Department of Molecular Neurochemistry, Medical University of Lodz, 92-215 Lodz, Poland.
Department of Pharmaceutical Toxicology, China Medical University, Shenyang 110122, China.
Int J Mol Sci. 2023 Feb 4;24(4):3120. doi: 10.3390/ijms24043120.
The family of myocyte enhancer factor 2 (MEF2) transcription factors comprises four highly conserved members that play an important role in the nervous system. They appear in precisely defined time frames in the developing brain to turn on and turn off genes affecting growth, pruning and survival of neurons. MEF2s are known to dictate neuronal development, synaptic plasticity and restrict the number of synapses in the hippocampus, thus affecting learning and memory formation. In primary neurons, negative regulation of MEF2 activity by external stimuli or stress conditions is known to induce apoptosis, albeit the pro or antiapoptotic action of MEF2 depends on the neuronal maturation stage. By contrast, enhancement of MEF2 transcriptional activity protects neurons from apoptotic death both in vitro and in preclinical models of neurodegenerative diseases. A growing body of evidence places this transcription factor in the center of many neuropathologies associated with age-dependent neuronal dysfunctions or gradual but irreversible neuron loss. In this work, we discuss how the altered function of MEF2s during development and in adulthood affecting neuronal survival may be linked to neuropsychiatric disorders.
肌细胞增强因子 2(MEF2)转录因子家族由四个高度保守的成员组成,它们在神经系统中起着重要作用。它们在发育中的大脑中以精确定义的时间框架出现,开启和关闭影响神经元生长、修剪和存活的基因。已知 MEF2 决定神经元发育、突触可塑性,并限制海马体中的突触数量,从而影响学习和记忆形成。在原代神经元中,已知外部刺激或应激条件对 MEF2 活性的负向调节会诱导细胞凋亡,尽管 MEF2 的促凋亡或抗凋亡作用取决于神经元成熟阶段。相比之下,增强 MEF2 的转录活性可保护神经元免受体外和神经退行性疾病的临床前模型中的凋亡死亡。越来越多的证据表明,这种转录因子处于许多与年龄相关的神经元功能障碍或逐渐但不可逆转的神经元丧失相关的神经病理学的中心。在这项工作中,我们讨论了 MEF2 在发育中和成年期的功能改变如何影响神经元存活,可能与神经精神疾病有关。