Evidence map›Paper›PMID 23539630›Full record

ArticleThe Journal of biological chemistry2013

Cannabinoid receptor 2 suppresses leukocyte inflammatory migration by modulating the JNK/c-Jun/Alox5 pathway.

Yi-Jie Liu, Hong-Bo Fan, Yi Jin, Chun-Guang Ren, Xiao-E Jia, Lei Wang, Yi Chen, Mei Dong, Kang-Yong Zhu, Zhi-Wei Dong and 5 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.0field-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

37 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
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  6. Observational
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  16. CB2 Agonist (AM1241) Improving Effect on Ovalbumin-Induced Asthma in Rats.Iranian journal of pharmaceutical research : IJPR · 2020
    Article
  17. Cannabinoids in Gynecological Diseases.Medical cannabis and cannabinoids · 2019
    Review
  18. Article
  19. Article
  20. 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

15 authors at 5 institutions in 2 countries.

Yi-Jie LiuState Key Laboratory for Medical Genomics, Shanghai Institute of Hematology, RuiJin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Hong-Bo Fan
Yi Jin
Chun-Guang Ren
Xiao-E Jia
Lei Wang
Yi Chen
Mei Dong
Kang-Yong Zhu
Zhi-Wei Dong
Bai-Xin Ye
Zhong Zhong
Min Deng
Ting Xi Liu
Ruibao Ren
Shanghai Institutes for Biological Sciences · CNShanghai Jiao Tong University · CNChinese Academy of Sciences · CNGlaxoSmithKline (China) · CNRuijin Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe role of cannabinoid receptor type 2 (Cnr2) in regulating immune function had been widely investigated, but the mechanism is not fully understood.

resultsCnr2 activation down-regulates 5-lipoxygenase (Alox5) expression by suppressing the JNK/c-Jun activation.

conclusionThe Cnr2-JNK-Alox5 axis modulates leukocyte inflammatory migration. SIGNIFICANCE: Linking two important regulators in leukocyte inflammatory migration and providing a potential therapeutic strategy for treating human inflammation-associated diseases. Inflammatory migration of immune cells is involved in many human diseases. Identification of molecular pathways and modulators controlling inflammatory migration could lead to therapeutic strategies for treating human inflammation-associated diseases. The role of cannabinoid receptor type 2 (Cnr2) in regulating immune function had been widely investigated, but the mechanism is not fully understood. Through a chemical genetic screen using a zebrafish model for leukocyte migration, we found that both an agonist of the Cnr2 and inhibitor of the 5-lipoxygenase (Alox5, encoded by alox5) inhibit leukocyte migration in response to acute injury. These agents have a similar effect on migration of human myeloid cells. Consistent with these results, we found that inactivation of Cnr2 by zinc finger nuclease-mediated mutagenesis enhances leukocyte migration, while inactivation of Alox5 blocks leukocyte migration. Further investigation indicates that there is a signaling link between Cnr2 and Alox5 and that alox5 is a target of c-Jun. Cnr2 activation down-regulates alox5 expression by suppressing the JNK/c-Jun activation. These studies demonstrate that Cnr2, JNK, and Alox5 constitute a pathway regulating leukocyte migration. The cooperative effect between the Cnr2 agonist and Alox5 inhibitor also provides a potential therapeutic strategy for treating human inflammation-associated diseases.

Indexed as

MAP Kinase Signaling SystemAnimalsAnimals, Genetically ModifiedArachidonate 5-LipoxygenaseBase SequenceCannabinoid Receptor AgonistsCell MovementGene Expression Regulation, EnzymologicGene Knockout TechniquesIndolesLeukocytesMolecular Sequence DataProtein BindingProto-Oncogene Proteins c-junReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2Arachidonate 5-LipoxygenaseCannabinoid Receptor AgonistsCnr2 protein, zebrafishIndolesJHW 015Proto-Oncogene Proteins c-junReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2Zebrafish ProteinsAlox5CB2Cell MigrationChemical BiologyChemical Genetic ScreenImmunologyLeukocyte MigrationSignal TransductionZebra Fish

Identifiers

PMID23539630
PMCPMC3650391
OpenAlexW2125103246

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.