An unusual potassium conductance protects <i>Caenorhabditis elegans</i> pharyngeal muscle rhythms against environmental noise

The nematode <i>Caenorhabditis elegans</i> feeds by rhythmic contraction and relaxation of a neuromuscular organ called the pharynx, which draws in and filters water and bacterial food. This behavior is driven by myogenic plateau potentials, long-lasting depolarizations of the pharyngeal muscle, which are timed by neuronal input from a dedicated pharyngeal nervous system. While the timing of these plateaus' initiation has received significant attention, their mechanisms of termination remain incompletely understood. In particular, it is unclear how plateaus resist early termination by hyperpolarizing current noise. Here, we present a computational model of pharyngeal plateaus against a noisy background. We propose that an unusual, rapidly inactivating potassium conductance confers exceptional noise robustness on the system. We further investigate the possibility that a similar mechanism in other systems permits switching between plateau and spiking behavior under noisy conditions.

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Journal
Proceedings of the National Academy of Sciences
Published
2025-04-03
DOI
https://doi.org/10.1073/pnas.2422709122
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
0.00

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article

An unusual potassium conductance protects Caenorhabditis elegans pharyngeal muscle rhythms against environmental noise

Piali Sengupta, Shawn R. Lockery, Eve Marder, Max Kenngott
Proceedings of the National Academy of Sciences
Genetics, Aging, and Longevity in Model Organisms
article

An unusual potassium conductance protects Caenorhabditis elegans pharyngeal muscle rhythms against environmental noise

Piali Sengupta, Shawn R. Lockery, Eve Marder, Max Kenngott
article en

Abstract

The nematode <i>Caenorhabditis elegans</i> feeds by rhythmic contraction and relaxation of a neuromuscular organ called the pharynx, which draws in and filters water and bacterial food. This behavior is driven by myogenic plateau potentials, long-lasting depolarizations of the pharyngeal muscle, which are timed by neuronal input from a dedicated pharyngeal nervous system. While the timing of these plateaus' initiation has received significant attention, their mechanisms of termination remain incompletely understood. In particular, it is unclear how plateaus resist early termination by hyperpolarizing current noise. Here, we present a computational model of pharyngeal plateaus against a noisy background. We propose that an unusual, rapidly inactivating potassium conductance confers exceptional noise robustness on the system. We further investigate the possibility that a similar mechanism in other systems permits switching between plateau and spiking behavior under noisy conditions.

Proceedings of the National Academy of SciencesVol. 122(14)
Brandeis University (US)
National Science Foundation, Kavli Foundation, National Institute of Neurological Disorders and Stroke, Division of Biological Infrastructure
Clean water and sanitation
Openalex Percentile: Top 94%
Genetics, Aging, and Longevity in Model Organisms
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