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PMID: 16289327 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Disruption of cerebellar granule cell development in the Pax6 mutant, Sey mouse.

Brain research. Developmental brain research ·Vol. 160 ·No. 2 ·2005-12-07 ·Pages 176-93

Swanson DJ, Tong Y, Goldowitz D

Abstract

The transcriptional regulator Pax6 is expressed in cerebellar granule cells and a mutation in that gene (Sey) has been shown to affect cerebellar development. We have defined novel phenotypes in the Sey/Sey cerebellum, indicating that the mutation of Pax6 alters granule cell behavior in vitro and also the interaction between granule cells and Purkinje cells in vivo. In culture, Sey/Sey granule cell precursors show the following abnormal phenotypes: enhanced proliferation, increased apoptotic cell death, and decreased number of morphologically differentiating beta-III tubulin-positive cells. There is an overlap in the populations of Sey/Sey cells that express markers for proliferation and neuronal differentiation indicating an abnormality in the transition between these states in granule cells. In vivo, Purkinje cell ectopias were found deep in the cerebellum and extending into the inferior colliculus. Coincident with this, Purkinje cell phenotype was the alteration in the pattern and levels of Reelin expression in granule cells of the external germinal layer (EGL). The finding of increased staining for Disabled-1, a signaling pathway intermediary that is normally downregulated by a Reelin signal, throughout the Purkinje cell population suggests that in the Sey/Sey cerebellum there is a disruption in Reelin signaling from the EGL to Purkinje cells. These findings suggest that Pax6 is critical for the proper differentiation of granule cells and their communication with developing Purkinje cells. Thus, through its guidance of granule cell development, Pax6 also has a strong influence on many of the cellular programs that guide the morphogenesis of the entire cerebellum.

MeSH Terms
Animals Bromodeoxyuridine/metabolism Calbindins Cell Adhesion Molecules, Neuronal/metabolism Cell Count/methods Cell Death/physiology Cell Proliferation Cells, Cultured Cerebellum/cytology,embryology Embryo, Mammalian Extracellular Matrix Proteins/metabolism Eye Proteins/genetics Gene Expression Regulation, Developmental/genetics,physiology Genotype Homeodomain Proteins/genetics Immunohistochemistry/methods In Situ Hybridization/methods Mice Mice, Neurologic Mutants Nerve Tissue Proteins/metabolism Neurons/physiology PAX6 Transcription Factor Paired Box Transcription Factors/genetics RNA, Messenger/biosynthesis Reelin Protein Repressor Proteins/genetics Reverse Transcriptase Polymerase Chain Reaction/methods S100 Calcium Binding Protein G/metabolism Serine Endopeptidases/metabolism Time Factors Tubulin/metabolism beta-Galactosidase
Chemicals
Calbindins Cell Adhesion Molecules, Neuronal Extracellular Matrix Proteins Eye Proteins Homeodomain Proteins Nerve Tissue Proteins PAX6 Transcription Factor Paired Box Transcription Factors Pax6 protein, mouse RNA, Messenger Reelin Protein Repressor Proteins S100 Calcium Binding Protein G Tubulin beta3 tubulin, mouse beta-Galactosidase Reln protein, mouse Serine Endopeptidases Bromodeoxyuridine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Swanson Douglas James
Department of Anatomy and Neurobiology, Center of Excellence in Genomics and Bioinformatics, University of Tennessee Health Sciences Center, 515 LINK Building, 855 Monroe Avenue, Memphis, TN 38163, USA. djswanson@utmem.edu
Tong Yiai
Goldowitz Dan
Article Info
Journal
Brain research. Developmental brain research
Abbr.
Brain Res Dev Brain Res
ISSN
0165-3806
Published
2005-12-07
Epub
2005-00-09
Pages
176-93
Language
English
Region
Netherlands
NLM ID
8908639
Subset
IM
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