ZFIN ID: ZDB-PUB-181008-2
Differential copper-induced death and regeneration of olfactory sensory neuron populations and neurobehavioral function in larval zebrafish
Ma, E.Y., Heffern, K., Cheresh, J., Gallagher, E.P.
Date: 2018
Source: Neurotoxicology   69: 141-151 (Journal)
Registered Authors: Gallagher, Evan P.
Keywords: copper, olfactory sensory neurons, transgenics, zebrafish
MeSH Terms:
  • Animals
  • Animals, Genetically Modified
  • Cell Death/drug effects
  • Cell Death/physiology
  • Cell Proliferation/drug effects
  • Cell Proliferation/physiology
  • Copper/toxicity*
  • Larva/drug effects
  • Larva/physiology
  • Nerve Regeneration/drug effects*
  • Nerve Regeneration/physiology
  • Odorants
  • Olfactory Mucosa/drug effects*
  • Olfactory Mucosa/physiology
  • Olfactory Receptor Neurons/drug effects*
  • Olfactory Receptor Neurons/physiology
  • Random Allocation
  • Smell/drug effects*
  • Smell/physiology
  • Water Pollutants, Chemical/toxicity*
  • Zebrafish
PubMed: 30292653 Full text @ Neurotoxicology
ABSTRACT
Fish rely heavily on their sense of smell to maintain behaviors essential for survival, such as predator detection and avoidance, prey selection, social behavior, imprinting, and homing to natal streams and spawning sites. Due to its direct contact with the outside environment, the peripheral olfactory system of fish is particularly susceptible to dissolved contaminants. In particular, environmental exposures to copper (Cu) can cause a rapid loss of olfactory function. In this study, confocal imaging of double-transgenic zebrafish larvae with differentially labeled ciliated and microvillous olfactory sensory neurons (OSNs) were used to examine cell death and regeneration following Cu exposure. Changes in cell morphologies were observed at varying degrees within both ciliated and microvillous OSNs, including the presence of round dense cell bodies, cell loss and fragmentation, retraction or loss of axons, disorganized cell arrangements, and loss of cells and fluorescence signal intensity, which are all indicators of cell death after Cu exposure. A marked loss of ciliated OSNs relative to microvillous OSNs occurred after exposure to low Cu concentrations for 3 hours, with some regeneration observed after 72 hours. At higher Cu concentrations and 24-h exposures, ciliated and microvillous OSNs were damaged with increased severity of injury with longer Cu exposures. Interestingly, microvillous, but not ciliated OSNs, regenerated rapidly within the 72-h time period of recovery after death from Cu exposure, suggesting that microvillous OSNs may be replaced in lieu of ciliated OSNs. An increase in bromodeoxyuridine labeling was observed 24 h after Cu-induced OSN death, suggesting that increased proliferation of the olfactory stem cells replaced the damaged OSNs. Olfactory behavioral analyses supported our imaging studies and revealed both initial loss and restoration of olfactory function after Cu exposures. In summary, our studies indicate that following zebrafish OSN damage by Cu, regeneration of microvillous OSNs may occur exceeding ciliated OSNs, likely via increased proliferation of the cellular reservoir of neuronal OSC precursors. Transgenic zebrafish are a valuable tool to study metal olfactory injury and recovery and to characterize sensitive olfactory neuron populations in fish exposed to environmental pollutants.
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