Evidence map›Paper›PMID 42723550›Full record

ArticleOrganogenesis2026

Amniotic fluid stem cells alleviate neuronal injury-related changes in spina bifida by inducing autophagy via regulating the FOXO1/STAT3 axis.

Cuicui Li, Hepu Lin, Hongwei Gao, Ning Liu, Yiwu Dai, Yongchun Luo

Abstract read
In one paragraph

Article in Organogenesis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Cuicui LiDepartment of Neurosurgery, The First Medical Center of the PLA General Hospital, Beijing, China.
Hepu LinDepartment of Neurosurgery, The First Medical Center of the PLA General Hospital, Beijing, China.
Hongwei GaoDepartment of Neurosurgery, The Seven Medical Center of the PLA General Hospital, Beijing, China.
Ning LiuDepartment of Neurosurgery, The Seven Medical Center of the PLA General Hospital, Beijing, China.
Yiwu DaiDepartment of Neurosurgery, The First Medical Center of the PLA General Hospital, Beijing, China.
Yongchun LuoDepartment of Neurosurgery, The First Medical Center of the PLA General Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spina bifida (SB) is associated with progressive spinal cord injury and limited therapeutic options for neural protection. Amniotic fluid stem cells (AFSCs) have shown regenerative potential, but their effects on SB-related neuronal injury and the underlying mechanisms remain unclear. In this study, we investigated whether AFSCs alleviate neuronal injury-related changes in SB rats through the modulation of autophagy via the FOXO1/STAT3 pathway. SB-like lesions were induced in neonatal rats, followed by the intramedullary injection of AFSCs or vehicle on postnatal day 1. Behavioral assessment was performed using Basso, Beattie, and Bresnahan locomotor scoring on days 2, 7, and 14 after injection, and lesion-centered lumbosacral spinal cord tissues were collected on day 15. AFSC treatment partially improved hindlimb locomotor scores and reduced neuronal injury-related alterations in SB rats. AFSCs also increased autophagy-associated markers, including LC3II/I and Beclin1, and reduced p62 mRNA expression in vivo and in neural stem cells isolated from SB rats. Mechanistically, AFSC treatment was associated with reduced FOXO1 and enhanced STAT3 signaling. FOXO1 overexpression or STAT3 inhibition attenuated AFSC-mediated effects, whereas siRNA-mediated FOXO1 knockdown enhanced these effects; combined STAT3 knockdown partially reversed the effects of FOXO1 silencing. These findings suggest that AFSCs alleviate SB-related neuronal injury-associated changes by regulating autophagy through the FOXO1/STAT3 axis. This study provides preclinical evidence for an experimental neuroprotective mechanism of AFSCs, although further validation is required before translational applicability can be considered.

Indexed as

Amniotic FluidAutophagyForkhead Box Protein O1NeuronsSpinal DysraphismSTAT3 Transcription FactorStem CellsAnimalsFemaleRatsRats, Sprague-DawleySignal TransductionForkhead Box Protein O1Foxo1 protein, ratStat3 protein, ratSTAT3 Transcription FactorAmniotic fluid stem cellsautophagyFOXO1neural stem cellsspina bifida

Identifiers

PMID42723550
PMCPMC13577246

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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.