<?xml version="1.0" encoding="UTF-8"?>
<OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/"
         xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"
         xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd">
<ListRecords>
<oai_dc:dc xmlns="http://www.openarchives.org/OAI/2.0/oai_dc/"
           xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/"
           xmlns:dc="http://purl.org/dc/elements/1.1/"
           xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"
           xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   	<dc:title>In Vivo regulation of Oligodendrocyte processor cell proliferation and differentiation by the AMPA-receptor Subunit GluA2</dc:title>
   	<dc:creator>Chen, Ting</dc:creator>
   	<dc:creator>Kula, Bartosz</dc:creator>
   	<dc:creator>Nagy, Balint ; https://orcid.org/0000-0002-4002-4686</dc:creator>
   	<dc:creator>Barzan, Ruxandra</dc:creator>
   	<dc:creator>Gall, Andrea</dc:creator>
   	<dc:creator>Ehrlich, Ingrid</dc:creator>
   	<dc:creator>Kukley, Maria</dc:creator>
   	<dc:subject>ddc:570</dc:subject>
   	<dc:description>The functional role of AMPA receptor (AMPAR)-mediated synaptic signaling between neurons and oligodendrocyte precursor cells (OPCs) remains enigmatic. We modified the properties of AMPARs at axon-OPC synapses in the mouse corpus callosum in vivo during the peak of myelination by targeting the GluA2 subunit. Expression of the unedited (Ca2+ permeable) or the pore-dead GluA2 subunit of AMPARs triggered proliferation of OPCs and reduced their differentiation into oligodendrocytes. Expression of the cytoplasmic C-terminal (GluA2(813-862)) of the GluA2 subunit (C-tail), a modification designed to affect the interaction between GluA2 and AMPAR-binding proteins and to perturb trafficking of GluA2-containing AMPARs, decreased the differentiation of OPCs without affecting their proliferation. These findings suggest that ionotropic and non-ionotropic properties of AMPARs in OPCs, as well as specific aspects of AMPAR-mediated signaling at axon-OPC synapses in the mouse corpus callosum, are important for balancing the response of OPCs to proliferation and differentiation cues. In the brain, oligodendrocyte precursor cells (OPCs) receive glutamatergic AMPA-receptor-mediated synaptic input from neurons. Chen et al. show that modifying AMPA-receptor properties at axon-OPC synapses alters proliferation and differentiation of OPCs. This expands the traditional view of synaptic transmission by suggesting neurons also use synapses to modulate behavior of glia.</dc:description>
   	<dc:publisher>Elsevier</dc:publisher>
   	<dc:date>2018</dc:date>
   	<dc:type>info:eu-repo/semantics/article</dc:type>
   	<dc:type>doc-type:Article</dc:type>
   	<dc:type>Article</dc:type>
   	<dc:type>http://purl.org/coar/resource_type/c_2df8fbb1</dc:type>
   	<dc:identifier>https://research-explorer.ista.ac.at/record/32</dc:identifier>
   	<dc:identifier>https://research-explorer.ista.ac.at/download/32/5703</dc:identifier>
   	<dc:source>Chen T, Kula B, Nagy B, et al. In Vivo regulation of Oligodendrocyte processor cell proliferation and differentiation by the AMPA-receptor Subunit GluA2. &lt;i&gt;Cell Reports&lt;/i&gt;. 2018;25(4):852-861.e7. doi:&lt;a href=&quot;https://doi.org/10.1016/j.celrep.2018.09.066&quot;&gt;10.1016/j.celrep.2018.09.066&lt;/a&gt;</dc:source>
   	<dc:language>eng</dc:language>
   	<dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/j.celrep.2018.09.066</dc:relation>
   	<dc:relation>info:eu-repo/semantics/altIdentifier/wos/000448219500005</dc:relation>
   	<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
</oai_dc:dc>
</ListRecords>
</OAI-PMH>
