Regulation of eosinophil-active cytokine production from human cord blood-derived mast cells

Guha Krishnaswamy, Kenton Hall, George Youngberg, Fred Hossler, David Johnson, William A. Block, Shau Ku Huang, Jim Kelley, David S. Chi

研究成果: 雜誌貢獻文章同行評審

19 引文 斯高帕斯(Scopus)

摘要

Human mast cells are multifunctional tissue-dwelling cells that play a crucial role in eosinophil-dependent disorders, such as asthma and parasitic diseases, by the secretion of eosinophil-active mediators. Mast cell-derived cytokines, generated in response to cross-linking of the high-affinity IgE receptor, can regulate eosinophil activation, survival, and chemotaxis. In this study, mast cells generated from human cord blood progenitors (stem cells) were studied for eosinophil-active inflammatory cytokine expression. Cord blood-derived mast cells (CBDMC) expressed typical intracellular scroll granules and microvilli-like structures on their cell surfaces, demonstrated the presence of tryptase, and elaborated prostaglandin D2 (PGD2) after cross-linkage of the high-affinity receptor for IgE (FcεRI). CBDMC expressed tumor necrosis factor-α (TNF-α) and the eosinophil-active growth factors, interleukin-5 (IL-5) and granulocyte-macrophage colony-stimulating factor (GM-CSF) after activation. (IL-1β greatly enhanced IgE-dependent production of these cytokines in response to FcεRI cross-linkage, suggesting a role for bystander/phagocytic cells in modulating mast cell function. In contrast, interferon-α (IFN-α) inhibited IL-5 and GM-CSF generation, and the glucocorticoid, dexamethasone (Dex), inhibited production of IL-5 and GM-CSF from CBDMC. A macrophage-mast cell-eosinophil axis may existin vivo that may be susceptible to pharmacologic manipulation.

原文英語
頁(從 - 到)379-388
頁數10
期刊Journal of Interferon and Cytokine Research
22
發行號3
DOIs
出版狀態已發佈 - 一月 1 2002
對外發佈Yes

ASJC Scopus subject areas

  • Immunology
  • Cell Biology
  • Virology

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