Evidence map›Paper›PMID 11245682›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2001

Extracellular ATP or ADP induce chemotaxis of cultured microglia through Gi/o-coupled P2Y receptors.

S Honda, Y Sasaki, K Ohsawa, Y Imai, Y Nakamura, K Inoue, S Kohsaka

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 234 papers.

0numbers the graph read from it
0cells of the map it votes in
234citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

234 citing papers in PubMed, 569 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Revisiting the critical roles of reactive microglia in traumatic brain injury.International journal of surgery (London, England) · 2025
    Review
  9. The Arp2/3 complex is required forbioRxiv : the preprint server for biology · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. ER and SOCE CaCell calcium · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. ER and SOCE CabioRxiv : the preprint server for biology · 2024
    Article
  18. Review
  19. Microglial Regulation of Sleep and Wakefulness.Advances in neurobiology · 2024
    Review
  20. Unraveling the enigma: housekeeping geneFrontiers in psychiatry · 2024
    Article

174 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

S HondaDepartment of Neurochemistry, National Institute of Neuroscience, 4-1-1 Ogawa-higashi, Kodaira, Tokyo 187-8502, Japan.
Y Sasaki
K Ohsawa
Y Imai
Y Nakamura
K Inoue
S Kohsaka
National Center of Neurology and Psychiatry · JPNational Institute of Health Sciences · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The initial microglial responses that occur after brain injury and in various neurological diseases are characterized by microglial accumulation in the affected sites of brain that results from the migration and proliferation of these cells. The early-phase signal responsible for this accumulation is likely to be transduced by rapidly diffusible factors. In this study, the possibility of ATP released from injured neurons and nerve terminals affecting cell motility was determined in rat primary cultured microglia. Extracellular ATP and ADP induced membrane ruffling and markedly enhanced chemokinesis in Boyden chamber assay. Further analyses using the Dunn chemotaxis chamber assay, which allows direct observation of cell movement, revealed that both ATP and ADP induced chemotaxis of microglia. The elimination of extracellular calcium or treatment with pyridoxalphosphate-6-azophenyl-2',4'-disulphonic acid, suramin, or adenosine-3'-phosphate-5'-phosphosulfate did not inhibit ATP- or ADP-induced membrane ruffling, whereas AR-C69931MX or pertussis toxin treatments clearly did so. As an intracellular signaling molecule underlying these phenomena, the small G-protein Rac was activated by ATP and ADP stimulation, and its activation was also inhibited by pretreatment with pertussis toxin. These results strongly suggest that membrane ruffling and chemotaxis of microglia induced by ATP or ADP are mediated by G(i/o)-coupled P2Y receptors.

Indexed as

Adenosine DiphosphateAdenosine MonophosphateAdenosine TriphosphateAnimalsCell MembraneCells, CulturedChemotaxisDiffusion Chambers, CultureExtracellular SpaceGTP-Binding Protein alpha Subunits, Gi-GoGTP-Binding ProteinsHeterotrimeric GTP-Binding ProteinsMicrogliaPertussis Toxinrac GTP-Binding ProteinsRatsAdenosine DiphosphateAdenosine MonophosphateAdenosine TriphosphatecangrelorGTP-Binding Protein alpha Subunits, Gi-GoGTP-Binding ProteinsHeterotrimeric GTP-Binding ProteinsPertussis Toxinrac GTP-Binding ProteinsReceptors, Purinergic P2Virulence Factors, Bordetella

Identifiers

PMID11245682
PMCPMC6762617
OpenAlexW1947551305

What OpenQuestion holds

Textmetadata
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.