<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>Araki M</dc:creator>
  <dc:creator>Araki K</dc:creator>
  <dc:creator>Miyazaki Y</dc:creator>
  <dc:creator>Iwamoto M</dc:creator>
  <dc:creator>Izui S</dc:creator>
  <dc:creator>Yamamura K</dc:creator>
  <dc:creator>Vassalli P</dc:creator>
  <dc:date>1996</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">E-selectin is a membrane protein expressed by endothelial cells activated by cytokines released during the inflammatory process; it plays an important role in neutrophil emigration into inflamed tissues. To further explore in vivo the function of E-selectin, we have generated transgenic mouse line expressing E-selectin under the control of a chicken beta-actin promoter. In these mice, the number of blood neutrophils was reduced, without any other obvious phenotype or tissue damage. These neutrophils, however, displayed two significant changes: first, an alteration in the levels of expression of two membrane receptors involved in neutrophil adhesion to endothelial cells, namely a marked increased in the Mac-1 antigen (CD11b/CD18) and a decrease in the Mel-14 antigen (L-selectin); second, an increased oxidative activity when compared to blood neutrophils of non-transgenic mice, as shown by their capacity to oxidize 2',7'-dichlorofluorescein (DCFH) into a fluorescent compound. These observations indicate that the binding of E-selection with neutrophils bearing its ligands promotes neutrophil activation in vivo.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/152405</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1006/bbrc.1996.1107</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/8713130</dc:relation>
  <dc:source>Biochemical and biophysical research communications. - 1996</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Actins</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Animals</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Base Sequence</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Bone Marrow</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Bone Marrow Cells</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">E-Selectin</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Fluorescence</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Liver</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Lymphocyte Activation</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Mice</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Mice, Transgenic</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Molecular Sequence Data</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Muscles</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Myocardium</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Neutrophil Activation</dc:subject>
  <dc:subject xmlns:ns16="xml" ns16:lang="en">Neutrophils</dc:subject>
  <dc:subject xmlns:ns17="xml" ns17:lang="en">Promoter Regions, Genetic</dc:subject>
  <dc:subject xmlns:ns18="xml" ns18:lang="en">Protein Binding</dc:subject>
  <dc:subject xmlns:ns19="xml" ns19:lang="en">RNA, Messenger</dc:subject>
  <dc:title xmlns:ns20="xml" ns20:lang="en">E-selectin binding promotes neutrophil activation in vivo in E-selectin transgenic mice.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
