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PDK1 regulates the generation of oligodendrocyte precursor cells at an early stage of mouse telencephalic development
Author(s) -
Watatani Kenji,
Hirabayashi Yusuke,
Itoh Yasuhiro,
Gotoh Yukiko
Publication year - 2012
Publication title -
genes to cells
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.912
H-Index - 115
eISSN - 1365-2443
pISSN - 1356-9597
DOI - 10.1111/j.1365-2443.2012.01591.x
Subject(s) - biology , oligodendrocyte , microbiology and biotechnology , stage (stratigraphy) , neuroscience , myelin , central nervous system , paleontology
During the development of the mouse telencephalon, multipotent neural precursor cells (NPCs) generate oligodendrocyte precursor cells (OPCs), progenitors restricted to the oligodendrocyte lineage, at various sites in a developmental stage‐dependent manner. Although substantial progress has been made in identifying the transcription factors that control the production of OPCs, the signaling pathways that regulate these transcription factors and the spatiotemporal pattern of OPC production have been only partially clarified. Here, we show that the serine–threonine kinase 3‐phosphoinositide‐dependent kinase 1 (PDK1) contributes to an early wave of OPC production in the developing mouse telencephalon. Ablation of PDK1 in NPCs resulted in a reduction in the number of OPCs positive for Sox10 and platelet‐derived growth factor receptor α (PDGFRα) within the neocortex and striatum at embryonic day (E) 15.5, but not at E18.5. Furthermore, pharmacological inhibition of phosphoinositide 3‐kinase (PI3K) or deletion of the PDK1 gene suppressed the generation of OPCs from NPCs induced by fibroblast growth factor (FGF) 2 in culture. These results implicate the PI3K–PDK1 pathway in the physiological regulation of OPC production in a developmental context‐dependent manner.