Project Summary
Chemical synapses are composed of paired pre- and post-synaptic terminals. Most of the excitatory
synapses reside on dendritic spines, a type of dendritic protrusion that hosts neurotransmitter receptors and
other postsynaptic specializations. Synapses are plastic and undergo short- and long-term modifications
during developmental refinement of neuronal circuitry, as well as during learning and memory. Synaptic
modifications involve both pre- and post-synaptic changes. At the postsynaptic site, directed trafficking of
neurotransmitter receptors to and from the membrane surface is believed to be a key event underlying long-
term potentiation (LTP) and depression (LTD), respectively. In addition, dendritic spines undergo rapid
changes in their morphology during plasticity. The underlying cellular mechanisms that control and regulate
these rapid changes in postsynaptic receptors and spine structures remain to be fully elucidated. The
cytoskeleton controls many, if not all, aspects of the motility of cellular structures. How the cytoskeleton
regulates postsynaptic structure, function, and modifications during plasticity, however, remains poorly
understood. This proposed study aims to investigate novel actin mechanisms that enable the development of
postsynaptic structure and specialization required for a functional synapse. Specifically, we will investigate
how actin crosslinking, (+) capping, and dynamic G-actin regulation work in concert to enable the elaboration
and maturation of dendritic spines as well as to regulate their remodeling during synaptic plasticity.
Furthermore, the study will a novel interaction between (+) end capping protein CP and Shank scaffolding
protein in coupling the actin-based structural changes and the development of the postsynaptic specialization.
Given that many neural disorders are associated with alterations in synaptic connections and plasticity, we
hope to gain a better understanding of the molecular and cellular mechanisms underlying synaptic plasticity,
which is of importance to our understanding of brain development and functions under both physiological and
pathological conditions.