Human mast cell line-1 (HMC-1) cells transfected with FcɛRIα are sensitive to IgE/antigen-mediated stimulation demonstrating selectivity towards cytokine production
Xia, YuXiu C., Sun, ShanShan, Kuek, Li Eon, Lopata, Andreas L., Hulett, Mark D., and Mackay, Graham A. (2011) Human mast cell line-1 (HMC-1) cells transfected with FcɛRIα are sensitive to IgE/antigen-mediated stimulation demonstrating selectivity towards cytokine production. International Immunopharmacology, 11 (8). pp. 1002-1011.
|PDF (Published Version) - Repository staff only - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader|
View at Publisher Website: http://dx.doi.org/10.1016/j.intimp.2011....
Mast cells play important roles in allergic and inflammatory diseases. Efforts to better understand human mast cell activation and develop novel inhibitory agents have been hampered by the lack of suitable human mast cell lines. The HMC-1 mast cell line has been extensively used, but lacks native expression of the human high-affinity IgE receptor FcɛRI limiting its applications.We have stably transfected HMC-1 cells with the IgE- binding alpha-subunit of FcɛRI to generate HMCα cells that are antigen-responsive. We have used flow cytometry, cell signaling assays, pharmacological pathway inhibitors and cell functional assays to characterize the properties of HMCα cells. IgE/antigen responses were compared with those of the adenosine receptor agonist NECA. Surface expression of FcεRI in HMCα cells was demonstrated and was enhanced by prior sensitization with IgE. Activation of HMCα cells with IgE/antigen did not produce degranulation, but did lead to release of numerous cytokines. Whilst there was no measurable increase of intracellular Ca2+ or marked general changes in protein tyrosine phosphorylation, IgE/antigen stimulation of HMCα cells enhanced phosphorylation of p38MAPK and Erk. Inhibitors of these pathways, as well as the src kinase inhibitor PP2, attenuated IgE/antigen-induced cytokine release. In summary, we have generated and characterized HMCα cells and show that they are a useful and relevant human mast cell model to examine FcɛRI stabilization, signaling and mediator release. We envisage that HMCα cells will have utility in understanding the importance of mast cells in human allergic disease and in assessing the activity of novel anti-allergic compounds.
|Item Type:||Article (Refereed Research - C1)|
|Keywords:||mast cells, FcεRI, IgE, adenosine, cytokines, MAPK|
|FoR Codes:||06 BIOLOGICAL SCIENCES > 0601 Biochemistry and Cell Biology > 060199 Biochemistry and Cell Biology not elsewhere classified @ 100%|
|SEO Codes:||92 HEALTH > 9201 Clinical Health (Organs, Diseases and Abnormal Conditions) > 920108 Immune System and Allergy @ 100%|
|Deposited On:||08 Jun 2011 09:16|
|Last Modified:||18 Oct 2013 01:12|
Last 12 Months: 0
|Citation Counts with External Providers:|
Repository Staff Only: item control page