Temporal distribution of distinct mast cell phenotypes during intestinal schistosomiasis in mice

被引:21
作者
De Jonge, F
Van Nassauw, L
Van Meir, F
Miller, HRP
Van Marck, E
Timmermans, JP
机构
[1] Univ Antwerp, RUCA, Dept Biomed Sci, Cell Biol & Histol Lab, B-2020 Antwerp, Belgium
[2] Univ Edinburgh, Royal Dick Sch Vet Studies, Dept Vet Clin Studies, Roslin, Midlothian, Scotland
[3] Univ Antwerp, Dept Med, Pathol Lab, Wilrijk, Belgium
关键词
mast cell subsets; Schistosoma mansoni; ileum; mast cell proteases; mouse;
D O I
10.1046/j.1365-3024.2002.00457.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mastocytosis is a common feature of helminth infection in most host species. We examined the temporal distribution and phenotype of mast cells during intestinal schistosomiasis in mice, using antibodies directed against histamine, a general mast cell marker, against mouse mast cell protease-1 (MMCP-1), a mucosal mast cell (MMC) marker, and against tryptase, a predominantly connective tissue mast cell (CTMC) marker. Ileal paraffin and/or cryosections of control, 8- and 15-week-infected mice were quantitatively analysed. In the intestinal wall of non- and unisexual infected mice, a few dispersed mast cells were detected. In infected mice, a transient increase of mast cells in the mucosa and a gradual increase in the outer muscle layer were observed. MMCP-1 expressing MMCs were predominantly present in the mucosa during the acute phase [8 weeks postinfection (p.i.)], while tryptase and histamine immunoreactivity demonstrated that two subsets of CTMCs were predominantly present in the outer muscle layer at 15 weeks p.i. (chronic phase). In conclusion, these results reveal that, in mice, both MMCs and CTMCs are involved in the inflammatory response during schistosomiasis. The recruitment of each mast cell population is time-dependent and occurs at different locations. These data suggest that mastocytosis is associated with motility-related gastrointestinal symptoms and egg excretion.
引用
收藏
页码:225 / 231
页数:7
相关论文
共 34 条
[1]  
ABE T, 1988, IMMUNOLOGY, V63, P181
[2]  
Bogers J, 2000, NEUROGASTROENT MOTIL, V12, P431, DOI 10.1046/j.1365-2982.2000.00219.x
[3]   IMMUNOPATHOLOGY OF SCHISTOSOMA-MANSONI INFECTION [J].
BOROS, DL .
CLINICAL MICROBIOLOGY REVIEWS, 1989, 2 (03) :250-269
[4]   LOCALIZATION OF RAT TRYPTASE TO A SUBSET OF THE CONNECTIVE-TISSUE TYPE OF MAST-CELL [J].
CHEN, Z ;
IRANI, AA ;
BRADFORD, TR ;
CRAIG, SS ;
NEWLANDS, G ;
MILLER, H ;
HUFF, T ;
SIMMONS, WH ;
SCHWARTZ, LB .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1993, 41 (07) :961-969
[5]  
DOENHOFF M, 1978, IMMUNOLOGY, V35, P771
[6]   IMMUNOLOGICAL CONTROL OF HEPATOTOXICITY AND PARASITE EGG EXCRETION IN SCHISTOSOMA-MANSONI INFECTIONS - STAGE SPECIFICITY OF THE REACTIVITY OF IMMUNE SERUM IN T-CELL DEPRIVED MICE [J].
DOENHOFF, MJ ;
PEARSON, S ;
DUNNE, DW ;
BICKLE, Q ;
LUCAS, S ;
BAIN, J ;
MUSALLAM, R ;
HASSOUNAH, O .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1981, 75 (01) :41-53
[7]  
DOMINGO EO, 1969, GASTROENTEROLOGY, V56, P231
[8]   Schistosomiasis [J].
El-Garem, AA .
DIGESTION, 1998, 59 (05) :589-605
[9]  
Friend DS, 1998, J IMMUNOL, V160, P5537
[10]   Alterations of intestinal motor responses to various stimuli after Nippostrongylus brasiliensis infection in rats:: role of mast cells [J].
Gay, J ;
Fioramonti, J ;
Garcia-Villar, R ;
Buéno, L .
NEUROGASTROENTEROLOGY AND MOTILITY, 2000, 12 (03) :207-214