Evidence map›Paper›PMID 29907159›Full record

ArticleJournal of neuroinflammation2018

JNK-mediated microglial DICER degradation potentiates inflammatory responses to induce dopaminergic neuron loss.

Qing Wang, Qian He, Yifei Chen, Wei Shao, Chao Yuan, Yizheng Wang

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Microglia as Therapeutic Target for Radiation-Induced Brain Injury.International journal of molecular sciences · 2022
    Review
  4. Review
  5. Article
  6. Review
  7. Dicer up-regulation by inhibition of specific proteolysis in differentiating monocytic cells.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  8. 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

6 authors at 1 institution in 1 country.

Qing WangCenter of Cognition and Brain Science, Beijing Institute of Medical Sciences, Beijing, 100000, People's Republic of China.
Qian HeCenter of Cognition and Brain Science, Beijing Institute of Medical Sciences, Beijing, 100000, People's Republic of China.
Yifei ChenCenter of Cognition and Brain Science, Beijing Institute of Medical Sciences, Beijing, 100000, People's Republic of China.
Wei ShaoCenter of Cognition and Brain Science, Beijing Institute of Medical Sciences, Beijing, 100000, People's Republic of China.
Chao YuanCenter of Cognition and Brain Science, Beijing Institute of Medical Sciences, Beijing, 100000, People's Republic of China.
Yizheng WangNational Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, 12 Middle Wulumuqi Road, Shanghai, 200040, People's Republic of China. yzwang@ion.ac.cn.
Fudan University · CN

Funding

Beijing Municipal Science and Technology Commission Z151100003915120Ministry of Science and Technology of the People's Republic of China 2015ZX09102005
6 · The paper itself

Abstract

backgroundAmplified inflammation is important for the progression of Parkinson's disease (PD). However, how this enhanced inflammation is regulated remains largely unknown. Deletion of DICER leads to progressive dopamine neuronal loss and induces gliosis. We hypothesized that the homeostasis of microglial DICER would be responsible for the amplified inflammation in the mouse model of PD.

methodsThe microglia or C57BL/6 mice were treated or injected with l-methyl-4-phenyl-l,2,3,6-tetrahydropyridine (MPTP) or 1-methyl-4-phenylpyridinium (MPP

resultsMicroglial DICER was phosphorylated at serine 1456 by c-jun N-terminal kinase (JNK) and downregulated in response to 1-methyl-4-phenylpyridinium (MPP

conclusionsJNK-mediated microglial DICER degradation potentiates inflammation to induce dopaminergic neuronal loss. Thus, preventing microglial DICER degradation could be a novel strategy for controlling neuroinflammation in PD.

Indexed as

1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineAnimalsAnimals, NewbornCells, CulturedCytokinesDEAD-box RNA HelicasesDisease Models, AnimalDopaminergic NeuronsEnzyme InhibitorsGene Expression RegulationImmunoprecipitationInflammationLipopolysaccharidesMAP Kinase Kinase 4MiceMice, Inbred C57BL1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineCytokinesDEAD-box RNA HelicasesDicer1 protein, mouseEnzyme InhibitorsLipopolysaccharidesMAP Kinase Kinase 4Ribonuclease IIITyrosine 3-MonooxygenaseDegradationDICERInflammationMicrogliaPhosphorylation

Identifiers

PMID29907159
PMCPMC6003208
OpenAlexW2808000886

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.