| Literature DB >> 30007419 |
Fangmiao Sun1, Jianzhi Zeng2, Miao Jing2, Jingheng Zhou3, Jiesi Feng2, Scott F Owen4, Yichen Luo5, Funing Li6, Huan Wang1, Takashi Yamaguchi7, Zihao Yong8, Yijing Gao7, Wanling Peng9, Lizhao Wang10, Siyu Zhang10, Jiulin Du6, Dayu Lin11, Min Xu9, Anatol C Kreitzer12, Guohong Cui3, Yulong Li13.
Abstract
Dopamine (DA) is a central monoamine neurotransmitter involved in many physiological and pathological processes. A longstanding yet largely unmet goal is to measure DA changes reliably and specifically with high spatiotemporal precision, particularly in animals executing complex behaviors. Here, we report the development of genetically encoded GPCR-activation-based-DA (GRABDA) sensors that enable these measurements. In response to extracellular DA, GRABDA sensors exhibit large fluorescence increases (ΔF/F0 ∼90%) with subcellular resolution, subsecond kinetics, nanomolar to submicromolar affinities, and excellent molecular specificity. GRABDA sensors can resolve a single-electrical-stimulus-evoked DA release in mouse brain slices and detect endogenous DA release in living flies, fish, and mice. In freely behaving mice, GRABDA sensors readily report optogenetically elicited nigrostriatal DA release and depict dynamic mesoaccumbens DA signaling during Pavlovian conditioning or during sexual behaviors. Thus, GRABDA sensors enable spatiotemporally precise measurements of DA dynamics in a variety of model organisms while exhibiting complex behaviors.Entities:
Keywords: GPCR; GRAB(DA); dopamine; sensor
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Year: 2018 PMID: 30007419 PMCID: PMC6092020 DOI: 10.1016/j.cell.2018.06.042
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582