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活化巨噬细胞不依赖超氧化物释放过氧化氢。

Superoxide-independent hydrogen peroxide release by activated macrophages.

作者信息

Russo M, Teixeira H C, Marcondes M C, Barbuto J A

机构信息

Departamento de Imunologia, Universidade de São Paulo, Brasil.

出版信息

Braz J Med Biol Res. 1989;22(10):1271-3.

PMID:2561630
Abstract

The present data show that freshly explanted BCG-activated mouse peritoneal macrophages release large quantities of hydrogen peroxide upon initial contact with a foreign substratum, without the requirement for other membrane stimuli such as phorbol diesters. The hydrogen peroxide detected under these conditions does not originate from extracellularly released superoxide, since 2 x 10(5) BCG-activated macrophages spontaneously released 1.6 nmol hydrogen peroxide but only 0.2 nmol superoxide. Thus, more than 90% of the hydrogen peroxide detected was not derived from extracellular superoxide dismutation. The dissociation between hydrogen peroxide and superoxide release was further demonstrated in cytochalasin B- or lidocaine-treated cells or in the absence of glucose. Under these conditions, hydrogen peroxide release was markedly inhibited while superoxide release was unaffected. These observations provide evidence that another metabolic pathway is involved in the generation and release of hydrogen peroxide during adherence and spreading of freshly explanted activated macrophages onto a substratum.

摘要

目前的数据表明,刚分离出的卡介苗激活的小鼠腹腔巨噬细胞在初次接触外来基质时会释放大量过氧化氢,无需其他膜刺激,如佛波酯。在这些条件下检测到的过氧化氢并非源自细胞外释放的超氧化物,因为2×10⁵个卡介苗激活的巨噬细胞自发释放1.6 nmol过氧化氢,但仅释放0.2 nmol超氧化物。因此,检测到的过氧化氢中超过90%并非来自细胞外超氧化物歧化反应。在细胞松弛素B或利多卡因处理的细胞中或在无葡萄糖的情况下,过氧化氢和超氧化物释放之间的解离得到进一步证实。在这些条件下,过氧化氢释放受到显著抑制,而超氧化物释放不受影响。这些观察结果提供了证据,表明在刚分离出的激活巨噬细胞黏附并铺展到基质上的过程中,另一种代谢途径参与了过氧化氢的生成和释放。

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