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肾脏中的NADPH氧化酶。

NADPH oxidases in the kidney.

作者信息

Gill Pritmohinder S, Wilcox Christopher S

机构信息

Angiogenesis Section, Lombardi Cancer Center, Cardiovascular-Kidney Institute and Division of Nephrology and Hypertension, Georgetown University, Washington, District of Columbia 20007, USA.

出版信息

Antioxid Redox Signal. 2006 Sep-Oct;8(9-10):1597-607. doi: 10.1089/ars.2006.8.1597.

Abstract

NADPH oxidases have a distinct cellular localization in the kidney. Reactive oxygen species (ROS) are produced in the kidney by fibroblasts, endothelial cells (EC), vascular smooth muscle cells (VSMC), mesangial cells (MCs), tubular cells, and podocyte cells. All components of the phagocytic NADPH oxidase, as well as the Nox-1 and -4, are expressed in the kidney, with a prominent expression in renal vessels, glomeruli, and podocytes, and cells of the thick ascending limb of the loop of Henle (TAL), macula densa, distal tubules, collecting ducts, and cortical interstitial fibroblasts. NADPH oxidase activity is upregulated by prolonged infusion of angiotensin II (Ang II) or a high salt diet. Since these are major factors underlying the development of hypertension, renal NADPH oxidase may have an important pathophysiological role. Indeed, recent studies with small interference RNAs (siRNAs) targeted to p22( phox ) implicate p22( phox ) in Ang II-induced activation of renal NADPH oxidase and the development of oxidative stress and hypertension, while studies with apocynin implicate activation of p47( phox ) in the development of nephropathy in a rat model of type 1 diabetes mellitus (DM). Experimental studies of the distribution, signaling, and function of NADPH oxidases in the kidney are described.

摘要

NADPH氧化酶在肾脏中有独特的细胞定位。肾脏中的成纤维细胞、内皮细胞(EC)、血管平滑肌细胞(VSMC)、系膜细胞(MCs)、肾小管细胞和足细胞可产生活性氧(ROS)。吞噬性NADPH氧化酶的所有成分以及Nox-1和Nox-4在肾脏中均有表达,在肾血管、肾小球、足细胞以及髓袢升支粗段(TAL)、致密斑、远曲小管、集合管和皮质间质成纤维细胞中表达尤为显著。通过长期输注血管紧张素II(Ang II)或高盐饮食可上调NADPH氧化酶的活性。由于这些是高血压发生发展的主要因素,肾脏NADPH氧化酶可能具有重要的病理生理作用。事实上,近期针对p22(phox)的小干扰RNA(siRNA)研究表明,p22(phox)参与Ang II诱导的肾脏NADPH氧化酶激活以及氧化应激和高血压的发展,而使用阿朴吗啡的研究表明,在1型糖尿病(DM)大鼠模型中,p47(phox)的激活参与了肾病的发展。本文描述了NADPH氧化酶在肾脏中的分布、信号传导和功能的实验研究。

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