Evidence map›Paper›PMID 28303030›Full record

ArticleScientific reports2017

Formyl peptide receptors promotes neural differentiation in mouse neural stem cells by ROS generation and regulation of PI3K-AKT signaling.

Liang Zhang, Guan Wang, Xingxing Chen, Xin Xue, Qiaonan Guo, Mingyong Liu, Jianhua Zhao

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

45 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Therapeutic potential of WKYMVm in diseases.Frontiers in pharmacology · 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

7 authors at 3 institutions in 1 country.

Liang ZhangDepartment of Spine Surgery, Daping Hospital, Third Military Medical University, Chongqing, 400042, China.
Guan WangDepartment of Spine Surgery, Daping Hospital, Third Military Medical University, Chongqing, 400042, China.
Xingxing ChenDepartment of Spine Surgery, Daping Hospital, Third Military Medical University, Chongqing, 400042, China.
Xin XueDepartment of Spine Surgery, Daping Hospital, Third Military Medical University, Chongqing, 400042, China.
Qiaonan GuoDepartment of Pathology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Mingyong LiuDepartment of Spine Surgery, Daping Hospital, Third Military Medical University, Chongqing, 400042, China. mingyong_liu@163.com.
Jianhua ZhaoDepartment of Spine Surgery, Daping Hospital, Third Military Medical University, Chongqing, 400042, China. zhaojianhua1964@yahoo.com.
Army Medical University · CNDaping Hospital · CNXinqiao Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to determine whether formyl peptide receptors (FPRs) regulated the differentiation of neural stem cells (NSCs). FPRs promote the migration of NSCs both in vitro and in vivo. However, the role of FPRs during differentiation of NSCs is unknown. Analysis by Western blot showed significantly increased expression of FPR1 and FPR2 during differentiation of NSCs. The activation of FPRs promotes NSCs to differentiate into neurons with more primary neurites and branch points and longer neurites per cell. Meanwhile, this activation also inhibits the differentiation of NSC into astrocytes. This bidirectional effect can be inhibited by the FPRs-specific inhibitor. Moreover, it was found that the activation of FPRs increased the generation of reactive oxygen species (ROS) and phosphorylation of AKT in the NSCs, while N-acetylcysteine and LY294002 inhibited the FPRs-stimulated increase in ROS generation and AKT phosphorylation, and blocked the FPRs-stimulated neural differentiation into neurons. Therefore, FPRs-stimulated neural differentiation was mediated via ROS and PI3K-AKT signaling pathways. Collectively, the present findings provided a novel insight into the functional role of FPRs in neurogenesis, with important implications for its potential use as a candidate for treating brain or spinal cord injury.

Indexed as

NeurogenesisUp-RegulationAcetylcysteineAnimalsAstrocytesCell DifferentiationCell ProliferationCells, CulturedChromonesMiceMorpholinesNeural Stem CellsNeuronsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReactive Oxygen Species2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-oneAcetylcysteineChromonesformyl peptide receptor 2, mouseFpr1 protein, mouseMorpholinesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReactive Oxygen SpeciesReceptors, Formyl Peptide

Identifiers

PMID28303030
PMCPMC5428260
OpenAlexW2593666679

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.