TrkB (tropomyosin-related kinase B) controls the assembly and maintenance of GABAergic synapses in the cerebellar cortex

• Published in: The Journal of neuroscience Vol. 31; no. 8; pp. 2769 - 2780
• Main Authors: Chen, Albert I, Nguyen, Cindy N, Copenhagen, David R, Badurek, Sylvia, Minichiello, Liliana, Ranscht, Barbara, Reichardt, Louis F
• Format: Journal Article
• Language: English
• Published: United States Society for Neuroscience 23.02.2011
• Subjects: Animals; Cell Adhesion - genetics; Cell Adhesion - physiology; Cell Differentiation - genetics; Cell Differentiation - physiology; Cerebellar Cortex - enzymology; Cerebellar Cortex - growth & development; gamma-Aminobutyric Acid - physiology; Interneurons - cytology; Interneurons - enzymology; Mice; Mice, Knockout; Mice, Transgenic; Receptor, trkB - physiology; Synapses - enzymology; Synapses - genetics; Synapses - physiology; Synaptic Transmission - genetics; Tropomyosin - physiology
• DOI: 10.1523/JNEUROSCI.4991-10.2011
• ISSN: 0270-6474

Inhibitory interneurons play a critical role in coordinating the activity of neural circuits. To explore the mechanisms that direct the organization of inhibitory circuits, we analyzed the involvement of tropomyosin-related kinase B (TrkB) in the assembly and maintenance of GABAergic inhibitory synapses between Golgi and granule cells in the mouse cerebellar cortex. We show that TrkB acts directly within each cell-type to regulate synaptic differentiation. TrkB is required not only for assembly, but also maintenance of these synapses and acts, primarily, by regulating the localization of synaptic constituents. Postsynaptically, TrkB controls the localization of a scaffolding protein, gephyrin, but acts at a step subsequent to the localization of a cell adhesion molecule, Neuroligin-2. Importantly, TrkB is required for the localization of an Ig superfamily cell adhesion molecule, Contactin-1, in Golgi and granule cells and the absence of Contactin-1 also results in deficits in inhibitory synaptic development. Thus, our findings demonstrate that TrkB controls the assembly and maintenance of GABAergic synapses and suggest that TrkB functions, in part, through promoting synaptic adhesion.