The Solomon H. Snyder Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Department of Pharmacology and Molecular Sciences, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Br J Pharmacol. 2019 Feb;176(4):583-593. doi: 10.1111/bph.14446. Epub 2018 Aug 23.
The transsulfuration pathway is a metabolic pathway where transfer of sulfur from homocysteine to cysteine occurs. The pathway leads to the generation of several sulfur metabolites, which include cysteine, GSH and the gaseous signalling molecule hydrogen sulfide (H S). Precise control of this pathway is critical for maintenance of optimal cellular function and, therefore, the key enzymes of the pathway, cystathionine β-synthase and cystathionine γ-lyase, are regulated at multiple levels. Disruption of the transsulfuration pathway contributes to the pathology of several conditions such as vascular dysfunction, Huntington's disease and during ageing. Treatment with donors of hydrogen sulfide and/or stimulation of this pathway have proved beneficial in several of these disorders. In this review, we focus on the regulation of the transsulfuration pathway pertaining to cysteine and H S, which could be targeted to develop novel therapeutics. LINKED ARTICLES: This article is part of a themed section on Chemical Biology of Reactive Sulfur Species. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v176.4/issuetoc.
硫转移途径是一种代谢途径,其中同型半胱氨酸中的硫转移到半胱氨酸上。该途径会产生几种硫代谢物,包括半胱氨酸、GSH 和气体信号分子硫化氢(H₂S)。该途径的精确控制对于维持最佳细胞功能至关重要,因此,该途径的关键酶,即胱硫醚β-合酶和胱硫醚γ-裂合酶,在多个水平上受到调节。硫转移途径的破坏会导致多种疾病的病理,如血管功能障碍、亨廷顿病和衰老。在这些疾病中,用硫化氢供体治疗和/或刺激该途径已被证明是有益的。在这篇综述中,我们重点关注与半胱氨酸和 H₂S 相关的硫转移途径的调节,这可能是开发新疗法的靶点。
本文是关于反应性硫物种的化学生物学的专题部分的一部分。要查看该部分中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v176.4/issuetoc.