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在炎症巨噬细胞对糊化固定红细胞的吞噬作用过程中,呼吸爆发活性受损。

Respiratory burst activity is impaired during phagocytosis of gelatinized fixed erythrocytes by inflammatory macrophages.

作者信息

Gudewicz P W, Blumenstock F A

机构信息

Department of Physiology, Albany Medical College of Union University, New York 12208.

出版信息

Inflammation. 1987 Dec;11(4):439-46. doi: 10.1007/BF00915987.

Abstract

The ability of immune and nonimmune opsonized gelatin-coated particles to stimulate respiratory burst activity by inflammatory macrophages was studied. The uptake and phagocytosis of 51Cr-labeled gelatin-coated fixed erythrocytes, opsonized with either specific IgG or purified plasma fibronectin, was measured in monolayer cultures of rat inflammatory peritoneal macrophages. Respiratory burst activity was evaluated in monolayers of rat inflammatory peritoneal macrophages by measuring: (1) luminol-dependent chemiluminescence and (2) the production of 14CO2 from the oxidation of [1-14C] glucose. Uptake of opsonized gelatin-coated, fixed erythrocytes resulted in no stimulation of chemiluminescence and only a limited stimulation of [1-14C] glucose oxidation. Respiratory burst activity produced by phorbol myristate acetate was not inhibited during the uptake of opsonized gelatin-coated particles. These data suggest that metabolic processes associated with macrophage respiratory burst activity may not be coupled to the ingestion of opsonized gelatin-coated fixed erythrocytes.

摘要

研究了免疫和非免疫调理的明胶包被颗粒刺激炎性巨噬细胞呼吸爆发活性的能力。在大鼠炎性腹腔巨噬细胞单层培养物中,测定了用特异性IgG或纯化的血浆纤连蛋白调理的51Cr标记的明胶包被固定红细胞的摄取和吞噬作用。通过测量以下指标评估大鼠炎性腹腔巨噬细胞单层中的呼吸爆发活性:(1) 鲁米诺依赖性化学发光和(2) [1-14C]葡萄糖氧化产生的14CO2。摄取调理的明胶包被固定红细胞不会刺激化学发光,对[1-14C]葡萄糖氧化的刺激也很有限。在摄取调理的明胶包被颗粒过程中,佛波酯肉豆蔻酸酯产生的呼吸爆发活性未受到抑制。这些数据表明,与巨噬细胞呼吸爆发活性相关的代谢过程可能与摄取调理的明胶包被固定红细胞无关。

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