Scn1a-GFP transgenic mouse revealed Nav1.1 expression in neocortical pyramidal tract projection neurons

Author:

Yamagata Tetsushi12,Ogiwara Ikuo23ORCID,Tatsukawa Tetsuya2,Suzuki Toshimitsu12,Otsuka Yuka1,Imaeda Nao1,Mazaki Emi2,Inoue Ikuyo2,Tokonami Natsuko2,Hibi Yurina1,Itohara Shigeyoshi4,Yamakawa Kazuhiro12ORCID

Affiliation:

1. Department of Neurodevelopmental Disorder Genetics, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences

2. Laboratory for Neurogenetics, RIKEN Center for Brain Science

3. Department of Physiology, Nippon Medical School

4. Laboratory for Behavioral Genetics, RIKEN Center for Brain Science

Abstract

Expressions of voltage-gated sodium channels Nav1.1 and Nav1.2, encoded by SCN1A and SCN2A genes, respectively, have been reported to be mutually exclusive in most brain regions. In juvenile and adult neocortex, Nav1.1 is predominantly expressed in inhibitory neurons while Nav1.2 is in excitatory neurons. Although a distinct subpopulation of layer V (L5) neocortical excitatory neurons were also reported to express Nav1.1, their nature has been uncharacterized. In hippocampus, Nav1.1 has been proposed to be expressed only in inhibitory neurons. By using newly generated transgenic mouse lines expressing Scn1a promoter-driven green fluorescent protein (GFP), here we confirm the mutually exclusive expressions of Nav1.1 and Nav1.2 and the absence of Nav1.1 in hippocampal excitatory neurons. We also show that Nav1.1 is expressed in inhibitory and a subpopulation of excitatory neurons not only in L5 but all layers of neocortex. By using neocortical excitatory projection neuron markers including FEZF2 for L5 pyramidal tract (PT) and TBR1 for layer VI (L6) cortico-thalamic (CT) projection neurons, we further show that most L5 PT neurons and a minor subpopulation of layer II/III (L2/3) cortico-cortical (CC) neurons express Nav1.1 while the majority of L6 CT, L5/6 cortico-striatal (CS), and L2/3 CC neurons express Nav1.2. These observations now contribute to the elucidation of pathological neural circuits for diseases such as epilepsies and neurodevelopmental disorders caused by SCN1A and SCN2A mutations.

Funder

Japan Society for the Promotion of Science

RIKEN Center for Brain Science

Japan Agency for Medical Research and Development

Ministry of Education, Culture, Sports, Science and Technology

Takeda Science Foundation

Kiyokun Foundation

Japan Epilepsy Research Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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