Novel Markers Reveal Subpopulations of Subplate Neurons in the Murine Cerebral Cortex

被引:110
作者
Hoerder-Suabedissen, Anna
Wang, Wei Zhi
Lee, Sheena
Davies, Kay E. [1 ]
Goffinet, Andre M. [2 ]
Rakic, Sonja [3 ]
Parnavelas, John [3 ]
Reim, Kerstin [4 ,5 ]
Nicolic, Margareta [6 ]
Paulsen, Ole
Molnar, Zoltan [1 ]
机构
[1] Univ Oxford, Dept Physiol Anat & Genet, MRC, Funct Genom Unit, Oxford OX1 3QX, England
[2] Catholic Univ Louvain, Dept Microbiol Immunol & Genet, Dev Neurobiol Unit, B-1348 Louvain, Belgium
[3] UCL, Dept Anat & Dev Biol, London WC1E 6BT, England
[4] Max Planck Inst Expt Med, Dept Mol Neurobiol, D-37075 Gottingen, Germany
[5] Max Planck Inst Expt Med, Ctr Mol Physiol Brain, D-37075 Gottingen, Germany
[6] Univ London Imperial Coll Sci Technol & Med, Sch Med, Dept Cellular & Mol Neurosci, London SW7 2AZ, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
CTGF; DDC; Nurr1; p35-KO; reeler mutant; subplate; EARLIEST GENERATED CELLS; CORTICAL DEVELOPMENT; WHITE-MATTER; POSTNATAL-DEVELOPMENT; PROJECTIONS; AXONS; ESTABLISHMENT; CONNECTIONS; COMPLEXINS; LAMINATION;
D O I
10.1093/cercor/bhn195
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The subplate lays the foundation of the developing cerebral cortex, and abnormalities have been suggested to contribute to various brain developmental disorders. The causal relationship between cellular pathologies and cognitive disorders remains unclear, and therefore, a better understanding of the role of subplate cells in cortical development is essential. Only by determining the molecular taxonomy of this diverse class of neurons can we identify the subpopulations that may contribute differentially to cortical development. We identified novel markers for murine subplate cells by comparing gene expression of subplate and layer 6 of primary visual and somatosensory cortical areas of postnatal day (P)8 old mice using a microarray-based approach. We examined the utility of these markers in well-characterized mutants (reeler, scrambler, and p35-KO) where the subplate is displaced in relation to the cortical plate. In situ hybridization or immunohistochemistry confirmed subplate-selective expression of complexin 3, connective tissue growth factor, nuclear receptor-related 1/Nr4a2, and monooxygenase Dbh-like 1 while transmembrane protein 163 also had additional expression in layer 5, and DOPA decarboxylase was also present in the white matter. Localization of marker-positive cells in the reeler and p35-KO cortices suggests different subpopulations of subplate cells. These new markers open up possibilities for further identification of subplate subpopulations in research and in neuropathological diagnosis.
引用
收藏
页码:1738 / 1750
页数:13
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