Semaphorin 3F Is Critical for Development of Limbic System Circuitry and Is Required in Neurons for Selective CNS Axon Guidance Events

• Published in: The Journal of neuroscience Vol. 23; no. 17; pp. 6671 - 6680
• Main Authors: Sahay, Amar, Molliver, Mark E, Ginty, David D, Kolodkin, Alex L
• Format: Journal Article
• Language: English
• Published: United States Soc Neuroscience 30.07.2003; Society for Neuroscience
• Subjects: Amygdala - metabolism; Animals; Axons - physiology; Cell Adhesion Molecules - metabolism; Central Nervous System - embryology; Central Nervous System - metabolism; Cranial Nerves - embryology; Cranial Nerves - metabolism; Development/Plasticity/Repair; Gene Targeting; Hippocampus - embryology; Hippocampus - metabolism; Ligands; Limbic System - embryology; Limbic System - metabolism; Membrane Proteins - deficiency; Membrane Proteins - genetics; Membrane Proteins - physiology; Mesencephalon - embryology; Mesencephalon - metabolism; Mice; Mice, Knockout; Mice, Mutant Strains; Nerve Net - embryology; Nerve Net - metabolism; Nerve Tissue Proteins - deficiency; Nerve Tissue Proteins - genetics; Nerve Tissue Proteins - metabolism; Nerve Tissue Proteins - physiology; Neurons - metabolism; Neuropilin-2 - deficiency; Neuropilin-2 - genetics; Neuropilin-2 - metabolism; Prosencephalon - embryology; Prosencephalon - metabolism; Synapsins - metabolism
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/jneurosci.23-17-06671.2003

Little is known about the role of class 3 semaphorins in the development of CNS circuitry. Several class 3 semaphorins, including semaphorin 3F (Sema3F) bind to the receptor neuropilin-2 to confer chemorepulsive responses in vitro. To understand the role of Sema3F in the establishment of neural circuitry in vivo, we have generated sema3F null and sema3F conditional mutant mice. Inspection of the peripheral nervous system in sema3F null mice reveals that Sema3F is essential for the proper organization of specific cranial nerve projections. Analysis of the CNS in sema3F null mice reveals a crucial role for Sema3F in the rostral forebrain, midbrain, and hippocampus in establishing specific Npn-2 (neuropilin-2)-expressing limbic tracts. Furthermore, we identify Sema3F and Npn-2 as the first guidance cue-receptor pair shown to be essential for controlling the development of amygdaloid circuitry. In addition, we provide genetic evidence in vertebrates for a neuronal requirement of a soluble axon guidance cue in CNS axon guidance. Our data reveal a requirement for neuronal Sema3F in the normal development of the anterior commissure in the ventral forebrain and infrapyramidal tract in the hippocampus. Thus, our results show that Sema3F is the principal ligand for Npn-2-mediated axon guidance events in vivo and is a critical determinant of limbic and peripheral nervous system circuitry.