PUBLICATION
Exposure to the aryl hydrocarbon receptor agonist dioxin disrupts formation of the muscle, nerves, and vasculature in the developing jaw
- Authors
- Cintrón-Rivera, L.G., Burns, N., Patel, R., Plavicki, J.
- ID
- ZDB-PUB-230904-51
- Date
- 2023
- Source
- Environmental pollution (Barking, Essex : 1987) 337: 122499 (Journal)
- Registered Authors
- Cintrón-Rivera, Layra, Plavicki, Jessica
- Keywords
- AHR, Craniofacial, Dioxin, Jaw, TCDD, Zebrafish
- MeSH Terms
-
- Animals
- Dioxins*/metabolism
- Dioxins*/toxicity
- Environmental Pollutants*/toxicity
- Female
- Humans
- Muscles/metabolism
- Persistent Organic Pollutants/metabolism
- Polychlorinated Dibenzodioxins*/metabolism
- Polychlorinated Dibenzodioxins*/toxicity
- Pregnancy
- Receptors, Aryl Hydrocarbon/metabolism
- Zebrafish/metabolism
- Zebrafish Proteins/genetics
- PubMed
- 37660771 Full text @ Environ. Pollut.
Citation
Cintrón-Rivera, L.G., Burns, N., Patel, R., Plavicki, J. (2023) Exposure to the aryl hydrocarbon receptor agonist dioxin disrupts formation of the muscle, nerves, and vasculature in the developing jaw. Environmental pollution (Barking, Essex : 1987). 337:122499.
Abstract
Human exposure to environmental pollutants can disrupt embryonic development and impact juvenile and adult health outcomes by adversely affecting cell and organ function. Notwithstanding, environmental contamination continues to increase due to industrial development, insufficient regulations, and the mobilization of pollutants as a result of extreme weather events. Dioxins are a class of structurally related persistent organic pollutants that are highly toxic, carcinogenic, and teratogenic. 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) is the most potent dioxin compound and has been shown to induce toxic effects in developing organisms by activating the aryl hydrocarbon receptor (AHR), a ligand activated transcription factor targeted by multiple persistent organic pollutants. Contaminant-induced AHR activation results in malformations of the craniofacial cartilages and neurocranium; however, the mechanisms mediating these phenotypes are not well understood. In this study, we utilized the optically transparent zebrafish model to elucidate novel cellular targets and potential transcriptional targets underlying TCDD-induced craniofacial malformations. To this end, we exposed zebrafish embryos at 4 h post fertilization to TCDD and employed a mixed-methods approach utilizing immunohistochemistry staining, transgenic reporter lines, fixed and in vivo confocal imaging, and timelapse microscopy to determine the targets mediating TCDD-induced craniofacial phenotypes. Our data indicates that embryonic TCDD exposure reduced jaw and pharyngeal arch Sox10+ chondrocytes and Tcf21+ pharyngeal mesoderm progenitors. Exposure to TCDD correspondingly led to a reduction in collagen type II deposition in Sox10+ domains. Embryonic TCDD exposure impaired development of tissues derived from or guided by Tcf21+ progenitors, namely: nerves, muscle, and vasculature. Specifically, TCDD exposure disrupted development of the hyoid and mandibular arch muscles, decreased neural innervation of the jaw, resulted in compression of cranial nerves V and VII, and led to jaw vasculature malformations. Collectively, these findings reveal novel structural targets and potential transcriptional targets of TCDD-induced toxicity, showcasing how contaminant exposures lead to congenital craniofacial malformations.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping