Evidence map›Paper›PMID 24891524›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2014

Visualization of the pH-dependent dynamic distribution of G2A in living cells.

Wanjun Lan, Satoshi Yamaguchi, Teruyasu Yamamoto, Shinya Yamahira, Modong Tan, Naoka Murakami, Jingyan Zhang, Motonao Nakamura, Teruyuki Nagamune

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

9 authors at 2 institutions in 2 countries.

Wanjun LanDepartment of Chemistry and Biotechnology and State Key Laboratory of Bioreactor Engineering, Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, Shanghai, China.
Satoshi YamaguchiDepartment of Chemistry and Biotechnology and.
Teruyasu YamamotoDepartment of Chemistry and Biotechnology and.
Shinya YamahiraDepartment of Bioengineering, Graduate School of Engineering, and.
Modong TanDepartment of Chemistry and Biotechnology and.
Naoka MurakamiDepartment of Biochemistry and Molecular Biology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan; and.
Jingyan ZhangState Key Laboratory of Bioreactor Engineering, Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, Shanghai, China.
Motonao NakamuraDepartment of Biochemistry and Molecular Biology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan; and.
Teruyuki NagamuneDepartment of Chemistry and Biotechnology and Department of Bioengineering, Graduate School of Engineering, and nagamune@bioeng.t.u-tokyo.ac.jp.
The University of Tokyo · JPEast China University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G2A (from G2 accumulation) receptor is a member of the proton-sensing G-protein coupled receptor (GPCR) family and induces signal transduction events that regulate the cell cycle, proliferation, oncogenesis, and immunity. The mechanism by which G2A-mediated signal transduction is regulated by the extracellular pH remains unresolved. Here, we first visualize the pH-dependent G2A distribution change in living cells by a sortase A-mediated pulse labeling technology: the short-peptide tag-fused human G2A on human embryo kidney HEK293T cell surfaces was labeled with a small fluorescent dye in the presence of lysophosphatidylcholine, and the labeled G2A was chased at acidic and neutral pHs in real time by microscope time course observations. G2A internalization from cell surfaces into intracellular compartments was observed to be inhibited under acidic pH conditions, and this inhibition was relieved at neutral pH. Additionally, the internalized G2A was redistributed onto cell surfaces by jumping from a neutral to an acidic pH. From quantitative image analysis data, we conclude the amount of G2A on the cell surface was controlled by suppressing the G2A internalization rate by one-tenth in response to the extracellular acidic pH, and this acidic pH-induced G2A accumulation on cell surfaces may be explained by proton-induced dissociation of G2A from endocytic machinery.

Indexed as

Fluorescent Antibody TechniqueFluorescent DyesAminoacyltransferasesBacterial ProteinsCell MembraneCysteine EndopeptidasesHEK293 CellsHumansHydrogen-Ion ConcentrationImage Processing, Computer-AssistedLysophosphatidylcholinesMicroscopy, ConfocalModels, StatisticalPeptide FragmentsPhagocytosisProtein TransportAminoacyltransferasesBacterial ProteinsCysteine EndopeptidasesFluorescent DyesLysophosphatidylcholinesPeptide FragmentsReceptors, G-Protein-Coupledsortase AGPCRinternalizationpH dependencepulse labeling

Identifiers

PMID24891524
PMCPMC5395726
OpenAlexW2045572548

What OpenQuestion holds

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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 OpenQuestion graph.