Intellectual disabilities (ID) and autism spectrum disorders (ASD) are highly prevalent. Seizures occur in 10- 30% of individuals with ASD, leading to lifelong disabilities. Treatments are largely lacking because these disorders are molecularly ill-defined. Large-scale genetic screens of families with ASD and ID have identified hundreds of risk genes. Compelling evidence suggests that the risk genes converge on a few key biological processes in neurons. Our grant focuses on two- the ?-catenin (?-cat)/ canonical Wnt pathway and synaptic function. ?-cat has dual functions in cadherin synaptic adhesion complexes and canonical Wnt signal transduction. Both pathways modulate synapse density and plasticity, as well as the formation and function of circuit networks in the brain. We propose that an optimal range of ?-cat levels and its associated pathways is essential; levels too high or low lead to deregulation and brain dysfunction. As support for this hypothesis, several human ID, ASD, and seizure linked genes are predicted to cause either loss- or gain-of-function of the ?-cat/ canonical Wnt pathway, highlighting the importance of elucidating the changes caused by aberrant ?-cat levels in the brain. Further, our recent studies show that targeted deletion in mouse neurons of adenomatous polyposis coli protein (APC), a major negative regulator of ?-cat levels in the canonical Wnt pathway, leads to cognitive and autistic-like disabilities and seizures. Synapse number, maturation and function are altered. Molecular alterations include excessive ?-cat and associated changes in Wnt target gene expression and cadherin synaptic adhesion complexes. We propose direct tests of the effects of aberrant ?-cat levels in the brain.
Aim 1 studies will use our new mouse line with ?-cat conditional overexpression in neurons to model gain-of-function.
Aim 2 studies will use our new mouse line with conditional deletion of ?-cat to model loss-of- function. We will define the cognitive and behavioral phenotypes, their severity, and the molecular and functional changes caused by high versus low ?-cat.
Aim3 studies will identify drug treatments that correct excessive ?-cat levels and test for amelioratio of cognitive deficits, autism-like behaviors and seizures in APC conditional knockout mice. We will also test for rectification of the molecular and functional alterations. Preliminary data provde strong support for our planned studies. All 3 Aims will use the same multidisciplinary approaches to define the behavioral, molecular and functional changes induced by aberrant ?-cat levels. This project will utilize the complementary expertise of the Jacob lab in synaptic biology and new genetic mouse models of cognitive and autism-like disabilities, with co-morbid seizures, and the Dulla lab in electrophysiological and network analysis. Our studies will elucidate how alterations in ?-cat contribute to the pathophysiology of ID, ASD and seizures on a molecular, synaptic, and circuit level. Our findings will also provide critical insights into the therapeutic potential of targeting ?-cat and its associated pathways and thereby inform the design of future therapeutic strategies for these neurodevelopmental disorders.

Public Health Relevance

Autism spectrum disorders (ASD) and intellectual disabilities (ID) are highly prevalent. Seizures are often co- morbid with autism. Effective therapeutic treatments are largely lacking because these disorders are not well defined molecularly. Emerging evidence suggests that ID and ASD-linked genes converge on a small number of key biological processes that predispose neurons to these disorders. Our planned studies will focus on two of these molecular networks. We will determine how their aberrant function contributes to the pathophysiology of ASD, ID, and seizures on molecular, synaptic, and circuit levels. Our findings will identify novel molecular targets and drug treatments to inform the design of future therapeutic strategies, with relevance to multiple ID, ASD and seizure-linked gene mutations.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
1R01MH106623-01A1
Application #
9026843
Study Section
Special Emphasis Panel (ZRG1-MDCN-P (57)S)
Program Officer
Winsky, Lois M
Project Start
2016-08-05
Project End
2021-04-30
Budget Start
2016-08-05
Budget End
2017-04-30
Support Year
1
Fiscal Year
2016
Total Cost
$520,996
Indirect Cost
$205,241
Name
Tufts University
Department
Neurosciences
Type
Schools of Medicine
DUNS #
039318308
City
Boston
State
MA
Country
United States
Zip Code
02111
Pirone, Antonella; Alexander, Jonathan M; Koenig, Jenny B et al. (2018) Social Stimulus Causes Aberrant Activation of the Medial Prefrontal Cortex in a Mouse Model With Autism-Like Behaviors. Front Synaptic Neurosci 10:35
Pirone, Antonella; Alexander, Jonathan; Lau, Lauren A et al. (2017) APC conditional knock-out mouse is a model of infantile spasms with elevated neuronal ?-catenin levels, neonatal spasms, and chronic seizures. Neurobiol Dis 98:149-157