Time course and magnitude of alpha-synuclein inclusion formation and nigrostriatal degeneration in the rat model of synucleinopathy triggered by intrastriatal α-synuclein preformed fibrils

Animal models that accurately recapitulate the accumulation of alpha-synuclein (α-syn) inclusions, progressive neurodegeneration of the nigrostriatal system and motor deficits can be useful tools for Parkinson's disease (PD) research. The preformed fibril (PFF) synucleinopathy model in rodents...

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Main Authors: Joseph R. Patterson, Megan F. Duffy, Christopher J. Kemp, Jacob W. Howe, Timothy J. Collier, Anna C. Stoll, Kathryn M. Miller, Pooja Patel, Nathan Levine, Darren J. Moore, Kelvin C. Luk, Sheila M. Fleming, Nicholas M. Kanaan, Katrina L. Paumier, Omar M.A. El-Agnaf, Caryl E. Sortwell
Format: Article
Language:English
Published: Elsevier 2019-10-01
Series:Neurobiology of Disease
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996119301937
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author Joseph R. Patterson
Megan F. Duffy
Christopher J. Kemp
Jacob W. Howe
Timothy J. Collier
Anna C. Stoll
Kathryn M. Miller
Pooja Patel
Nathan Levine
Darren J. Moore
Kelvin C. Luk
Sheila M. Fleming
Nicholas M. Kanaan
Katrina L. Paumier
Omar M.A. El-Agnaf
Caryl E. Sortwell
spellingShingle Joseph R. Patterson
Megan F. Duffy
Christopher J. Kemp
Jacob W. Howe
Timothy J. Collier
Anna C. Stoll
Kathryn M. Miller
Pooja Patel
Nathan Levine
Darren J. Moore
Kelvin C. Luk
Sheila M. Fleming
Nicholas M. Kanaan
Katrina L. Paumier
Omar M.A. El-Agnaf
Caryl E. Sortwell
Time course and magnitude of alpha-synuclein inclusion formation and nigrostriatal degeneration in the rat model of synucleinopathy triggered by intrastriatal α-synuclein preformed fibrils
Neurobiology of Disease
Alpha-Synuclein
Preformed fibrils
Synucleinopathy
Parkinson's disease
author_facet Joseph R. Patterson
Megan F. Duffy
Christopher J. Kemp
Jacob W. Howe
Timothy J. Collier
Anna C. Stoll
Kathryn M. Miller
Pooja Patel
Nathan Levine
Darren J. Moore
Kelvin C. Luk
Sheila M. Fleming
Nicholas M. Kanaan
Katrina L. Paumier
Omar M.A. El-Agnaf
Caryl E. Sortwell
author_sort Joseph R. Patterson
title Time course and magnitude of alpha-synuclein inclusion formation and nigrostriatal degeneration in the rat model of synucleinopathy triggered by intrastriatal α-synuclein preformed fibrils
title_short Time course and magnitude of alpha-synuclein inclusion formation and nigrostriatal degeneration in the rat model of synucleinopathy triggered by intrastriatal α-synuclein preformed fibrils
title_full Time course and magnitude of alpha-synuclein inclusion formation and nigrostriatal degeneration in the rat model of synucleinopathy triggered by intrastriatal α-synuclein preformed fibrils
title_fullStr Time course and magnitude of alpha-synuclein inclusion formation and nigrostriatal degeneration in the rat model of synucleinopathy triggered by intrastriatal α-synuclein preformed fibrils
title_full_unstemmed Time course and magnitude of alpha-synuclein inclusion formation and nigrostriatal degeneration in the rat model of synucleinopathy triggered by intrastriatal α-synuclein preformed fibrils
title_sort time course and magnitude of alpha-synuclein inclusion formation and nigrostriatal degeneration in the rat model of synucleinopathy triggered by intrastriatal α-synuclein preformed fibrils
publisher Elsevier
series Neurobiology of Disease
issn 1095-953X
publishDate 2019-10-01
description Animal models that accurately recapitulate the accumulation of alpha-synuclein (α-syn) inclusions, progressive neurodegeneration of the nigrostriatal system and motor deficits can be useful tools for Parkinson's disease (PD) research. The preformed fibril (PFF) synucleinopathy model in rodents generally displays these PD-relevant features, however, the magnitude and predictability of these events is far from established. We therefore sought to optimize the magnitude of α-syn accumulation and nigrostriatal degeneration, and to understand the time course of both. Rats were injected unilaterally with different quantities of α-syn PFFs (8 or 16 μg of total protein) into striatal sites selected to concentrate α-syn inclusion formation in the substantia nigra pars compacta (SNpc). Rats displayed an α-syn PFF quantity-dependent increase in the magnitude of ipsilateral SNpc inclusion formation at 2 months and bilateral loss of nigral dopamine neurons at 6 months. Unilateral 16 μg PFF injection also resulted in modest sensorimotor deficits in forelimb adjusting steps associated with degeneration at 6 months. Bilateral injection of 16 μg α-syn PFFs resulted in symmetric bilateral degeneration equivalent to the ipsilateral nigral degeneration observed following unilateral 16 μg PFF injection (~50% loss). Bilateral PFF injections additionally resulted in alterations in several gait analysis parameters. These α-syn PFF parameters can be applied to generate a reproducible synucleinopathy model in rats with which to study pathogenic mechanisms and vet potential disease-modifying therapies.
