Stem cell factor programs the mast cell activation phenotype.

نویسندگان

  • Tomonobu Ito
  • Daniel Smrž
  • Mi-Yeon Jung
  • Geethani Bandara
  • Avanti Desai
  • Šárka Smržová
  • Hye Sun Kuehn
  • Michael A Beaven
  • Dean D Metcalfe
  • Alasdair M Gilfillan
چکیده

Mast cells, activated by Ag via FcεRI, release an array of proinflammatory mediators that contribute to allergic disorders, such as asthma and anaphylaxis. The KIT ligand, stem cell factor (SCF), is critical for mast cell expansion, differentiation, and survival, and under acute conditions, it enhances mast cell activation. However, extended SCF exposure in vivo conversely protects against fatal Ag-mediated anaphylaxis. In investigating this dichotomy, we identified a novel mode of regulation of the mast cell activation phenotype through SCF-mediated programming. We found that mouse bone marrow-derived mast cells chronically exposed to SCF displayed a marked attenuation of FcεRI-mediated degranulation and cytokine production. The hyporesponsive phenotype was not a consequence of altered signals regulating calcium flux or protein kinase C, but of ineffective cytoskeletal reorganization with evidence implicating a downregulation of expression of the Src kinase Hck. Collectively, these findings demonstrate a major role for SCF in the homeostatic control of mast cell activation with potential relevance to mast cell-driven disease and the development of novel approaches for the treatment of allergic disorders.

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عنوان ژورنال:
  • Journal of immunology

دوره 188 11  شماره 

صفحات  -

تاریخ انتشار 2012