Localization of protease-activated receptors-1 and-2 in human mast cells: Indications for an amplified mast cell degranulation cascade

被引:106
作者
D'Andrea, MR [1 ]
Rogahn, CJ [1 ]
Andrade-Gordon, P [1 ]
机构
[1] RW Johnson Pharmaceut Res Inst, Spring House, PA 19477 USA
关键词
double immunofluorescence; exocytosis; immunohistochemistry; mast cells; mast cell tryptase; protease-activated receptor-1; protease-activated receptor-2;
D O I
10.3109/10520290009064152
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Protease-activated receptors (PARs) belong to a family of G-coupled seven transmembrane receptors that are activated by a proteolytic cleavage of their N-termini, Recent studies suggest the involvement of protease-activated receptors-1 and -2 (PAR-1, PAR-2) activators in mast cell degranulation in various physiological and pathophysiological processes in inflammatory responses. Although PAR-1 and PAR-2 activating proteases, thrombin and tryptase, have been associated with mast cell activation, PAR-1 and PAR-2 have not been localized within these cells. We describe here the localization of PAR-1 and PAR-2 in mast cells from various normal human tissues using immunohistochemical and double immunofluorescence techniques. The presence of these receptors on the membrane may explain the actions of accessible extracellular thrombin and tryptase for mast cell activation, In addition to the membrane labeling, these receptors are also localized on the membrane of the intracellular tryptase-positive granules, which may function to sustain further mast cell degranulation upon exocytosis, The localization of these two receptors in mast cells suggests a novel mechanism for controlling mast cell activation through regulation of PAR-1 and PAR-2.
引用
收藏
页码:85 / 90
页数:6
相关论文
共 34 条
[1]   Ligand cross-reactivity within the protease-activated receptor family [J].
Blackhart, BD ;
Emilsson, K ;
Nguyen, D ;
Teng, W ;
Martelli, AJ ;
Nystedt, S ;
Sundelin, J ;
Scarborough, RM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (28) :16466-16471
[2]  
Bohm SK, 1996, BIOCHEM J, V314, P1009
[3]  
BRADDING P, 1995, IMMUNOPHARMACOLOGY R, P53
[4]  
Buckley MG, 1998, J PATHOL, V186, P67
[5]  
BURGESS TL, 1987, ANNU REV CELL BIOL, V3, P243, DOI 10.1146/annurev.cb.03.110187.001331
[6]   Thrombin functions as an inflammatory mediator through activation of its receptor [J].
Cirino, G ;
Cicala, C ;
Bucci, MR ;
Sorrentino, L ;
Maraganore, JM ;
Stone, SR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (03) :821-827
[7]  
CRAIG SS, 1989, LAB INVEST, V60, P147
[8]  
D'Andrea MR, 1998, J HISTOCHEM CYTOCHEM, V46, P157
[9]  
DANDREA MR, 1998, THESIS RUTGERS U PIS
[10]  
DVORAK AM, 1985, LAB INVEST, V53, P45