Evidence map›Paper›PMID 40606270›Full record

ReviewFrontiers in cellular neuroscience2025

Research progress on the mechanisms of endogenous neural stem cell differentiation in spinal cord injury repair.

Tianwei Wang, Qing Han, Shi Lv, Li-Ping Zhang, Hengrui Li, Jian Liu, Jinyi Kuang, Bao-Liang Sun, Jing-Yi Sun

Abstract readReview
In one paragraph

Review in Frontiers in cellular neuroscience, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. 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

9 authors.

Tianwei WangDepartment of Neurology, The Second Affiliated Hospital, Shandong First Medical University and Shandong Academy of Medical Sciences, Taian, China.
Qing HanDepartment of Neurology, The Second Affiliated Hospital, Shandong First Medical University and Shandong Academy of Medical Sciences, Taian, China.
Shi LvDepartment of Neurology, The Second Affiliated Hospital, Shandong First Medical University and Shandong Academy of Medical Sciences, Taian, China.
Li-Ping ZhangDepartment of Neurology, The Second Affiliated Hospital, Shandong First Medical University and Shandong Academy of Medical Sciences, Taian, China.
Hengrui LiDepartment of Neurology, The Second Affiliated Hospital, Shandong First Medical University and Shandong Academy of Medical Sciences, Taian, China.
Jian LiuDepartment of Neurology, The Second Affiliated Hospital, Shandong First Medical University and Shandong Academy of Medical Sciences, Taian, China.
Jinyi KuangDepartment of Neurology, The Second Affiliated Hospital, Shandong First Medical University and Shandong Academy of Medical Sciences, Taian, China.
Bao-Liang SunDepartment of Neurology, The Second Affiliated Hospital, Shandong First Medical University and Shandong Academy of Medical Sciences, Taian, China.
Jing-Yi SunDepartment of Spinal Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinal cord injury (SCI) is a devastating condition with limited self-repair capacity, resulting in long-term disabilities. Endogenous neural stem cells (eNSCs), which are present in the adult central nervous system (CNS), hold significant potential for repairing neural damage following SCI. These cells can proliferate, migrate to the injury site, and differentiate into various neural cell types, including neurons and glial cells. However, after SCI, eNSCs predominantly differentiate into astrocytes, with minimal neuronal differentiation, thereby hindering effective neural regeneration. This review summarizes the key mechanisms underlying the differentiation of eNSCs into neurons, focusing on the molecular signaling pathways that regulate their fate, including the Notch, Wnt/β-catenin, Sonic Hedgehog, and PI3K/Akt pathways. It also discusses the microenvironment's role, including factors such as hypoxia, extracellular matrix components, and inflammatory cytokines, which influence eNSCs differentiation. The review also highlights potential therapeutic strategies to enhance eNSCs differentiation into neurons, including biomaterials and multimodal approaches that combine pharmacological, physical, and tissue engineering techniques. Despite progress in understanding eNSCs biology and signaling mechanisms, challenges remain in optimizing therapeutic strategies for SCI repair. Future research should focus on overcoming these limitations, emphasizing refining treatment timing, drug delivery systems, and the development of personalized therapies to promote effective neural regeneration and functional recovery after SCI.

Indexed as

biomaterialsendogenous neural stem cellsneural differentiation mechanismsneural regenerationsignaling pathwaysspinal cord injury

Identifiers

PMID40606270
PMCPMC12213763

What Socratic 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 Socratic graph.