<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>Leoni, Cristina</dc:creator>
  <dc:creator>Montagner, Sara</dc:creator>
  <dc:creator>Rinaldi, Andrea</dc:creator>
  <dc:creator>Bertoni, Francesco</dc:creator>
  <dc:creator>Polletti, Sara</dc:creator>
  <dc:creator>Balestrieri, Chiara</dc:creator>
  <dc:creator>Monticelli, Silvia</dc:creator>
  <dc:date>2017-02-06</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">DNA methylation and specifically the DNA methyltransferase enzyme DNMT3A are  involved in the pathogenesis of a variety of hematological diseases and in regulating the  function of immune cells. Although altered DNA methylation patterns and mutations in  DNMT3A correlate with mast cell proliferative disorders in humans, the role of DNA  methylation in mast cell biology is not understood. By using mast cells lacking Dnmt3a,  we found that this enzyme is involved in restraining mast cell responses to acute and  chronic stimuli, both in vitro and in vivo. The exacerbated mast cell responses observed  in the absence of Dnmt3a were recapitulated or enhanced by treatment with the  demethylating agent 5-aza-2′-deoxycytidine as well as by down-modulation of Dnmt1  expression, further supporting the role of DNA methylation in regulating mast cell  activation. Mechanistically, these effects were in part mediated by the dysregulated  expression of the scaffold protein IQGAP2, which is characterized by the ability to  regulate a wide variety of biological processes. Altogether, our data demonstrate that  DNMT3A and DNA methylation are key modulators of mast cell responsiveness to acute  and chronic stimulation.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/318903</dc:identifier>
  <dc:identifier>https://n2t.net/ark:/12658/srd1318903</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/318903/files/Leoni_PNAS_2017.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1073/pnas.1616420114</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1318903</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. - 2017, vol. 114, no. 8, p. E1490-E1499</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">DNA methylation</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Epigenetics</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Inflammation</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Mast cells</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns5="xml" ns5:lang="en">Dnmt3a restrains mast cell inflammatory responses</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_5794</dc:type>
</oai_dc:dc>
