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Rapid and persistent modulation of actin dynamics regulates
postsynaptic reorganization underlying bidirectional plasticity
Yasunori Hayashi
Abstract
The synapse is a highly organized cellular specialization, that reorganizes
structure and composition according to input strength both positively and
negatively. But the mechanisms orchestrating these changes remain elusive.
Actin serves as both cytoskeleton and scaffold for various postsynaptic
proteins and exists in a dynamic equilibrium between F-actin and G-actin,
which is bidirectionally modulated by various cellular signals. This makes
actin a plausible locus for bidirectional reorganization of structure and
molecules. A newly innovated FRET-based live imaging technique that monitors
F-actin/G-actin equilibrium revealed that a tetanic stimulation causes a
rapid and persistent shift of actin equilibrium towards F-actin. This
enlarges dendritic spines and increases the postsynaptic binding capacity.
In contrast, prolonged low frequency stimulation shifts the equilibrium
towards G-actin, resulting in a loss of postsynaptic actin and spine
structure. This bidirectional regulation of actin is actively involved in
postsynaptic assembly-disassembly and serves as a substrate for
bidirectional synaptic plasticity.
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