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Human voltage-gated Na(+) and K(+) channel properties underlie sustained fast AP signaling
Human cortical pyramidal neurons are large, have extensive dendritic trees, and yet have unexpectedly fast input-output properties: Rapid subthreshold synaptic membrane potential changes are reliably encoded in timing of action potentials (APs). Here, we tested whether biophysical properties of volt...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569700/ https://www.ncbi.nlm.nih.gov/pubmed/37824607 http://dx.doi.org/10.1126/sciadv.ade3300 |
Sumario: | Human cortical pyramidal neurons are large, have extensive dendritic trees, and yet have unexpectedly fast input-output properties: Rapid subthreshold synaptic membrane potential changes are reliably encoded in timing of action potentials (APs). Here, we tested whether biophysical properties of voltage-gated sodium (Na(+)) and potassium (K(+)) currents in human pyramidal neurons can explain their fast input-output properties. Human Na(+) and K(+) currents exhibited more depolarized voltage dependence, slower inactivation, and faster recovery from inactivation compared with their mouse counterparts. Computational modeling showed that despite lower Na(+) channel densities in human neurons, the biophysical properties of Na(+) channels resulted in higher channel availability and contributed to fast AP kinetics stability. Last, human Na(+) channel properties also resulted in a larger dynamic range for encoding of subthreshold membrane potential changes. Thus, biophysical adaptations of voltage-gated Na(+) and K(+) channels enable fast input-output properties of large human pyramidal neurons. |
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