<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>Mayoral, Ramon J.</dc:creator>
  <dc:creator>Deho, Lorenzo</dc:creator>
  <dc:creator>Rusca, Nicole</dc:creator>
  <dc:creator>Bartonicek, Nenad</dc:creator>
  <dc:creator>Saini, Harpreet Kaur</dc:creator>
  <dc:creator>Enright, Anton J.</dc:creator>
  <dc:creator>Monticelli, Silvia</dc:creator>
  <dc:date>2011-10-12</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Mast cells have essential effector and immunoregulatory functions in IgE-associated  allergic disorders and certain innate and adaptive immune responses, but the role of  miRNAs in regulating mast cell functions is almost completely unexplored. To examine  the role of the activation-induced miRNA miR-221 in mouse mast cells, we developed  robust lentiviral systems for miRNA overexpression and depletion. While miR-221  favored mast cell adhesion and migration towards SCF or antigen in trans-well migration  assays, as well as cytokine production and degranulation in response to IgE-antigen  complexes, neither miR-221 overexpression, nor its ablation, interfered with mast cell  differentiation. Transcriptional profiling of miR-221-overexpressing mast cells revealed  modulation of many transcripts, including several associated with the cytoskeleton;  indeed, miR-221 overexpression was associated with reproducible increases in cortical  actin in mast cells, and with altered cellular shape and cell cycle in murine fibroblasts.  Our bioinformatics analysis showed that this effect was likely mediated by the composite  effect of miR-221 on many primary and secondary targets in resting cells. Indeed, miR- 221-induced cellular alterations could not be recapitulated by knockdown of one of the  major targets of miR-221. We propose a model in which miR-221 has two different roles  in mast cells: in resting cells, basal levels of miR-221 contribute to the regulation of the  cell cycle and cytoskeleton, a general mechanism probably common to other miR-221- expressing cell types, such as fibroblasts. Vice versa, upon induction in response to  mast cell stimulation, miR-221 effects are mast cell-specific and activation-dependent,  contributing to the regulation of degranulation, cytokine production and cell adherence.  Our studies provide new insights into the roles of miR-221 in mast cell biology, and  identify novel mechanisms that may contribute to mast cell-related pathological  conditions, such as asthma, allergy and mastocytosis.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://n2t.net/ark:/12658/srd1319041</dc:identifier>
  <dc:identifier>https://susi.usi.ch/global/documents/319041</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/319041/files/mayoral_pone_2011.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0026133</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1319041</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>Plos one. - 2011, vol. 6, no. 10, p. e26133</dc:source>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">MiR-221 influences effector functions and actin cytoskeleton in mast cells</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
