» Articles » PMID: 22127979

Retinoic Acid Signaling Regulates Sonic Hedgehog and Bone Morphogenetic Protein Signalings During Genital Tubercle Development

Abstract

Retinoic acid (RA) plays pivotal roles in organogenesis, and both excessive and reduced amounts of RA cause developmental abnormalities. Reproductive organs are susceptible to teratogen toxigenicity, and the genital tubercle (GT) is one such representative organ. The physiological function of endogenous RA signaling and the mechanisms of RA-induced teratogenicity are poorly understood during the GT development. The objective of this study is to understand the developmental and teratogenic roles of RA during GT development by analyzing genetically modified mouse models. We found dynamic patterns of gene expression for the RA-synthesizing enzyme, Raldh2, and for the RA-catabolizing enzyme, Cyp26b1, during GT development. Rarb, an indicator gene for RA signaling, starts its expression in the prospective corpus cavernosum penis and in the urethral plate epithelium (UE), which plays central roles during GT development. Excessive RA signaling in Cyp26b1(-/-) mutants leads to abnormal extents of cell proliferation and differentiation during GT development, and also upregulates expression of growth factor signalings. They include Sonic hedgehog (Shh) signaling and Bone morphogenetic protein (Bmp) signaling, which are expressed in the UE and its bilateral mesenchyme. RA signaling positively regulatesShh and Bmp4 expression during GT development as testified also by the experiment of RA administration and analyses of loss-of-function of RA signaling mutants. Thus, RA signaling is involved in the developmental cascade necessary for UE formation and GT development.

Citing Articles

Lateral Motor Column specific expression of Sonic Hedgehog contributes to maintenance and scaling of pMN progenitor cell populations during oligodendrogenesis.

Starikov L, Ghinia-Tegla M, Kottmann A Res Sq. 2024; .

PMID: 38798533 PMC: 11118686. DOI: 10.21203/rs.3.rs-4249282/v1.


The role of p63 in embryonic external genitalia outgrowth in mice.

Tanaka K, Matsumaru D, Suzuki K, Yamada G, Miyagawa S Dev Growth Differ. 2023; 65(2):132-140.

PMID: 36680528 PMC: 11520970. DOI: 10.1111/dgd.12840.


Exploration of the DARTable Genome- a Resource Enabling Data-Driven NAMs for Developmental and Reproductive Toxicity Prediction.

Janowska-Sejda E, Adeleye Y, Currie R Front Toxicol. 2022; 3:806311.

PMID: 35295108 PMC: 8915813. DOI: 10.3389/ftox.2021.806311.


An ontology for developmental processes and toxicities of neural tube closure.

Heusinkveld H, Staal Y, Baker N, Daston G, Knudsen T, Piersma A Reprod Toxicol. 2020; 99:160-167.

PMID: 32926990 PMC: 10083840. DOI: 10.1016/j.reprotox.2020.09.002.


Sonic Hedgehog Signaling Is Required for Cyp26 Expression during Embryonic Development.

El Shahawy M, Reibring C, Hallberg K, Neben C, Marangoni P, Harfe B Int J Mol Sci. 2019; 20(9).

PMID: 31072004 PMC: 6540044. DOI: 10.3390/ijms20092275.


References
1.
Feil R, Wagner J, Metzger D, Chambon P . Regulation of Cre recombinase activity by mutated estrogen receptor ligand-binding domains. Biochem Biophys Res Commun. 1997; 237(3):752-7. DOI: 10.1006/bbrc.1997.7124. View

2.
Wu X, Ferrara C, Shapiro E, Grishina I . Bmp7 expression and null phenotype in the urogenital system suggest a role in re-organization of the urethral epithelium. Gene Expr Patterns. 2009; 9(4):224-30. PMC: 2653601. DOI: 10.1016/j.gep.2008.12.005. View

3.
Morgan E, Nguyen S, Scott V, Stadler H . Loss of Bmp7 and Fgf8 signaling in Hoxa13-mutant mice causes hypospadia. Development. 2003; 130(14):3095-109. DOI: 10.1242/dev.00530. View

4.
Yashiro K, Zhao X, Uehara M, Yamashita K, Nishijima M, Nishino J . Regulation of retinoic acid distribution is required for proximodistal patterning and outgrowth of the developing mouse limb. Dev Cell. 2004; 6(3):411-22. DOI: 10.1016/s1534-5807(04)00062-0. View

5.
Ribes V, Wang Z, Dolle P, Niederreither K . Retinaldehyde dehydrogenase 2 (RALDH2)-mediated retinoic acid synthesis regulates early mouse embryonic forebrain development by controlling FGF and sonic hedgehog signaling. Development. 2005; 133(2):351-61. DOI: 10.1242/dev.02204. View