header logo image header logo text
Downloads Login
Research
General Information
ZIRC
ZFIN ID: ZDB-PUB-130708-44
Maintenance of Melanophore Morphology and Survival Is Cathepsin and vps11 Dependent in Zebrafish
Clancey, L.F., Beirl, A.J., Linbo, T.H., and Cooper, C.D.
Date: 2013
Source: PLoS One   8(5): e65096 (Journal)
Registered Authors: Beirl, Alisha, Cooper, Cynthia, Linbo, Tor
Keywords: none
MeSH Terms:
  • Animals
  • Autophagy/drug effects
  • Autophagy/genetics
  • Caspases/metabolism
  • Cathepsins/genetics*
  • Cathepsins/metabolism
  • Cell Survival/drug effects
  • Cell Survival/genetics
  • Chromosome Mapping
  • Chromosomes
  • Enzyme Activation/drug effects
  • Enzyme Inhibitors/pharmacology
  • Gene Expression Regulation
  • Macrolides/pharmacology
  • Melanophores/cytology*
  • Melanophores/drug effects
  • Melanophores/metabolism*
  • Mutation
  • Organ Specificity/genetics
  • Vesicular Transport Proteins/genetics*
  • Vesicular Transport Proteins/metabolism
  • Zebrafish/genetics*
  • Zebrafish/metabolism
  • Zebrafish Proteins/genetics*
  • Zebrafish Proteins/metabolism
PubMed: 23724125 Full text @ PLoS One
FIGURES
ABSTRACT

Here, we characterize a Danio rerio zebrafish pigment cell mutant (melanophore integrity mutant), which displays a defect in maintenance of melanophore and iridophore number. Mapping and candidate gene analysis links the melanophore integrity mutant mutation to the vacuolar protein sorting 11 (vps11w66) gene. Quantification of vps11w66 chromatophores during larval stages suggests a decrease in number as compared to wildtype siblings. TUNEL analysis and treatment with the caspase inhibitor, zVAD-fmk, indicate that vps11w66chromatophore death is caspase independent. Western blot analysis of PARP-1 cleavage patterns in mutant lysates suggests that increases in pH dependent cathepsin activity is involved in the premature chromatophore death observed in vps11w66 mutants. Consistently, treatment with ALLM and Bafilomycin A1 (cathepsin/calpain and vacuolar-type H+-ATPase inhibitors, respectively), restore normal melanophore morphology and number in vps11w66 mutants. Last, LC3B western blot analysis indicates an increase in autophagosome marker, LC3B II in vps11w66 mutants as compared to wildtype control, but not in ALLM or Bafilomycin A1 treated mutants. Taken together, these data suggest that vps11 promotes normal melanophore morphology and survival by inhibiting cathepsin release and/or activity.

ADDITIONAL INFORMATION