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Minimal requirements for a neuron to co-regulate many properties and the implications for ion channel correlations and robustness
Open accessPreprint — published as 10.7554/elife.72875 · Paper page
Abstract
Neurons regulate their excitability by adjusting their ion channel levels. Degeneracy – achieving equivalent outcomes (excitability) using different solutions (channel combinations) – facilitates this regulation by enabling a disruptive change in one channel to be offset by compensatory changes in other channels. But neurons must co-regulate many properties. Pleiotropy – the impact of one channel on more than one property – complicates regulation because a compensatory ion channel change that restores one property to its target value often disrupts other properties. How then does a neuron simultaneously regulate multiple properties? Here we demonstrate that of the many channel combinations producing the target value for one property (the single-output solution set), few combinations produce the target value for other properties. Combinations producing the target value for two or more properties (the multi-output solution set) correspond to the intersection between single-output solution sets. Properties can be effectively co-regulated only if the number of adjustable channels ( n in ) exceeds the number of regulated properties ( n out ). Ion channel correlations emerge during homeostatic regulation when the dimensionality of solution space ( n in – n out ) is low. Even if each property can be regulated to its target value when considered in isolation, regulation as a whole fails if single-output solution sets do not intersect. Our results also highlight that ion channels must be co-adjusted with different ratios to regulate different properties, which suggests that each error signal drives modulatory changes independently, despite those changes ultimately affecting the same ion channels.
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Metadata
- Authors
- Yang, J., Shakil, H., Ratté, S., & Prescott, S. A.
- Affiliations
- University of Toronto (CA)
- Great Ormond Street Hospital (GB)
- Venue
- eLife
- Publisher
- openRxiv
- Published
- 2020-12-04
- Volume
- 11
- ISSN
- 2050-084X (ISSN-L)
- PMC
- PMC8986315
- OpenAlex
- W4220827944
- Cited by
- 41
- References
- 1
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 12 · 2023: 14 · 2022: 4 · 2021: 1
- FWCI
- 2.94
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- eLife (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- University of Toronto
- Hospital for Sick Children
- Canadian Institutes of Health Research (167276)
- Natural Sciences and Engineering Research Council of Canada
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Physical Sciences › Physics and Astronomy › Statistical and Nonlinear Physics › stochastic dynamics and bifurcation
- Keywords
- neuronal excitability, ion channel modulation, degeneracy, pleiotropy, homeostatic regulation, solution space, error signal, robustness
- MeSH terms
- Homeostasis, Ion Channels, Neurons
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