Evidence map›Paper›PMID 29116599›Full record

ArticleCell biochemistry and biophysics2018

The Class-A GPCR Dopamine D2 Receptor Forms Transient Dimers Stabilized by Agonists: Detection by Single-Molecule Tracking.

Rinshi S Kasai, Shuichi V Ito, Ryo M Awane, Takahiro K Fujiwara, Akihiro Kusumi

Open access · hybridAbstract read
In one paragraph

Article in Cell biochemistry and biophysics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

48 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
  2. Article
  3. FDA Drug Repurposing Uncovers Modulators of Dopamine DJournal of medicinal chemistry · 2025
    Article
  4. Article
  5. Stabilized DNature communications · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Antiparallel dimer structure of CELSR cadherin in solution revealed by high-speed atomic force microscopy.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  18. The World of GPCR dimers - Mapping dopamine receptor DComputational and structural biotechnology journal · 2023
    Article
  19. Choosing the Probe for Single-Molecule Fluorescence Microscopy.International journal of molecular sciences · 2022
    Review
  20. 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

5 authors at 1 institution in 1 country.

Rinshi S KasaiInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, 606-8507, Japan.
Shuichi V ItoInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, 606-8507, Japan.
Ryo M AwaneInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, 606-8507, Japan.
Takahiro K FujiwaraCenter for Meso-Bio Single-Molecule Imaging (CeMI), Institute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University, Kyoto, 606-8507, Japan.
Akihiro KusumiInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, 606-8507, Japan. akihiro.kusumi@OIST.jp.
Kyoto University · JP

Funding

Core Research for Evolutional Science and Technology JPMJCR14W2Japan Society for the Promotion of Science 15H01212Japan Society for the Promotion of Science 16H04775Japan Society for the Promotion of Science 16H06386Japan Society for the Promotion of Science 17K07333Japan Society for the Promotion of Science 24115511Japan Society for the Promotion of Science 24247029Japan Society for the Promotion of Science 26115707Japan Society for the Promotion of Science 26870292
6 · The paper itself

Abstract

Whether class-A G-protein coupled receptors (GPCRs) exist and work as monomers or dimers has drawn extensive attention. A class-A GPCR dopamine D2 receptor (D2R) is involved in many physiological and pathological processes and diseases, indicating its critical role in proper functioning of neuronal circuits. In particular, D2R homodimers might play key roles in schizophrenia development and amphetamine-induced psychosis. Here, using single-molecule imaging, we directly tracked single D2R molecules in the plasma membrane at a physiological temperature of 37 °C, and unequivocally determined that D2R forms transient dimers with a lifetime of 68 ms in its resting state. Agonist addition prolonged the dimer lifetime by a factor of ~1.5, suggesting the possibility that transient dimers might be involved in signaling.

Indexed as

AnimalsCell MembraneCHO CellsCricetinaeCricetulusDiffusionDimerizationFluorescent DyesHalf-LifeHumansPhotobleachingReceptors, Dopamine D2DRD2 protein, humanFluorescent DyesReceptors, Dopamine D2Cultured cellDimerizationDopamine receptorG protein-coupled receptor (GPCR)Plasma membraneSingle-molecule biophysics

Identifiers

PMID29116599
PMCPMC5913388
OpenAlexW2767999265

What OpenQuestion 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 OpenQuestion graph.