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Nonlinear Mixed Selectivity Supports Reliable Neural Computation

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Specialty Biology
Date 2020 Feb 19
PMID 32069273
Citations 31
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Abstract

Neuronal activity in the brain is variable, yet both perception and behavior are generally reliable. How does the brain achieve this? Here, we show that the conjunctive coding of multiple stimulus features, commonly known as nonlinear mixed selectivity, may be used by the brain to support reliable information transmission using unreliable neurons. Nonlinearly mixed feature representations have been observed throughout primary sensory, decision-making, and motor brain areas. In these areas, different features are almost always nonlinearly mixed to some degree, rather than represented separately or with only additive (linear) mixing, which we refer to as pure selectivity. Mixed selectivity has been previously shown to support flexible linear decoding for complex behavioral tasks. Here, we show that it has another important benefit: in many cases, it makes orders of magnitude fewer decoding errors than pure selectivity even when both forms of selectivity use the same number of spikes. This benefit holds for sensory, motor, and more abstract, cognitive representations. Further, we show experimental evidence that mixed selectivity exists in the brain even when it does not enable behaviorally useful linear decoding. This suggests that nonlinear mixed selectivity may be a general coding scheme exploited by the brain for reliable and efficient neural computation.

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References
1.
Zhang Y, Sharpee T . A Robust Feedforward Model of the Olfactory System. PLoS Comput Biol. 2016; 12(4):e1004850. PMC: 4827830. DOI: 10.1371/journal.pcbi.1004850. View

2.
Eichler K, Li F, Litwin-Kumar A, Park Y, Andrade I, Schneider-Mizell C . The complete connectome of a learning and memory centre in an insect brain. Nature. 2017; 548(7666):175-182. PMC: 5806122. DOI: 10.1038/nature23455. View

3.
Fusi S, Miller E, Rigotti M . Why neurons mix: high dimensionality for higher cognition. Curr Opin Neurobiol. 2016; 37:66-74. DOI: 10.1016/j.conb.2016.01.010. View

4.
Sergio L, Kalaska J . Changes in the temporal pattern of primary motor cortex activity in a directional isometric force versus limb movement task. J Neurophysiol. 1998; 80(3):1577-83. DOI: 10.1152/jn.1998.80.3.1577. View

5.
Olshausen B, Field D . Emergence of simple-cell receptive field properties by learning a sparse code for natural images. Nature. 1996; 381(6583):607-9. DOI: 10.1038/381607a0. View