| Literature DB >> 30922875 |
Jiesi Feng1, Changmei Zhang2, Julieta E Lischinsky3, Miao Jing4, Jingheng Zhou5, Huan Wang6, Yajun Zhang7, Ao Dong1, Zhaofa Wu6, Hao Wu8, Weiyu Chen2, Peng Zhang9, Jing Zou10, S Andrew Hires10, J Julius Zhu11, Guohong Cui5, Dayu Lin12, Jiulin Du2, Yulong Li13.
Abstract
Norepinephrine (NE) is a key biogenic monoamine neurotransmitter involved in a wide range of physiological processes. However, its precise dynamics and regulation remain poorly characterized, in part due to limitations of available techniques for measuring NE in vivo. Here, we developed a family of GPCR activation-based NE (GRABNE) sensors with a 230% peak ΔF/F0 response to NE, good photostability, nanomolar-to-micromolar sensitivities, sub-second kinetics, and high specificity. Viral- or transgenic-mediated expression of GRABNE sensors was able to detect electrical-stimulation-evoked NE release in the locus coeruleus (LC) of mouse brain slices, looming-evoked NE release in the midbrain of live zebrafish, as well as optogenetically and behaviorally triggered NE release in the LC and hypothalamus of freely moving mice. Thus, GRABNE sensors are robust tools for rapid and specific monitoring of in vivo NE transmission in both physiological and pathological processes.Entities:
Keywords: GPCR; GRABNE; neurotransmitter; norepinephrine; sensor
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Year: 2019 PMID: 30922875 PMCID: PMC6533151 DOI: 10.1016/j.neuron.2019.02.037
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173