Li Wei-Peng, Liu Gui-Yu, Wang Shi-Yun, Hu Jiao, Ji Wen-Juan, Zhu Jun-Ming, Chang Qing-Yu, Li Tian-Yi, Wei Guo-Rong, Shang Jian-Qing, Li Hong-Zhan, Peng Fu-Hua, Zhao Yun-Yan, Su Xiao-Hong, Xie Wei
Department of Neurology, Southern Medical University Hospital of Integrated Traditional Chinese and Western Medicine, Southern Medical University, Guangzhou 510317, China.
School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, China.
Research (Wash D C). 2025 Aug 7;8:0818. doi: 10.34133/research.0818. eCollection 2025.
Chronic stress exposure is a potent risk factor for anxiety, disrupting adaptive responses and increasing vulnerability. Astrocytes, as essential regulators of synaptic function and neuroimmune homeostasis, are implicated in mood regulation and neuropsychiatric pathogenesis. However, the precise molecular mechanisms of astrocytes involved in stress-induced anxiety remain poorly understood. In this study, we reveal a pivotal role of astrocytic brain-derived neurotrophic factor (BDNF) in modulating anxiety sensitivity through coordinated regulation with hippocampal CA1 neurons. Chronic restraint stress induces anxiety-like behaviors and disrupts presynaptic glutamatergic transmission in hippocampal CA1 neurons, with astrocytes potentially playing a central regulatory role in a Ca-dependent manner. Pharmacological manipulation confirms the involvement of BDNF/TrkB signaling, while knockdown of astrocytic BDNF further impairs synaptic function and exacerbates stress-induced anxiety. Transcriptomic analysis suggests interferon-related signaling pathways as potential downstream effectors, amplifying anxiety sensitivity through altered astrocytic activation and neuroimmune dynamics. Our study provides critical mechanistic insights into astrocytic regulation of anxiety sensitivity and highlights astrocytic BDNF as a promising therapeutic target for stress-related anxiety disorders.
长期暴露于应激是焦虑的一个重要风险因素,它会破坏适应性反应并增加易感性。星形胶质细胞作为突触功能和神经免疫稳态的重要调节因子,参与情绪调节和神经精神疾病的发病机制。然而,星形胶质细胞参与应激诱导焦虑的精确分子机制仍知之甚少。在本研究中,我们揭示了星形胶质细胞源性脑源性神经营养因子(BDNF)在通过与海马CA1神经元协同调节来调节焦虑敏感性方面的关键作用。慢性束缚应激诱导焦虑样行为,并破坏海马CA1神经元的突触前谷氨酸能传递,星形胶质细胞可能以钙依赖方式发挥核心调节作用。药理学操作证实了BDNF/TrkB信号通路的参与,而敲低星形胶质细胞BDNF会进一步损害突触功能并加剧应激诱导的焦虑。转录组分析表明干扰素相关信号通路是潜在的下游效应器,通过改变星形胶质细胞激活和神经免疫动态来放大焦虑敏感性。我们的研究为星形胶质细胞对焦虑敏感性的调节提供了关键的机制见解,并强调星形胶质细胞BDNF作为应激相关焦虑症的一个有前景的治疗靶点。