<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>Monticelli, Silvia</dc:creator>
  <dc:creator>Leoni, Cristina</dc:creator>
  <dc:date>2017-11-29</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Mast cells are tissue-resident, innate immune cells present in most tissues of the body  and are important effector and immunomodulatory cells. Differentiated mast cells typically  are characterized by the surface expression of the receptors KIT and FcεRI, the latter  especially being important for stimulation through IgE antibodies, although these cells  have the ability to respond to a wide variety of environmental signals, to which they can  variably react by releasing pre-stored or de novo–synthesized mediators or both. Since  mast cells terminate their differentiation in their tissue of residence in response to specific  microenvironmental cues, each tissue may comprise unique mast cell subtypes, and  responses are tailored to the danger signals that are likely to be encountered in each  anatomical location. From a transcriptional point of view, these cells therefore must be  endowed with epigenetic and transcriptional programs that allow them to maintain a stable  identity and at the same time allow sufficient plasticity to adapt to different environmental  challenges. In this commentary, we highlight some of the recent findings that advanced  our understanding of the transcriptional and epigenetic programs regulating mast cell  functions.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/318993</dc:identifier>
  <dc:identifier>https://localhost:5000/ark:/12658/srd1318993</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/318993/files/Monticelli_F1000R_2017.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.12688/f1000research.12384.1</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1318993</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>F1000 research. - 2017, vol. 6, p. 2064</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Mast cell response</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Transcription factors</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Epigenetic control</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns4="xml" ns4:lang="en">Epigenetic and transcriptional control of mast cell responses</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
