Department of Neurology, Huadong Hospital, Fudan University, 221 West Yan An Road, Shanghai, 200040, China.
Department of Neurology, Huadong Hospital, Fudan University, 221 West Yan An Road, Shanghai, 200040, China.
Behav Brain Res. 2021 May 21;406:113227. doi: 10.1016/j.bbr.2021.113227. Epub 2021 Mar 5.
Major depressive disorders (MDD) is one of the most common mental illness in the world. Recently, brain mA /m (fat mass- and obesity-associated gene Fto) was found that exerted an important role in regulating gene expression involved in stress related depression. However, the potential mechanism of Fto on depression still remains elusive. This study investigated the role of Fto and its downstream signaling pathway in hippocampus on chronic restraint stress induced depressive-like behaviors.
C57BL/6 mice weighing 20-22 g were randomly divided into 4 groups (Control, Control + Fto-ov, Stress, Stress + Fto-ov). Mice were exposed to chronic restraint stress for 3 consecutive weeks to induce depression model. Mice in the Fto-ov groups were stereotaxic injected with Recombinant Adeno-associated Virus lentivirus (Fto) in hippocampus followed by stress procedure. Depressive-like behaviors were detected after stress procedure. Western blot was used to test hippocampal Fto, p-CaMKII and p-CREB expression. Post synaptic density protein 95 (PSD95) and synaptophysin levels were detected by PCR. Golgi-Cox staining was used to appraise dendritic spine density and branches. Synaptic morphology in hippocampus was determined by electron microscopy.
We demonstrated that chronic restraint stress induced depressive-like behaviors, decreased protein expression of Fto, p-CaMKII and p-CREB, reduced levels of synaptic plasticity markers (synaptophysin and PSD95) in hippocampus. Moreover, chronic restraint stress led to synaptic morphology alterations (reduced dendritic spine density and number of branches; thinned postsynaptic density). However, these molecules changes and morphology alterations were reversed by stereotaxic injected recombinant adeno-associated Fto-overexpression virus in hippocampus.
This study found that the modulation of Fto on CaMKII/CREB signaling pathway plays a key role in hippocampal synaptic plasticity, and then ameliorated chronic restraint stress induced depressive-like behaviors.
重度抑郁症(MDD)是世界上最常见的精神疾病之一。最近,发现大脑 mA/m(肥胖相关基因 Fto)在调节与应激相关的抑郁相关基因表达中发挥着重要作用。然而,Fto 对抑郁的潜在机制仍不清楚。本研究探讨了 Fto 及其下游信号通路在海马体中对慢性束缚应激诱导的抑郁样行为的作用。
体重 20-22 克的 C57BL/6 小鼠随机分为 4 组(对照组、对照组+Fto-ov、应激组、应激组+Fto-ov)。连续 3 周对小鼠进行慢性束缚应激以诱导抑郁模型。Fto-ov 组小鼠立体定向注射重组腺相关病毒慢病毒(Fto)至海马体,然后进行应激程序。应激程序后检测抑郁样行为。Western blot 检测海马体 Fto、p-CaMKII 和 p-CREB 表达。通过 PCR 检测突触后密度蛋白 95(PSD95)和突触小体蛋白水平。高尔基-考克斯染色评估树突棘密度和分支。电子显微镜观察海马突触形态。
我们发现慢性束缚应激诱导了抑郁样行为,降低了海马体 Fto、p-CaMKII 和 p-CREB 的蛋白表达,降低了突触可塑性标志物(突触小体蛋白和 PSD95)的水平。此外,慢性束缚应激导致了突触形态的改变(减少了树突棘密度和分支数量;突触后密度变薄)。然而,这些分子变化和形态改变可以通过立体定向注射重组腺相关 Fto 过表达病毒在海马体中得到逆转。
本研究发现 Fto 对 CaMKII/CREB 信号通路的调节在海马体突触可塑性中起着关键作用,从而改善了慢性束缚应激诱导的抑郁样行为。