Research Axis
Brain and Child Development Axis
Research Theme
Neurodevelopmental diseases
Address
CHUSJ - Centre de Recherche
Phone
514 345-4931 #2867
In the cerebral cortex, neural networks consist of two broad classes of neurons: excitatory projection neurons, which use glutamate as neurotransmitter, and inhibitory local-circuit interneurons, comprising about 20-30% of all cortical neurons, which primarily use gamma-aminobutyric acid-GABA as a neurotransmitter. Although a minor cell population compared to glutamatergic neurons, GABAergic interneurons play a vital role in modulating neuronal excitability and integration, and in the generation of temporal synchrony and oscillations among networks of glutamatergic neurons. In addition, the development of GABAergic inhibition has recently been shown to play a key role in critical period plasticity of cortical circuits. Critical periods represent epochs of heightened brain plasticity during which experience can produce permanent, large-scale changes in neuronal circuits. By regulating critical period plasticity, GABAergic interneurons may influence how experience shapes the brain during early life and adolescence. To date our understanding of the molecular mechanisms regulating GABAergic synapse development is still in its infancy.
Disruption of the balance between excitatory and inhibitory synaptic activities is believed to cause diseases such as autism and epilepsy. Alteration in the maturation of the GABAergic network thus might be a critical determinant of these neurodevelopmental disorders. Understanding the cellular and molecular mechanisms governing GABAergic circuit development is the first essential step towards a better comprehension of how abnormalities in this process can occur, thereby leading to aberrant cortical development and function. The overall goal of my laboratory is to study the molecular mechanisms regulating GABAergic synapse development, by using a combination of molecular, imaging, electrophysiological and behavioural techniques.
We currently focus on the following three questions:
- Molecular pathways regulating GABAergic synapse maturation in the postnatal brain;
- Mechanisms linking experience to GABAergic synapse maturation in primary visual cortex;
- Alterations of GABAergic circuit development in animal models of neurodevelopment diseases.