NaV1.1 is essential for proprioceptive signaling and motor behaviors

  1. Cyrrus M Espino
  2. Cheyanne M Lewis
  3. Serena Ortiz
  4. Miloni S Dalal
  5. Snigdha Garlapalli
  6. Kaylee M Wells
  7. Darik A O'Neil
  8. Katherine A Wilkinson
  9. Theanne N Griffith  Is a corresponding author
  1. University of California, Davis, United States
  2. San Jose State University, United States
  3. Rutgers, The State University of New Jersey, United States
  4. Marine Biological Laboratory, United States

Abstract

The voltage-gated sodium channel (NaV), NaV1.1, is well-studied in the central nervous system; conversely, its contribution to peripheral sensory neuron function is more enigmatic. Here, we identify a new role for NaV1.1 in mammalian proprioception. RNAscope analysis and in vitro patch clamp recordings in genetically identified mouse proprioceptors show ubiquitous channel expression and significant contributions to intrinsic excitability. Notably, genetic deletion of NaV1.1 in sensory neurons caused profound and visible motor coordination deficits in conditional knockout mice of both sexes, similar to conditional Piezo2-knockout animals, suggesting this channel is a major contributor to sensory proprioceptive transmission. Ex vivo muscle afferent recordings from conditional knockout mice found that loss of NaV1.1 leads to inconsistent and unreliable proprioceptor firing characterized by action potential failures during static muscle stretch; conversely, afferent responses to dynamic vibrations were unaffected. This suggests that while a combination of Piezo2 and other NaV isoforms are sufficient to elicit activity in response to transient stimuli, NaV1.1 is required for transmission of receptor potentials generated during sustained muscle stretch. Impressively, recordings from afferents of heterozygous conditional knockout animals were similarly impaired, and heterozygous conditional knockout mice also exhibited motor behavioral deficits. Thus, NaV1.1 haploinsufficiency in sensory neurons impairs both proprioceptor function and motor behaviors. Importantly, human patients harboring NaV1.1 loss-of-function mutations often present with motor delays and ataxia; therefore, our data suggest sensory neuron dysfunction contributes to the clinical manifestations of neurological disorders in which NaV1.1 function is compromised. Collectively, we present the first evidence that NaV1.1 is essential for mammalian proprioceptive signaling and behaviors.

Data availability

Source Data files have been uploaded to Mendeley for all figures (https://data.mendeley.com/datasets/kt23th75v9). Code has been uploaded to GitHub (https://github.com/doctheagrif/Current-Clamp-Matlab-Code_O-Neil-DA). A key resources table with specific organism and reagent information has been included in the methods section.

The following data sets were generated

Article and author information

Author details

  1. Cyrrus M Espino

    Department of Physiology and Membrane Biology, University of California, Davis, Davis, United States
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-2708-4577
  2. Cheyanne M Lewis

    Department of Physiology and Membrane Biology, University of California, Davis, Davis, United States
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-0057-2047
  3. Serena Ortiz

    Department of Biological Science, San Jose State University, San Jose, United States
    Competing interests
    The authors declare that no competing interests exist.
  4. Miloni S Dalal

    Department of Pharmacology, Physiology, and Neuroscience, Rutgers, The State University of New Jersey, Newark, United States
    Competing interests
    The authors declare that no competing interests exist.
  5. Snigdha Garlapalli

    Undergraduate program in Psychology, University of California, Davis, Davis, United States
    Competing interests
    The authors declare that no competing interests exist.
  6. Kaylee M Wells

    Neurobiology, Marine Biological Laboratory, Woods Hole, United States
    Competing interests
    The authors declare that no competing interests exist.
  7. Darik A O'Neil

    Neurobiology, Marine Biological Laboratory, Woods Hole, United States
    Competing interests
    The authors declare that no competing interests exist.
  8. Katherine A Wilkinson

    Department of Biological Science, San Jose State University, San Jose, United States
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-2692-5533
  9. Theanne N Griffith

    Department of Physiology and Membrane Biology, University of California, Davis, Davis, United States
    For correspondence
    tgriffith@ucdavis.edu
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-0090-6286

