The two major inhibitory synaptic transmitters, GABA and glycine, gate anion currents whose direction and magnitude are determined primarily by the distribution of chloride ions (Cl-) on either side of the neuronal membrane. This Cl- distribution s surprisingly difficult to determine. Each neuron seems to have a unique reversal potential for currents gated by GABAA receptors (EGABA), and recently EGABA has been shown to vary at different subcellular regions of the same neuron. These findings are hard to reconcile with the idea that one of two equilibrative cation-Cl cotransporters determine the Cl- distribution, because such a scheme links the Cl- distribution to the K and Na distributions, and should lead to an extremely uniform and predictable EGABA. ++ In the last grant cycle, we found a candidate explanation for the variability of EGABA: Cl is displaced by anionic - macromolecules in the cytoplasm and extracellular space. This is congruent with the concentration of impermeant anions in the cytoplasm, and the density of variably-sulfated glycosaminoglycans that largely comprise the matrix filling the extracellular space. The distribution of Cl- by charge displacement is analogous to the distribution of Styrofoam packing peanuts in a shipping box, where the shipped contents are the anionic macromolecules, the box is the neuronal membrane, and the peanuts are Cl-. Cl- distribution by displacement has interesting and testable predictions that we will begin to explore here. First, Cl- microdomains would be created if the distribution of anionic macromolecules is not uniform. Intracellular Cl microdomains would alter EGABA locally, while extracellular Cl domains would primarily affect -- the local GABAA conductance. Conceivably then, every GABAA synapse could have a unique reversal potential and conductance, which would permit the read-out of the enormous amount of information that could be stored in the distribution of Cl-displacing anionic macromolecules. The second prediction is that disruption of the extracellular matrix after brain injury, for example by the activation of matrix metalloproteases, would increase extracellular Cl-. Equilibrative co-transport of Cl-, cations, and water would then increase intracellular volume - a new mechanism for cytotoxic edema. We will test these predictions using perforated patch recordings and novel high-resolution Cl- reporting tools. These tools include transgenic mice with inducible expression of more sensitive ratiometric fluorescent Cl- fluorophores. We are also developing, as part of a collaborative BRAIN U01, fusions of these new Cl- fluorophores to the intracellular and extracellular faces of GABAA receptors. These fluorophores provide the sensitivity, stability and spatial resolution to rigorously test the Cl- microdomain hypothesis and the pathogenesis of cytotoxic edema using multi-photon and newly-developed very-long-term imaging technologies.

Public Health Relevance

GABA and glycine are the major inhibitory neurotransmitters, but accumulating evidence indicates that rather than creating 'go / no go' signals, these neurotransmitters create a whole spectrum of signals, from 'definitely yes' through 'maybe' to 'no'. We predict that intra- and extracellular structural matrices bind clusters of negative charges that serve to modulate the currents gated by GABA and glycine at individual synaptic connections between nerve cells. In this proposal, we will test this hypothesis using new detectors created expressly for this purpose in the NIH BRAIN tool creation project.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS040109-18
Application #
9391709
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Leenders, Miriam
Project Start
2000-04-01
Project End
2020-12-31
Budget Start
2018-01-01
Budget End
2018-12-31
Support Year
18
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02114
Glykys, Joseph; Dzhala, Volodymyr; Egawa, Kiyoshi et al. (2017) Chloride Dysregulation, Seizures, and Cerebral Edema: A Relationship with Therapeutic Potential. Trends Neurosci 40:276-294
Glykys, Joseph; Staley, Kevin J (2016) Developmental Decrease of Neuronal Chloride Concentration Is Independent of Trauma in Thalamocortical Brain Slices. PLoS One 11:e0158012
Glykys, Joseph; Staley, Kevin J (2015) Diazepam effect during early neonatal development correlates with neuronal Cl(.). Ann Clin Transl Neurol 2:1055-70
Staley, Kevin (2015) Molecular mechanisms of epilepsy. Nat Neurosci 18:367-72
Dzhala, Volodymyr; Staley, Kevin J (2015) Acute and chronic efficacy of bumetanide in an in vitro model of posttraumatic epileptogenesis. CNS Neurosci Ther 21:173-80
Glykys, J; Dzhala, V; Egawa, K et al. (2014) Response to comments on ""Local impermeant anions establish the neuronal chloride concentration"". Science 345:1130
Delpire, Eric; Staley, Kevin J (2014) Novel determinants of the neuronal Cl(-) concentration. J Physiol 592:4099-114
Glykys, J; Dzhala, V; Egawa, K et al. (2014) Local impermeant anions establish the neuronal chloride concentration. Science 343:670-5
Dzhala, Volodymyr; Valeeva, Guzel; Glykys, Joseph et al. (2012) Traumatic alterations in GABA signaling disrupt hippocampal network activity in the developing brain. J Neurosci 32:4017-31
Talos, Delia M; Sun, Hongyu; Kosaras, Bela et al. (2012) Altered inhibition in tuberous sclerosis and type IIb cortical dysplasia. Ann Neurol 71:539-51

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