Department of Brain and Cognitive Sciences, Ewha Womans University, 11-1 Daehyun-Dong, Seodaemoon-Gu, Seoul, 03760, Republic of Korea.
Department of Chemistry and Nano Science, Ewha Womans University, Seoul, 03760, Republic of Korea.
Mol Neurobiol. 2019 Dec;56(12):8537-8556. doi: 10.1007/s12035-019-01689-4. Epub 2019 Jul 2.
Chronic stress induces persistent depressive behaviors. Stress-induced transcriptional alteration over the homeostatic range in stress hormone-sensitive brain regions is believed to underlie long-lasting depressive behaviors. However, the detailed mechanisms by which chronic stress causes those adaptive changes are not clearly understood. In the present study, we investigated whether epigenetic changes regulate stress-induced depressive behaviors. We found that chronic stress in mice downregulates the epigenetic factors HDAC2 and SUV39H1 in the hippocampus. A series of follow-up analyses including ChIP assay and siRNA-mediated functional analyses reveal that glucocorticoids released by stress cumulatively increase Mkp-1 expression in the hippocampus, and increased Mkp-1 then debilitates p-CREB and PPARγ, which in turn suppress the epigenetic factors HDAC2 and SUV39H1. Furthermore, HDAC2 and SUV39H1 normally suppress the transcription of the Mkp-1, and therefore the reduced expression of HDAC2 and SUV39H1 increases Mkp-1 expression. Accordingly, repeated stress progressively strengthens a vicious cycle of the Mkp-1 signaling cascade that facilitates depressive behaviors. These results suggest that the hippocampal stress adaptation system comprising HDAC2/SUV39H1-regulated Mkp-1 signaling network determines the vulnerability to chronic stress and the maintenance of depressive behaviors.
慢性应激会导致持续的抑郁行为。人们认为,应激激素敏感脑区中稳态范围内的应激诱导转录改变是导致持久抑郁行为的基础。然而,慢性应激导致这些适应性变化的详细机制尚不清楚。在本研究中,我们研究了表观遗传变化是否调节应激诱导的抑郁行为。我们发现,小鼠慢性应激会下调海马中的表观遗传因子 HDAC2 和 SUV39H1。一系列后续分析,包括 ChIP 测定和 siRNA 介导的功能分析表明,应激释放的糖皮质激素在海马中累积增加了 Mkp-1 的表达,而增加的 Mkp-1 则削弱了 p-CREB 和 PPARγ,进而抑制了表观遗传因子 HDAC2 和 SUV39H1。此外,HDAC2 和 SUV39H1 通常会抑制 Mkp-1 的转录,因此 HDAC2 和 SUV39H1 的表达减少会增加 Mkp-1 的表达。因此,反复的应激会逐渐加强 Mkp-1 信号级联的恶性循环,从而促进抑郁行为。这些结果表明,包含 HDAC2/SUV39H1 调节的 Mkp-1 信号网络的海马应激适应系统决定了对慢性应激的易感性和抑郁行为的维持。