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辅酶 A 的病理生理学作用。

The Pathophysiological Role of CoA.

机构信息

Department of Pharmaceutical Biochemistry, Faculty of Pharmacy, Medical University of Gdansk, 80-211 Gdańsk, Poland.

Department of Biochemistry, Faculty of Medicine, Medical University of Gdansk, 80-211 Gdansk, Poland.

出版信息

Int J Mol Sci. 2020 Nov 28;21(23):9057. doi: 10.3390/ijms21239057.

Abstract

The importance of coenzyme A (CoA) as a carrier of acyl residues in cell metabolism is well understood. Coenzyme A participates in more than 100 different catabolic and anabolic reactions, including those involved in the metabolism of lipids, carbohydrates, proteins, ethanol, bile acids, and xenobiotics. However, much less is known about the importance of the concentration of this cofactor in various cell compartments and the role of altered CoA concentration in various pathologies. Despite continuous research on these issues, the molecular mechanisms in the regulation of the intracellular level of CoA under pathological conditions are still not well understood. This review summarizes the current knowledge of (a) CoA subcellular concentrations; (b) the roles of CoA synthesis and degradation processes; and (c) protein modification by reversible CoA binding to proteins (CoAlation). Particular attention is paid to (a) the roles of changes in the level of CoA under pathological conditions, such as in neurodegenerative diseases, cancer, myopathies, and infectious diseases; and (b) the beneficial effect of CoA and pantethine (which like CoA is finally converted to Pan and cysteamine), used at pharmacological doses for the treatment of hyperlipidemia.

摘要

辅酶 A(CoA)作为细胞代谢中酰基残基载体的重要性是众所周知的。CoA 参与了 100 多种不同的分解代谢和合成代谢反应,包括涉及脂质、碳水化合物、蛋白质、乙醇、胆汁酸和外源性化合物代谢的反应。然而,人们对这种辅助因子在各种细胞区室中的浓度的重要性以及 CoA 浓度改变在各种病理中的作用知之甚少。尽管对这些问题进行了持续的研究,但在病理条件下调节细胞内 CoA 水平的分子机制仍未得到很好的理解。这篇综述总结了(a)CoA 亚细胞浓度的现有知识;(b)CoA 合成和降解过程的作用;以及(c)通过可逆的 CoA 与蛋白质结合对蛋白质进行修饰(CoAlation)。特别关注(a)在病理条件下 CoA 水平变化的作用,如神经退行性疾病、癌症、肌肉疾病和传染病;以及(b)CoA 和泛硫乙胺(与 CoA 一样最终转化为 Pan 和半胱氨酸)在药理学剂量下用于治疗高血脂的有益作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1da3/7731229/f8f026b292c9/ijms-21-09057-g001.jpg

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