» Articles » PMID: 33304906

Zebrafish Models of Craniofacial Malformations: Interactions of Environmental Factors

Overview
Specialty Cell Biology
Date 2020 Dec 11
PMID 33304906
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

The zebrafish is an appealing model organism for investigating the genetic (G) and environmental (E) factors, as well as their interactions (GxE), which contribute to craniofacial malformations. Here, we review zebrafish studies on environmental factors involved in the etiology of craniofacial malformations in humans including maternal smoking, alcohol consumption, nutrition and drug use. As an example, we focus on the (cleft) palate, for which the zebrafish ethmoid plate is a good model. This review highlights the importance of investigating ExE interactions and discusses the variable effects of exposure to environmental factors on craniofacial development depending on dosage, exposure time and developmental stage. Zebrafish also promise to be a good tool to study novel craniofacial teratogens and toxin mixtures. Lastly, we discuss the handful of studies on gene-alcohol interactions using mutant sensitivity screens and reverse genetic techniques. We expect that studies addressing complex interactions (ExE and GxE) in craniofacial malformations will increase in the coming years. These are likely to uncover currently unknown mechanisms with implications for the prevention of craniofacial malformations. The zebrafish appears to be an excellent complementary model with high translational value to study these complex interactions.

Citing Articles

Zebrafish Models for Skeletal and Extraskeletal Osteogenesis Imperfecta Features: Unveiling Pathophysiology and Paving the Way for Drug Discovery.

Masiero C, Aresi C, Forlino A, Tonelli F Calcif Tissue Int. 2024; 115(6):931-959.

PMID: 39320469 PMC: 11607041. DOI: 10.1007/s00223-024-01282-5.


Toxicity and Metabolomic Dysfunction Invoked by Febrifugin, a Harmful Component of Edible Nut of .

Zhang X, Song Q, Zheng H, Wang R, Zhang Q Int J Mol Sci. 2024; 25(17).

PMID: 39273700 PMC: 11396426. DOI: 10.3390/ijms25179753.


Loss-of-function of the Zinc Finger Homeobox 4 () gene underlies a neurodevelopmental disorder.

Maria Del Rocio P, Palomares Bralo M, Vanhooydonck M, Hamerlinck L, Dhaene E, Leimbacher S medRxiv. 2024; .

PMID: 39148819 PMC: 11326360. DOI: 10.1101/2024.08.07.24311381.


Early stress exposure on zebrafish development: effects on survival, malformations and molecular alterations.

Valcarce D, Selles-Egea A, Riesco M, De Garnica M, Martinez-Fernandez B, Herraez M Fish Physiol Biochem. 2024; 50(4):1545-1562.

PMID: 38743196 PMC: 11286684. DOI: 10.1007/s10695-024-01355-0.


Transforming growth factor beta signaling and craniofacial development: modeling human diseases in zebrafish.

Fox S, Waskiewicz A Front Cell Dev Biol. 2024; 12:1338070.

PMID: 38385025 PMC: 10879340. DOI: 10.3389/fcell.2024.1338070.


References
1.
Finer L, Zolna M . Declines in Unintended Pregnancy in the United States, 2008-2011. N Engl J Med. 2016; 374(9):843-52. PMC: 4861155. DOI: 10.1056/NEJMsa1506575. View

2.
Spoorendonk K, Peterson-Maduro J, Renn J, Trowe T, Kranenbarg S, Winkler C . Retinoic acid and Cyp26b1 are critical regulators of osteogenesis in the axial skeleton. Development. 2008; 135(22):3765-74. DOI: 10.1242/dev.024034. View

3.
Massarsky A, Abdel A, Glazer L, Levin E, Di Giulio R . Exposure to 1,2-Propanediol Impacts Early Development of Zebrafish (Danio rerio) and Induces Hyperactivity. Zebrafish. 2017; 14(3):216-222. DOI: 10.1089/zeb.2016.1400. View

4.
Jiang Q, Lu D, Wang F, Zhang Y, Cao L, Gui Y . Folic acid supplement rescues ethanol-induced developmental defects in the zebrafish embryos. Acta Biochim Biophys Sin (Shanghai). 2020; 52(5):536-545. DOI: 10.1093/abbs/gmaa030. View

5.
Pardo-Martin C, Allalou A, Medina J, Eimon P, Wahlby C, Yanik M . High-throughput hyperdimensional vertebrate phenotyping. Nat Commun. 2013; 4:1467. PMC: 3573763. DOI: 10.1038/ncomms2475. View