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Short Communication E-Cadherin restricts mast cell degranulation in mice

机译:短通信钙粘蛋白限制肥大细胞脱粒的老鼠

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Crosslinking of FcεRI-bound IgE triggers the release of a large number of biologically active, potentially anaphylactic compounds by mast cells. FcεRI activation ought to be well-controlled to restrict adverse activation. As mast cells are embedded in tissues, adhesion molecules may contribute to limiting premature activation. Here, we report that E-Cadherin serves that purpose. Having confirmed that cultured mast cells express E-Cadherin, a mast-cell-specific E-Cadherin deficiency, Mcpt5-Cre E-Cdhfl/fl mice, was used to analyze mast cell degranulation in vitro and in vivo. Cultured peritoneal mast cells from Mcpt5-Cre E-Cdhfl/fl mice were normal with respect to many parameters but showed much-enhanced degranulation in three independent assays. Soluble E-Cadherin reduced the degranulation of control cells. The release of some newly synthesized inflammatory cytokines was decreased by E-Cadherin deficiency. Compared to controls, Mcpt5-Cre E-Cdhfl/fl mice reacted much stronger to IgE-dependent stimuli, developing anaphylactic shock. We suggest E-Cadherin-mediated tissue interactions restrict mast cell degranulation to prevent their precocious activation.
机译:交联的FcεRI-bound IgE触发释放大量的生物活性,潜在过敏性肥大细胞的化合物。FcεRI激活应该控制限制不良激活。嵌入在组织粘附分子有助于限制过早激活。在这里,我们报告上皮型服务目的。mast-cell-specific细胞钙粘蛋白表达钙粘蛋白缺乏,Mcpt5-Cre E-Cdhfl / fl老鼠,被用来分析肥大细胞脱粒体外和体内。从Mcpt5-Cre E-Cdhfl / fl老鼠正常对许多参数,但显示提高了在三个独立的脱粒化验。控制细胞的脱粒。一些新合成炎性细胞因子减少钙缺乏症。控制,Mcpt5-Cre E-Cdhfl / fl老鼠的反应IgE-dependent刺激越强,发展过敏性休克。E-Cadherin-mediated组织相互作用限制肥大细胞脱颗粒,防止他们早熟的激活。

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