CREB Regulates Experience-Dependent Spine Formation and Enlargement in Mouse Barrel Cortex.

Neural Plast

Laboratory of Psychobiology, Santa Lucia Foundation, 00143 Rome, Italy ; Institute of Cell Biology and Neurobiology (IBCN), National Research Council, 00015 Rome, Italy.

Published: March 2016

Experience modifies synaptic connectivity through processes that involve dendritic spine rearrangements in neuronal circuits. Although cAMP response element binding protein (CREB) has a key function in spines changes, its role in activity-dependent rearrangements in brain regions of rodents interacting with the surrounding environment has received little attention so far. Here we studied the effects of vibrissae trimming, a widely used model of sensory deprivation-induced cortical plasticity, on processes associated with dendritic spine rearrangements in the barrel cortex of a transgenic mouse model of CREB downregulation (mCREB mice). We found that sensory deprivation through prolonged whisker trimming leads to an increased number of thin spines in the layer V of related barrel cortex (Contra) in wild type but not mCREB mice. In the barrel field controlling spared whiskers (Ipsi), the same trimming protocol results in a CREB-dependent enlargement of dendritic spines. Last, we demonstrated that CREB regulates structural rearrangements of synapses that associate with dynamic changes of dendritic spines. Our findings suggest that CREB plays a key role in dendritic spine dynamics and synaptic circuits rearrangements that account for new brain connectivity in response to changes in the environment.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436461PMC
http://dx.doi.org/10.1155/2015/651469DOI Listing

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