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タイトル: | Viable Neuronopathic Gaucher Disease Model in Medaka (Oryzias latipes) Displays Axonal Accumulation of Alpha-Synuclein. |
著者: | Uemura, Norihito https://orcid.org/0000-0002-6251-0810 (unconfirmed) Koike, Masato Ansai, Satoshi https://orcid.org/0000-0003-2683-0160 (unconfirmed) Kinoshita, Masato https://orcid.org/0000-0003-3936-7371 (unconfirmed) Ishikawa-Fujiwara, Tomoko Matsui, Hideaki Naruse, Kiyoshi Sakamoto, Naoaki Uchiyama, Yasuo Todo, Takeshi Takeda, Shunichi Yamakado, Hodaka Takahashi, Ryosuke https://orcid.org/0000-0002-1407-9640 (unconfirmed) |
著者名の別形: | 上村, 紀仁 木下, 政人 内山, 安男 藤堂, 剛 武田, 俊一 山門, 穂高 髙橋, 良輔 |
発行日: | 2-Apr-2015 |
出版者: | Public Library of Science |
誌名: | PLOS genetics |
巻: | 11 |
号: | 4 |
論文番号: | e1005065 |
抄録: | Homozygous mutations in the glucocerebrosidase (GBA) gene result in Gaucher disease (GD), the most common lysosomal storage disease. Recent genetic studies have revealed that GBA mutations confer a strong risk for sporadic Parkinson's disease (PD). To investigate how GBA mutations cause PD, we generated GBA nonsense mutant (GBA-/-) medaka that are completely deficient in glucocerebrosidase (GCase) activity. In contrast to the perinatal death in humans and mice lacking GCase activity, GBA-/- medaka survived for months, enabling analysis of the pathological progression. GBA-/- medaka displayed the pathological phenotypes resembling human neuronopathic GD including infiltration of Gaucher cell-like cells into the brains, progressive neuronal loss, and microgliosis. Detailed pathological findings represented lysosomal abnormalities in neurons and alpha-synuclein (α-syn) accumulation in axonal swellings containing autophagosomes. Unexpectedly, disruption of α-syn did not improve the life span, formation of axonal swellings, neuronal loss, or neuroinflammation in GBA-/- medaka. Taken together, the present study revealed GBA-/- medaka as a novel neuronopathic GD model, the pahological mechanisms of α-syn accumulation caused by GCase deficiency, and the minimal contribution of α-syn to the pathogenesis of neuronopathic GD. |
記述: | パーキンソン病の解明に役立つメダカの作製に成功 -メダカが神経変性疾患の研究に貢献できる可能性- 京都大学プレスリリース. 2015-04-09. |
著作権等: | c 2015 Uemura et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
URI: | http://hdl.handle.net/2433/197174 |
DOI(出版社版): | 10.1371/journal.pgen.1005065 |
PubMed ID: | 25835295 |
関連リンク: | https://www.kyoto-u.ac.jp/ja/research-news/2015-04-09 |
出現コレクション: | 学術雑誌掲載論文等 |
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