Unreliable homeostatic action potential broadening in cultured dissociated neurons

  1. Carl-Ludwig-Institute of Physiology, Faculty of Medicine, Leipzig University, Leipzig, Germany
  2. Division of Pulmonary and Critical Care Medicine, Department of Medicine, Oregon Health and Science University, Portland, United States
  3. Section of Pulmonary and Critical Care Medicine, VA Portland Health Care System, Portland, United States
  4. Institute for Developmental Biology and Neurobiology, Johannes Gutenberg University, Mainz, Germany
  5. Unité de Neurobiologie des canaux Ioniques et de la Synapse (UNIS), UMR_S 1072, INSERM, Aix-Marseille Université, Marseille, France
  6. MRC Centre for Neurodevelopmental Disorders, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, United Kingdom
  7. Centre for Developmental Neurobiology, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London, United Kingdom
  8. Institute of Neuroanatomy, Mannheim Center for Translational Neuroscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany
  9. Institute of Anatomy and Cell Biology, Johannes Kepler University, Linz, Austria

Peer review process

Not revised: This Reviewed Preprint includes the authors’ original preprint (without revision), an eLife assessment, and public reviews.

Read more about eLife’s peer review process.

Editors

  • Reviewing Editor
    Teresa Giraldez
    Universidad de La Laguna, La Laguna, Spain
  • Senior Editor
    Lu Chen
    Stanford University, Stanford, United States of America

Reviewer #1 (Public review):

Summary:

Ritzau-Jost et al. investigate the potential contribution of AP broadening in homeostatic upregulation of neuronal network activity with a specific focus on dissociated neuronal cultures. In cultures obtained from a few brain regions from mice or rats using different culture conditions and examined by different laboratories, AP half-width remained stable despite chronic activity block with TTX. The finding suggests that AP width is not significantly modulated by changes in sodium channel activity.

Strengths:

The collaborative nature of the study amongst the neuronal culture experts and the rigorous electrophysiological assessments provides for a compelling support of the main conclusion.

Weaknesses:

Given the negative nature of the results, a couple of remaining issues (such as the cell density of cultures and the presentation of imaging experiments with a voltage sensor) warrant further consideration. In addition, a discussion of the reasons for the seeming stability of AP half-width to sodium channel modulation might help extend the scope of the study beyond the presentation of a negative conclusion.

Reviewer #2 (Public review):

Summary:

This study reexamined the idea that action potential broadening serves as a homeostatic mechanism to compensate for changes in network activity. The key finding was that, while action potential broadening does occur in certain neurons - such as CA3 pyramidal cells-it is far from a universal response. This is important because it helps resolve longstanding discrepancies in the field, thereby contributing to a better understanding of network dynamics. The replication of these findings across multiple laboratories further strengthened the study's rigor.

Strengths:

Mechanisms of network homeostasis are essential to understand network dynamics.

Weaknesses:

No weaknesses were noted by this reviewer.

Reviewer #3 (Public review):

Summary:

The manuscript "Unreliable homeostatic action potential broadening in cultured dissociated neurons" by Ritzau-Jost et al. investigates action potential (AP) broadening as a mechanism underlying homeostatic synaptic plasticity. Given the existing variability in the literature concerning AP broadening, the authors address an important and timely research question of considerable interest to the field.

The study systematically demonstrates cell-type- and model-specific AP broadening in hippocampal neurons after chronic treatment with either tetrodotoxin (TTX) or glutamatergic transmission blockers. The findings indicate AP broadening in CA3 pyramidal neurons in organotypic cultures after TTX treatment, but notably not in dissociated hippocampal neurons under identical conditions. However, blocking glutamatergic neurotransmission caused AP broadening in dissociated hippocampal neurons. Moreover, extensive evaluations in neocortical dissociated cultures robustly challenge previous findings by revealing a lack of AP broadening following TTX treatment. Additionally, the proposed role of BK-type potassium channels in mediating AP broadening is convincingly questioned through complementary electrophysiological and voltage-imaging experiments.

Strengths:

The manuscript exhibits an outstanding experimental design, employing state-of-the-art techniques and a rigorous multi-lab validation approach that greatly enhances scientific reliability. The experimental results are meticulously illustrated, and the conclusions drawn are justified and supported by the presented data. Furthermore, the manuscript is comprehensively and clearly written.

Weaknesses:

Concerning the statistical analyses employed, it is advisable to consider the Kruskal-Wallis test with corrections for multiple comparisons when evaluating more than two experimental groups.

  1. Howard Hughes Medical Institute
  2. Wellcome Trust
  3. Max-Planck-Gesellschaft
  4. Knut and Alice Wallenberg Foundation