Pathophysiology of lysosomal storage disease and lysophagy
Project/Area Number |
15H05673
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Research Category |
Grant-in-Aid for Young Scientists (A)
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Allocation Type | Single-year Grants |
Research Field |
Pediatrics
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Research Institution | Kawasaki Medical School (2016) Osaka University (2015) |
Principal Investigator |
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Project Period (FY) |
2015-04-01 – 2017-03-31
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Project Status |
Completed (Fiscal Year 2016)
|
Budget Amount *help |
¥24,310,000 (Direct Cost: ¥18,700,000、Indirect Cost: ¥5,610,000)
Fiscal Year 2016: ¥7,150,000 (Direct Cost: ¥5,500,000、Indirect Cost: ¥1,650,000)
Fiscal Year 2015: ¥17,160,000 (Direct Cost: ¥13,200,000、Indirect Cost: ¥3,960,000)
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Keywords | リソソーム蓄積病 / オートファジー / EPG5 / VPS33A / リソソーム |
Outline of Final Research Achievements |
(i) Intracellular accumulation of cholesterol that is often observed in lysosomal storage diseases affects lysosomal membrane permeability. We identified a candidate molecule which works for ubiquitin ligase in the autophagic process following lysosomal membrane rupture. (ii) We analyzed skin fibroblasts from patients of Vici syndrome, which is caused by mutations of EPG5 gene, and elucidated that EPG5 functions for the fusion step between autophagosome and lysosome. (iii) Using whole exome sequencing, we established a novel syndrome which is caused by mutations of VPS33A gene (Mucopolysaccharidosis Plus Syndrome, OMIM #617303), and reported a part of pathophysiology of this new disease. Altogether we proved that not only undegraded substrates of lysosomal enzymes but also membrane lipid contents and intracellular vesicular trafficking are complicatedly implicated in the pathophysiology of lysosomal storage diseases.
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Report
(3 results)
Research Products
(1 results)
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[Journal Article] Mutation in VPS33A affects metabolism of glycosaminoglycans: a new type of mucopolysaccharidosis with severe systemic symptoms2017
Author(s)
Kondo H, Maksimova N, Otomo T*,Kato H, Imai A, Asano Y, Kobayashi K, Nojima S, Nakaya A, Hamada Y, Irahara K, Gurinova E, Sukhomyasova A, Nogovicina A, Savvina M, Yoshimori T, Ozono K Sakai N*
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Journal Title
Human Molecular Genetics
Volume: 26
Pages: 173-183
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research / Acknowledgement Compliant