Beyond IgE: Alternative Mast Cell Activation Across Different Disease States
Open Access
- 22 February 2020
- journal article
- review article
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 21 (4), 1498
- https://doi.org/10.3390/ijms21041498
Abstract
Mast cells are often regarded through the lens of IgE-dependent reactions as a cell specialized only for anti-parasitic and type I hypersensitive responses. However, recently many researchers have begun to appreciate the expansive repertoire of stimuli that mast cells can respond to. After the characterization of the interleukin (IL)-33/suppression of tumorigenicity 2 (ST2) axis of mast cell activation—a pathway that is independent of the adaptive immune system—researchers are revisiting other stimuli to induce mast cell activation and/or subsequent degranulation independent of IgE. This discovery also underscores that mast cells act as important mediators in maintaining body wide homeostasis, especially through barrier defense, and can thus be the source of disease as well. Particularly in the gut, inflammatory bowel diseases (Crohn’s disease, ulcerative colitis, etc.) are characterized with enhanced mast cell activity in the context of autoimmune disease. Mast cells show phenotypic differences based on tissue residency, which could manifest as different receptor expression profiles, allowing for unique mast cell responses (both IgE and non-IgE mediated) across varying tissues as well. This variety in receptor expression suggests mast cells respond differently, such as in the gut where immunosuppressive IL-10 stimulates the development of food allergy or in the lungs where transforming growth factor-β1 (TGF-β1) can enhance mast cell IL-6 production. Such differences in receptor expression illustrate the truly diverse effector capabilities of mast cells, and careful consideration must be given toward the phenotype of mast cells observed in vitro. Given mast cells’ ubiquitous tissue presence and their capability to respond to a broad spectrum of non-IgE stimuli, it is expected that mast cells may also contribute to the progression of autoimmune disorders and other disease states such as metastatic cancer through promoting chronic inflammation in the local tissue microenvironment and ultimately polarizing toward a unique Th17 immune response. Furthermore, these interconnected, atypical activation pathways may crosstalk with IgE-mediated signaling differently across disorders such as parasitism, food allergies, and autoimmune disorders of the gut. In this review, we summarize recent research into familiar and novel pathways of mast cells activation and draw connections to clinical human disease.Keywords
This publication has 100 references indexed in Scilit:
- Dietary gluten triggers concomitant activation of CD4 + and CD8 + αβ T cells and γδ T cells in celiac diseaseProceedings of the National Academy of Sciences of the United States of America, 2013
- Activation and regulation of the inflammasomesNature Reviews Immunology, 2013
- Regulatory T Cells Enhance Mast Cell Production of IL-6 via Surface-Bound TGF-βThe Journal of Immunology, 2012
- Host innate recognition of an intestinal bacterial pathogen induces TRIF-dependent protective immunityThe Journal of Experimental Medicine, 2011
- NLRP3 inflammasome plays a key role in the regulation of intestinal homeostasisInflammatory Bowel Diseases, 2011
- Inflammatory Bowel Disease-Associated Interleukin-33 Is Preferentially Expressed in Ulceration-Associated MyofibroblastsThe American Journal of Pathology, 2010
- IL-33 Is Produced by Mast Cells and Regulates IgE-Dependent InflammationPLOS ONE, 2010
- The NLRP3 inflammasome functions as a negative regulator of tumorigenesis during colitis-associated cancerThe Journal of Experimental Medicine, 2010
- Homeostatic Role of Transforming Growth Factor-β in the Oral Cavity and Esophagus of Mice and Its Expression by Mast Cells in These TissuesThe American Journal of Pathology, 2009
- Neuropeptides activate human mast cell degranulation and chemokine productionImmunology, 2008