| Literature DB >> 32572460 |
Isabel Del Pino1,2, Chiara Tocco3, Elia Magrinelli3,4, Andrea Marcantoni5, Celeste Ferraguto3, Giulia Tomagra5, Michele Bertacchi3, Christian Alfano3, Xavier Leinekugel1, Andreas Frick1, Michèle Studer3.
Abstract
The formation of functional cortical maps in the cerebral cortex results from a timely regulated interaction between intrinsic genetic mechanisms and electrical activity. To understand how transcriptional regulation influences network activity and neuronal excitability within the neocortex, we used mice deficient for Nr2f1 (also known as COUP-TFI), a key determinant of primary somatosensory (S1) area specification during development. We found that the cortical loss of Nr2f1 impacts on spontaneous network activity and synchronization of S1 cortex at perinatal stages. In addition, we observed alterations in the intrinsic excitability and morphological features of layer V pyramidal neurons. Accordingly, we identified distinct voltage-gated ion channels regulated by Nr2f1 that might directly influence intrinsic bioelectrical properties during critical time windows of S1 cortex specification. Altogether, our data suggest a tight link between Nr2f1 and neuronal excitability in the developmental sequence that ultimately sculpts the emergence of cortical network activity within the immature neocortex.Entities:
Keywords: Nr2f1/COUP-TFI; intrinsic excitability; layer V pyramidal neurons; somatosensory cortex; spontaneous activity
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Year: 2020 PMID: 32572460 DOI: 10.1093/cercor/bhaa137
Source DB: PubMed Journal: Cereb Cortex ISSN: 1047-3211 Impact factor: 5.357