2004
DOI: 10.1053/j.gastro.2004.04.004
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Mouse mast cell protease-1 is required for the enteropathy induced by gastrointestinal helminth infection in the mouse

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Cited by 73 publications
(76 citation statements)
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“…The MMC subset undergoes massive hyperplasia in the infected intestinal mucosa, while the CTMC population remains sparse and located predominantly in the intestinal serosal region. Mechanistically, mast cells have been shown to participate in intestinal expulsion of Trichinella by elaboration of the chymase mMCP-1 (26,27). This observation was consistent with the functional importance of the expanded MMC subpopulation in this tissue in the initial responses to this early stage of T. spiralis infection.…”
Section: Mouse Mast Cell Tryptase Mmcp-6 Is a Critical Link Between Asupporting
confidence: 74%
“…The MMC subset undergoes massive hyperplasia in the infected intestinal mucosa, while the CTMC population remains sparse and located predominantly in the intestinal serosal region. Mechanistically, mast cells have been shown to participate in intestinal expulsion of Trichinella by elaboration of the chymase mMCP-1 (26,27). This observation was consistent with the functional importance of the expanded MMC subpopulation in this tissue in the initial responses to this early stage of T. spiralis infection.…”
Section: Mouse Mast Cell Tryptase Mmcp-6 Is a Critical Link Between Asupporting
confidence: 74%
“…Some of the positive immunomodulatory functions of mast cells that have been proposed based on in vitro studies have been confirmed in vivo using mast cell knock-in mice 1,54,[57][58][59][60][61][62][63][64][65][66][67][68][69][70] or in mice lacking specific mast-cell-associated proteases [26][27][28][32][33][34] or lacking specific protease enzymatic activity 11 (Table 1 ). In many of these studies, the end points assessed included the recruitment of particular immune cells, such as granulocytes 28,32,33,[57][58][59][60][61]63,64,[67][68][69][70] , DCs 62,64,65,71 or various subpopulations of lymphocytes 64,67,70,72 .…”
Section: Positive Immunomodulatory Functions In Vivomentioning
confidence: 93%
“…If that mediator is selectively expressed by mast cells, and if its deletion does not significantly influence the expression of other mastcell products, then it is possible to draw conclusions about the role of that mast-cell product in vivo. For example, mice that lack mouse mast-cell protease-1 (mMCP-1) [26][27][28] , mMCP-4 29,30 , mMCP-6 [31][32][33] , or mouse mast cell-carboxypeptidase A (mMC-CPA) 34 , or that have a mutated mMC-CPA that essentially lacks enzymatic activity 11 , have been used to analyze whether the absence of these proteases (or their enzymatic activity) influences other aspects of the mast-cell phenotype, such as content of other stored mediators, as well as to define the functions of such mast-cell-associated proteases in vivo.…”
Section: Other Approachesmentioning
confidence: 99%
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“…179 Mast cells on the other hand contribute to worm expulsion through the release of various proteases that serve to loosen tight junctions between epithelial cells, thus aiding in the shedding of embedded worms, notably during T. spiralis infection. [180][181][182] However, mast cells appear to be unessential for the expulsion of N. brasiliensis infection, [183][184][185] illustrating the context-specific nature of these responses. Goblet cells also secrete several molecules in addition to mucins that contribute to expulsion.…”
Section: Expulsionmentioning
confidence: 99%