IL-15 induces mast cell migration via a pertussis toxin-sensitive receptor
Autor: | H. Patrick McNeil, Michael Grimm, Hong Wei Wang, Nicodemus Tedla, Hunt Je, Nicole E. Jackson, T Hampartzoumian, Carolyn L. Geczy, Andrew M. Collins |
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Rok vydání: | 2005 |
Předmět: |
medicine.medical_treatment
Immunology Biology Pertussis toxin Antibodies Cell Degranulation Mice Immune system Cell Movement medicine Animals Humans Immunology and Allergy Mast Cells Interleukin 5 Cells Cultured Interleukin-15 Mice Inbred BALB C Degranulation Mast cell Cell biology Interleukin 33 Cytokine medicine.anatomical_structure Pertussis Toxin Interleukin 15 Female |
Zdroj: | European Journal of Immunology. 35:2376-2385 |
ISSN: | 1521-4141 0014-2980 |
Popis: | IL-15 induces proliferation, inhibits apoptosis and increases IL-4 production in murine mast cells. There is evidence that these activities are mediated via the uncharacterised receptor, IL-15R-X, rather than the classical three-chain IL-15 receptor. Effects of IL-15 on important aspects of mast cell biology, such as migration and degranulation, are unknown. We report that IL-15 induces migration of murine and human mast cells in a dose-dependent and biphasic manner, with peaks of migration occurring at approximately 10(-15) and approximately 10(-9) M. The potency of the response was similar to that induced by other well-established mast cell chemoattractants. Competition assays performed with murine and human mast cells indicate that both peaks of migration are due to chemotaxis. Pre-treatment of cells with pertussis toxin (PTX), a guanine nucleotide-binding regulatory protein (G-protein) inhibitor, resulted in complete inhibition of murine mast cell migration at approximately 10(-15) M IL-15, and human mast cell migration at approximately 10(-15) and approximately 10(-9) M. This demonstrates that murine and human mast cells express a PTX-sensitive receptor, activated in response to IL-15. Additionally, IL-15 did not induce degranulation in murine mast cells. Locally-produced IL-15 may contribute to mast cell recruitment during inflammatory responses, thereby acting as a linking cytokine between innate and adaptive arms of the immune system. |
Databáze: | OpenAIRE |
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