header logo image header logo text
Downloads Login
Research
General Information
ZIRC
ZFIN ID: ZDB-PUB-001019-9
Programmed cell death in zebrafish Rohon Beard neurons is influenced by TrkC1/NT-3 signaling
Williams, J.A., Barrios, A., Gatchalian, C., Rubin, L., Wilson, S.W., and Holder, N.
Date: 2000
Source: Developmental Biology   226(2): 220-230 (Journal)
Registered Authors: Barrios, Arantza, Gatchalian, Christine, Holder, Nigel, Williams, Juliet, Wilson, Steve
Keywords: Rohon Beard neurons; programmed cell death; TrkC1; NT-3
MeSH Terms:
  • Animals
  • Apoptosis/drug effects
  • Apoptosis/physiology*
  • Caspases/physiology
  • Cell Differentiation
  • Cells, Cultured
  • Ganglia, Spinal/cytology
  • In Situ Nick-End Labeling
  • Nerve Tissue Proteins/drug effects
  • Nerve Tissue Proteins/physiology*
  • Neurons, Afferent/classification
  • Neurons, Afferent/cytology*
  • Neurons, Afferent/drug effects
  • Neurotrophin 3/pharmacology
  • Neurotrophin 3/physiology*
  • Receptor, trkC/drug effects
  • Receptor, trkC/physiology*
  • Signal Transduction
  • Zebrafish/anatomy & histology
  • Zebrafish/growth & development*
PubMed: 11023682 Full text @ Dev. Biol.
FIGURES
ABSTRACT
Rohon Beard (RB) cells are embryonic primary sensory neurons that are removed by programmed cell death during larval development in zebrafish. RB somatosensory functions are taken over by neurons of the dorsal root ganglia (DRG), suggesting that RB cell death may be triggered by the differentiation of these ganglia, as has been proposed to be the case in Xenopus. However, here we show that the timing of RB cell death correlates with reduced expression of trkC1, the receptor for neurotrophin NT-3, but not with the appearance of DRG, which differentiate only after most RB cells die. trkC1 is expressed in subpopulations of RB neurons during development, and cell death is initiated only in trkC1-negative neurons, suggesting a role for TrkC1 and its ligand, NT-3, in RB cell survival. In support of this, antibodies that deplete NT-3 induce RB cell death while exogenous application of NT-3 reduces death. In addition, we show that RB cell death can be prevented using a caspase inhibitor, zVADfmk, showing that during normal development, RB cells die by a caspase-dependent programmed cell death pathway possibly triggered by reduced signaling via TrkC1.
ADDITIONAL INFORMATION