In the central nervous system, proteins experience mechanical cues that vary widely across developmental stage, cell type and location, and physiological state. When acting on membrane embedded ion-channel proteins, mechanical forces can modulate the ionic flux produced by the physiological activator or can directly gate the channel. In this application, we explore the hypothesis that mechanical forces can open NMDA receptors in the absence of the endogenous neurotransmitter glutamate. NMDA receptors are glutamate-gated excitatory receptors that are widely expressed at synaptic and extrasynaptic sites in brain and spinal cord, where they play key roles in physiology and pathology of excitatory synaptic development and plasticity. These key functions rely on unique biophysical properties such as, among others, slow kinetics, large calcium permeability, voltage-dependent Mg2+ block. In this application, we propose to pursue two interrelated aims. The first will be done in recombinant receptors and will examine the type and intensity of force that can gate the channel, the biophysical properties of the force-induced current (kinetics, conductance, permeability, etc.), and how the channel senses the mechanical cue.
The second aim will be done in endogenous receptors (primary cultured neurons) and will begin to explore possible roles of mechanically gated NMDA receptor currents in physiologic and pathologic conditions. In both aims, we will use electrophysiology and optical methods to monitor NMDA receptor response, total and calcium current, to experimentally-controlled mechanical perturbations. These experiments will delineate what kind of mechanical forces can activate NMDA receptors and how the signals produced by force and by glutamate compare, and will help to predict the physiological and pathological situations where mechanical forces can shape neuronal function specifically by gating NMDA receptor currents. Given that the mechanosensitivity of NMDA receptor signals is yet uncharted, the results will lay the groundwork necessary to understand how NMDA receptors contribute to the impact of mechanical forces on synaptic function and dysfunction.

Public Health Relevance

NMDA receptors are glutamate-gated excitatory ion-channels with critical roles in the development of central nervous system and remain important throughout lifespan for the normal function of cells and circuits across the brain and spinal cord. Their dysfunction has been implicated in severe developmental and psychiatric conditions, including schizophrenia, addiction, and chronic pain, and also in debilitating neuropathologies such as stroke, Alzheimer's, Parkinson's, and Huntington's diseases; and they may also contribute to psychiatric and neurologic effects associated with brain and spinal cord trauma, which may include shaken baby syndrome, concussions, and combat, sports, and automobile injuries. This application explores the hypothesis that mechanical stimuli can activate the NMDA receptors in the absence of neurotransmission and aims to characterize the mechanically-activated signals and thus to provide the basic knowledge necessary to design new therapeutic approaches.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21NS098385-01
Application #
9168784
Study Section
Biophysics of Neural Systems Study Section (BPNS)
Program Officer
Silberberg, Shai D
Project Start
2016-08-15
Project End
2018-07-31
Budget Start
2016-08-15
Budget End
2017-07-31
Support Year
1
Fiscal Year
2016
Total Cost
$199,375
Indirect Cost
$74,375
Name
State University of New York at Buffalo
Department
Biochemistry
Type
Schools of Medicine
DUNS #
038633251
City
Buffalo
State
NY
Country
United States
Zip Code
14260
Iacobucci, Gary J; Popescu, Gabriela K (2018) Kinetic models for activation and modulation of NMDA receptor subtypes. Curr Opin Physiol 2:114-122
Maneshi, Mohammad Mehdi; Maki, Bruce; Gnanasambandam, Radhakrishnan et al. (2017) Mechanical stress activates NMDA receptors in the absence of agonists. Sci Rep 7:39610
Bajpai, Vivek K; Kerosuo, Laura; Tseropoulos, Georgios et al. (2017) Reprogramming Postnatal Human Epidermal Keratinocytes Toward Functional Neural Crest Fates. Stem Cells 35:1402-1415
Iacobucci, Gary J; Popescu, Gabriela K (2017) Resident Calmodulin Primes NMDA Receptors for Ca2+-Dependent Inactivation. Biophys J 113:2236-2248
Iacobucci, Gary J; Popescu, Gabriela K (2017) NMDA receptors: linking physiological output to biophysical operation. Nat Rev Neurosci 18:236-249