<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>Volpe, Silvia</dc:creator>
  <dc:creator>Thelen, Sylvia</dc:creator>
  <dc:creator>Pertel. Thomas</dc:creator>
  <dc:creator>Lohse, Martin J.</dc:creator>
  <dc:creator>Thelen, Marcus</dc:creator>
  <dc:date>2010-04-15</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Background: Migration of mammalian cells is a complex cell type and environment specific process. Migrating  hematopoietic cells assume a rapid amoeboid like movement when exposed to gradients of chemoattractants.  The underlying signaling mechanisms remain controversial with respect to localization and distribution of  chemotactic receptors within the plasma membrane and the role of PI 3-kinase activity in cell polarization.  Methodology/Principal Findings: We present a novel model for the investigation of human leukocyte migration.  Monocytic THP-1 cells transfected with the a2A-adrenoceptor (a2AAR) display comparable signal transduction  responses, such as calcium mobilization, MAP-kinase activation and chemotaxis, to the noradrenaline homlogue  UK 14’304 as when stimulated with CCL2, which binds to the endogenous chemokine receptor CCR2. Time-lapse  video microcopy reveals that chemotactic receptors remain evenly distributed over the plasma membrane and  that their internalization is not required for migration. Measurements of intramolecular fluorescence resonance  energy transfer (FRET) of a2AAR-YFP/CFP suggest a uniform activation of the receptors over the entire plasma  membrane. Nevertheless, PI 3-kinse activation is confined to the leading edge. When reverting the gradient of  chemoattractant by moving the dispensing micropipette, polarized monocytes – in contrast to neutrophils – rapidly  flip their polarization axis by developing a new leading edge at the previous posterior side. Flipping of the  polarization axis is accompanied by re-localization of PI-3-kinase activity to the new leading edge. However,  reversal of the polarization axis occurs in the absence of PI 3-kinase activation. Conclusions/Significance:  Accumulation and internalization of chemotactic receptors at the leading edge is dispensable for cell migration.  Furthermore, uniformly distributed receptors allow the cells to rapidly reorient and adapt to changes in the  attractant cue. Polarized monocytes, which display typical amoeboid like motility, can rapidly develop a new  leading edge facing the highest chemoattractant concentration at any site of the plasma membrane, including the  uropod. The process appears to be independent of PI 3-kinase activity.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/318925</dc:identifier>
  <dc:identifier>https://localhost:5000/ark:/12658/srd1318925</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/318925/files/volpe_plosone_2010.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0010159</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1318925</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>Plos one. - 2010, vol. 5, no. 4, p. e10159</dc:source>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Polarization of migrating monocytic cells is independent of PI 3-Kinase activity</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
