Lateral habenula IL-10 controls GABA A receptor trafficking and modulates depression susceptibility after maternal separation

• Published in: Brain, behavior, and immunity Vol. 122; p. 122
• Main Authors: Ding, Ruxuan, Tang, Ying, Cao, Guoxin, Mai, Yunlin, Fu, Yixin, Ren, Zhiheng, Li, Wenfu, Hou, Jiawei, Sun, Shizhu, Chen, Bingqing, Han, Xiaojiao, He, Zelei, Ye, Jiang-Hong, Zhou, Lihua, Fu, Rao
• Format: Journal Article
• Language: English
• Published: Netherlands 01.11.2024
• Subjects: Animals; Cytokines - metabolism; Depression - metabolism; Disease Susceptibility - metabolism; Female; Habenula - metabolism; Interleukin-10 - metabolism; Male; Maternal Deprivation; Mice; Mice, Inbred C57BL; Neurons - metabolism; Phosphatidylinositol 3-Kinases - metabolism; Protein Transport - physiology; Receptors, GABA-A - metabolism; Signal Transduction - physiology; Depression susceptibility; Lateral habenula; Maternal separation; GABA(A) receptor; Gephyrin; Interlukin-10
• ISSN: 1090-2139

Maternal separation (MS), a form of early life adversity, increases the risk of psychiatric disorders in adulthood by intricately linking cytokines and mood-regulating brain circuits. The Lateral Habenula (LHb) encodes aversive experiences, contributes to negative moods, and is pivotal in depression development. However, the precise impact of MS on LHb cytokine signaling and synaptic plasticity remains unclear. We reported that adolescent MS offspring mice displayed susceptibility to depression behavioral phylotypes, with neuronal hyperactivity and an imbalance in pro-inflammatory and anti-inflammatory cytokines in the LHb. Moreover, the decreased IL-10 level negatively correlated with depressive-like behaviors in susceptible mice. Functionally, LHb IL-10 overexpression restored decreased levels of PI3K, phosphorylated AKT (pAKT), gephyrin, and membrane GABA receptor proteins while reducing abnormally elevated GSK3β and Fos expression, rescuing the MS-induced depression. Conversely, LHb neuronal IL-10 receptor knockdown in naive mice increased Fos expression and elicited depression-like symptoms, potentially through impaired membrane GABA receptor trafficking by suppressing the PI3K/pAKT/gephyrin cascades. Hence, this work establishes a mechanism by which MS promotes susceptibility to adolescent depression by impeding the critical role of IL-10 signaling on neuronal GABA receptor function.