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Functional Characterization and Expression Analysis of the Proteinase-Activated Receptor-2 in Human Cutaneous Mast Cells.

Authors :
Moormann, Corinna
Artuc, Metin
Pohl, Elena
Varga, Georg
Buddenkotte, Jörg
Vergnolle, Nathalie
Brehler, Randolf
Henz, Beate M.
Schneider, Stefan W.
Luger, Thomas A.
Steinhoff, Martin
Source :
Journal of Investigative Dermatology. Apr2006, Vol. 126 Issue 4, p746-755. 10p. 5 Diagrams, 5 Graphs.
Publication Year :
2006

Abstract

Proteinase-activated receptor-2 (PAR2) belongs to a new G protein-coupled receptor subfamily activated by serine proteinases. PAR2 has been demonstrated to play a role during inflammation and immune response in different tissues including the skin. We examined whether PAR2 is functionally expressed by cutaneous human primary skin mast cells (HPMC) and the human mast cell line 1 (HMC-1). Reverse transcription-polymerase chain reaction and FACS analysis show expression of PAR2 both at the RNA and protein level. HPMCs and HMC-1 also express PAR1, PAR3, and PAR4. Ca-mobilization studies demonstrate functional PAR2 expressed by human skin mast cells, as shown by natural and synthetic PAR2 agonists. PAR2 agonists induced histamine release from HPMC indicating a role of PAR2 in regulating inflammatory and immune responses by skin mast cells. Double-immunofluorescence staining reveals colocalization of PAR2 with tryptase in the majority of human skin mast cells. In conclusion, trypsin and tryptase as well as specific agonists for PAR2 were able to induce Ca2+ mobilization in HPMCs, and agonists of PAR2 induce the release of histamine from these cells. Thus, PAR2 may be an important regulator of skin mast cell function during cutaneous inflammation and hypersensitivity.Journal of Investigative Dermatology (2006) 126, 746–755. doi:10.1038/sj.jid.5700169; published online 9 February 2006 [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0022202X
Volume :
126
Issue :
4
Database :
Academic Search Index
Journal :
Journal of Investigative Dermatology
Publication Type :
Academic Journal
Accession number :
20179555
Full Text :
https://doi.org/10.1038/sj.jid.5700169