Seeding of protein aggregation causes cognitive impairment in rat model of cortical synucleinopathy
- 26 August 2019
- journal article
- research article
- Published by Wiley in Movement Disorders
- Vol. 34 (11) , 1699-1710
Abstract
Background: Cortical α‐synuclein pathology plays a role in the development of cognitive dysfunction in both Parkinson's disease and dementia with Lewy bodies, although the causative cellular lesions have remained unclear. We aimed to address causal links between α‐synuclein‐driven pathology in the cerebral cortex and the development of cognitive impairments using new experimental models.Methods: Neuronal overexpression of human α‐synuclein was induced in the rat medial prefrontal cortex using viral vectors. This was combined with inoculations of preformed fibrils of human α‐synuclein in some animals. Rats were evaluated with tests probing prefrontal cognitive functions (delayed matching/nonmatching to position and 5‐choice serial reaction time task). Patterns of neuropathology were characterized immunohistochemically.Results: Neither α‐synuclein overexpression nor the fibril seeds alone yielded any behavioral phenotype. In contrast, combining the 2 approaches produced significant impairments in working memory, attention, and inhibitory control. All animals injected with α‐synuclein vectors exhibited high immunoreactivity for human α‐synuclein in the medial prefrontal cortex and its primary projection targets. However, only when this overexpression was combined with fibril inoculations did animals exhibit large, proteinase K‐resistant and Ser129‐phosphorylated α‐synuclein intraneuronal inclusions in the medial prefrontal cortex and its closely interconnected brain regions. The inclusions were associated with distorted dendritic morphologies and partial neuronal loss in the targeted cortical areas.Conclusions: Cortical overexpression of human α‐synuclein is not sufficient to produce cognitive dysfunction, whereas combining this overexpression with fibril seeds yields both cognitive and histopathological phenotypes that are relevant to human Lewy body disease. © 2019 International Parkinson and Movement Disorder SocietyKeywords
Funding Information
- Åhlén-stiftelsen
- Parkinsonfonden
- Vetenskapsrådet
- Wenner-Gren Foundation
This publication has 62 references indexed in Scilit:
- The neural and genetic basis of executive function: Attention, cognitive flexibility, and response inhibitionPharmacology Biochemistry and Behavior, 2014
- Executive dysfunction in P arkinson's disease: A reviewJournal of Neuropsychology, 2013
- Pathological α-Synuclein Transmission Initiates Parkinson-like Neurodegeneration in Nontransgenic MiceScience, 2012
- Functional brain imaging of cognitive dysfunction in Parkinson's diseaseJournal of Neurology, Neurosurgery & Psychiatry, 2012
- Intracerebral inoculation of pathological α-synuclein initiates a rapidly progressive neurodegenerative α-synucleinopathy in miceJournal of Experimental Medicine, 2012
- Exogenous α-Synuclein Fibrils Induce Lewy Body Pathology Leading to Synaptic Dysfunction and Neuron DeathNeuron, 2011
- Proteomics Analysis Identifies Phosphorylation-dependent α-Synuclein Protein InteractionsMolecular & Cellular Proteomics, 2008
- Evaluation of α-synuclein immunohistochemical methods used by invited expertsActa Neuropathologica, 2008
- Double dissociation between hippocampal and prefrontal lesions on an operant delayed matching task and a water maze reference memory taskBehavioural Brain Research, 2006
- Medial prefrontal and neostriatal lesions disrupt performance in an operant delayed alternation task in ratsBehavioural Brain Research, 1999