Key Laboratory of Mental Health of the Ministry of Education, Guangdong-Hong Kong-Macao Greater Bay Area Center for Brain Science and Brain-Inspired Intelligence, Guangdong-Hong Kong Joint Laboratory for Psychiatric Disorders, Guangdong Province Key Laboratory of Psychiatric Disorders, Guangdong Basic Research Center of Excellence for Integrated Traditional and Western Medicine for Qingzhi Diseases, Department of Neurobiology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, 510515, China.
Microbiome Medicine Center, Department of Laboratory Medicine, Zhujiang Hospital, Southern Medical University, Guangzhou, 510260, China.
Adv Sci (Weinh). 2024 Nov;11(41):e2403389. doi: 10.1002/advs.202403389. Epub 2024 Sep 12.
Lysosomes are important cellular structures for human health as centers for recycling, signaling, metabolism and stress adaptation. However, the potential role of lysosomes in stress-related emotions has long been overlooked. Here, it is found that lysosomal morphology in astrocytes is altered in the medial prefrontal cortex (mPFC) of susceptible mice after chronic social defeat stress. A screen of lysosome-related genes revealed that the expression of the mucolipin 1 gene (Mcoln1; protein: mucolipin TRP channel 1) is decreased in susceptible mice and depressed patients. Astrocyte-specific knockout of mucolipin TRP channel 1 (TRPML1) induced depressive-like behaviors by inhibiting lysosomal exocytosis-mediated adenosine 5'-triphosphate (ATP) release. Furthermore, this stress response of astrocytic lysosomes is mediated by the transcription factor EB (TFEB), and overexpression of TRPML1 rescued depressive-like behaviors induced by astrocyte-specific knockout of TFEB. Collectively, these findings reveal a lysosomal stress-sensing signaling pathway contributing to the development of depression and identify the lysosome as a potential target organelle for antidepressants.
溶酶体是人类健康的重要细胞结构,作为回收、信号转导、代谢和应激适应的中心。然而,溶酶体在与应激相关的情绪中的潜在作用长期以来一直被忽视。在这里,研究人员发现,慢性社交挫败应激后,易感小鼠的内侧前额叶皮层(mPFC)中的星形胶质细胞中的溶酶体形态发生改变。溶酶体相关基因的筛选显示,易感小鼠和抑郁患者中粘脂素 1 基因(Mcoln1;蛋白:粘脂素 TRP 通道 1)的表达降低。星形胶质细胞特异性敲除粘脂素 TRP 通道 1(TRPML1)通过抑制溶酶体胞吐作用介导的三磷酸腺苷(ATP)释放,诱导出类似抑郁的行为。此外,星形胶质细胞溶酶体的这种应激反应是由转录因子 EB(TFEB)介导的,过表达 TRPML1 可挽救星形胶质细胞特异性敲除 TFEB 诱导的类似抑郁的行为。总的来说,这些发现揭示了一种溶酶体应激感应信号通路,有助于抑郁症的发展,并确定溶酶体作为抗抑郁药的潜在靶细胞器。