Evidence map›Paper›PMID 40640216›Full record

ArticleNature communications2025

A high-performance genetically encoded sensor for cellular imaging of PKC activity in vivo.

Takaki Yahiro, Landon Bayless-Edwards, James A Jones, Yizhou Zhuo, Lei Ma, Maozhen Qin, Tianyi Mao, Haining Zhong

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Adenosine in the Brain: Recent Progress on Detection, Function, and Translation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Takaki Yahiro *Vollum Institute, Oregon Health and Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0001-7396-5442
Landon Bayless-Edwards *Vollum Institute, Oregon Health and Science University, Portland, OR, USA.ORCID http://orcid.org/0000-0001-8053-7673
James A JonesVollum Institute, Oregon Health and Science University, Portland, OR, USA.
Yizhou ZhuoVollum Institute, Oregon Health and Science University, Portland, OR, USA.
Lei MaVollum Institute, Oregon Health and Science University, Portland, OR, USA.
Maozhen QinVollum Institute, Oregon Health and Science University, Portland, OR, USA.
Tianyi MaoVollum Institute, Oregon Health and Science University, Portland, OR, USA. mao@ohsu.edu.ORCID http://orcid.org/0000-0002-3532-8319
Haining ZhongVollum Institute, Oregon Health and Science University, Portland, OR, USA. zhong@ohsu.edu.ORCID http://orcid.org/0000-0002-7109-4724

Funding

Multiplex imaging of neuronal activity and signaling dynamics underlying learning in discrete amygdala circuits of behaving mice.R01NS104944 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI LI, BO, MAO, TIANYI · 2018 to 2022
$5.0M
Genetic and physiological dissection of the circuit mechanisms in the striatum.R01NS081071 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI MAO, TIANYI · 2013 to 2023
$3.6M
Sensing and manipulating neuromodulatory signaling in vivoRF1MH130784 · NIMH · OREGON HEALTH & SCIENCE UNIVERSITY · PI ZHONG, HAINING · 2023 to 2023
$2.6M
Neuromodulation in the striatumR01NS127013 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI Haining Zhong · 2022 to 2026
$1.9M
Intracellular signaling mechanisms underlying opioid modulation of painF30DA057838 · NIDA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Landon Bayless-Edwards · 2023 to 2026
$203k
NIDA NIH HHS F30 DA057838NIMH NIH HHS RF1 MH130784NINDS NIH HHS R01 NS081071NINDS NIH HHS R01 NS104944NINDS NIH HHS R01 NS127013U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) RF1MH130784U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS081071U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS104944U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS127013U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse (NIDA) F30DA057838
6 · The paper itself

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.

Indexed as

Biosensing TechniquesProtein Kinase CAnimalsGTP-Binding Protein alpha Subunits, Gq-G11HEK293 CellsHumansLocomotionMaleMiceMotor CortexNeuronsPhosphorylationReceptor, Muscarinic M3Signal TransductionGTP-Binding Protein alpha Subunits, Gq-G11Protein Kinase CReceptor, Muscarinic M3

Identifiers

PMID40640216
PMCPMC12246085

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.