Evidence map›Paper›PMID 28780733›Full record

ArticleNeurochemical research2017

Brain-Derived Neurotrophic Factor Increases Synaptic Protein Levels via the MAPK/Erk Signaling Pathway and Nrf2/Trx Axis Following the Transplantation of Neural Stem Cells in a Rat Model of Traumatic Brain Injury.

Tao Chen, Yu Wu, Yuzi Wang, Jigao Zhu, Haiying Chu, Li Kong, Liangwei Yin, Haiying Ma

Abstract read
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In one paragraph

Article in Neurochemical research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
2.6field-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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Article
  6. Review
  7. Article
  8. Article
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  10. Article
  11. Review
  12. Article
  13. Potential Neuroprotective Role of Neurotrophin in Traumatic Brain Injury.CNS & neurological disorders drug targets · 2024
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Differential contribution of TrkB and p75Frontiers in molecular neuroscience · 2023
    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

8 authors at 2 institutions in 1 country.

Tao ChenDepartment of Neurosurgery, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, China.
Yu WuDepartment of Histology and Embryology, Dalian Medical University, Dalian, 116044, China.
Yuzi WangDepartment of Histology and Embryology, Dalian Medical University, Dalian, 116044, China.
Jigao ZhuDepartment of Histology and Embryology, Dalian Medical University, Dalian, 116044, China.
Haiying ChuDepartment of Histology and Embryology, Dalian Medical University, Dalian, 116044, China.
Li KongDepartment of Histology and Embryology, Dalian Medical University, Dalian, 116044, China.
Liangwei YinDepartment of Oncology, Dalian Central Hospital, Dalian, 116033, Liaoning, China. lwyin2008@163.com.
Haiying MaDepartment of Histology and Embryology, Dalian Medical University, Dalian, 116044, China. hyma20060602@aliyun.com.
Dalian Medical University · CNDalian Municipal Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain-derived neurotrophic factor (BDNF) plays an important role in promoting the growth, differentiation, survival and synaptic stability of neurons. Presently, the transplantation of neural stem cells (NSCs) is known to induce neural repair to some extent after injury or disease. In this study, to investigate whether NSCs genetically modified to encode the BDNF gene (BDNF/NSCs) would further enhance synaptogenesis, BDNF/NSCs or naive NSCs were directly engrafted into lesions in a rat model of traumatic brain injury (TBI). Immunohistochemistry, western blotting and RT-PCR were performed to detect synaptic proteins, BDNF-TrkB and its downstream signaling pathways, at 1, 2, 3 or 4 weeks after transplantation. Our results showed that BDNF significantly increased the expression levels of the TrkB receptor gene and the phosphorylation of the TrkB protein in the lesions. The expression levels of Ras, phosphorylated Erk1/2 and postsynaptic density protein-95 were elevated in the BDNF/NSCs-transplanted groups compared with those in the NSCs-transplanted groups throughout the experimental period. Moreover, the nuclear factor (erythroid-derived 2)-like 2/Thioredoxin (Nrf2/Trx) axis, which is a specific therapeutic target for the treatment of injury or cell death, was upregulated by BDNF overexpression. Therefore, we determined that the increased synaptic proteins level implicated in synaptogenesis might be associated with the activation of the MAPK/Erk1/2 signaling pathway and the upregulation of the antioxidant agent Trx modified by BDNF-TrkB following the BDNF/NSCs transplantation after TBI.

Indexed as

AnimalsBrain-Derived Neurotrophic FactorBrain Injuries, TraumaticDisease Models, AnimalEmbryonic Stem CellsMaleMAP Kinase Signaling SystemMitogen-Activated Protein Kinase KinasesNeural Stem CellsNF-E2-Related Factor 2RatsRats, WistarStem Cell TransplantationSynapsesThioredoxinsBrain-Derived Neurotrophic FactorMitogen-Activated Protein Kinase KinasesNfe2l2 protein, ratNF-E2-Related Factor 2ThioredoxinsTxn1 protein, ratBrain-derived neurotrophic factorDifferentiationMAPK/ErkPSD-95SynaptogenesisThioredoxinTransplantationTraumatic brain injuryTrkB

Identifiers

PMID28780733
OpenAlexW2743076159

What Socratic 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 Socratic graph.