Improved green and red GRAB sensors for monitoring spatiotemporal serotonin release in vivo

The serotonergic system plays important roles in both physiological and pathological processes, and is a therapeutic target for many psychiatric disorders. Although several genetically encoded GFP-based serotonin (5-HT) sensors were recently developed, their sensitivities and spectral profiles are r...

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Veröffentlicht in:Nature methods 2024-04, Vol.21 (4), p.692-702
Hauptverfasser: Deng, Fei, Wan, Jinxia, Li, Guochuan, Dong, Hui, Xia, Xiju, Wang, Yipan, Li, Xuelin, Zhuang, Chaowei, Zheng, Yu, Liu, Laixin, Yan, Yuqi, Feng, Jiesi, Zhao, Yulin, Xie, Hao, Li, Yulong
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Sprache:eng
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Zusammenfassung:The serotonergic system plays important roles in both physiological and pathological processes, and is a therapeutic target for many psychiatric disorders. Although several genetically encoded GFP-based serotonin (5-HT) sensors were recently developed, their sensitivities and spectral profiles are relatively limited. To overcome these limitations, we optimized green fluorescent G-protein-coupled receptor (GPCR)-activation-based 5-HT (GRAB 5-HT ) sensors and developed a red fluorescent GRAB 5-HT sensor. These sensors exhibit excellent cell surface trafficking and high specificity, sensitivity and spatiotemporal resolution, making them suitable for monitoring 5-HT dynamics in vivo. Besides recording subcortical 5-HT release in freely moving mice, we observed both uniform and gradient 5-HT release in the mouse dorsal cortex with mesoscopic imaging. Finally, we performed dual-color imaging and observed seizure-induced waves of 5-HT release throughout the cortex following calcium and endocannabinoid waves. In summary, these 5-HT sensors can offer valuable insights regarding the serotonergic system in both health and disease. Deng et al. expand the toolbox of neurotransmitter sensors with high-sensitivity green and red genetically encoded serotonin sensors. These are suitable for in vivo applications, as demonstrated in a variety of applications in mice.
ISSN:1548-7091
1548-7105
1548-7105
DOI:10.1038/s41592-024-02188-8