» Articles » PMID: 35394423

Completion of Neural Crest Cell Production and Emigration is Regulated by Retinoic-acid-dependent Inhibition of BMP Signaling

Overview
Journal Elife
Specialty Biology
Date 2022 Apr 8
PMID 35394423
Authors
Affiliations
Soon will be listed here.
Abstract

Production and emigration of neural crest cells is a transient process followed by the emergence of the definitive roof plate. The mechanisms regulating the end of neural crest ontogeny are poorly understood. Whereas early crest development is stimulated by mesoderm-derived retinoic acid, we report that the end of the neural crest period is regulated by retinoic acid synthesized in the dorsal neural tube. Inhibition of retinoic acid signaling in the neural tube prevents the normal upregulation of BMP inhibitors in the nascent roof plate and prolongs the period of BMP responsiveness which otherwise ceases close to roof plate establishment. Consequently, neural crest production and emigration are extended well into the roof plate stage. In turn, extending the activity of neural crest-specific genes inhibits the onset of retinoic acid synthesis in roof plate suggesting a mutual repressive interaction between neural crest and roof plate traits. Although several roof plate-specific genes are normally expressed in the absence of retinoic acid signaling, roof plate and crest markers are co-expressed in single cells and this domain also contains dorsal interneurons. Hence, the cellular and molecular architecture of the roof plate is compromised. Collectively, our results demonstrate that neural tube-derived retinoic acid, via inhibition of BMP signaling, is an essential factor responsible for the end of neural crest generation and the proper segregation of dorsal neural lineages.

Citing Articles

Bone morphogenetic protein (BMP) signaling determines neuroblastoma cell fate and sensitivity to retinoic acid.

Pan M, Zhang Y, Wright W, Liu X, Passaia B, Currier D Nat Commun. 2025; 16(1):2036.

PMID: 40021625 PMC: 11871043. DOI: 10.1038/s41467-025-57185-y.


Epithelial-mesenchymal crosstalk: the scriptwriter of craniofacial morphogenesis.

Lu J, Peng B, Wang W, Zou Y Front Cell Dev Biol. 2024; 12:1497002.

PMID: 39583201 PMC: 11582012. DOI: 10.3389/fcell.2024.1497002.


Retinoic acid, an essential component of the roof plate organizer, promotes the spatiotemporal segregation of dorsal neural fates.

Rekler D, Ofek S, Kagan S, Friedlander G, Kalcheim C Development. 2024; 151(19).

PMID: 39250350 PMC: 11463963. DOI: 10.1242/dev.202973.


Valproic acid-induced teratogenicity is driven by senescence and prevented by Rapamycin in human spinal cord and animal models.

Pietrogrande G, Shaker M, Stednitz S, Soheilmoghaddam F, Aguado J, Morrison S Mol Psychiatry. 2024; 30(3):986-998.

PMID: 39227432 PMC: 11835743. DOI: 10.1038/s41380-024-02732-0.


A Spatio-Temporal-Dependent Requirement of Sonic Hedgehog in the Early Development of Sclerotome-Derived Vertebrae and Ribs.

Kahane N, Dahan-Barda Y, Kalcheim C Int J Mol Sci. 2024; 25(11).

PMID: 38891790 PMC: 11171667. DOI: 10.3390/ijms25115602.


References
1.
Chizhikov V, Millen K . Roof plate-dependent patterning of the vertebrate dorsal central nervous system. Dev Biol. 2004; 277(2):287-95. DOI: 10.1016/j.ydbio.2004.10.011. View

2.
Reijntjes S, Blentic A, Gale E, Maden M . The control of morphogen signalling: regulation of the synthesis and catabolism of retinoic acid in the developing embryo. Dev Biol. 2005; 285(1):224-37. DOI: 10.1016/j.ydbio.2005.06.019. View

3.
Holguera I, Desplan C . Neuronal specification in space and time. Science. 2018; 362(6411):176-180. PMC: 6368964. DOI: 10.1126/science.aas9435. View

4.
Martinez-Morales P, Diez Del Corral R, Olivera-Martinez I, Quiroga A, Das R, Barbas J . FGF and retinoic acid activity gradients control the timing of neural crest cell emigration in the trunk. J Cell Biol. 2011; 194(3):489-503. PMC: 3153641. DOI: 10.1083/jcb.201011077. View

5.
Lara-Ramirez R, Zieger E, Schubert M . Retinoic acid signaling in spinal cord development. Int J Biochem Cell Biol. 2013; 45(7):1302-13. DOI: 10.1016/j.biocel.2013.04.002. View