نتایج جستجو برای: synuclein

تعداد نتایج: 7040  

Journal: :Brain sciences 2018
Manuel Menéndez-González Huber S Padilla-Zambrano Cristina Tomás-Zapico Benjamin Fernández García

This concept article aims to show the rationale of targeting extracellular α-Synuclein (α-Syn) from cerebrospinal fluid (CSF) as a new strategy to remove this protein from the brain in Parkinson's disease (PD). Misfolding and intracellular aggregation of α-synuclein into Lewy bodies are thought to be crucial in the pathogenesis of PD. Recent research has shown that small amounts of monomeric an...

Journal: :EMBO reports 2010
Frédéric Darios Violeta Ruipérez Inmaculada López Jose Villanueva Luis M Gutierrez Bazbek Davletov

Alpha-synuclein is a synaptic modulatory protein implicated in the pathogenesis of Parkinson disease. The precise functions of this small cytosolic protein are still under investigation. alpha-Synuclein has been proposed to regulate soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) proteins involved in vesicle fusion. Interestingly, alpha-synuclein fails to interact ...

2003
Amy B. Manning-Boğ Alison L. McCormack Maya G. Purisai Laurel M. Bolin Donato A. Di Monte

-Synuclein is likely to play a role in neurodegenerative processes, including the degeneration of nigrostriatal dopaminergic neurons that underlies Parkinson’s disease. However, the toxicological properties of -synuclein remain relatively unknown. Here, the relationship between -synuclein expression and neuronal injury was studied in mice exposed to the herbicide paraquat. Paraquat neurotoxicit...

2004
Doris L. Fortin Matthew D. Troyer Ken Nakamura Shin-ichiro Kubo Malcolm D. Anthony Robert H. Edwards

-Synuclein contributes to the pathogenesis of Parkinson’s disease (PD), but its precise role in the disorder and its normal function remain poorly understood. Consistent with a presumed role in neurotransmitter release and its prominent deposition in the dystrophic neurites of PD, -synuclein localizes almost exclusively to the nerve terminal. In brain extracts, however, -synuclein behaves as a ...

Journal: :The Lancet. Neurology 2011
Kostas Vekrellis Maria Xilouri Evangelia Emmanouilidou Hardy J Rideout Leonidas Stefanis

Substantial genetic, neuropathological, and biochemical evidence implicates the presynaptic neuronal protein α-synuclein in Parkinson's disease and related Lewy body disorders. How dysregulation of α-synuclein leads to neurodegeneration is, however, unclear. Soluble oligomeric, but not fully fibrillar, α-synuclein is thought to be toxic. The major neuronal target of aberrant α-synuclein might b...

2011
Arianna Bellucci Laura Navarria Elisa Falarti Michela Zaltieri Federica Bono Ginetta Collo Maria Grazia Cristina Missale PierFranco Spano

Alpha-synuclein, the major component of Lewy bodies, is thought to play a central role in the onset of synaptic dysfunctions in Parkinson's disease (PD). In particular, α-synuclein may affect dopaminergic neuron function as it interacts with a key protein modulating dopamine (DA) content at the synapse: the DA transporter (DAT). Indeed, recent evidence from our "in vitro" studies showed that α-...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2014
Giuseppe Ronzitti Giovanna Bucci Marco Emanuele Damiana Leo Tatyana D Sotnikova Liudmila V Mus Camille H Soubrane Mark L Dallas Agnes Thalhammer Lorenzo A Cingolani Sumiko Mochida Raul R Gainetdinov Gary J Stephens Evelina Chieregatti

α-Synuclein is thought to regulate neurotransmitter release through multiple interactions with presynaptic proteins, cytoskeletal elements, ion channels, and synaptic vesicles membrane. α-Synuclein is abundant in the presynaptic compartment, and its release from neurons and glia has been described as responsible for spreading of α-synuclein-derived pathology. α-Synuclein-dependent dysregulation...

2014
Guobin Li Haiying Yang Dezhang Zhu Hui Huang Guoyuan Liu Peng Lun

Chaperone-mediated autophagy (CMA) is involved in wild-type α-synuclein degradation in Parkinson's disease (PD), and LAMP2A and Hsc 70 have recently been indicated to be deregulated by microRNAs. To recognize the regularory role of miR-320a in CMA and the possible role in α-synuclein degradation, in the present study, we examined the targeting and regulating role of miR-320 in Hsc 70 expression...

2014
David J. Busch Paul A. Oliphint Rylie B. Walsh Susan M. L. Banks Wendy S. Woods Julia M. George Jennifer R. Morgan

Parkinson's disease is associated with multiplication of the α-synuclein gene and abnormal accumulation of the protein. In animal models, α-synuclein overexpression broadly impairs synaptic vesicle trafficking. However, the exact steps of the vesicle trafficking pathway affected by excess α-synuclein and the underlying molecular mechanisms remain unknown. Therefore we acutely increased synuclei...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2013
Abid Oueslati Bernard L Schneider Patrick Aebischer Hilal A Lashuel

An increase in α-synuclein levels due to gene duplications/triplications or impaired degradation is sufficient to trigger its aggregation and cause familial Parkinson disease (PD). Therefore, lowering α-synuclein levels represents a viable therapeutic strategy for the treatment of PD and related synucleinopathies. Here, we report that Polo-like kinase 2 (PLK2), an enzyme up-regulated in synucle...

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