4.8 Article

Functional and ultrastructural analysis of reafferent mechanosensation in larval zebrafish

期刊

CURRENT BIOLOGY
卷 32, 期 1, 页码 176-+

出版社

CELL PRESS
DOI: 10.1016/j.cub.2021.11.007

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资金

  1. National Institutes of Health [U19NS104653, R43 OD024879, 2R44OD024879]
  2. National Science Foundation [IIS-1912293]
  3. Simons Foundation [SCGB 542973]
  4. Human Frontier Science Program [RGP0033/2014, LT000805/2019-L]
  5. European Molecular Biology Organization [ALTF 202-2019]
  6. Max Planck Foundation
  7. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany's Excellence Strategy within the framework of the Munich Cluster for Systems Neurology [EXC 2145, 390857198]

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The study provides detailed characterization of how hair cells in zebrafish larvae can discriminate between reafferent and exafferent signals, revealing factors that influence lateral line sensitivity. Through dye labeling, organ circuit reconstruction, and investigation of neural signals, the core mechanism of internal stimulus suppression is uncovered.
All animals need to differentiate between exafferent stimuli, which are caused by the environment, and reafferent stimuli, which are caused by their own movement. In the case of mechanosensation in aquatic animals, the exafferent inputs are water vibrations in the animal's proximity, which need to be distinguishable from the reafferent inputs arising from fluid drag due to locomotion. Both of these inputs are detected by the lateral line, a collection of mechanosensory organs distributed along the surface of the body. In this study, we characterize in detail how hair cells-the receptor cells of the lateral line-in zebrafish larvae discriminate between such reafferent and exafferent signals. Using dye labeling of the lateral line nerve, we visualize two parallel descending inputs that can influence lateral line sensitivity. We combine functional imaging with ultra-structural EM circuit reconstruction to show that cholinergic signals originating from the hindbrain transmit efference copies (copies of the motor command that cancel out self-generated reafferent stimulation during locomotion) and that dopaminergic signals from the hypothalamus may have a role in threshold modulation, both in response to locomotion and salient stimuli. We further gain direct mechanistic insight into the core components of this circuit by loss-of-function perturbations using targeted ablations and gene knockouts. We propose that this simple circuit is the core implementation of mechanosensory reafferent suppression in these young animals and that it might form the first instantiation of state-dependent modulation found at later stages in development.

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