<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>Moore, Thomas L.</dc:creator>
  <dc:creator>Hauser, Daniel</dc:creator>
  <dc:creator>Gruber, Thomas</dc:creator>
  <dc:creator>Rothen-Rutishauser, Barbara</dc:creator>
  <dc:creator>Lattuada, Marco</dc:creator>
  <dc:creator>Petri-Fink, Alke</dc:creator>
  <dc:creator>Lyck, Ruth</dc:creator>
  <dc:date>2017-06-07</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">A major hurdle in the development of biomedical nanoparticles (NP) is understanding  how they interact with complex biological systems and navigate biological barriers to  arrive at pathological targets. It is becoming increasingly evident that merely controlling  particle physicochemical properties may not be sufficient to mediate particle  biodistribution in dynamic environments. Thus, researchers are increasingly turning  toward more complex but likewise more physiological in vitro systems to study  particle–-cell/particle–system interactions. An emerging paradigm is to utilize naturally  migratory cells to act as so-called “Trojan horses” or cellular shuttles. We report here  the use of monocytes/macrophages to transport NP across a confluent endothelial cell  layer using a microfluidic in vitro model. With a custom-built flow chamber, we showed  that physiological shear stress, when compared to low flow or static conditions,  increased NP uptake by macrophages. We further provided a mathematical  explanation for the effect of flow on NP uptake, namely that the physical exposure  times of NP to cells is dictated by shear stress (i.e., flow rate) and results in increased  particle uptake under flow. This study was extended to a multicellular, hydrodynamic in  vitro model. Because monocytes are cells that naturally translocate across biological  barriers, we utilized a monocyte/macrophage cell line as cellular NP transporters  across an endothelial layer. In this exploratory study, we showed that  monocyte/macrophage cells adhere to an endothelial layer and dynamically interact  with the endothelial cells. The monocytes/macrophages took up NP and diapedesed  across the endothelial layer with NP accumulating within the cellular uropod. These  data illustrate that monocytes/macrophages may therefore act as active shuttles to  deliver particles across endothelial barriers.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/305497</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/305497/files/lat_csm.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/305497/files/lat_csm_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1021/acsami.7b03479</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>ACS Applied Materials &amp; Interfaces. - 2017, vol. 9, no. 22, p. 18501–18511</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Cellular shuttles: monocytes/macrophages exhibit transendothelial transport of nanoparticles under physiological flow</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
