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诱导型一氧化氮合酶的细胞保护机制。

Cellular Protective Mechanisms Of Inducible Nitric Oxide Synthase.

机构信息

Department of Surgery, University of Pittsburgh, USA.

出版信息

Redox Biol. 2015 Aug;5:418. doi: 10.1016/j.redox.2015.09.026. Epub 2015 Dec 30.

Abstract

The inducible nitric oxide synthase (iNOS) is expressed constitutively but also induced in a number of epithelial cell types. iNOS regulates a number of cellular processes in these cell types without exerting toxicity. Among these functions is protection from cellular injury mediated by pro-apoptotic signals. We have had long-standing interest in the cell protective roles of iNOS in hepatocytes. We demonstrated that the upregulation of iNOS protects hepatocytes and the liver from TNF-mediated toxicity. This includes the inhibition of caspase activity through s-nitrosation. However, some of the effects are mediated through cGMP. Exploration into the mechanisms of the cGMP-mediated protection identified a role for the iNOS/NO/cGMP pathway in the activation of ADAM17 (TACE), which is a sheddase that cleaves a number of cell surface receptors including TNF receptor type 1 (TNFR1). The activation is associated with the phosphorylation of TACE. The iNOS/NO/cGMP/TACE pathway can be augmented by PDE5 inhibitors and reduce organ injury in the setting of sepsis. The implications go beyond acute pathophysiology and may be important to the mechanisms of iNOS in promoting aggressive cancers.

摘要

诱导型一氧化氮合酶 (iNOS) 在许多上皮细胞类型中持续表达,但也可被诱导。iNOS 在这些细胞类型中调节许多细胞过程而不会产生毒性。其中的功能之一是保护细胞免受促凋亡信号介导的细胞损伤。我们对 iNOS 在肝细胞中的细胞保护作用一直很感兴趣。我们证明,iNOS 的上调可保护肝细胞和肝脏免受 TNF 介导的毒性。这包括通过 s-亚硝基化抑制半胱天冬酶活性。然而,一些作用是通过 cGMP 介导的。对 cGMP 介导的保护机制的探索确定了 iNOS/NO/cGMP 途径在 ADAM17(TACE)激活中的作用,TACE 是一种剪切酶,可切割包括 TNF 受体 1 (TNFR1) 在内的许多细胞表面受体。这种激活与 TACE 的磷酸化有关。PDE5 抑制剂可增强 iNOS/NO/cGMP/TACE 途径,并可减少脓毒症时的器官损伤。其影响不仅限于急性病理生理学,对于 iNOS 促进侵袭性癌症的机制可能很重要。

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