Spatial and temporal expression of Wnt and Dickkopf genes during murine lens development
- PMID: 15053977
- DOI: 10.1016/j.modgep.2003.11.002
Spatial and temporal expression of Wnt and Dickkopf genes during murine lens development
Abstract
Recent studies indicate a role for Wnt signalling in regulating lens cell differentiation (Stump et al., 2003). To further our understanding of this, we investigated the expression patterns of Wnts and Wnt signalling regulators, the Dickkopfs (Dkks), during murine lens development. In situ hybridisation showed that Wnt5a, Wnt5b, Wnt7a, Wnt7b, Wnt8a and Wnt8b genes are expressed throughout the early lens primordia. At embryonic day 14.5 (E14.5), Wnt5a, Wnt5b, Wnt7a, Wnt8a and Wnt8b are reduced in the primary fibres, whereas Wnt7b remains strongly expressed. This trend persists up to E15.5. At later embryonic stages, Wnt expression is predominantly localised to the epithelium and elongating cells at the lens equator. As fibre differentiation progresses, Wnt expression becomes undetectable in the cells of the lens cortex. The one exception is Wnt7b, which continues to be weakly expressed in cortical fibres. This pattern of expression continues through to early postnatal stages. However, by postnatal day 21 (P21), expression of all Wnts is distinctly weaker in the central lens epithelium compared with the equatorial region. This is most notable for Wnt5a, which is barely detectable in the central lens epithelium at P21. Dkk1, Dkk2 and Dkk3 have similar patterns of expression to each other and to the majority of the Wnts during lens development. This study shows that multiple Wnt and Dkk genes are expressed during lens development. Expression is predominantly in the epithelial compartment but is also associated, particularly in the case of Wnt7b, with early events in fibre differentiation.
Similar articles
-
Conditional mutations of beta-catenin and APC reveal roles for canonical Wnt signaling in lens differentiation.Invest Ophthalmol Vis Sci. 2009 Oct;50(10):4794-806. doi: 10.1167/iovs.09-3567. Epub 2009 Jun 10. Invest Ophthalmol Vis Sci. 2009. PMID: 19515997
-
Characterisation of the Wnt antagonists and their response to conditionally activated Wnt signalling in the developing mouse forebrain.Brain Res Dev Brain Res. 2004 Nov 25;153(2):261-70. doi: 10.1016/j.devbrainres.2004.09.008. Brain Res Dev Brain Res. 2004. PMID: 15527894
-
Wnt signaling enhances FGF2-triggered lens fiber cell differentiation.Development. 2004 Apr;131(8):1813-24. doi: 10.1242/dev.01060. Epub 2004 Mar 17. Development. 2004. PMID: 15084465
-
Growth factor regulation of lens development.Dev Biol. 2005 Apr 1;280(1):1-14. doi: 10.1016/j.ydbio.2005.01.020. Dev Biol. 2005. PMID: 15766743 Review.
-
The lens epithelium in ocular health and disease.Int J Biochem Cell Biol. 2010 Dec;42(12):1945-63. doi: 10.1016/j.biocel.2010.09.012. Epub 2010 Sep 29. Int J Biochem Cell Biol. 2010. PMID: 20883819 Review.
Cited by
-
Characterization of Lgr6+ Cells as an Enriched Population of Hair Cell Progenitors Compared to Lgr5+ Cells for Hair Cell Generation in the Neonatal Mouse Cochlea.Front Mol Neurosci. 2018 May 14;11:147. doi: 10.3389/fnmol.2018.00147. eCollection 2018. Front Mol Neurosci. 2018. PMID: 29867341 Free PMC article.
-
Interactions between lens epithelial and fiber cells reveal an intrinsic self-assembly mechanism.Dev Biol. 2014 Jan 15;385(2):291-303. doi: 10.1016/j.ydbio.2013.10.030. Epub 2013 Nov 8. Dev Biol. 2014. PMID: 24211762 Free PMC article.
-
Pax6 is essential for lens fiber cell differentiation.Development. 2009 Aug;136(15):2567-78. doi: 10.1242/dev.032888. Epub 2009 Jul 1. Development. 2009. PMID: 19570848 Free PMC article.
-
BAC-Dkk3-EGFP transgenic mouse: an in vivo analytical tool for Dkk3 expression.J Biomed Biotechnol. 2012;2012:973140. doi: 10.1155/2012/973140. Epub 2012 Jul 15. J Biomed Biotechnol. 2012. PMID: 22910798 Free PMC article.
-
Dkk1, -2, and -3 expression in mouse craniofacial development.J Mol Histol. 2005 Jun;36(5):367-72. doi: 10.1007/s10735-005-9008-3. Epub 2005 Sep 30. J Mol Histol. 2005. PMID: 16195809
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials