Evidence map›Paper›PMID 38995011›Full record

ArticleCells2024

Regeneration of Propriospinal Axons in Rat Transected Spinal Cord Injury through a Growth-Promoting Pathway Constructed by Schwann Cells Overexpressing GDNF.

Xiaolong Du, Shengqi Zhang, Aytak Khabbaz, Kristen Lynn Cohen, Yihong Zhang, Samhita Chakraborty, George M Smith, Hongxing Wang, Amol P Yadav, Naikui Liu and 1 more

Abstract read
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Biomaterials and cell-based therapy post spinal cord injury.Journal of translational medicine · 2025
    Review
  6. 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

11 authors.

Xiaolong DuDepartment of Neurological Surgery, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Shengqi ZhangDepartment of Neurological Surgery, Indiana University School of Medicine, Indianapolis, IN 46202, USA.ORCID 0009-0008-9208-6724
Aytak KhabbazDepartment of Neurological Surgery, Indiana University School of Medicine, Indianapolis, IN 46202, USA.ORCID 0000-0001-7758-0953
Kristen Lynn CohenDepartment of Neurological Surgery, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Yihong ZhangDepartment of Neurological Surgery, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Samhita ChakrabortyDepartment of Neurological Surgery, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
George M SmithShriners Hospitals Pediatric Research Center, School of Medicine, Temple University, Philadelphia, PA 19140, USA.
Hongxing WangDepartment of Rehabilitation Medicine, Zhongda Hospital Southeast University, Nanjing 210009, China.ORCID 0000-0001-5962-9717
Amol P YadavDepartment of Biomedical Engineering, the University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Naikui LiuDepartment of Neurological Surgery, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Lingxiao DengDepartment of Neurological Surgery, Indiana University School of Medicine, Indianapolis, IN 46202, USA.ORCID 0000-0002-1293-8325

Funding

Plasticity of spinal L3 propriospinal neurons in urination recovery after thoracic SCIR21NS130241 · NINDS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENG, LINGXIAO · 2022 to 2022
$436k
IND DEPT HLTH 55051, 74247, 74244NIH HHS R21NS130241US ARMY HT94252310700
6 · The paper itself

Abstract

Unsuccessful axonal regeneration in transected spinal cord injury (SCI) is mainly attributed to shortage of growth factors, inhibitory glial scar, and low intrinsic regenerating capacity of severely injured neurons. Previously, we constructed an axonal growth permissive pathway in a thoracic hemisected injury by transplantation of Schwann cells overexpressing glial-cell-derived neurotrophic factor (SCs-GDNF) into the lesion gap as well as the caudal cord and proved that this novel permissive bridge promoted the regeneration of descending propriospinal tract (dPST) axons across and beyond the lesion. In the current study, we subjected rats to complete thoracic (T11) spinal cord transections and examined whether these combinatorial treatments can support dPST axons' regeneration beyond the transected injury. The results indicated that GDNF significantly improved graft-host interface by promoting integration between SCs and astrocytes, especially the migration of reactive astrocyte into SCs-GDNF territory. The glial response in the caudal graft area has been significantly attenuated. The astrocytes inside the grafted area were morphologically characterized by elongated and slim process and bipolar orientation accompanied by dramatically reduced expression of glial fibrillary acidic protein. Tremendous dPST axons have been found to regenerate across the lesion and back to the caudal spinal cord which were otherwise difficult to see in control groups. The caudal synaptic connections were formed, and regenerated axons were remyelinated. The hindlimb locomotor function has been improved.

Indexed as

AxonsGlial Cell Line-Derived Neurotrophic FactorNerve RegenerationSchwann CellsSpinal Cord InjuriesAnimalsAstrocytesFemaleRatsRats, Sprague-DawleyGlial Cell Line-Derived Neurotrophic Factordescending propriospinal axonfunctional recoveryglial-cell-derived neurotrophic factorglial responseglial scarregenerationSchwann cellspinal cord injuryspinal transectiontransplantation

Identifiers

PMID38995011
PMCPMC11240522

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.