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Voltage-Gated Ion Channels Are Transcriptional Targets of Sox10 during Oligodendrocyte Development.
Peters, Christian; Aberle, Tim; Sock, Elisabeth; Brunner, Jessica; Küspert, Melanie; Hillgärtner, Simone; Wüst, Hannah M; Wegner, Michael.
Affiliation
  • Peters C; Institut für Biochemie, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
  • Aberle T; Institut für Biochemie, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
  • Sock E; Institut für Biochemie, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
  • Brunner J; Institut für Biochemie, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
  • Küspert M; Institut für Biochemie, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
  • Hillgärtner S; Institut für Biochemie, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
  • Wüst HM; Institut für Biochemie, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
  • Wegner M; Institut für Biochemie, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
Cells ; 13(13)2024 Jul 07.
Article in En | MEDLINE | ID: mdl-38995010
ABSTRACT
The transcription factor Sox10 is an important determinant of oligodendroglial identity and influences oligodendroglial development and characteristics at various stages. Starting from RNA-seq data, we here show that the expression of several voltage-gated ion channels with known expression and important function in oligodendroglial cells depends upon Sox10. These include the Nav1.1, Cav2.2, Kv1.1, and Kir4.1 channels. For each of the four encoding genes, we found at least one regulatory region that is activated by Sox10 in vitro and at the same time bound by Sox10 in vivo. Cell-specific deletion of Sox10 in oligodendroglial cells furthermore led to a strong downregulation of all four ion channels in a mouse model and thus in vivo. Our study provides a clear functional link between voltage-gated ion channels and the transcriptional regulatory network in oligodendroglial cells. Furthermore, our study argues that Sox10 exerts at least some of its functions in oligodendrocyte progenitor cells, in myelinating oligodendrocytes, or throughout lineage development via these ion channels. By doing so, we present one way in which oligodendroglial development and properties can be linked to neuronal activity to ensure crosstalk between cell types during the development and function of the central nervous system.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oligodendroglia / SOXE Transcription Factors Limits: Animals / Humans Language: En Journal: Cells Year: 2024 Document type: Article Affiliation country: Alemania Country of publication: Suiza

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oligodendroglia / SOXE Transcription Factors Limits: Animals / Humans Language: En Journal: Cells Year: 2024 Document type: Article Affiliation country: Alemania Country of publication: Suiza