Mast cell histamine promotes the immunoregulatory activity of myeloid-derived suppressor cells
Autor: | Hannah B. Zellner, Rebecca K. Martin, Harry D. Bear, Sheela R. Damle, Lauren Folgosa, John J. Ryan, Sheinei J. Saleem, Giang-Kim T. Nguyen, Daniel H. Conrad, Anne-Marie Irani |
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Rok vydání: | 2014 |
Předmět: |
Cell Survival
Immunology Histamine Antagonists Translational & Clinical Immunology Biology behavioral disciplines and activities Mice chemistry.chemical_compound Th2 Cells Mediator Immune system medicine Animals Immunology and Allergy Mast Cells Receptor ARG1 Cell Proliferation Interleukin-13 Cell Biology Mast cell humanities Mice Mutant Strains medicine.anatomical_structure chemistry Tumor progression Myeloid-derived Suppressor Cell Receptors Histamine Interleukin-4 Histamine |
Zdroj: | Journal of Leukocyte Biology. 96:151-159 |
ISSN: | 1938-3673 0741-5400 |
DOI: | 10.1189/jlb.5a1213-644r |
Popis: | It has been shown recently that MCs are required for differential regulation of the immune response by granulocytic versus monocytic MDSCs. Granulocytic MDSCs promoted parasite clearance, whereas monocytic MDSCs enhanced tumor progression; both activities were abrogated in MC-deficient mice. Herein, we demonstrate that the lack of MCs also influences MDSC trafficking. Preferential trafficking to the liver was not seen in MC-deficient mice. In addition, evidence that the MC mediator histamine was important in MDSC trafficking and activation is also shown. MDSCs express HR1–3. Blockade of these receptors by HR1 or HR2 antagonists reversed the histamine enhancement of MDSC survival and proliferation observed in cell culture. In addition, histamine differentially influenced Arg1 and iNOS gene expression in MDSCs and greatly enhanced IL-4 and IL-13 message, especially in granulocytic MDSCs. Evidence that histamine influenced activity seen in vitro translated to in vivo when HR1 and HR2 antagonists blocked the effect of MDSCs on parasite expulsion and tumor metastasis. All of these data support the MDSC-mediated promotion of Th2 immunity, leading to the suggestion that allergic-prone individuals would have elevated MDSC levels. This was directly demonstrated by looking at the relative MDSC levels in allergic versus control patients. Monocytic MDSCs trended higher, whereas granulocytic MDSCs were increased significantly in allergic patients. Taken together, our studies indicate that MCs and MC-released histamine are critical for MDSC-mediated immune regulation, and this interaction should be taken into consideration for therapeutic interventions that target MDSCs. |
Databáze: | OpenAIRE |
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