首页> 外文期刊>Biochimica et Biophysica Acta. Molecular and cell biology of Lipids >Increased cyclooxygenase-2 and 5-lipoxygenase activating protein expression in peritoneal macrophages during ovalbumin immunization of mice and cytosolic phospholipase A_2 activation after antigen challenge
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Increased cyclooxygenase-2 and 5-lipoxygenase activating protein expression in peritoneal macrophages during ovalbumin immunization of mice and cytosolic phospholipase A_2 activation after antigen challenge

机译:小鼠卵清蛋白免疫过程中腹腔巨噬细胞中环氧合酶2和5-脂氧合酶激活蛋白的表达增加以及抗原攻击后胞浆磷脂酶A_2的激活

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摘要

The present study investigates phenotypic and functional differentiation of peritoneal macrophages during ovalbumin-induced subcutaneous immunization of mice. For the first time we show that, in mouse peritoneal macrophages, ovalbumin immunization induces an increase in cyclooxygenase-2 (COX-2) and 5-lipoxygenase activating protein (FLAP) expression whereas it inhibits cytosolic phospholipase A_2 (cPLA2) expression. The study of arachidonic acid (AA) metabolism in peritoneal macrophages from control (cPM) and ovalbumin-immunized (iPM) mice shows that the reduced cPLA2 expression is correlated to a reduced basal AA metabolism, but is not a limiting factor for the opsonized zymosan-, PMA-, or A23187-triggered AA metabolism. We also show that in vitro ovalbumin challenge induce, only in iPM, cPLA2 activation through phosphorylation of serine residues, via a mechanism involving MAP kinases, and through increased intracellular calcium concentrations, leading to eicosanoid production. In parallel, we report that, in peritoneal macrophages, ovalbumin immunization induces the expression of CD23, the low affinity receptor for IgEs known for its involvement in allergic diseases. Thus, the modified expression of the enzymes involved in AA metabolism and the difference of response of cPM and iPM toward the antigen are important elements to understand the underlying mechanism of ovalbumin-induced allergic responses.
机译:本研究调查卵清蛋白诱导的小鼠皮下免疫过程中腹膜巨噬细胞的表型和功能分化。首次显示,在小鼠腹膜巨噬细胞中,卵清蛋白免疫诱导了环氧合酶2(COX-2)和5-脂氧合酶激活蛋白(FLAP)表达的增加,而抑制了胞质磷脂酶A_2(cPLA2)的表达。对照(cPM)和卵清蛋白免疫(iPM)小鼠腹膜巨噬细胞中花生四烯酸(AA)代谢的研究表明,降低的cPLA2表达与基础的AA代谢降低有关,但不是调理酵母聚糖的限制因素-,PMA-或A23187触发的AA代谢。我们还表明,体外卵清蛋白激发仅在iPM中通过丝氨酸残基的磷酸化,通过涉及MAP激酶的机制以及通过增加的细胞内钙浓度而导致cPLA2激活,从而导致类花生酸的产生。同时,我们报道,在腹膜巨噬细胞中,卵清蛋白免疫诱导CD23的表达,CD23是对IgE的低亲和力受体,以其参与过敏性疾病而闻名。因此,参与AA代谢的酶的修饰表达以及cPM和iPM对抗原的反应差异是了解卵清蛋白诱导的过敏反应的潜在机制的重要因素。

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