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尿路上皮细胞通过激活 Duox1 产生过氧化氢。

Urothelial cells produce hydrogen peroxide through the activation of Duox1.

机构信息

Department of Physiology, Semmelweis University, Budapest, Hungary.

出版信息

Free Radic Biol Med. 2010 Dec 15;49(12):2040-8. doi: 10.1016/j.freeradbiomed.2010.09.027.

Abstract

Hydrogen peroxide (H(2)O(2)) has important messenger and effector functions in the plant and animal kingdom. Phagocytes produce H(2)O(2) to kill pathogens, and epithelial cells of large airways have also been reported to produce H(2)O(2) for signaling and host defense purposes. In this report, we show for the first time that urothelial cells produce H(2)O(2) in response to a calcium signal. Using a gene-deficient mouse model we also demonstrate that H(2)O(2) is produced by the NADPH oxidase Duox1, which is expressed in the mouse urothelium. In contrast, we found no evidence for the expression of lactoperoxidase, an enzyme that has been shown to cooperate with Duox enzymes. We also found that specific activation of TRPV4 calcium channels elicits a calcium signal and stimulates H(2)O(2) production in urothelial cells. Furthermore, we detected altered pressure responses in the urinary bladders of Duox1 knockout animals. Our results raise the possibility that mechanosensing in epithelial cells involves calcium-dependent H(2)O(2) production similar to that observed in plants.

摘要

过氧化氢 (H₂O₂) 在植物和动物王国中具有重要的信使和效应功能。吞噬细胞产生 H₂O₂ 来杀死病原体,而大气道的上皮细胞也被报道为了信号传递和宿主防御的目的而产生 H₂O₂。在本报告中,我们首次表明尿路上皮细胞会产生 H₂O₂ 以响应钙信号。我们还使用基因缺失小鼠模型证明 H₂O₂ 是由 NADPH 氧化酶 Duox1 产生的,Duox1 在小鼠尿路上皮中表达。相比之下,我们没有发现乳过氧化物酶表达的证据,乳过氧化物酶是一种已被证明与 Duox 酶合作的酶。我们还发现,特定激活 TRPV4 钙通道会引发钙信号并刺激尿路上皮细胞产生 H₂O₂。此外,我们在 Duox1 基因敲除动物的膀胱中检测到压力反应改变。我们的结果提出了一种可能性,即在上皮细胞中机械感觉可能涉及类似于在植物中观察到的钙依赖性 H₂O₂ 产生。

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