Evidence map›Paper›PMID 35566353›Full record

ArticleMolecules (Basel, Switzerland)2022

Establishment of a Cell Model for Dynamic Monitoring of Intracellular Calcium Concentration and High-Throughput Screening of P2Y2 Regulators.

Mingda Wu, Cheng Hu, Jingsong Liu, Chuannan Wu, Xueying Liu, Feng Hao, Wenliang Li

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. 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
0.1field-weighted citation impact, top 59% of its field
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, 2 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

Mingda WuCollege of Laboratory Medicine, Jilin Medical University, Jilin 132000, China.ORCID 0000-0002-1259-9298
Cheng HuCollege of Laboratory Medicine, Jilin Medical University, Jilin 132000, China.
Jingsong LiuDepartment of Thoracic Surgery, The Affiliated Hospital of Xuzhou Medical University, Xuzhou 221000, China.
Chuannan WuThe Municipal Hospital Affiliated to Xuzhou Medical University, Xuzhou 221000, China.
Xueying LiuSchool of Medical Technology, Beihua University, Jilin 132000, China.
Feng HaoCollege of Laboratory Medicine, Jilin Medical University, Jilin 132000, China.ORCID 0000-0002-2238-8654
Wenliang LiJilin Collaborative Innovation Center for Antibody Engineering, Jilin Medical University, Jilin 132000, China.
Jilin Medical University · CNXuzhou Medical College · CNBeihua University · CNYanbian University · CN

Funding

National Natural Science Foundation of China 81601234Science and Technology Project of Traditional Chinese Medicine of Jilin Province 2021092Starting fund for doctoral research of Jilin Medical College JYBS2021013lkthe grant of Jilin Province Development and Reform Commission 2021C039-3the Grant of Jilin Province Science & Technology Committee 20180101194JCthe Project of Jilin provincial Department of Education JJKH20220462KJthe Project of Jilin provincial Department of Education JJKH20220473SK
6 · The paper itself

Abstract

P2Y receptors are G-protein-coupled receptors (GPCRs) for extracellular nucleotides. The P2Y2 receptor subtype is expressed in a variety of cell types and plays an important role in physiological and pathophysiological processes such as inflammatory responses and neuropathic pain. Based on this, the P2Y2 has been identified as an important drug target. The specificity of current P2Y2 receptor modulators is relatively poor, and currently, specific and efficient P2Y2 receptor modulators and efficient screening strategies are lacking. In this study, a cell model based on calcium-activated chloride channels (CaCCs) was established that can detect changes in intracellular calcium concentrations and can be used to high-throughput screen for P2Y2 receptor-specific regulators. This screening strategy is suitable for screening of most G-protein-coupled receptor regulators that mediate increases in intracellular calcium signals. The cell model consists of three components that include the endogenously expressed P2Y2 receptor protein, the exogenously expressed calcium-activated chloride channel Anoctamin-1 (Ano1), and a yellow fluorescent protein mutant expressed within the cell that is highly sensitive to iodine ions. This model will allow for high-throughput screening of GPCR regulators that mediate increased intracellular calcium signaling using the calcium-activated transport of iodide ions by Ano1. We verified the ability of the model to detect intracellular calcium ion concentration using fluorescence quenching kinetic experiments by applying existing P2Y2 agonists and inhibitors to validate the screening function of the model, and we also evaluated the performance of the model in the context of high-throughput screening studies. The experimental results revealed that the model could sensitively detect intracellular calcium ion concentration changes and that the model was accurate in regard to detecting P2Y2 modulators. The resultant value of the Z-factor was 0.69, thus indicating that the model possesses good sensitivity and specificity.

Indexed as

CalciumHigh-Throughput Screening AssaysCalcium SignalingNucleotidesReceptors, Purinergic P2Y2CalciumNucleotidesReceptors, Purinergic P2Y2calcium concentrationGPCRshigh-throughput screeningP2Y2regulators

Identifiers

PMID35566353
PMCPMC9103248
OpenAlexW4229369109

What Socratic holds

Textmetadata
LicenceCC BY
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.