2016
DOI: 10.1126/science.aaf7560
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Imprinting and recalling cortical ensembles

Abstract: Neuronal ensembles are coactive groups of neurons that may represent emergent building blocks of neural circuits. They could be formed by Hebbian plasticity, whereby synapses between coactive neurons are strengthened. Here we report that repetitive activation with two-photon optogenetics of neuronal populations in visual cortex of awake mice generates artificially induced ensembles which recur spontaneously after being imprinted and do not disrupt preexistent ones. Moreover, imprinted ensembles can be recalled… Show more

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Cited by 260 publications
(370 citation statements)
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“…Another application emerged with (i) the discovery of high responsivity of red light–driven opsins to two-photon illumination, enabling single-cell resolution optogenetics in brain tissue (63), and (ii) integration of red light–excited control with blue light–excited readout (via genetically encoded activity sensors such as GCaMP Ca 2+ reporters). Enabling these in vivo all-optical play-in/read-out experiments (50, 7578) has opened the door to tuning optogenetic control in order to match timing and amplitude of naturally occurring activity in the same circuit elements (3, 76), and more broadly to keeping stimulation attuned to native dynamics and events in real time through closed-loop and activity-guided strategies (50, 7478). Many opsins are now available for redshifted excitation, including not just VChR1 and C1V1 but also the VChR1-based ReaChR (79) as well as MChR1 (80), Chrimson (65), and bReaCHES (77) (with ChETA modifications for speed).…”
Section: Spectral Propertiesmentioning
confidence: 99%
“…Another application emerged with (i) the discovery of high responsivity of red light–driven opsins to two-photon illumination, enabling single-cell resolution optogenetics in brain tissue (63), and (ii) integration of red light–excited control with blue light–excited readout (via genetically encoded activity sensors such as GCaMP Ca 2+ reporters). Enabling these in vivo all-optical play-in/read-out experiments (50, 7578) has opened the door to tuning optogenetic control in order to match timing and amplitude of naturally occurring activity in the same circuit elements (3, 76), and more broadly to keeping stimulation attuned to native dynamics and events in real time through closed-loop and activity-guided strategies (50, 7478). Many opsins are now available for redshifted excitation, including not just VChR1 and C1V1 but also the VChR1-based ReaChR (79) as well as MChR1 (80), Chrimson (65), and bReaCHES (77) (with ChETA modifications for speed).…”
Section: Spectral Propertiesmentioning
confidence: 99%
“…8D, see also Supplemental Information). When combined with light-sensitive optogenetic actuators, patterned illumination can perturb electrical activity with near cellular resolution (Baker et al, 2016; Carrillo-Reid et al, 2016; Packer et al, 2015; Papagiakoumou et al, 2010; Rickgauer et al, 2014). …”
Section: Considerations Of Interventional Experimental Designmentioning
confidence: 99%
“…Later, if these patterns or their noisy versions are used to provoke the network, it settles on the original patterns after several rounds of activation updates on the recurrent weights (recall), thus stored patterns act as attractors. It is of high importance that the existence of such networks has been experimentally validated in the visual cortex of awake mice by optogenetic methods 36 . Some versions of the learning rule allow for iterative learning without catastrophic forgetting and enable palimpsest memory.…”
Section: Introductionmentioning
confidence: 99%