| Literature DB >> 34942116 |
Zhaofa Wu1, Kaikai He2, Yue Chen3, Hongyu Li4, Sunlei Pan5, Bohan Li2, Tingting Liu4, Fengxue Xi6, Fei Deng2, Huan Wang2, Jiulin Du4, Miao Jing3, Yulong Li7.
Abstract
The purinergic transmitter ATP (adenosine 5'-triphosphate) plays an essential role in both the central and peripheral nervous systems, and the ability to directly measure extracellular ATP in real time will increase our understanding of its physiological functions. Here, we developed a sensitive GPCR activation-based ATP sensor called GRABATP1.0, with a robust fluorescence response to extracellular ATP when expressed in several cell types. This sensor has sub-second kinetics, has ATP affinity in the range of tens of nanomolar, and can be used to localize ATP release with subcellular resolution. Using this sensor, we monitored ATP release under a variety of in vitro and in vivo conditions, including stimuli-induced and spontaneous ATP release in primary hippocampal cultures, injury-induced ATP release in a zebrafish model, and lipopolysaccharides-induced ATP-release events in individual astrocytes in the mouse cortex. Thus, the GRABATP1.0 sensor is a sensitive, versatile tool for monitoring ATP release and dynamics under both physiological and pathophysiological conditions.Entities:
Keywords: ATP; GPCR; GRAB; fluorescent sensors; genetically encoded; imaging; injury; neuroinflammation; purinergic signaling
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Year: 2021 PMID: 34942116 DOI: 10.1016/j.neuron.2021.11.027
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173