» Articles » PMID: 22180728

Lhx2 and Lhx9 Determine Neuronal Differentiation and Compartition in the Caudal Forebrain by Regulating Wnt Signaling

Overview
Journal PLoS Biol
Specialty Biology
Date 2011 Dec 20
PMID 22180728
Citations 64
Authors
Affiliations
Soon will be listed here.
Abstract

Initial axial patterning of the neural tube into forebrain, midbrain, and hindbrain primordia occurs during gastrulation. After this patterning phase, further diversification within the brain is thought to proceed largely independently in the different primordia. However, mechanisms that maintain the demarcation of brain subdivisions at later stages are poorly understood. In the alar plate of the caudal forebrain there are two principal units, the thalamus and the pretectum, each of which is a developmental compartment. Here we show that proper neuronal differentiation of the thalamus requires Lhx2 and Lhx9 function. In Lhx2/Lhx9-deficient zebrafish embryos the differentiation process is blocked and the dorsally adjacent Wnt positive epithalamus expands into the thalamus. This leads to an upregulation of Wnt signaling in the caudal forebrain. Lack of Lhx2/Lhx9 function as well as increased Wnt signaling alter the expression of the thalamus specific cell adhesion factor pcdh10b and lead subsequently to a striking anterior-posterior disorganization of the caudal forebrain. We therefore suggest that after initial neural tube patterning, neurogenesis within a brain compartment influences the integrity of the neuronal progenitor pool and border formation of a neuromeric compartment.

Citing Articles

Conserved multisensory integration of social cues in the thalamus.

Anneser L, Kappel J iScience. 2025; 28(1):111678.

PMID: 39868040 PMC: 11761278. DOI: 10.1016/j.isci.2024.111678.


Secreted Frizzled-Related Protein 1a regulates hematopoietic development in a dose-dependent manner.

Ide A, Carpenter K, Elaswad M, Opria K, Marcellin K, Gilliland C bioRxiv. 2025; .

PMID: 39829913 PMC: 11741364. DOI: 10.1101/2025.01.10.632371.


Molecular mechanisms of libido influencing semen quality in geese through the hypothalamic-pituitary-testicular-external genitalia axis.

He Z, Liu T, He X, Song Y, Li G, Li X Poult Sci. 2025; 104(2):104756.

PMID: 39753050 PMC: 11754076. DOI: 10.1016/j.psj.2024.104756.


Small molecule valproic acid enhances ventral patterning of human neural tube organoids by regulating Wnt and Shh signalling.

Zheng Y, Zhang F, Nie H, Li X, Xun J, Fu J Cell Prolif. 2024; 58(1):e13737.

PMID: 39164046 PMC: 11693559. DOI: 10.1111/cpr.13737.


StaVia: spatially and temporally aware cartography with higher-order random walks for cell atlases.

Stassen S, Kobashi M, Lam E, Huang Y, Ho J, Tsia K Genome Biol. 2024; 25(1):224.

PMID: 39152459 PMC: 11328412. DOI: 10.1186/s13059-024-03347-y.


References
1.
Cerda G, Thomas J, Allende M, Karlstrom R, Palma V . Electroporation of DNA, RNA, and morpholinos into zebrafish embryos. Methods. 2006; 39(3):207-11. DOI: 10.1016/j.ymeth.2005.12.009. View

2.
Scholpp S, Lumsden A . Building a bridal chamber: development of the thalamus. Trends Neurosci. 2010; 33(8):373-80. PMC: 2954313. DOI: 10.1016/j.tins.2010.05.003. View

3.
Redies C, Ast M, Nakagawa S, Takeichi M, MartInez-de-la-Torre M, Puelles L . Morphologic fate of diencephalic prosomeres and their subdivisions revealed by mapping cadherin expression. J Comp Neurol. 2000; 421(4):481-514. DOI: 10.1002/(sici)1096-9861(20000612)421:4<481::aid-cne3>3.0.co;2-h. View

4.
Murakami T, Hijikata T, Matsukawa M, Ishikawa H, Yorifuji H . Zebrafish protocadherin 10 is involved in paraxial mesoderm development and somitogenesis. Dev Dyn. 2005; 235(2):506-14. DOI: 10.1002/dvdy.20622. View

5.
Bulfone A, Puelles L, Porteus M, Frohman M, Martin G, Rubenstein J . Spatially restricted expression of Dlx-1, Dlx-2 (Tes-1), Gbx-2, and Wnt-3 in the embryonic day 12.5 mouse forebrain defines potential transverse and longitudinal segmental boundaries. J Neurosci. 1993; 13(7):3155-72. PMC: 6576688. View