Literature DB >> 23630284

Intermediate intrinsic diversity enhances neural population coding.

Shreejoy J Tripathy1, Krishnan Padmanabhan, Richard C Gerkin, Nathaniel N Urban.   

Abstract

Cell-to-cell variability in molecular, genetic, and physiological features is increasingly recognized as a critical feature of complex biological systems, including the brain. Although such variability has potential advantages in robustness and reliability, how and why biological circuits assemble heterogeneous cells into functional groups is poorly understood. Here, we develop analytic approaches toward answering how neuron-level variation in intrinsic biophysical properties of olfactory bulb mitral cells influences population coding of fluctuating stimuli. We capture the intrinsic diversity of recorded populations of neurons through a statistical approach based on generalized linear models. These models are flexible enough to predict the diverse responses of individual neurons yet provide a common reference frame for comparing one neuron to the next. We then use Bayesian stimulus decoding to ask how effectively different populations of mitral cells, varying in their diversity, encode a common stimulus. We show that a key advantage provided by physiological levels of intrinsic diversity is more efficient and more robust encoding of stimuli by the population as a whole. However, we find that the populations that best encode stimulus features are not simply the most heterogeneous, but those that balance diversity with the benefits of neural similarity.

Keywords:  generalized linear models; intrinsic biophysics; ion channels; neural variability; stimulus coding

Mesh:

Substances:

Year:  2013        PMID: 23630284      PMCID: PMC3657795          DOI: 10.1073/pnas.1221214110

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  42 in total

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  53 in total

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8.  Adenosine A1 receptor activates background potassium channels and modulates information processing in olfactory bulb mitral cells.

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9.  Optimized Parallel Coding of Second-Order Stimulus Features by Heterogeneous Neural Populations.

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