» Articles » PMID: 25233141

The Development and Growth of Tissues Derived from Cranial Neural Crest and Primitive Mesoderm is Dependent on the Ligation Status of Retinoic Acid Receptor γ: Evidence That Retinoic Acid Receptor γ Functions to Maintain Stem/progenitor Cells in The...

Overview
Journal Stem Cells Dev
Date 2014 Sep 19
PMID 25233141
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Retinoic acid (RA) signaling is important to normal development. However, the function of the different RA receptors (RARs)--RARα, RARβ, and RARγ--is as yet unclear. We have used wild-type and transgenic zebrafish to examine the role of RARγ. Treatment of zebrafish embryos with an RARγ-specific agonist reduced somite formation and axial length, which was associated with a loss of hoxb13a expression and less-clear alterations in hoxc11a or myoD expression. Treatment with the RARγ agonist also disrupted formation of tissues arising from cranial neural crest, including cranial bones and anterior neural ganglia. There was a loss of Sox 9-immunopositive neural crest stem/progenitor cells in the same anterior regions. Pectoral fin outgrowth was blocked by RARγ agonist treatment. However, there was no loss of Tbx-5-immunopositive lateral plate mesodermal stem/progenitor cells and the block was reversed by agonist washout or by cotreatment with an RARγ antagonist. Regeneration of the caudal fin was also blocked by RARγ agonist treatment, which was associated with a loss of canonical Wnt signaling. This regenerative response was restored by agonist washout or cotreatment with the RARγ antagonist. These findings suggest that RARγ plays an essential role in maintaining stem/progenitor cells during embryonic development and tissue regeneration when the receptor is in its nonligated state.

Citing Articles

Targeting Androgen, Thyroid Hormone, and Vitamin A and D Receptors to Treat Prostate Cancer.

Hantusch B, Kenner L, Stanulovic V, Hoogenkamp M, Brown G Int J Mol Sci. 2024; 25(17).

PMID: 39273194 PMC: 11394715. DOI: 10.3390/ijms25179245.


Molecular Interactions of Selective Agonists and Antagonists with the Retinoic Acid Receptor γ.

Powala K, Zolek T, Brown G, Kutner A Int J Mol Sci. 2024; 25(12).

PMID: 38928275 PMC: 11203493. DOI: 10.3390/ijms25126568.


Deregulation of All- Retinoic Acid Signaling and Development in Cancer.

Brown G Int J Mol Sci. 2023; 24(15).

PMID: 37569466 PMC: 10419198. DOI: 10.3390/ijms241512089.


Retinoic acid receptor regulation of decision-making for cell differentiation.

Brown G Front Cell Dev Biol. 2023; 11:1182204.

PMID: 37082619 PMC: 10110968. DOI: 10.3389/fcell.2023.1182204.


Targeting the Retinoic Acid Pathway to Eradicate Cancer Stem Cells.

Brown G Int J Mol Sci. 2023; 24(3).

PMID: 36768694 PMC: 9916838. DOI: 10.3390/ijms24032373.


References
1.
Grandel H, Brand M . Zebrafish limb development is triggered by a retinoic acid signal during gastrulation. Dev Dyn. 2011; 240(5):1116-26. DOI: 10.1002/dvdy.22461. View

2.
Geraudie J, Borday Birraux V . Posterior hoxa genes expression during zebrafish bony fin ray development and regeneration suggests their involvement in scleroblast differentiation. Dev Genes Evol. 2003; 213(4):182-6. DOI: 10.1007/s00427-003-0307-y. View

3.
Gudas L . Retinoids induce stem cell differentiation via epigenetic changes. Semin Cell Dev Biol. 2013; 24(10-12):701-5. PMC: 3849227. DOI: 10.1016/j.semcdb.2013.08.002. View

4.
Suemori H, Noguchi S . Hox C cluster genes are dispensable for overall body plan of mouse embryonic development. Dev Biol. 2001; 220(2):333-42. DOI: 10.1006/dbio.2000.9651. View

5.
Oliveira E, Casado M, Raldua D, Soares A, Barata C, Pina B . Retinoic acid receptors' expression and function during zebrafish early development. J Steroid Biochem Mol Biol. 2013; 138:143-51. DOI: 10.1016/j.jsbmb.2013.03.011. View