Funding

Burroughs Wellcome Fund

  • Theanne N Griffith

National Institute of General Medical Sciences (5T32GM099608-10)

  • Cyrrus M Espino

National Institute of General Medical Sciences (1T32GM1144303-01A1)

  • Cyrrus M Espino

National Institute of General Medical Sciences (5SC3GM127195)

  • Katherine A Wilkinson

National Institute of General Medical Sciences (5R25GM71381)

  • Serena Ortiz

National Institute of Neurological Disorders and Stroke (R25NS063307)

  • Kaylee M Wells
  • Darik A O'Neil

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Reviewing Editor

  1. Alexander Theodore Chesler, National Institutes of Health, United States

Ethics

Animal experimentation: Animal use was conducted according to guidelines from the National Institutes of Health's Guide for the Care and Use of Laboratory Animals and was approved by the Institutional Animal Care and Use Committee of Rutgers University-Newark (PROTO201900161), UC Davis (#21947 and #22438) and San José State University (#990, ex vivo muscle recordings).

Version history

  1. Received: May 2, 2022
  2. Preprint posted: May 6, 2022 (view preprint)
  3. Accepted: October 21, 2022
  4. Accepted Manuscript published: October 24, 2022 (version 1)
  5. Version of Record published: November 7, 2022 (version 2)

Copyright

© 2022, Espino et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 2,244
    views
  • 317
    downloads
  • 12
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Cyrrus M Espino
  2. Cheyanne M Lewis
  3. Serena Ortiz
  4. Miloni S Dalal
  5. Snigdha Garlapalli
  6. Kaylee M Wells
  7. Darik A O'Neil
  8. Katherine A Wilkinson
  9. Theanne N Griffith
(2022)
NaV1.1 is essential for proprioceptive signaling and motor behaviors
eLife 11:e79917.
https://doi.org/10.7554/eLife.79917

Share this article

https://doi.org/10.7554/eLife.79917

Further reading

    1. Neuroscience
    Juan Jose Rodriguez Gotor, Kashif Mahfooz ... John F Wesseling
    Research Article

    Vesicles within presynaptic terminals are thought to be segregated into a variety of readily releasable and reserve pools. The nature of the pools and trafficking between them is not well understood, but pools that are slow to mobilize when synapses are active are often assumed to feed pools that are mobilized more quickly, in a series. However, electrophysiological studies of synaptic transmission have suggested instead a parallel organization where vesicles within slowly and quickly mobilized reserve pools would separately feed independent reluctant- and fast-releasing subdivisions of the readily releasable pool. Here, we use FM-dyes to confirm the existence of multiple reserve pools at hippocampal synapses and a parallel organization that prevents intermixing between the pools, even when stimulation is intense enough to drive exocytosis at the maximum rate. The experiments additionally demonstrate extensive heterogeneity among synapses in the relative sizes of the slowly and quickly mobilized reserve pools, which suggests equivalent heterogeneity in the numbers of reluctant and fast-releasing readily releasable vesicles that may be relevant for understanding information processing and storage.

    1. Evolutionary Biology
    2. Neuroscience
    Daniel Thiel, Luis Alfonso Yañez Guerra ... Gáspár Jékely
    Research Article

    Neuropeptides are ancient signaling molecules in animals but only few peptide receptors are known outside bilaterians. Cnidarians possess a large number of G protein-coupled receptors (GPCRs) – the most common receptors of bilaterian neuropeptides – but most of these remain orphan with no known ligands. We searched for neuropeptides in the sea anemone Nematostella vectensis and created a library of 64 peptides derived from 33 precursors. In a large-scale pharmacological screen with these peptides and 161 N. vectensis GPCRs, we identified 31 receptors specifically activated by 1 to 3 of 14 peptides. Mapping GPCR and neuropeptide expression to single-cell sequencing data revealed how cnidarian tissues are extensively connected by multilayer peptidergic networks. Phylogenetic analysis identified no direct orthology to bilaterian peptidergic systems and supports the independent expansion of neuropeptide signaling in cnidarians from a few ancestral peptide-receptor pairs.