<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>Rusca, Nicole</dc:creator>
  <dc:creator>Dehò, Lorenzo</dc:creator>
  <dc:creator>Montagner, Sara</dc:creator>
  <dc:creator>Zielinski, Christina E.</dc:creator>
  <dc:creator>Sica, Antonio</dc:creator>
  <dc:creator>Sallusto, Federica</dc:creator>
  <dc:creator>Monticelli, Silvia</dc:creator>
  <dc:date>2012-10-12</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The transcription factor NF-κB regulates the expression of a broad number of genes central to  immune and inflammatory responses. We identified a new molecular network that comprises  specifically the NF-κB family member NF-κB1 (p50) and miR-146a, and we show that in mast  cells it contributes to the regulation of cell homeostasis and survival, while in T lymphocytes it  modulates T cell memory formation. Increased mast cell survival was due to unbalanced  expression of pro- and antiapoptotic factors and particularly to the complete inability of p50- deleted mast cells to induce expression of miR-146a, which in the context of mast cell survival  acted as a proapoptotic factor. Interestingly, in a different cellular context, namely, human and  mouse primary T lymphocytes, miR-146a and NF-κB p50 did not influence cell survival or  cytokine production but rather T cell expansion and activation in response to T cell receptor  (TCR) engagement. Our data identify a new molecular network important in modulating  adaptive and innate immune responses and show how the same activation-induced microRNA  (miRNA) can be similarly regulated in different cell types even in response to different stimuli  but can still determine very different outcomes, likely depending on the specific transcriptome.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://n2t.net/ark:/12658/srd1318847</dc:identifier>
  <dc:identifier>https://susi.usi.ch/global/documents/318847</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/318847/files/Rusca_MCB_2012.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1128/MCB.00824-12</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1318847</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Molecular and cellular biology. - 2012, vol. 32, no. 21, p. 4432-4444</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">MicroRNA</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">T lymphocytes</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Mast cells</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Immunological memory</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Activation survival</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">miR-146a and NF-κB1 regulate mast cell survival and T lymphocyte differentiation</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
