Synuclein Model Overview
Alpha-synuclein (α-synuclein; α-syn) is major pathogenic protein found in Lewy bodies in the substantia nigra pars compacta and other brain regions in Parkinson's disease (PD). For this Parkinson's disease model, we perform stereotaxic inoculation of recombinant preformed fibrils (PFFs) of human α-syn into the brains of M83 transgenic mice [B6;C3-Tg( Prnp SNCA A53T )83Vle/J] with α-syn overexpression or murine α-syn into the brains of non-transgenic, wild-type (B6-C3H) mice.
Our validated injection sites are Striatum +/- Overlying Cortex or Medial Forebrain Bundle (MFB).
The rationale for targeting the Striatum +/- Overlying Cortex includes:
- It is the injection site originally reported (Luk et al., J. Exp. Med., 209: 975-986, 2011; doi: 10.1084/jem.20112457; Luk et al., Science, 338: 949-953, 2012; doi: 10.1126/science.1227157)
- The dopaminergic nerve terminals in the striatum originate from neurons in the substantia nigra
- Injection into the overlying cerebral cortex increases the extent alpha-synuclein pathology in the brain
Our rationale for targeting the MFB includes:
- It is a tract directly connected to the substantia nigra and ventral tegmental area, and is often targeted in toxin-based models of human Parkinson's disease (e.g. 6-hyroxydopamine [6-OHDA])
- It serves as a "hub" for projections from many other brain regions, thereby serving as an excellent seeding location to facilitate spreading of alpha-synuclein pathology to distant brain regions
- This model results in significant loss of dopaminergic neurons in the substantia nigra and associated motor deficits
A significant advantage of this animal model of Parkinson's disease is the it reproduces many aspects of the human disease, including:
- Highly reproducible spreading of alpha-synuclein in a well-defined spatiotemporal pattern, resulting in extensive alpha-synuclein pathology in neuronal cell bodies and neurites
- Strong neuroinflammation (microgliosis and astrogliosis)
- Neurodegeneration with loss of tyrosine hydroxylase positive neurons in the substantia nigra & regional brain atrophy
- Measurable motor function changes
- Amenable to disease modification via therapeutic intervention
Synuclein Model Generation
A general schema for synuclein PFF animal model generation is:
We have in-licensed the M83 transgenic (tg) mice. As a Preclinical Neuroscience CRO, we maintain a well-established breeding colony of these transgenic alpha-synuclein mice in-house at Biospective, allowing us to conduct large-scale (>100 mice) studies.
For this specific rodent model, we breed and age M83+/- male mice to 8-12 weeks-of-age. Alternatively, we use wild-type (B6-C3H) mice at 8-12 weeks-of-age. We then perform stereotaxic injection of sonicated, recombinant human alpha-synuclein PFFs into the target region. We use digital stereotaxic devices with automated microinjectors for high accuracy & precision.
This animal model is highly reproducible with a nearly 100% success rate of synuclein PFF seeding.
Our Synuclein Mouse Model Validated Measures
- Body weight
- Clinical scores
- Motor function tests
- MRI brain atrophy (Read More in our Presentation - Brain atrophy analysis in rodent models of neurodegenerative diseases)
- Neurofilament Light measures in plasma & CSF
- Immunohistochemistry & multiplex immunofluorescence (Read More in our Presentation - Microglial activation in an α-synuclein mouse model of Parkinson's disease)
Learn more about our characterization of this model, our validated measures, and our Preclinical Neuroscience CRO services.