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Expression of the inhibitory Ly49E receptor is not critically involved in the immune response against cutaneous, pulmonary or liver tumours

Authors :
Tessa Kerre
Jessica Filtjens
Els Van Ammel
Aline Van Acker
Jiri Keirsse
Bart Vandekerckhove
Jo A. Van Ginderachter
Jean Plum
Tom Taghon
Sylvie Taveirne
Georges Leclercq
Department of Bio-engineering Sciences
Cellular and Molecular Immunology
Faculty of Sciences and Bioengineering Sciences
Physiology
Source :
SCIENTIFIC REPORTS, Scientific Reports
Publication Year :
2016
Publisher :
Nature Publishing Group, 2016.

Abstract

Natural killer (NK) lymphocytes are part of the innate immune system and are important in immune protection against tumourigenesis. NK cells display a broad repertoire of activating and inhibitory cell surface receptors that regulate NK cell activity. The Ly49 family of NK receptors is composed of several members that recognize major histocompatibility complex class I (MHC-I) or MHC-I-related molecules. Ly49E is a unique inhibitory member, being triggered by the non-MHC-I-related protein urokinase plasminogen activator (uPA) in contrast to the known MHC-I-triggering of the other inhibitory Ly49 receptors. Ly49E also has an uncommon expression pattern on NK cells, including high expression on liver DX5− NK cells. Furthermore, Ly49E is the only Ly49 member expressed by epidermal γδ T cells. As γδ T cells and/or NK cells have been shown to be involved in the regulation of cutaneous, pulmonary and liver malignancies and as uPA is involved in tumourigenesis, we investigated the role of the inhibitory Ly49E receptor in the anti-tumour immune response. We demonstrate that, although Ly49E is highly expressed on epidermal γδ T cells and liver NK cells, this receptor does not play a major role in the control of skin tumour formation or in lung and liver tumour development.

Details

Language :
English
ISSN :
20452322
Database :
OpenAIRE
Journal :
SCIENTIFIC REPORTS, Scientific Reports
Accession number :
edsair.doi.dedup.....cbf6ce56c2c5263452ffc4cf77fa9ec6
Full Text :
https://doi.org/10.1038/srep30564