Molecular Mechanisms of Synapse Assembly and Plasticity

The major goal of the research in our lab is to understand the mechanisms by which synapses are formed and modified. In the nervous system, the elemental means of communication between cells is synaptic transmission. Essential to the high speed and efficiency by which neurons communicate is the exquisite molecular organization of the pre- and postsynaptic apparatus. At the presynaptic compartment, neurotransmitter-laden vesicles are poised at active zones, ready for immediate release, and the calcium channels necessary for triggering exocytosis are spatially linked to the secretory machinery. At the postsynaptic membrane, neurotransmitter receptors form high-density clusters which are directly apposed to the active zones. Thus, proper development and functioning of synaptic junctions requires positional information, which coordinates the correct placement of pre- and postsynaptic elements. Once synapses are formed, it is the ability of synaptic connections to strengthen or to weaken which is believed to be central to the processes of learning and memory, and the restoration of synaptic connectivity after a traumatic injury.

In the lab we are using a multidisciplinary approach that includes genetics, confocal and electron microscopy, electrophysiology and molecular biology to identify the proteins required to scaffold the synapse and to regulate it's molding during plasticity. Much of our studies are carried out using a Drosophila glutamatergic synapse model that has a high degree of evolutionary conservation with excitatory synapses in the mammalian brain. Using these approaches are unraveling fundamental mechanisms for synapse formation and synapse dynamics, including the role of scaffolding proteins in shaping and regulating the growth of synapses, synaptic formation “signaling molecules”, such as WNTs, which are well-recognized factors for early embryonic pattern formation but with novel roles in synapse development and plasticity, the role of exosomes in trans-synaptic communication, and the trafficking of RNAs which are prime substrates for forming postsynaptic building blocks. Our genetic studies have led to important discoveries in the field that are accelerating our knowledge of synapse development and plasticity and which are significantly contributing to our understanding of neurological disorders, such as dystonia, muscular dystrophies, and accelerated aging.

A postdoctoral position is available to study in this laboratory. Contact Dr. Budnik for additional details.