Journal article
Astrocyte-secreted glypican 4 regulates release of neuronal pentraxin 1 from axons to induce functional synapse formation
- Abstract:
- The generation of precise synaptic connections between developing neurons is critical to the formation of functional neural circuits. Astrocyte-secreted glypican 4 induces formation of active excitatory synapses by recruiting AMPA glutamate receptors to the postsynaptic cell surface. We now identify the molecular mechanism of how glypican 4 exerts its effect. Glypican 4 induces release of the AMPA receptor clustering factor neuronal pentraxin 1 from presynaptic terminals by signaling through presynaptic protein tyrosine phosphatase receptor δ. Pentraxin then accumulates AMPA receptors on the postsynaptic terminal forming functional synapses. Our findings reveal a signaling pathway that regulates synaptic activity during central nervous system development and demonstrates a role for astrocytes as organizers of active synaptic connections by coordinating both pre and post synaptic neurons. As mutations in glypicans are associated with neurological disorders, such as autism and schizophrenia, this signaling cascade offers new avenues to modulate synaptic function in disease.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 8.4MB, Terms of use)
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- Publisher copy:
- 10.1016/j.neuron.2017.09.053
Authors
- Publisher:
- Elsevier
- Journal:
- Neuron More from this journal
- Volume:
- 96
- Issue:
- 2
- Pages:
- 428-445.e13
- Publication date:
- 2017-10-11
- Acceptance date:
- 2017-09-27
- DOI:
- EISSN:
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1097-4199
- ISSN:
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0896-6273
- Pmid:
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29024665
- Language:
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English
- Keywords:
- Pubs id:
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pubs:737202
- UUID:
-
uuid:d763ee05-ba52-46e7-9f5e-e1dcf3a6ae2a
- Local pid:
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pubs:737202
- Source identifiers:
-
737202
- Deposit date:
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2018-12-07
Terms of use
- Copyright holder:
- MRC Laboratory of Molecular Biology
- Copyright date:
- 2017
- Notes:
- © 2017 MRC Laboratory of Molecular Biology. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
- Licence:
- CC Attribution (CC BY)
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