<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" 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:creator>Vaquié, Adrien</dc:creator>
  <dc:creator>Sauvain, Alizée</dc:creator>
  <dc:creator>Duman, Mert</dc:creator>
  <dc:creator>Nocera, Gianluigi</dc:creator>
  <dc:creator>Egger, Boris</dc:creator>
  <dc:creator>Meyenhofer, Felix</dc:creator>
  <dc:creator>Falquet, Laurent</dc:creator>
  <dc:creator>Bartesaghi, Luca</dc:creator>
  <dc:creator>Chrast, Roman</dc:creator>
  <dc:creator>Lamy, Christophe M.</dc:creator>
  <dc:creator>Bang, Seokyoung</dc:creator>
  <dc:creator>Lee, Seung-Ryeol</dc:creator>
  <dc:creator>Jeon, Noo Li</dc:creator>
  <dc:creator>Ruff, Sophie</dc:creator>
  <dc:creator>Jacob, Claire</dc:creator>
  <dc:date>2019-06-11</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">After a peripheral nerve lesion, distal ends of injured axons disintegrate into small  fragments that are subsequently cleared by Schwann cells and later by macrophages.  Axonal debris clearing is an early step of the repair process that facilitates  regeneration. We show here that Schwann cells promote distal cut axon disintegration  for timely clearing. By combining cell-based and in vivo models of nerve lesion with  mouse genetics, we show that this mechanism is induced by distal cut axons, which  signal to Schwann cells through PlGF mediating the activation and upregulation of  VEGFR1 in Schwann cells. In turn, VEGFR1 activates Pak1, leading to the formation  of constricting actomyosin spheres along unfragmented distal cut axons to mediate  their disintegration. Interestingly, oligodendrocytes can acquire a similar behavior as  Schwann cells by enforced expression of VEGFR1. These results thus identify  controllable molecular cues of a neuron-glia crosstalk essential for timely clearing of  damaged axons.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/307916</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307916/files/jac_iai.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307916/files/jac_iai_sm.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307916/files/taba.txt</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307916/files/tabb.txt</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307916/files/tabc.txt</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/j.celrep.2019.05.060</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Cell Reports. - 2019, vol. 27, no. 11, p. 3152-3166.e7</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Injured axons instruct schwann cells to build constricting actin spheres to accelerate axonal disintegration</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
