Evidence map›Paper›PMID 35429110›Full record

ArticleJournal of cellular and molecular medicine2022

MiR-130a-3p regulates neural stem cell differentiation in vitro by targeting Acsl4.

Wen Li, Bo-Quan Shan, He-Yan Zhao, Hui He, Mei-Ling Tian, Xiang Cheng, Jian-Bing Qin, Guo-Hua Jin

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. MicroRNAs and synaptic dysfunction in Parkinson's disease.Molecular therapy. Nucleic acids · 2025
    Review
  5. Article
  6. Article
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  8. Review
  9. Article
  10. Review
  11. The Role of Epigenetics in Neuroinflammatory-Driven Diseases.International journal of molecular sciences · 2022
    Review
  12. 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

8 authors at 1 institution in 1 country.

Wen LiDepartment of Human Anatomy, Institute of Neurobiology, Nantong University, Nantong, China.ORCID 0000-0003-2402-6769
Bo-Quan ShanDepartment of Human Anatomy, Institute of Neurobiology, Nantong University, Nantong, China.
He-Yan ZhaoDepartment of Human Anatomy, Institute of Neurobiology, Nantong University, Nantong, China.
Hui HeDepartment of Human Anatomy, Institute of Neurobiology, Nantong University, Nantong, China.
Mei-Ling TianDepartment of Human Anatomy, Institute of Neurobiology, Nantong University, Nantong, China.
Xiang ChengDepartment of Human Anatomy, Institute of Neurobiology, Nantong University, Nantong, China.
Jian-Bing QinDepartment of Human Anatomy, Institute of Neurobiology, Nantong University, Nantong, China.
Guo-Hua JinDepartment of Human Anatomy, Institute of Neurobiology, Nantong University, Nantong, China.
Ministry of Education of the People's Republic of China · CN

Funding

Graduate Scientific Research Innovation Program of Jiangsu Province KYCX19 2066Priority Academic Program Development of Jiangsu Higher Education Institutions 03081023The Science and Technology Program of Nantong City JC2020024
6 · The paper itself

Abstract

In the adult mammalian brain, neural stem cells (NSCs) are the precursor cells of neurons that contribute to nervous system development, regeneration, and repair. MicroRNAs (miRNAs) are small non-coding RNAs that regulate cell fate determination and differentiation by negatively regulating gene expression. Here, we identified a post-transcriptional mechanism, centred around miR-130a-3p that regulated NSC differentiation. Importantly, overexpressing miR-130a-3p promoted NSC differentiation into neurons, whereas inhibiting miR-130a-3p function reduced the number of neurons. Then, the quantitative PCR, Western blot and dual-luciferase reporter assays showed that miR-130a-3p negatively regulated acyl-CoA synthetase long-chain family member 4 (Acsl4) expression. Additionally, inhibition of Acsl4 promoted NSC differentiation into neurons, whereas silencing miR-130a-3p partially suppressed the neuronal differentiation induced by inhibiting Acsl4. Furthermore, overexpressing miR-130a-3p or inhibiting Acsl4 increased the levels of p-AKT, p-GSK-3β and PI3K. In conclusion, our results suggested that miR-130a-3p targeted Acsl4 to promote neuronal differentiation of NSCs via regulating the Akt/PI3K pathway. These findings may help to develop strategies for stem cell-mediated treatment for central nervous system diseases.

Indexed as

MicroRNAsNeural Stem CellsAnimalsCell DifferentiationGlycogen Synthase Kinase 3 betaMammalsNervous SystemPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktGlycogen Synthase Kinase 3 betaMicroRNAsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktAcsl4Akt/PI3K signalling pathwaydifferentiationMiR-130a-3pneural stem cells

Identifiers

PMID35429110
PMCPMC9077303
OpenAlexW4223999356

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.