Pacitti Dario, Scotton Chris J, Kumar Vinod, Khan Haroon, Wark Peter A B, Torregrossa Roberta, Hansbro Philip M, Whiteman Matthew
Institute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter, United Kingdom.
Priority Research Centre for Healthy Lungs and Hunter Medical Research Institute, The University of Newcastle, Newcastle, Australia.
Antioxid Redox Signal. 2021 Sep 1;35(7):551-579. doi: 10.1089/ars.2021.0039. Epub 2021 Jun 1.
Hydrogen sulfide (HS) is a gaseous signaling molecule involved in a plethora of physiological and pathological processes. It is primarily synthesized by cystathionine-β-synthase, cystathionine-γ-lyase, and 3-mercaptopyruvate sulfurtransferase as a metabolite of the transsulfuration pathway. HS has been shown to exert beneficial roles in lung disease acting as an anti-inflammatory and antiviral and to ameliorate cell metabolism and protect from oxidative stress. HS interacts with transcription factors, ion channels, and a multitude of proteins post-translational modifications through S-persulfidation ("sulfhydration"). Perturbation of endogenous HS synthesis and/or levels have been implicated in the development of accelerated lung aging and diseases, including asthma, chronic obstructive pulmonary disease, and fibrosis. Furthermore, evidence indicates that persulfidation is decreased with aging. Here, we review the use of HS as a biomarker of lung pathologies and discuss the potential of using HS-generating molecules and synthesis inhibitors to treat respiratory diseases. Furthermore, we provide a critical appraisal of methods of detection used to quantify HS concentration in biological samples and discuss the challenges of characterizing physiological and pathological levels. Considerations and caveats of using HS delivery molecules, the choice of generating molecules, and concentrations are also reviewed. . 35, 551-579.
硫化氢(HS)是一种气态信号分子,参与众多生理和病理过程。它主要由胱硫醚-β-合酶、胱硫醚-γ-裂解酶和3-巯基丙酮酸硫转移酶作为转硫途径的代谢产物合成。已表明HS在肺部疾病中发挥有益作用,具有抗炎和抗病毒作用,并能改善细胞代谢和抵御氧化应激。HS通过S-亚磺化(“硫氢化”)与转录因子、离子通道以及众多蛋白质的翻译后修饰相互作用。内源性HS合成和/或水平的扰动与加速肺衰老和疾病的发生有关,包括哮喘、慢性阻塞性肺疾病和纤维化。此外,有证据表明亚磺化随着衰老而减少。在这里,我们综述了HS作为肺部疾病生物标志物的应用,并讨论了使用产生HS的分子和合成抑制剂治疗呼吸系统疾病的潜力。此外,我们对用于量化生物样品中HS浓度的检测方法进行了批判性评估,并讨论了表征生理和病理水平的挑战。还综述了使用HS递送分子的注意事项和警告、产生分子的选择以及浓度。. 35, 551 - 579。