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The detection of ADAM8 protein on cells of the human immune system and the demonstration of its expression on peripheral blood B cells, dendritic cells and monocyte subsets

Richens, Joanna; Fairclough, Lucy; Ghaemmaghami, Amir M.; Mahdavi, Jafar; Shakib, Farouk; Sewell, Herbert F.

Authors

Joanna Richens

Jafar Mahdavi

Farouk Shakib

Herbert F. Sewell



Abstract

A disintegrin and metalloprotease (ADAM) proteins have wide ranging functions, including proteolytic cleavage of cell surface molecules, cell fusion, cell adhesion and intracellular signalling. Recent evidence suggests the involvement of ADAM8 in allergic responses. For instance, ADAM8 is amongst a number of genes up-regulated in experimentally induced asthma in animals. In order to further define the involvement of ADAM8 in allergic responses, we sought in the first instance to examine its distribution on human peripheral blood B cells, resting and activated T cells, monocyte subsets and monocyte derived dendritic cells. Here we demonstrate for the first time ADAM8 protein expression on B cells and dendritic cells, and its higher expression on CD142+CD16- monocytes compared to CD14+CD16+ cells. Immature dendritic cells expressed low levels of ADAM8 when treated with a combination of GM-CSF and IL-4, but stimulation with LPS resulted in a higher level of expression, which was TLR-4 independent. Up-regulation of ADAM8 expression on dendritic cells was also observed after stimulation with TNF-α, but not after stimulation with anti-CD40. The demonstration of ADAM8 expression on these cells provides an opportunity for addressing the potential role of inhaled protease allergens, such as Der p 1, in modulating ADAM8 functions, particularly with regards to innate immune responses by dendritic cells and IgE synthesis by B cells. © 2006 Elsevier GmbH. All rights reserved.

Citation

Richens, J., Fairclough, L., Ghaemmaghami, A. M., Mahdavi, J., Shakib, F., & Sewell, H. F. (2007). The detection of ADAM8 protein on cells of the human immune system and the demonstration of its expression on peripheral blood B cells, dendritic cells and monocyte subsets. Immunobiology, 212(1), 29-38. https://doi.org/10.1016/j.imbio.2006.06.012

Journal Article Type Article
Publication Date Mar 5, 2007
Deposit Date Jan 3, 2023
Journal Immunobiology
Print ISSN 0171-2985
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 212
Issue 1
Pages 29-38
DOI https://doi.org/10.1016/j.imbio.2006.06.012
Public URL https://nottingham-repository.worktribe.com/output/3097605