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Journal Article

γ-Protocadherins Are Targeted to Subsets of Synapses and Intracellular Organelles in Neurons

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Frank,  Marcus
Department of Molecular Embryology, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

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Citation

Phillips, G. R., Tanaka, H., Frank, M., Elste, A., Fidler, L., Benson, D. L., et al. (2003). γ-Protocadherins Are Targeted to Subsets of Synapses and Intracellular Organelles in Neurons. Journal of Neuroscience, 23(12), 5096-5104.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002B-951F-8
Abstract
The clustered protocadherins (Pcdhs) comprise >50 putative synaptic recognition molecules that are related to classical cadherins and highly expressed in the nervous system. Pcdhs are organized into three gene clusters (α, β and γ). Within the α and γ clusters, three exons encode the cytoplasmic domain for each Pcdh, making these domains identical within a cluster. Using an antibody to the Pcdh-γ constant cytoplasmic domain, we find that all interneurons in cultured hippocampal neurons express high levels of Pcdh-γs in a nonsynaptic distribution. In contrast, only 48% of pyramidal-like cells expressed appreciable levels of these molecules. In these cells, Pcdh-γs were associated with a subset of excitatory synapses in which they may mediate presynaptic to postsynaptic recognition in concert with classical cadherins. Immunogold localization in hippocampal tissue showed Pcdh-γs at some synapses, in nonsynaptic plasma membranes, and in axonal and dendritic tubulovesicular structures, indicating that they may be exchanged among synapses and intracellular compartments. Our results show that although Pcdh-γs can be synaptic molecules, synapses form lacking Pcdh-γs. Thus, Pcdh-γs and their relatives may be late additions to the classical cadherin-based synaptic adhesive scaffold; their presence in intracellular compartments suggests a role in modifying synaptic physiology or stability.