Neurexins in serotonergic neurons regulate neuronal survival, serotonin transmission, and complex mouse behaviors

Author:

Cheung Amy123ORCID,Konno Kotaro4,Imamura Yuka5,Matsui Aya6,Abe Manabu7,Sakimura Kenji7ORCID,Sasaoka Toshikuni8ORCID,Uemura Takeshi910,Watanabe Masahiko4ORCID,Futai Kensuke12ORCID

Affiliation:

1. Department of Neurobiology, University of Massachusetts Chan Medical School

2. Brudnick Neuropsychiatric Research Institute, University of Massachusetts

3. Medical Scientist Training Program, University of Massachusetts

4. Department of Anatomy, Faculty of Medicine, Hokkaido University

5. Departments of Pharmacology and Biochemistry & Molecular Biology, Institute for Personalized Medicine, Pennsylvania State University College of Medicine, 500 University Drive

6. Vollum Institute, Oregon Health & Science University

7. Department of Animal Model Development, Brain Research Institute, Niigata University

8. Department of Comparative and Experimental Medicine, Brain Research Institute, Niigata University

9. Division of Gene Research, Research Center for Advanced Science, Shinshu University

10. Institute for Biomedical Sciences, Interdisciplinary Cluster for Cutting Edge Research, Shinshu University

Abstract

Extensive serotonin (5-hydroxytryptamine, 5-HT) innervation throughout the brain corroborates 5-HT’s modulatory role in numerous cognitive activities. Volume transmission is the major mode for 5-HT transmission but mechanisms underlying 5-HT signaling are still largely unknown. Abnormal brain 5-HT levels and function have been implicated in autism spectrum disorder (ASD). Neurexin (Nrxn) genes encode presynaptic cell adhesion molecules important for the regulation of synaptic neurotransmitter release, notably glutamatergic and GABAergic transmission. Mutations in Nrxn genes are associated with neurodevelopmental disorders including ASD. However, the role of Nrxn genes in the 5-HT system is poorly understood. Here, we generated a mouse model with all three Nrxn genes disrupted specifically in 5-HT neurons to study how Nrxns affect 5-HT transmission. Loss of Nrxns in 5-HT neurons reduced the number of serotonin neurons in the early postnatal stage, impaired 5-HT release, and decreased 5-HT release sites and serotonin transporter expression. Furthermore, 5-HT neuron-specific Nrxn knockout reduced sociability and increased depressive-like behavior. Our results highlight functional roles for Nrxns in 5-HT neurotransmission, 5-HT neuron survival, and the execution of complex behaviors.

Funder

National Institutes of Health

Publisher

eLife Sciences Publications, Ltd

Subject

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

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