Mice lacking alpha-synuclein are resistant to mitochondrial toxins.
Explore this paper's citation graph
Summary
It is found that alpha-synuclein-deficient mice are resistant to MPTP-induced degeneration of dopaminergic neurons and are also resistant to both malonate and 3-nitropropionic acid neurotoxicity.
- Type
- article
- Published
- 2006-03-01
- Cited by
- 209
- References
- 67
- Access
- Open access
- OpenAlex
- https://openalex.org/W1975722154
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:6724694
Keywords
Alpha-synuclein, Biology, Alpha (finance), Neuroscience, Parkinson's disease
References
- Dopamine mediates striatal malonate toxicity via dopamine transporter‐dependent generation of reactive oxygen species and D2 but not D1 receptor activation
- Kinetic Stabilization of the α-Synuclein Protofibril by a Dopamine-α-Synuclein Adduct
- The herbicide paraquat causes up-regulation and aggregation of alpha-synuclein in mice: paraquat and alpha-synuclein.
- Nuclear translocation and transcription regulation by the membrane-associated guanylate kinase CASK/LIN-2
- Induction of α-Synuclein Aggregation by Intracellular Nitrative Insult
- The A53T alpha-synuclein mutation increases iron-dependent aggregation and toxicity.
- Dopamine Modulates the Susceptibility of Striatal Neurons to 3-Nitropropionic Acid in the Rat Model of Huntington’s Disease
- Mice Deficient in Cellular Glutathione Peroxidase Show Increased Vulnerability to Malonate, 3-Nitropropionic Acid, and 1-Methyl-4-Phenyl-1,2,5,6-Tetrahydropyridine
- Behavioral and neurochemical effects of wild-type and mutated human alpha-synuclein in transgenic mice.
- Alpha-synuclein and neurodegenerative diseases
- GluR1 Glutamate Receptor Subunit Is Regulated Differentially in the Primate Basal Ganglia Following Nigrostriatal Dopamine Denervation
- A Drosophila model of Parkinson's disease
- Dopamine-dependent neurotoxicity of α-synuclein: A mechanism for selective neurodegeneration in Parkinson disease
- Reversal of motor impairments in parkinsonian rats by continuous intrastriatal delivery of l-dopa using rAAV-mediated gene transfer
- Mice lacking alpha-synuclein have an attenuated loss of striatal dopamine following prolonged chronic MPTP administration.
- MPTP induces alpha‐synuclein aggregation in the substantia nigra of baboons
- 6-Hydroxydopamine injections into the nigrostriatal pathway attenuate striatal malonate and 3-nitropropionic acid lesions.
- α-Synuclein phosphorylation controls neurotoxicity and inclusion formation in a Drosophila model of Parkinson disease
- Creatine increase survival and delays motor symptoms in a transgenic animal model of Huntington's disease.
- Proteasome Inhibition Alters Neural Mitochondrial Homeostasis and Mitochondria Turnover*
Cited by
- Untersuchung des Expressionsmusters und der Neuropathologie konditionaler Mausmodelle des Morbus Parkinson
- Adult neurogenesis in Parkinson’s disease
- Interaction between Neuromelanin and Alpha-Synuclein in Parkinson’s Disease
- shRNA targeting α-synuclein prevents neurodegeneration in a Parkinson's disease model.
- Mitochondrial importance in Alzheimer's, Huntington's and Parkinson's diseases.
- Mécanismes moléculaires et de signalisation induits par le stress oxydatif dans des modèles in vivo de la maladie de Parkinson chez la drosophile : intoxication au paraquat et expression de l'α-synucléine
- PROTEOMIC ANALYSIS OF DOPAMINE OXIDATION INDUCED MODIFICATIONS TO MITOCHONDRIAL PROTEINS: IMPLICATIONS FOR PARKINSON'S DISEASE
- Role of glutathione s-transferase pi in neuronal protection under oxidative stress and proteasome inhibition relevance to Parkinson’s disease
- Mitochondrial Involvement in Neurodegeneration and Aging
- Neurodegeneration in Parkinson's disease: genetics enlightens physiopathology.
- Ubiquitin-proteasome system dysfunction in experimental models of Parkinson's disease
- Signal Transduction Pathways Modulated by the PD-causative Gene LRRK2
- Alpha-synuclein in the neurodegenerative mechanisms of Parkinson's disease and dementia with Lewy bodies
- Genetic mouse models of neurodegenerative diseases.
- Redox imbalance in Parkinson's disease.
- Regional lysosomal malfunction underlies the selectivity of alpha-synuclein neurodegeneration
- Over‐expression of alpha‐synuclein in the nervous system enhances axonal degeneration after peripheral nerve lesion in a transgenic mouse strain
- Deletion of Herp facilitates degradation of cytosolic proteins
- Mitochondrial alterations in Parkinson’s disease: new clues
- Limelight on Alpha-Synuclein: Pathological and Mechanistic Implications in Neurodegeneration
Related papers
- Cloning and Characterization of Rat BAT3 cDNA
- EFFECT OF THE NEMATODE PHASMARHABDITIS HERMAPHRODITA ON YOUNG STAGES OF THE PEST SLUG ARION LUSITANICUS
- HLA-B-associated transcript 3 (Bat3)/Scythe is essential for p300-mediated acetylation of p53.
- Anthoxanthum Mosaic Virus
- Ecological and evolutionary importance of neighbors in the grass Anthoxanthum odoratum
- European Sweet Vernal Grasses (Anthoxanthum: Poaceae, Pooideae, Aveneae): A Morphometric Taxonomical Approach
- Memoirs: The Structure and Biology of Schizoneura Lanigera, Hausmann or Woolly Aphis of the Apple Tree: Part I.--The Apterous Viviparous Female
- HSV-1 strain McKrae is more neuroinvasive than HSV-1 KOS after corneal or vaginal inoculation in mice
- The evolutionary history of placodes: a molecular genetic investigation of the larvacean urochordate Oikopleura dioica
- Viral Pathogens and the Advantage of Sex in the Perennial Grass Anthoxanthum odoratum [and Discussion]