Department of Natural Sciences, University of Pernambuco, Garanhuns, Brazil.
Laboratory of Molecular Biology of Pathogens, Federal University of São Paulo, São Paulo, Brazil; Department of Microbiology, Immunology and Parasitology, Federal University of São Paulo, São Paulo, Brazil.
Mol Immunol. 2023 Aug;160:150-160. doi: 10.1016/j.molimm.2023.06.010. Epub 2023 Jul 10.
Global warming is changing the distribution of different pathogens around the globe, and humans are more susceptible to new or re-emerging infections. The human response to microbes is complex and involves different mechanisms of the immune system. Regulation of gene expression of immunity genes and of metabolism of immune cells are essential in this process. Both mechanisms could be regulated by protein lysine acetylation that will control chromatin structure affecting gene expression or key enzyme activity involved in cellular processes. Protein acetylation is crucial for the immunity and involves two families of enzymes: lysine acetyltransferases (KATs), which will promote protein acetylation, and lysine deacetylases (KDACs) that will reduce this modification. Lysine deacetylases are divided into Zinc-dependent or HDACs and NAD -dependent, or Sirtuins. These enzymes are in the nucleus, cytosol, and mitochondria of mammalian cells affecting different cellular pathways, such as metabolism, gene expression, DNA repair, cell proliferation, and apoptosis, opening the opportunity to explore these proteins as drug targets in different diseases, including cancer and neurodegenerative illness. Although widely explored in chronic diseases, very little is known about the role of Sirtuins during host response against microbes' infection. In this review we aim to explore the most recent literature evidencing a role for these enzymes during host responses to viruses, bacterial and protozoan infections, pointing out how these proteins can be manipulated by these pathogens to progress in the infection. Moreover, we will uncover the potential of host KDACs as therapeutic targets to prevent infections by activating effector immune functions.
全球变暖正在改变全球不同病原体的分布,人类更容易受到新的或重新出现的感染。人类对微生物的反应是复杂的,涉及免疫系统的不同机制。免疫基因的表达和免疫细胞的代谢调节在这个过程中至关重要。这两种机制都可以通过蛋白赖氨酸乙酰化来调节,它将控制染色质结构,影响基因表达或参与细胞过程的关键酶活性。蛋白乙酰化对免疫至关重要,涉及两类酶:促进蛋白乙酰化的赖氨酸乙酰转移酶(KATs),和降低这种修饰的赖氨酸去乙酰化酶(KDACs)。赖氨酸去乙酰化酶分为锌依赖性或 HDACs 和 NAD 依赖性或 Sirtuins。这些酶存在于哺乳动物细胞的核、细胞质和线粒体中,影响不同的细胞途径,如代谢、基因表达、DNA 修复、细胞增殖和细胞凋亡,为探索这些蛋白作为不同疾病(包括癌症和神经退行性疾病)的药物靶点提供了机会。尽管在慢性疾病中得到了广泛的研究,但关于 Sirtuins 在宿主对抗微生物感染的反应中的作用知之甚少。在这篇综述中,我们旨在探讨最近的文献证据,证明这些酶在宿主对病毒、细菌和原生动物感染的反应中的作用,指出这些蛋白如何被这些病原体操纵以促进感染的进展。此外,我们将揭示宿主 KDACs 作为治疗靶点的潜力,通过激活效应免疫功能来预防感染。