<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>Strowig, Till</dc:creator>
  <dc:creator>Rongvaux, Anthony</dc:creator>
  <dc:creator>Rathinam, Chozhavendan</dc:creator>
  <dc:creator>Takizawa, Hitoshi</dc:creator>
  <dc:creator>Borsotti, Chiara</dc:creator>
  <dc:creator>Philbrick, William</dc:creator>
  <dc:creator>Eynon, Elizabeth E.</dc:creator>
  <dc:creator>Manz, Markus G.</dc:creator>
  <dc:creator>Flavell, Richard A.</dc:creator>
  <dc:date>2011-07-25</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Transplantation of human hematopoietic stem cells into severely immunocompromised newborn mice allows the  development of a human hematopoietic and immune system in vivo. NOD/scid/γc−/− (NSG) and BALB/c Rag2−/ −γc−/− mice are the most commonly used mouse strains for this purpose and a number of studies have  demonstrated the high value of these model systems in areas spanning from basic to translational research.  However, limited cross-reactivity of many murine cytokines on human cells and residual host immune function  against the xenogeneic grafts results in defective development and maintenance of human cells in vivo. Whereas  NSG mice have higher levels of absolute human engraftment than similar mice on a BALB/c background, they  have a shorter lifespan and NOD ES cells are unsuitable for the complex genetic engineering that is required to  improve human hematopoiesis and immune responses by transgenesis or knockin of human genes. We have  generated mice that faithfully express a transgene of human signal regulatory protein alpha (SIRPa), a receptor  that negatively regulates phagocytosis, in Rag2−/−γc−/− mice on a mixed 129/BALB/c background, which can  easily be genetically engineered. These mice allow significantly increased engraftment and maintenance of human  hematopoietic cells reaching levels comparable to NSG mice. Furthermore, we found improved functionality of the  human immune system in these mice. In summary, hSIRPa-transgenic Rag2−/−γc−/− mice represent a unique  mouse strain supporting high levels of human cell engraftment, which can easily be genetically manipulated.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/318781</dc:identifier>
  <dc:identifier>https://n2t.net/ark:/12658/srd1318781</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/318781/files/strowig_pnas_2011.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1073/pnas.1109769108</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1318781</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Proceedings of the national academy of sciences of the United States of America. - 2011, vol. 108, no. 32, p. 13218-13223</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">CD34+</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">cellxenorejection</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns3="xml" ns3:lang="en">Transgenic expression of human signal regulatory protein alpha in Rag2−/−γc −/− mice improves engraftment of human hematopoietic cells in humanized mice</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
