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Neuromuscular degeneration and locomotor deficit in a Drosophila model of mucopolysaccharidosis VII is attenuated by treatment with resveratrol
- Source :
- Disease Models & Mechanisms, Disease Models & Mechanisms, Vol 11, Iss 11 (2018)
- Publication Year :
- 2018
- Publisher :
- The Company of Biologists Ltd, 2018.
-
Abstract
- Mucopolysaccharidosis VII (MPS VII) is a recessively inherited lysosomal storage disorder caused by β-glucuronidase enzyme deficiency. The disease is characterized by widespread accumulation of non-degraded or partially degraded glycosaminoglycans, leading to cellular and multiple tissue dysfunctions. The patients exhibit diverse clinical symptoms, and eventually succumb to premature death. The only possible remedy is the recently approved enzyme replacement therapy, which is an expensive, invasive and lifelong treatment procedure. Small-molecule therapeutics for MPS VII have so far remained elusive primarily due to lack of molecular insights into the disease pathogenesis and unavailability of a suitable animal model that can be used for rapid drug screening. To address these issues, we developed a Drosophila model of MPS VII by knocking out the CG2135 gene, the fly β-glucuronidase orthologue. The CG2135−/− fly recapitulated cardinal features of MPS VII, such as reduced lifespan, progressive motor impairment and neuropathological abnormalities. Loss of dopaminergic neurons and muscle degeneration due to extensive apoptosis was implicated as the basis of locomotor deficit in this fly. Such hitherto unknown mechanistic links have considerably advanced our understanding of the MPS VII pathophysiology and warrant leveraging this genetically tractable model for deeper enquiry about the disease progression. We were also prompted to test whether phenotypic abnormalities in the CG2135−/− fly can be attenuated by resveratrol, a natural polyphenol with potential health benefits. Indeed, resveratrol treatment significantly ameliorated neuromuscular pathology and restored normal motor function in the CG2135−/− fly. This intriguing finding merits further preclinical studies for developing an alternative therapy for MPS VII. This article has an associated First Person interview with the first author of the paper.<br />Summary: The authors generate a new Drosophila model of MPS VII, which offers insights into the pathophysiology of this disease, and also uncovers the therapeutic potential of resveratrol in treating MPS VII.
- Subjects :
- 0301 basic medicine
Mucopolysaccharidosis
Neuroscience (miscellaneous)
Neuromuscular Junction
lcsh:Medicine
Medicine (miscellaneous)
Mucopolysaccharidosis VII
Disease
Resveratrol
Motor Activity
Bioinformatics
General Biochemistry, Genetics and Molecular Biology
Neuromuscular degeneration
03 medical and health sciences
chemistry.chemical_compound
Immunology and Microbiology (miscellaneous)
lcsh:Pathology
Medicine
Animals
Drosophila Proteins
Humans
Amino Acid Sequence
Glucuronidase
business.industry
lcsh:R
Dopaminergic
fungi
Dros
Enzyme replacement therapy
medicine.disease
Phenotype
Pathophysiology
Disease Models, Animal
030104 developmental biology
Drosophila melanogaster
chemistry
Gene Targeting
β-glucuronidase
business
lcsh:RB1-214
Research Article
Subjects
Details
- Language :
- English
- ISSN :
- 17548411 and 17548403
- Volume :
- 11
- Issue :
- 11
- Database :
- OpenAIRE
- Journal :
- Disease Models & Mechanisms
- Accession number :
- edsair.doi.dedup.....17fc7fb0b38b3f6f0fc9a6ba87766f99