Parvalbumin(+) interneurons obey unique connectivity rules and establish a powerful lateral-inhibition microcircuit in dentate gyrus.
Parvalbumin(+) interneurons obey unique connectivity rules and establish a powerful lateral-inhibition microcircuit in dentate gyrus.
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DOI:
10.1038/s41467-018-06899-3
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发表时间:
2018-11-02
影响因子:
16.6
通讯作者:
Jonas P
中科院分区:
文献类型:
--
作者:
Espinoza C;Guzman SJ;Zhang X;Jonas P
Parvalbumin-positive (PV+) GABAergic interneurons in hippocampal microcircuits are thought to play a key role in several higher network functions, such as feedforward and feedback inhibition, network oscillations, and pattern separation. Fast lateral inhibition mediated by GABAergic interneurons may implement a winner-takes-all mechanism in the hippocampal input layer. However, it is not clear whether the functional connectivity rules of granule cells (GCs) and interneurons in the dentate gyrus are consistent with such a mechanism. Using simultaneous patch-clamp recordings from up to seven GCs and up to four PV+ interneurons in the dentate gyrus, we find that connectivity is structured in space, synapse-specific, and enriched in specific disynaptic motifs. In contrast to the neocortex, lateral inhibition in the dentate gyrus (in which a GC inhibits neighboring GCs via a PV+ interneuron) is ~ 10-times more abundant than recurrent inhibition (in which a GC inhibits itself). Thus, unique connectivity rules may enable the dentate gyrus to perform specific higher-order computations. GABAergic interneurons are known to provide inhibition to allow computational function of neuronal network. Here, Espinoza and colleagues show that connectivity of granule cells and interneurons in the dentate gyrus of mouse hippocampus are consistent with the circuit architecture capable of performing a winners-take-all mechanism.
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DOI:
10.1523/jneurosci.6044-08.2009
发表时间:
2009-06-10
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
de Almeida L;Idiart M;Lisman JE
通讯作者:
Lisman JE
影响因子:
16.2
作者:
Danielson NB;Turi GF;Ladow M;Chavlis S;Petrantonakis PC;Poirazi P;Losonczy A
通讯作者:
Losonczy A
影响因子:
56.9
作者:
Galarreta, M;Hestrin, S
通讯作者:
Hestrin, S
影响因子:
16.2
作者:
Geiger, JRP;Lubke, J;Jonas, P
通讯作者:
Jonas, P
影响因子:
16.6
作者:
Cayco-Gajic NA;Clopath C;Silver RA
通讯作者:
Silver RA