How inhibitory neurons increase information transmission under threshold modulation.
How inhibitory neurons increase information transmission under threshold modulation.
复制标题
抑制性神经元如何在阈值调制下增加信息传递。
DOI:
10.1016/j.celrep.2021.109158
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发表时间:
2021-05-25
期刊:
影响因子:
8.8
通讯作者:
Sharpee TO
中科院分区:
文献类型:
--
作者:
Hsu WM;Kastner DB;Baccus SA;Sharpee TO
Modulation of neuronal thresholds is ubiquitous in the brain. Phenomena such as figure-ground segmentation, motion detection, stimulus anticipation, and shifts in attention all involve changes in a neuron’s threshold based on signals from larger scales than its primary inputs. However, this modulation reduces the accuracy with which neurons can represent their primary inputs, creating a mystery as to why threshold modulation is so widespread in the brain. We find that modulation is less detrimental than other forms of neuronal variability and that its negative effects can be nearly completely eliminated if modulation is applied selectively to sparsely responding neurons in a circuit by inhibitory neurons. We verify these predictions in the retina where we find that inhibitory amacrine cells selectively deliver modulation signals to sparsely responding ganglion cell types. Our findings elucidate the central role that inhibitory neurons play in maximizing information transmission under modulation. Modulation of neuronal thresholds is ubiquitous in the brain but reduces the accuracy of neural signaling. Hsu et al. show that the negative impact of threshold modulation can be almost completely eliminated when modulation is not delivered uniformly to all neurons but only to a subset and via inhibitory neurons.
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影响因子:
25
作者:
Goris, Robbe L. T.;Movshon, J. Anthony;Simoncelli, Eero P.
通讯作者:
Simoncelli, Eero P.
影响因子:
16.2
作者:
Kato HK;Chu MW;Isaacson JS;Komiyama T
通讯作者:
Komiyama T
DOI:
10.1523/jneurosci.4036-12.2012
发表时间:
2012-11-14
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
Doi E;Gauthier JL;Field GD;Shlens J;Sher A;Greschner M;Machado TA;Jepson LH;Mathieson K;Gunning DE;Litke AM;Paninski L;Chichilnisky EJ;Simoncelli EP
通讯作者:
Simoncelli EP
影响因子:
16.2
作者:
Baccus, SA;Meister, M
通讯作者:
Meister, M
影响因子:
4.3
作者:
Brinkman, Braden A. W.;Weber, Alison I.;Shea-Brown, Eric
通讯作者:
Shea-Brown, Eric