» Articles » PMID: 24631632

The Different Effects on Cranial and Trunk Neural Crest Cell Behaviour Following Exposure to a Low Concentration of Alcohol in Vitro

Overview
Journal Arch Oral Biol
Specialty Dentistry
Date 2014 Mar 18
PMID 24631632
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Embryonic neural crest cells give rise to large regions of the face and peripheral nervous system. Exposure of these cells to high alcohol concentrations leads to cell death in the craniofacial region resulting in facial defects. However, the effects of low concentrations of alcohol on neural crest cells are not clear. In this study, cranial neural crest cells from Xenopus laevis were cultured in an ethanol concentration approximately equivalent to one drink. Techniques were developed to study various aspects of neural crest cell behaviour and a number of cellular parameters were quantified. In the presence of alcohol, a significant number of cranial neural crest cells emigrated from the explant on fibronectin but the liberation of individual cells was delayed. The cells also remained close to the explant and their morphology changed. Cranial neural crest cells did not grow on Type 1 collagen. For the purposes of comparison, the behaviour of trunk neural crest cells was also studied. The presence of alcohol correlated with increased retention of single cells on fibronectin but left other parameters unchanged. The behaviour of trunk neural crest cells growing on Type 1 collagen in the presence of alcohol did not differ from controls. Low concentrations of alcohol therefore significantly affected both cranial and trunk neural crest cells, with a wider variety of effects on cells from the cranial as opposed to the trunk region. The results suggest that low concentrations of alcohol may be more detrimental to early events in organ formation than currently suspected.

Citing Articles

Exosome-shuttled miR-126 mediates ethanol-induced disruption of neural crest cell-placode cell interaction by targeting SDF1.

Li Y, Cai T, Liu H, Liu J, Chen S, Fan H Toxicol Sci. 2023; 195(2):184-201.

PMID: 37490477 PMC: 10801442. DOI: 10.1093/toxsci/kfad068.


Neural crest cells and fetal alcohol spectrum disorders: Mechanisms and potential targets for prevention.

Chen S, Kannan M Pharmacol Res. 2023; 194:106855.

PMID: 37460002 PMC: 10528842. DOI: 10.1016/j.phrs.2023.106855.


Effect of Embryonic Alcohol Exposure on Craniofacial and Skin Melanocyte Development: Insights from Zebrafish ().

Azimian Zavareh P, Silva P, Gimhani N, Atukorallaya D Toxics. 2022; 10(9).

PMID: 36136509 PMC: 9501518. DOI: 10.3390/toxics10090544.


Up-regulation of microRNA-34a mediates ethanol-induced impairment of neural crest cell migration in vitro and in zebrafish embryos through modulating epithelial-mesenchymal transition by targeting Snail1.

Fan H, Li Y, Yuan F, Lu L, Liu J, Feng W Toxicol Lett. 2022; 358:17-26.

PMID: 35038560 PMC: 9058190. DOI: 10.1016/j.toxlet.2022.01.004.


Neural crest metabolism: At the crossroads of development and disease.

Bhattacharya D, Khan B, Simoes-Costa M Dev Biol. 2021; 475:245-255.

PMID: 33548210 PMC: 10171235. DOI: 10.1016/j.ydbio.2021.01.018.