Abstract
Mast cells have long been recognized as the critical tissue-based effector cells in IgE-mediated allergic diseases. Ligation of the high-affinity receptor for IgE (FcεRI), constitutively expressed on mast cells, promotes cell activation and immediate release and production of pro-inflammatory mediators. Besides these positive signals, FcεRI aggregation has recently been understood to generate negative intracellular signals capable of limiting mast cell functional responses. This review is aimed at providing a summary of the mechanisms through which FcεRI engagement can generate negative signals and regulate mast-cell function. Similar mechanisms are employed by other receptors expressed by immune cells, such as T cell and B cell receptors, pointing to a general concept in negative immunoreceptor signaling.
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Abbreviations
- BMMC:
-
bone marrow-derived mast cell
- CIN85:
-
Cbl-interacting protein of 85 kDa
- ERK:
-
extracellular signal-regulated kinase
- FcεRI:
-
high-affinity receptor for IgE
- ITAM:
-
immunoreceptor tyrosine-based activation motif
- ITIM:
-
immunoreceptor tyrosine-based inhibitory motif
- LAB:
-
linker for activation of B cell
- LAT:
-
linker for activation of T cell
- MAPK:
-
mitogen-activated protein kinase
- PI3K:
-
phosphatidylinositol 3-kinase
- PLC:
-
phospholipase C
- PTK:
-
protein tyrosine kinase
- PTEN:
-
phosphatase and tensin homologue deleted on chromosome 10
- RTK:
-
tyrosine kinase receptor
- SHIP:
-
SH2 domain-containing inositol-polyphosphate 5-phosphatase
- SHP:
-
SH2 domain-containing protein tyrosine phosphatase
- SLP-76:
-
SH2-containing leukocyte protein of 76 kDa
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Molfetta, R., Peruzzi, G., Santoni, A. et al. Negative signals from FcεRI engagement attenuate mast cell functions. Arch. Immunol. Ther. Exp. 55, 219–229 (2007). https://doi.org/10.1007/s00005-007-0028-4
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DOI: https://doi.org/10.1007/s00005-007-0028-4