A multicolor suite for deciphering population coding of calcium and cAMP in vivo

Tatsushi Yokoyama(Kyoto University), Satoshi Manita(University of Yamanashi), Hiroyuki Uwamori(RIKEN Center for Brain Science), Mio Tajiri(The University of Tokyo), Itaru Imayoshi(Kyoto University), Sho Yagishita(The University of Tokyo), Masanori Murayama(RIKEN Center for Brain Science), K. Kitamura(University of Yamanashi), Masayuki Sakamoto(Kyoto University)
Nature Methods
March 21, 2024
Cited by 38Open Access
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Abstract

Abstract cAMP is a universal second messenger regulated by various upstream pathways including Ca 2+ 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 Ca 2+ indicator RCaMP3 allowed simultaneous measurement of population patterns in Ca 2+ and cAMP in hundreds of neurons. We found Ca 2+ -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 Ca 2+ , GPCR and cAMP signaling at single-cell resolution both in vitro and in vivo.


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