Localized Induction of Wild-Type and Mutant Alpha-Synuclein Aggregation Reveals Propagation along Neuroanatomical Tracts

Author:

Ayers Jacob I.1,Riffe Cara J.1,Sorrentino Zachary A.1,Diamond Jeffrey1,Fagerli Eric1,Brooks Mieu1,Galaleldeen Ahmad23,Hart P. John34,Giasson Benoit I.1

Affiliation:

1. Department of Neuroscience, Center for Translational Research in Neurodegenerative Disease, McKnight Brain Institute, University of Florida, Gainesville, Florida, USA

2. Department of Biological Sciences, St. Mary's University, San Antonio, Texas, USA

3. Department of Biochemistry and X-Ray Crystallography Core Laboratory, University of Texas Health Science Center, San Antonio, Texas, USA

4. Department of Veterans Affairs, Geriatric Research, Education, and Clinical Center, South Texas Health Care System, San Antonio, Texas, USA

Abstract

The accumulation of alpha-synuclein (αS) inclusions is a hallmark feature of Parkinson's disease (PD) and PD-related diseases. Recently, a number of studies have demonstrated similarities between the prion protein and αS, including its ability to spread along neuroanatomical tracts throughout the central nervous system (CNS). However, there are caveats in each of these studies in which the injection routes used had the potential to result in a widespread dissemination of the αS-containing inocula, making it difficult to precisely define the mechanisms of spread. In this study, we assessed the spread of pathology following a localized induction of αS inclusions in the lumbar spinal cord following a unilateral injection in the sciatic nerve. Using this paradigm, we demonstrated the ability for αS inclusion spread and/or induction along neuroanatomical tracts within the CNS of two αS-overexpressing mouse models.

Funder

HHS | NIH | National Institute of Neurological Disorders and Stroke

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference65 articles.

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