<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu W</submitter><funding>Innovative Research Group Project of the National Natural Science Foundation of China</funding><funding>National Medical Research Council Singapore</funding><pagination>44</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9575256</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Aberrant aggregation of α-synuclein (α-syn) is a key pathological feature of Parkinson's disease (PD), but the precise role of intestinal α-syn in the progression of PD is unclear. In a number of genetic Drosophila models of PD, α-syn was frequently ectopically expressed in the neural system to investigate the pathobiology.&lt;h4>Method&lt;/h4>We investigated the potential role of intestinal α-syn in PD pathogenesis using a Drosophila model. Human α-syn was overexpressed in Drosophila guts, and life span, survival, immunofluorescence and climbing were evaluated. Immunofluorescence, Western blotting and reactive oxygen species (ROS) staining were performed to assess the effects of intestinal α-syn on intestinal dysplasia. High-throughput RNA and 16S rRNA gene sequencing, quanti</pubmed_abstract><journal>Translational neurodegeneration</journal><pubmed_title>Intestine-derived α-synuclein initiates and aggravates pathogenesis of Parkinson's disease in Drosophila.</pubmed_title><pmcid>PMC9575256</pmcid><funding_grant_id>STAR</funding_grant_id><funding_grant_id>31501175</funding_grant_id><funding_grant_id>OF LCG 000207</funding_grant_id><pubmed_authors>Tan EK</pubmed_authors><pubmed_authors>Lim KL</pubmed_authors><pubmed_authors>Liu W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Intestine-derived α-synuclein initiates and aggravates pathogenesis of Parkinson's disease in Drosophila.</name><description>&lt;h4>Background&lt;/h4>Aberrant aggregation of α-synuclein (α-syn) is a key pathological feature of Parkinson's disease (PD), but the precise role of intestinal α-syn in the progression of PD is unclear. In a number of genetic Drosophila models of PD, α-syn was frequently ectopically expressed in the neural system to investigate the pathobiology.&lt;h4>Method&lt;/h4>We investigated the potential role of intestinal α-syn in PD pathogenesis using a Drosophila model. Human α-syn was overexpressed in Drosophila guts, and life span, survival, immunofluorescence and climbing were evaluated. Immunofluorescence, Western blotting and reactive oxygen species (ROS) staining were performed to assess the effects of intestinal α-syn on intestinal dysplasia. High-throughput RNA and 16S rRNA gene sequencing, quanti</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2026-05-27T19:09:21.961Z</modification><creation>2025-02-19T03:22:59.307Z</creation></dates><accession>S-EPMC9575256</accession><cross_references><pubmed>36253844</pubmed><doi>10.1186/s40035-022-00318-w</doi></cross_references></HashMap>