<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Lu L</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Parkinson's disease (PD) is the second most common neurodegenerative disease after Alzheimer's dementia. Mitochondrial dysfunction is involved in the pathology of PD. Coiled-coil-helix-coiled-coil-helix domain-containing 2 (CHCHD2) was identified as associated with autosomal dominant PD. However, the mechanism of CHCHD2 in PD remains unclear.&lt;h4>Methods&lt;/h4>Short hairpin RNA (ShRNA)-mediated CHCHD2 knockdown or lentivirus-mediated CHCHD2 overexpression was performed to investigate the impact of CHCHD2 on mitochondrial morphology and function in neuronal tumor cell lines represented with human neuroblastoma (SHSY5Y) and HeLa cells. Blue-native polyacrylamide gel electrophoresis (PAGE) and two-dimensional sodium dodecyl sulfate-PAGE analysis were used to illustrate the rol</pubmed_abstract><journal>Chinese medical journal</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9532036</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>CHCHD2 maintains mitochondrial contact site and cristae organizing system stability and protects against mitochondrial dysfunction in an experimental model of Parkinson's disease.</pubmed_title><pmcid>PMC9532036</pmcid><pubmed_authors>Zhou M</pubmed_authors><pubmed_authors>Qiu J</pubmed_authors><pubmed_authors>Xu P</pubmed_authors><pubmed_authors>Xiao Y</pubmed_authors><pubmed_authors>Guo W</pubmed_authors><pubmed_authors>Dai W</pubmed_authors><pubmed_authors>Mao H</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Mo M</pubmed_authors><pubmed_authors>Lu L</pubmed_authors><pubmed_authors>Wu Z</pubmed_authors><pubmed_authors>Pei Z</pubmed_authors><pubmed_authors>Zhu X</pubmed_authors><pubmed_authors>Chen X</pubmed_authors></additional><is_claimable>false</is_claimable><name>CHCHD2 maintains mitochondrial contact site and cristae organizing system stability and protects against mitochondrial dysfunction in an experimental model of Parkinson's disease.</name><description>&lt;h4>Background&lt;/h4>Parkinson's disease (PD) is the second most common neurodegenerative disease after Alzheimer's dementia. Mitochondrial dysfunction is involved in the pathology of PD. Coiled-coil-helix-coiled-coil-helix domain-containing 2 (CHCHD2) was identified as associated with autosomal dominant PD. However, the mechanism of CHCHD2 in PD remains unclear.&lt;h4>Methods&lt;/h4>Short hairpin RNA (ShRNA)-mediated CHCHD2 knockdown or lentivirus-mediated CHCHD2 overexpression was performed to investigate the impact of CHCHD2 on mitochondrial morphology and function in neuronal tumor cell lines represented with human neuroblastoma (SHSY5Y) and HeLa cells. Blue-native polyacrylamide gel electrophoresis (PAGE) and two-dimensional sodium dodecyl sulfate-PAGE analysis were used to illustrate the rol</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2025-04-19T17:36:05.414Z</modification><creation>2025-04-19T17:36:05.414Z</creation></dates><accession>S-EPMC9532036</accession><cross_references><pubmed>35830185</pubmed><doi>10.1097/CM9.0000000000002053</doi></cross_references></HashMap>