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  Role of cell metabolism in the pathophysiology of brain size-associated neurodevelopmental disorders.

Xing, L., Huttner, W., & Namba, T. (2024). Role of cell metabolism in the pathophysiology of brain size-associated neurodevelopmental disorders. Neurobiology of disease, 199: 106607. doi:10.1016/j.nbd.2024.106607.

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Xing, Lei1, Autor           
Huttner, Wieland1, Autor           
Namba, Takashi1, Autor           
Affiliations:
1Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              

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 Zusammenfassung: Cell metabolism is a key regulator of human neocortex development and evolution. Several lines of evidence indicate that alterations in neural stem/progenitor cell (NPC) metabolism lead to abnormal brain development, particularly brain size-associated neurodevelopmental disorders, such as microcephaly. Abnormal NPC metabolism causes impaired cell proliferation and thus insufficient expansion of NPCs for neurogenesis. Therefore, the production of neurons, which is a major determinant of brain size, is decreased and the size of the brain, especially the size of the neocortex, is significantly reduced. This review discusses recent progress understanding NPC metabolism, focusing in particular on glucose metabolism, fatty acid metabolism and amino acid metabolism (e.g., glutaminolysis and serine metabolism). We provide an overview of the contributions of these metabolic pathways to brain development and evolution, as well as to the etiology of neurodevelopmental disorders. Furthermore, we discuss the advantages and disadvantages of various experimental models to study cell metabolism in the developing brain.

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 Datum: 2024-09-01
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
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 Identifikatoren: DOI: 10.1016/j.nbd.2024.106607
Anderer: cbg-8767
PMID: 39029564
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Titel: Neurobiology of disease
  Andere : Neurobiol Dis
Genre der Quelle: Zeitschrift
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Seiten: - Band / Heft: 199 Artikelnummer: 106607 Start- / Endseite: - Identifikator: -