Neuronal Adaptation and Plasticity after Chronic Disuse

NIH RePORTER · NIH · R01 · $595,386 · view on reporter.nih.gov ↗

Abstract

ABSTRACT Homeostatic regulation of excitability and synaptic efficacy works in conjunction with acutely induced Hebbian plasticity to maintain neuron firing within limits and thus preserve network stability and information flow. There is general agreement that homeostatic plasticity can affect intrinsic properties (action potential duration controlling neurotransmission) or synaptic properties (unitary synaptic current amplitude, for example) and involves diverse molecular mechanisms. Dysfunctional homeostasis has been invoked as a basis for brain diseases such as autism spectrum disorders (ASD). Despite major effort, the molecular underpinnings of various forms of homeostatic adaptation are still not clear. In this project, we will examine various aspects of neuronal homeostasis with relevance to neuropsychiatric disorders. The first question is how neuronal inactivity initiates local signaling near postsynaptic CaV1 channels and causes propagation of signals to the nucleus to regulate alternative mRNA splicing (AS) and thus affect spike duration. We will extend our findings on how one ASD-related gene (CACNA1C, L-type Ca2+ channel subunit) controls the expression of another (KCNMA1, BK channel subunit). Our data suggest that signaling to the nucleus via bCaMKK (encoded by CAMKK2) plays a critical role in AS through effects on localization of the splice factor Nova-2. In another subproject, we will clarify how the same activity silencing affects synaptic properties, and the striking switchover of postsynaptic glutamate receptors from Ca2+-impermeable to Ca2+-permeable AMPA receptors. We will decipher how various signaling pathways, generating both negative and positive feedback, work in coordination to trigger a damped oscillatory response of synaptic properties following TTX silencing, a novel observation from our group. We will take studies of homeostasis to recurrent circuits in cultured hippocampal slices, using an all-optical approach to visualize reallocation of presynaptic weights following inactivity and their postsynaptic consequences. Each of the Aims are of relevance to disease states such as ASD and schizophrenia. Using a mouse model of Timothy Syndrome, a rare form of ASD, we will probe how physiological phenomena are altered in a pathogenic setting, for example exploring why inactivity-driven BK splicing is much more severe in Timothy Syndrome neurons and probing how this affects higher order functions of relevance to ASD.

Key facts

NIH application ID
10117282
Project number
5R01MH071739-18
Recipient
NEW YORK UNIVERSITY SCHOOL OF MEDICINE
Principal Investigator
RICHARD W TSIEN
Activity code
R01
Funding institute
NIH
Fiscal year
2021
Award amount
$595,386
Award type
5
Project period
2004-07-16 → 2025-01-31