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Progenitor Hyperpolarization Regulates the Sequential Generation of Neuronal Subtypes in the Developing Neocortex
Author(s) -
Ilaria Vitali,
Sabine Fièvre,
Ludovic Telley,
Polina Oberst,
Sebastiano Bariselli,
Laura Frangeul,
Natalia Baumann,
John J. McMahon,
Esther Klingler,
Riccardo Bocchi,
Jozsef Z. Kiss,
Camilla Bellone,
Debra L. Silver,
Denis Jabaudon
Publication year - 2018
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2018.06.036
Subject(s) - corticogenesis , biology , progenitor cell , neocortex , hyperpolarization (physics) , progenitor , neuroscience , wnt signaling pathway , neural stem cell , microbiology and biotechnology , ganglionic eminence , stem cell , signal transduction , chemistry , nuclear magnetic resonance spectroscopy , organic chemistry
During corticogenesis, ventricular zone progenitors sequentially generate distinct subtypes of neurons, accounting for the diversity of neocortical cells and the circuits they form. While activity-dependent processes are critical for the differentiation and circuit assembly of postmitotic neurons, how bioelectrical processes affect nonexcitable cells, such as progenitors, remains largely unknown. Here, we reveal that, in the developing mouse neocortex, ventricular zone progenitors become more hyperpolarized as they generate successive subtypes of neurons. Experimental in vivo hyperpolarization shifted the transcriptional programs and division modes of these progenitors to a later developmental status, with precocious generation of intermediate progenitors and a forward shift in the laminar, molecular, morphological, and circuit features of their neuronal progeny. These effects occurred through inhibition of the Wnt-beta-catenin signaling pathway by hyperpolarization. Thus, during corticogenesis, bioelectric membrane properties are permissive for specific molecular pathways to coordinate the temporal progression of progenitor developmental programs and thus neocortical neuron diversity.

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