Abstract
AbstractcAMP is a universal second messenger regulated by various upstream pathways including Ca2+ and G-protein-coupled receptors (GPCRs). To decipher in vivo cAMP dynamics, we rationally designed cAMPinG1, a sensitive genetically encoded green cAMP indicator that outperformed its predecessors in both dynamic range and cAMP affinity. Two-photon cAMPinG1 imaging detected cAMP transients in the somata and dendritic spines of neurons in the mouse visual cortex on the order of tens of seconds. In addition, multicolor imaging with a sensitive red Ca2+ indicator RCaMP3 allowed simultaneous measurement of population patterns in Ca2+ and cAMP in hundreds of neurons. We found Ca2+-related cAMP responses that represented specific information, such as direction selectivity in vision and locomotion, as well as GPCR-related cAMP responses. Overall, our multicolor suite will facilitate analysis of the interaction between the Ca2+, GPCR and cAMP signaling at single-cell resolution both in vitro and in vivo.
Funder
MEXT | JST | Precursory Research for Embryonic Science and Technology
Japan Agency for Medical Research and Development
MEXT | Japan Society for the Promotion of Science
Japan Society for the Promotion of Science London
Inamori Foundation
Takeda Science Foundation
Tokyo Biochemical Research Foundation
Brain Science Foundation
Konica Minolta Imaging Science Foundation
Mochida Memorial Foundation for Medical and Pharmaceutical Research
KOSÉ Cosmetology Research Foundation
ACT-X-JST
MEXT | RIKEN
MEXT | JST | Core Research for Evolutional Science and Technology
Publisher
Springer Science and Business Media LLC
Cited by
3 articles.
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