Prolonged glial expression of Sox4 in the CNS leads to architectural cerebellar defects and ataxia.

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Prolonged glial expression of Sox4 in the CNS leads to architectural cerebellar defects and ataxia. / Hoser, Melanie; Baader, Stephan L; Bösl, Maria; Ihmer, Alice; Wegner, Michael; Sock, Elisabeth.

in: J NEUROSCI, Jahrgang 27, Nr. 20, 20, 2007, S. 5495-5505.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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Hoser M, Baader SL, Bösl M, Ihmer A, Wegner M, Sock E. Prolonged glial expression of Sox4 in the CNS leads to architectural cerebellar defects and ataxia. J NEUROSCI. 2007;27(20):5495-5505. 20.

Bibtex

@article{e57019d7b29c4898baf6f98eb5ce2084,
title = "Prolonged glial expression of Sox4 in the CNS leads to architectural cerebellar defects and ataxia.",
abstract = "Sox proteins of group C are strongly expressed in the developing nervous system and have been associated with maturation of neurons and glia. Here, we overexpressed the group C protein Sox4 in transgenic mice under the control of the human GFAP promoter. Transgene expression was detected in radial glia and astrocytes throughout the CNS. The transgenic mice were ataxic and exhibited hydrocephaly as well as cerebellar malformations. In the cerebellum, fissures were not formed and neuronal layering was dramatically disturbed. Nevertheless, all neuronal cell types of the cerebellum were present as well as cells with characteristics of early radial glia, astrocytes, and oligodendrocytes. However, radial glia failed to migrate into the position normally taken by Bergmann glia and did not extend radial fibers toward the pial surface. The cerebellar malformations can therefore be explained by the absence of functional Bergmann glia. We conclude that Sox4 expression counteracts differentiation of radial glia and has to be downregulated before full maturation can occur.",
author = "Melanie Hoser and Baader, {Stephan L} and Maria B{\"o}sl and Alice Ihmer and Michael Wegner and Elisabeth Sock",
year = "2007",
language = "Deutsch",
volume = "27",
pages = "5495--5505",
journal = "J NEUROSCI",
issn = "0270-6474",
publisher = "Society for Neuroscience",
number = "20",

}

RIS

TY - JOUR

T1 - Prolonged glial expression of Sox4 in the CNS leads to architectural cerebellar defects and ataxia.

AU - Hoser, Melanie

AU - Baader, Stephan L

AU - Bösl, Maria

AU - Ihmer, Alice

AU - Wegner, Michael

AU - Sock, Elisabeth

PY - 2007

Y1 - 2007

N2 - Sox proteins of group C are strongly expressed in the developing nervous system and have been associated with maturation of neurons and glia. Here, we overexpressed the group C protein Sox4 in transgenic mice under the control of the human GFAP promoter. Transgene expression was detected in radial glia and astrocytes throughout the CNS. The transgenic mice were ataxic and exhibited hydrocephaly as well as cerebellar malformations. In the cerebellum, fissures were not formed and neuronal layering was dramatically disturbed. Nevertheless, all neuronal cell types of the cerebellum were present as well as cells with characteristics of early radial glia, astrocytes, and oligodendrocytes. However, radial glia failed to migrate into the position normally taken by Bergmann glia and did not extend radial fibers toward the pial surface. The cerebellar malformations can therefore be explained by the absence of functional Bergmann glia. We conclude that Sox4 expression counteracts differentiation of radial glia and has to be downregulated before full maturation can occur.

AB - Sox proteins of group C are strongly expressed in the developing nervous system and have been associated with maturation of neurons and glia. Here, we overexpressed the group C protein Sox4 in transgenic mice under the control of the human GFAP promoter. Transgene expression was detected in radial glia and astrocytes throughout the CNS. The transgenic mice were ataxic and exhibited hydrocephaly as well as cerebellar malformations. In the cerebellum, fissures were not formed and neuronal layering was dramatically disturbed. Nevertheless, all neuronal cell types of the cerebellum were present as well as cells with characteristics of early radial glia, astrocytes, and oligodendrocytes. However, radial glia failed to migrate into the position normally taken by Bergmann glia and did not extend radial fibers toward the pial surface. The cerebellar malformations can therefore be explained by the absence of functional Bergmann glia. We conclude that Sox4 expression counteracts differentiation of radial glia and has to be downregulated before full maturation can occur.

M3 - SCORING: Zeitschriftenaufsatz

VL - 27

SP - 5495

EP - 5505

JO - J NEUROSCI

JF - J NEUROSCI

SN - 0270-6474

IS - 20

M1 - 20

ER -