoform of DNAJB6 (DNAJB6(S)) had been decreased in the striatum of a mouse model of Parkinson's disease (PD) induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). DNAJB6, one of the heat shock proteins, has been implicated in the pathogenesis of PD. In this study, we explored the cytoprotective effect of DNAJB6(S) against 1-methyl-4-phenylpyridinium ion- (MPP&lt;sup>+&lt;/sup>-) induced apoptosis and the underlying molecular mechanisms in cultured LN18 cells from astrocytic tumors. We observed that MPP&lt;sup>+&lt;/sup> significantly reduced the cell viability and induced apoptosis in LN18 glioblastoma cells. DNAJB6(S) protected LN18 cells against MPP&lt;sup>+&lt;/sup>-induced apoptosis not only by suppressing Bax cleavage but also by inhibiting a seri</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017</publication><modification>2025-04-18T19:22:48.779Z</modification><creation>2019-03-27T02:37:11Z</creation></dates><accession>S-EPMC5322441</accession><cross_references><pubmed>28280525</pubmed><doi>10.1155/2017/7982389</doi></cross_references></HashMap>