Task-dependent changes in cross-level coupling between single neurons and oscillatory activity in multiscale networks.
Task-dependent changes in cross-level coupling between single neurons and oscillatory activity in multiscale networks.
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DOI:
10.1371/journal.pcbi.1002809
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发表时间:
2012
影响因子:
4.3
通讯作者:
Carmena JM
中科院分区:
文献类型:
--
作者:
Canolty RT;Ganguly K;Carmena JM
Understanding the principles governing the dynamic coordination of functional brain networks remains an important unmet goal within neuroscience. How do distributed ensembles of neurons transiently coordinate their activity across a variety of spatial and temporal scales? While a complete mechanistic account of this process remains elusive, evidence suggests that neuronal oscillations may play a key role in this process, with different rhythms influencing both local computation and long-range communication. To investigate this question, we recorded multiple single unit and local field potential (LFP) activity from microelectrode arrays implanted bilaterally in macaque motor areas. Monkeys performed a delayed center-out reach task either manually using their natural arm (Manual Control, MC) or under direct neural control through a brain-machine interface (Brain Control, BC). In accord with prior work, we found that the spiking activity of individual neurons is coupled to multiple aspects of the ongoing motor beta rhythm (10–45 Hz) during both MC and BC, with neurons exhibiting a diversity of coupling preferences. However, here we show that for identified single neurons, this beta-to-rate mapping can change in a reversible and task-dependent way. For example, as beta power increases, a given neuron may increase spiking during MC but decrease spiking during BC, or exhibit a reversible shift in the preferred phase of firing. The within-task stability of coupling, combined with the reversible cross-task changes in coupling, suggest that task-dependent changes in the beta-to-rate mapping play a role in the transient functional reorganization of neural ensembles. We characterize the range of task-dependent changes in the mapping from beta amplitude, phase, and inter-hemispheric phase differences to the spike rates of an ensemble of simultaneously-recorded neurons, and discuss the potential implications that dynamic remapping from oscillatory activity to spike rate and timing may hold for models of computation and communication in distributed functional brain networks. How is the functional role of a particular neuron established within an ensemble? The concept of a neural tuning curve – the mapping from input variables such as movement direction to output firing rate – has proven useful in investigating neural function. However, prior work shows that tuning curves are not fixed but may be remapped as a function of task demands – presumably via high-level mechanisms of cognitive control. How is this accomplished? Brain rhythms may play a causal role in this process, but the coupling of single cells to network activity remains poorly understood. We investigated the coupling between rhythmic beta activity and spiking as macaques performed two different tasks. This coupling can be described in terms of a function that maps oscillatory amplitude and phase to instantaneous spike rate. Similarly to direction tuning, this “internal” tuning curve also exhibits task-dependent changes. We characterize these changes across a large ensemble of simultaneously-recorded cells, and consider some of the neuro-computational implications presented by cross-level coupling between single cells and large-scale networks. In particular, relative to the slow time-scale of behavior, the observed beta-to-rate mappings may prove useful for modulating winner-take-all dynamics on intermediate time-scales and relative spike timing on fast time-scales.
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DOI:
10.1073/pnas.1011284108
发表时间:
2011-07-05
影响因子:
11.1
作者:
Buffalo, Elizabeth A.;Fries, Pascal;Desimone, Robert
通讯作者:
Desimone, Robert
DOI:
10.1073/pnas.0308538101
发表时间:
2004-06-29
影响因子:
11.1
作者:
Brovelli, A;Ding, MZ;Bressler, SL
通讯作者:
Bressler, SL
影响因子:
4.3
作者:
Friston K
通讯作者:
Friston K
影响因子:
25
作者:
Fujisawa, Shigeyoshi;Amarasingham, Asohan;Buzsaki, Gyoergy
通讯作者:
Buzsaki, Gyoergy
影响因子:
16.2
作者:
Dean HL;Hagan MA;Pesaran B
通讯作者:
Pesaran B