A quantitative in vivo assay for craniofacial developmental toxicity of histone deacetylases

Toxicol Lett. 2021 May 15:342:20-25. doi: 10.1016/j.toxlet.2021.02.005. Epub 2021 Feb 10.

Abstract

Many bony features of the face develop from endochondral ossification of preexisting collagen-rich cartilage structures. The proper development of these cartilage structures is essential to the morphological formation of the face. The developmental programs governing the formation of the pre-bone facial cartilages are sensitive to chemical compounds that disturb histone acetylation patterns and chromatin structure. We have taken advantage of this fact to develop a quantitative morphological assay of craniofacial developmental toxicity based on the distortion and deterioration of facial cartilage structures in zebrafish larvae upon exposure to increasing concentrations of several well-described histone deacetylase inhibitors. In this assay, we measure the angle formed by the developing ceratohyal bone as a precise, sensitive and quantitative proxy for the overall developmental status of facial cartilages. Using the well-established developmental toxicant and histone deacetylase-inhibiting compound valproic acid along with 12 structurally related compounds, we demonstrate the applicability of the ceratohyal angle assay to investigate structure-activity relationships.

Keywords: Craniofacial development; Developmental and reproductive toxicology; Embryonic development; Histone deacetylase inhibition; Neural crest; Osteogenesis; Toxicity assay; Valproic acid; Zebrafish.

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Antibiotics, Antineoplastic / toxicity
  • Anticonvulsants / toxicity
  • Antifungal Agents / toxicity
  • Butyrates / toxicity*
  • Collagen Type II / genetics
  • Collagen Type II / metabolism*
  • Craniofacial Abnormalities / chemically induced*
  • Gene Expression Regulation, Developmental / drug effects
  • Genes, Reporter
  • Histone Deacetylases / metabolism*
  • Hydroxamic Acids / toxicity*
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Peptides / toxicity*
  • Red Fluorescent Protein
  • Valproic Acid / toxicity
  • Zebrafish

Substances

  • Antibiotics, Antineoplastic
  • Anticonvulsants
  • Antifungal Agents
  • Butyrates
  • Collagen Type II
  • Hydroxamic Acids
  • Luminescent Proteins
  • Peptides
  • pivalyloxymethyl butyrate
  • trapoxin A
  • trichostatin A
  • Valproic Acid
  • Histone Deacetylases