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烷基过氧化氢还原酶亚基C(AhpC)可保护细菌和人类细胞免受活性氮中间体的侵害。

Alkyl hydroperoxide reductase subunit C (AhpC) protects bacterial and human cells against reactive nitrogen intermediates.

作者信息

Chen L, Xie Q W, Nathan C

机构信息

Seaver Laboratory, Department of Medicine, Cornell University Medical College, New York, New York 10021, USA.

出版信息

Mol Cell. 1998 May;1(6):795-805. doi: 10.1016/s1097-2765(00)80079-9.

Abstract

In Salmonella typhimurium, ahpC encodes subunit C of alkyl hydroperoxide reductase, an enzyme that reduces organic peroxides. Here, we asked if ahpC could protect cells from reactive nitrogen intermediates (RNI). Salmonella disrupted in ahpC became hypersusceptible to RNI. ahpC from either Mycobacterium tuberculosis or S. typhimurium fully complemented the defect. Unlike protection against cumene hydroperoxide, protection afforded by ahpC against RNI was independent of the reducing flavoprotein, AhpF. Mycobacterial ahpC protected human cells from necrosis and apoptosis caused by RNI delivered exogenously or produced endogenously by transfected nitric oxide synthase. Resistance to RNI appears to be a physiologic function of ahpC. ahpC is the most widely distributed gene known that protects cells directly from RNI, and provides an enzymatic defense against an element of antitubercular immunity.

摘要

在鼠伤寒沙门氏菌中,ahpC编码烷基过氧化氢还原酶的C亚基,该酶可还原有机过氧化物。在此,我们探究了ahpC是否能保护细胞免受活性氮中间体(RNI)的伤害。ahpC基因缺失的沙门氏菌对RNI变得高度敏感。来自结核分枝杆菌或鼠伤寒沙门氏菌的ahpC完全弥补了这一缺陷。与对氢过氧化异丙苯的保护作用不同,ahpC对RNI的保护作用不依赖于还原性黄素蛋白AhpF。分枝杆菌的ahpC保护人类细胞免受外源性递送或转染的一氧化氮合酶内源性产生的RNI所导致的坏死和凋亡。对RNI的抗性似乎是ahpC的一种生理功能。ahpC是已知最广泛分布的基因,可直接保护细胞免受RNI的伤害,并提供针对抗结核免疫要素的酶促防御。

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