<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>Mazzotti, Chiara</dc:creator>
  <dc:creator>Gagliostro, Vincenzo</dc:creator>
  <dc:creator>Bosisio, Daniela</dc:creator>
  <dc:creator>Del Prete, Annalisa</dc:creator>
  <dc:creator>Tiberio, Laura</dc:creator>
  <dc:creator>Thelen, Marcus</dc:creator>
  <dc:creator>Sozzani, Silvano</dc:creator>
  <dc:date>2017-10-06</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">C-C chemokine receptor-like 2 (CCRL2) is a non-signaling seven-transmembrane domain (7-TMD)  receptor related to the atypical chemokine receptor (ACKR) family. ACKRs bind chemokines but do not  activate G protein-dependent signaling or cell functions. ACKRs were shown to regulate immune  functions in vivo by their ability to scavenge chemokines from the local environment. This study was  performed to investigate whether CCRL2 shares two of the main characteristics of ACKRs, namely the  ability to internalize and scavenge the ligands. Cell membrane analysis of CCRL2-transfected cells  revealed a weak, constitutive, ligand-independent internalization, and recycling of CCRL2, with a  kinetics that was slower than those observed with ACKR3, a prototypic ACKR, or other chemotactic  signaling receptors [i.e., chemokine-like receptor 1 and C-X-C motif chemokine receptor 2].  Intracellularly, CCRL2 colocalized with early endosome antigen 1-positive and Rab5-positive vesicles  and with recycling compartments mainly characterized by Rab11-positive vesicles. CCRL2-transfected  cells and activated mouse blood endothelial cells, that endogenously express CCRL2, were used to  investigate the scavenging ability of CCRL2. These experiments confirmed the ability of CCRL2 to bind  chemerin, the only recognized ligand, but excluded the ability of CCRL2 to perform scavenging.  Collectively, these results identify unique functional properties for this member of the non-signaling 7- TMD receptor family.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/319167</dc:identifier>
  <dc:identifier>https://localhost:5000/ark:/12658/srd1319167</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/319167/files/Mazzotti_FI_2017.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3389/fimmu.2017.01233</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1319167</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>Frontiers in immunology. - 2017, vol. 8, p. 1233</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Chemokine</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Endocytosis</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">G protein-coupled receptor</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Intracellular trafficking</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Scavenger receptor</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Atypical chemokine receptor</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Chemerin</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns8="xml" ns8:lang="en">The atypical receptor CCRL2 (C-C Chemokine Receptor-Like 2) does not act as a decoy receptor in endothelial cells</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
