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Publication : Astrocyte-mediated regulation of BLA(WFS1) neurons alleviates risk-assessment deficits in DISC1-N mice.

First Author  Zhou X Year  2024
Journal  Neuron PubMed ID  38642554
Mgi Jnum  J:348662 Mgi Id  MGI:7639615
Doi  10.1016/j.neuron.2024.03.028 Citation  Zhou X, et al. (2024) Astrocyte-mediated regulation of BLA(WFS1) neurons alleviates risk-assessment deficits in DISC1-N mice. Neuron
abstractText  Assessing and responding to threats is vital in everyday life. Unfortunately, many mental illnesses involve impaired risk assessment, affecting patients, families, and society. The brain processes behind these behaviors are not well understood. We developed a transgenic mouse model (disrupted-in-schizophrenia 1 [DISC1]-N) with a disrupted avoidance response in risky settings. Our study utilized single-nucleus RNA sequencing and path-clamp coupling with real-time RT-PCR to uncover a previously undescribed group of glutamatergic neurons in the basolateral amygdala (BLA) marked by Wolfram syndrome 1 (WFS1) expression, whose activity is modulated by adjacent astrocytes. These neurons in DISC1-N mice exhibited diminished firing ability and impaired communication with the astrocytes. Remarkably, optogenetic activation of these astrocytes reinstated neuronal excitability via D-serine acting on BLA(WFS1) neurons' NMDA receptors, leading to improved risk-assessment behavior in the DISC1-N mice. Our findings point to BLA astrocytes as a promising target for treating risk-assessment dysfunctions in mental disorders.
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