Author
Listed:
- Takaki Yahiro
(Oregon Health and Science University)
- Landon Bayless-Edwards
(Oregon Health and Science University)
- James A. Jones
(Oregon Health and Science University)
- Yizhou Zhuo
(Oregon Health and Science University)
- Lei Ma
(Oregon Health and Science University)
- Maozhen Qin
(Oregon Health and Science University)
- Tianyi Mao
(Oregon Health and Science University)
- Haining Zhong
(Oregon Health and Science University)
Abstract
Neuromodulators impose powerful control over brain function via their regulation of intracellular signaling through G-protein coupled receptors. In contrast to those of Gs and Gi pathways, in vivo imaging of the signaling events downstream of Gq-coupled receptors remains challenging. Here, we introduce CKAR3, a genetically encoded fluorescence lifetime sensor that reports the activity of protein kinase C (PKC), a major downstream effector of the Gq pathway. CKAR3 exhibits a lifetime dynamic range 5-fold larger than any existing PKC sensor. It specifically detects PKC phosphorylation with seconds kinetics without perturbing neuronal functions. In vivo two-photon lifetime imaging of CKAR3 reveals tonic PKC activity in cortical neurons. Animal locomotion elicits robust PKC activity in sparse neuronal ensembles in the motor cortex. Both basal and locomotion-elicited PKC activities are in part mediated by muscarinic acetylcholine receptors. Overall, CKAR3 enables interrogation of Gq signaling dynamics mediated by PKC in behaving animals.
Suggested Citation
Takaki Yahiro & Landon Bayless-Edwards & James A. Jones & Yizhou Zhuo & Lei Ma & Maozhen Qin & Tianyi Mao & Haining Zhong, 2025.
"A high-performance genetically encoded sensor for cellular imaging of PKC activity in vivo,"
Nature Communications, Nature, vol. 16(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-61729-7
DOI: 10.1038/s41467-025-61729-7
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