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Ion Channel Functions in Early Brain Development

期刊

TRENDS IN NEUROSCIENCES
卷 43, 期 2, 页码 103-114

出版社

CELL PRESS
DOI: 10.1016/j.tins.2019.12.004

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资金

  1. National Institute of Neurological Disorders and Stroke (NINDS) [R01 NS35129, R01NS032457]
  2. National Institute of Mental Health (NIMH) [U01MH106883]
  3. Allen Discovery Center program through the Paul G. Allen Frontiers Group
  4. NINDS [F32NS100033801, K99NS112604]

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During prenatal brain development, ion channels are ubiquitous across several cell types, including progenitor cells and migrating neurons but their function has not been clear. In the past, ion channel dysfunction has been primarily studied in the context of postnatal, differentiated neurons that fire action potentials - notably ion channels mutated in the epilepsies - yet data now support a surprising role in prenatal human brain disorders as well. Modem gene discovery approaches have identified defective ion channels in individuals with cerebral cortex malformations, which reflect abnormalities in early-to-middle stages of embryonic development (prior to ubiquitous action potentials). These human genetics studies and recent in utero animal modeling work suggest that precise control of ionic flux (calcium, sodium, and potassium) contributes to in utero developmental processes such as neural proliferation, migration, and differentiation.

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