TY - JOUR
T1 - Orchestrated experience-driven Arc responses are disrupted in a mouse model of Alzheimer's disease
AU - Rudinskiy, Nikita
AU - Hawkes, Jonathan M.
AU - Betensky, Rebecca A.
AU - Eguchi, Megumi
AU - Yamaguchi, Shun
AU - Spires-Jones, Tara L.
AU - Hyman, Bradley T.
N1 - Funding Information:
We thank A. Muzikansky (Harvard), B. Urbanc and B. Cohen (Drexel) for their help with statistical analysis. We also thank all the members of the Hyman laboratory for their input, discussions and help with the equipment. N.R. is supported by the fellowships from the Swiss National Science Foundation and the Swiss Foundation for Grants in Biology and Medicine. This research is supported by a gift from the Gilbert fund, grants from the US National Institutes of Health (AG033670 to T.L.S.-J. and AG08487 to B.T.H.) and a grant from the Harvard NeuroDiscovery Center to R.A.B.
PY - 2012/10
Y1 - 2012/10
N2 - Experience-induced expression of immediate-early gene Arc (also known as Arg3.1) is known to be important for consolidation of memory. Using in vivo longitudinal multiphoton imaging, we found orchestrated activity-dependent expression of Arc in the mouse extrastriate visual cortex in response to a structured visual stimulation. In wild-type mice, the amplitude of the Arc response in individual neurons strongly predicted the probability of reactivation by a subsequent presentation of the same stimulus. In a mouse model of Alzheimer's disease, this association was markedly disrupted in the cortex, specifically near senile plaques. Neurons in the vicinity of plaques were less likely to respond, but, paradoxically, there were stronger responses in those few neurons around plaques that did respond. To the extent that the orchestrated pattern of Arc expression reflects nervous system responses to and physiological consolidation of behavioral experience, the disruption in Arc patterns reveals plaque-associated interference with neural network integration.
AB - Experience-induced expression of immediate-early gene Arc (also known as Arg3.1) is known to be important for consolidation of memory. Using in vivo longitudinal multiphoton imaging, we found orchestrated activity-dependent expression of Arc in the mouse extrastriate visual cortex in response to a structured visual stimulation. In wild-type mice, the amplitude of the Arc response in individual neurons strongly predicted the probability of reactivation by a subsequent presentation of the same stimulus. In a mouse model of Alzheimer's disease, this association was markedly disrupted in the cortex, specifically near senile plaques. Neurons in the vicinity of plaques were less likely to respond, but, paradoxically, there were stronger responses in those few neurons around plaques that did respond. To the extent that the orchestrated pattern of Arc expression reflects nervous system responses to and physiological consolidation of behavioral experience, the disruption in Arc patterns reveals plaque-associated interference with neural network integration.
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U2 - 10.1038/nn.3199
DO - 10.1038/nn.3199
M3 - Article
C2 - 22922786
AN - SCOPUS:84866725335
SN - 1097-6256
VL - 15
SP - 1422
EP - 1429
JO - Nature Neuroscience
JF - Nature Neuroscience
IS - 10
ER -