Ripple-selective GABAergic projection cells in the hippocampus.
Ripple-selective GABAergic projection cells in the hippocampus.
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DOI:
10.1016/j.neuron.2022.04.002
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发表时间:
2022-06-15
期刊:
影响因子:
16.2
通讯作者:
Soltesz, Ivan
中科院分区:
文献类型:
--
作者:
Szabo, Gergely G.;Farrell, Jordan S.;Dudok, Barna;Hou, Wen-Hsien;Ortiz, Anna L.;Varga, Csaba;Moolchand, Prannath;Gulsever, Cafer Ikbal;Gschwind, Tilo;Dimidschstein, Jordane;Capogna, Marco;Soltesz, Ivan
Ripples are brief high-frequency electrographic events with important roles in episodic memory. However, the in vivo circuit mechanisms coordinating ripple-related activity among local and distant neuronal ensembles are not well understood. Here we define key characteristics of a long-distance projecting GABAergic cell group in the mouse hippocampus that selectively exhibits high-frequency firing during ripples while staying largely silent during theta-associated states when most other GABAergic cells are active. The high ripple-associated firing commenced before ripple onset and reached its maximum before ripple peak, with the signature theta-off, ripple-on firing pattern being preserved across awake and sleep states. Controlled by septal GABAergic, cholinergic, and CA3 glutamatergic inputs, these ripple-selective cells innervate parvalbumin and cholecystokinin-expressing local interneurons while also targeting a variety of extra-hippocampal regions. These results demonstrate the existence of a hippocampal GABAergic circuit element that is uniquely positioned to coordinate ripple-related neuronal dynamics across neuronal assemblies. Szabo et al. identify a subset of hippocampal GABAergic cells with long-range projections and unique activity dynamics. Theta-OFF/Ripple-ON (TORO) cells are virtually silent during locomotion- and REM sleep theta but fire vigorously during sharp wave-ripples. TORO cells receive CA3 glutamatergic, septal GABAergic and inhibitory cholinergic inputs and target interneurons.
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