Department of Pathophysiology, School of Basic Medical Sciences, Xuzhou Medical University, Xuzhou, China.
J Physiol Biochem. 2023 Nov;79(4):685-693. doi: 10.1007/s13105-023-00978-w. Epub 2023 Aug 7.
Neuronal death occurs in various physiological and pathological processes, and apoptosis, necrosis, and ferroptosis are three major forms of neuronal death. Neuronal apoptosis, necrosis, and ferroptosis are widely identified to involve the progress of stroke, Parkinson's disease, and Alzheimer's disease. A growing body of evidence has pointed out that neuronal death is tightly associated with expression of related genes and alteration of signaling molecules. In addition, recently, epigenetics has been increasingly focused on as a vital regulatory mechanism for neuronal apoptosis, necrosis, and ferroptosis, providing a new direction for treating nervous system diseases. Moreover, growing researches suggest that histone methylation or demethylation is involved in the processes of neuronal apoptosis, necrosis, and ferroptosis. These researches may imply that studying the potential roles of histone methylation is essential for treating the nervous system diseases. Here, we review potential roles of histone methylation and demethylation in neuronal death, which may give us a new direction in treating the nervous system diseases.
神经元死亡发生在各种生理和病理过程中,细胞凋亡、坏死和铁死亡是神经元死亡的三种主要形式。神经元凋亡、坏死和铁死亡广泛涉及中风、帕金森病和阿尔茨海默病的进展。越来越多的证据指出,神经元死亡与相关基因的表达和信号分子的改变密切相关。此外,最近,表观遗传学作为神经元凋亡、坏死和铁死亡的重要调控机制越来越受到关注,为治疗神经系统疾病提供了新的方向。此外,越来越多的研究表明,组蛋白甲基化或去甲基化参与了神经元凋亡、坏死和铁死亡的过程。这些研究可能意味着,研究组蛋白甲基化的潜在作用对于治疗神经系统疾病至关重要。在这里,我们综述了组蛋白甲基化和去甲基化在神经元死亡中的潜在作用,这可能为我们治疗神经系统疾病提供新的方向。