topic Alpha-Synuclein
Preformed fibrils
Synucleinopathy
Parkinson's disease
url http://www.sciencedirect.com/science/article/pii/S0969996119301937
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spelling doaj-758f84c3154542e3af56b5659a3f143d2021-03-22T12:48:24ZengElsevierNeurobiology of Disease1095-953X2019-10-01130104525Time course and magnitude of alpha-synuclein inclusion formation and nigrostriatal degeneration in the rat model of synucleinopathy triggered by intrastriatal α-synuclein preformed fibrilsJoseph R. Patterson0Megan F. Duffy1Christopher J. Kemp2Jacob W. Howe3Timothy J. Collier4Anna C. Stoll5Kathryn M. Miller6Pooja Patel7Nathan Levine8Darren J. Moore9Kelvin C. Luk10Sheila M. Fleming11Nicholas M. Kanaan12Katrina L. Paumier13Omar M.A. El-Agnaf14Caryl E. Sortwell15Department of Translational Neuroscience, Michigan State University, Grand Rapids, MI, USA; Corresponding author.Department of Translational Neuroscience, Michigan State University, Grand Rapids, MI, USA; Neuroscience Program, Michigan State University, East Lansing, MI, USADepartment of Translational Neuroscience, Michigan State University, Grand Rapids, MI, USADepartment of Translational Neuroscience, Michigan State University, Grand Rapids, MI, USADepartment of Translational Neuroscience, Michigan State University, Grand Rapids, MI, USA; Neuroscience Program, Michigan State University, East Lansing, MI, USA; Mercy Health Hauenstein Neuroscience Medical Center, Grand Rapids, MI, USADepartment of Translational Neuroscience, Michigan State University, Grand Rapids, MI, USA; Department of Pharmacology and Toxicology, Michigan State University, East Lansing, MI, USADepartment of Translational Neuroscience, Michigan State University, Grand Rapids, MI, USA; Neuroscience Program, Michigan State University, East Lansing, MI, USADepartment of Translational Neuroscience, Michigan State University, Grand Rapids, MI, USACenter of Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI, USACenter of Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI, USACenter for Neurodegenerative Disease Research, Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USACollege of Pharmacy, Northeast Ohio Medical University, Rootstown, OH, USADepartment of Translational Neuroscience, Michigan State University, Grand Rapids, MI, USA; Neuroscience Program, Michigan State University, East Lansing, MI, USA; Mercy Health Hauenstein Neuroscience Medical Center, Grand Rapids, MI, USADepartment of Translational Neuroscience, Michigan State University, Grand Rapids, MI, USANeurological Disorders Researcher Center, Qatar Biomedical Research Institute (QBRI), Hamad Bin Khalifa University (HBKU), Qatar Foundation, Doha, QatarDepartment of Translational Neuroscience, Michigan State University, Grand Rapids, MI, USA; Neuroscience Program, Michigan State University, East Lansing, MI, USA; Mercy Health Hauenstein Neuroscience Medical Center, Grand Rapids, MI, USAAnimal models that accurately recapitulate the accumulation of alpha-synuclein (α-syn) inclusions, progressive neurodegeneration of the nigrostriatal system and motor deficits can be useful tools for Parkinson's disease (PD) research. The preformed fibril (PFF) synucleinopathy model in rodents generally displays these PD-relevant features, however, the magnitude and predictability of these events is far from established. We therefore sought to optimize the magnitude of α-syn accumulation and nigrostriatal degeneration, and to understand the time course of both. Rats were injected unilaterally with different quantities of α-syn PFFs (8 or 16 μg of total protein) into striatal sites selected to concentrate α-syn inclusion formation in the substantia nigra pars compacta (SNpc). Rats displayed an α-syn PFF quantity-dependent increase in the magnitude of ipsilateral SNpc inclusion formation at 2 months and bilateral loss of nigral dopamine neurons at 6 months. Unilateral 16 μg PFF injection also resulted in modest sensorimotor deficits in forelimb adjusting steps associated with degeneration at 6 months. Bilateral injection of 16 μg α-syn PFFs resulted in symmetric bilateral degeneration equivalent to the ipsilateral nigral degeneration observed following unilateral 16 μg PFF injection (~50% loss). Bilateral PFF injections additionally resulted in alterations in several gait analysis parameters. These α-syn PFF parameters can be applied to generate a reproducible synucleinopathy model in rats with which to study pathogenic mechanisms and vet potential disease-modifying therapies.http://www.sciencedirect.com/science/article/pii/S0969996119301937Alpha-SynucleinPreformed fibrilsSynucleinopathyParkinson's disease