Evidence map›Paper›PMID 40604953›Full record

ArticleEuropean journal of medical research2025

Intermediate cell states in spermatogonial stem cell differentiation: enhancing neurogenesis and angiogenesis in spinal cord injury.

Xinyu Guo, Hao Yang, Haihong Zhang

Abstract read
In one paragraph

Article in European journal of medical research, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

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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

3 authors.

Xinyu GuoDepartment of Orthopedics, The Second Hospital of Lanzhou University, Lanzhou, China.
Hao YangTranslational Medicine Center, Hong Hui Hospital, Xi'an Jiaotong University, Xi'an, China.
Haihong ZhangDepartment of Orthopedics, The Second Hospital of Lanzhou University, Lanzhou, China. lzuzhanghh@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSpermatogonial stem cells (SSCs) can differentiate into various cell types, including neurons. This study sought to evaluate the therapeutic effects of SSC-derived spinal cord neurons for spinal cord injury (SCI).

methodsSSCs derived from rats were differentiated into spinal cord neurons. HUVECs were treated with SSC-conditioned medium (CM). Phase contrast imaging and immunofluorescence were used to evaluate the efficiency of neural transdifferentiation. The expression of glial cell-specific genes and angiogenic factors was detected by qRT-PCR. HUVEC migration was assessed using wound healing assay. Transdifferentiated spinal cord neurons were transplanted into SCI rats. The neural recovery of rats was assessed by immunofluorescence, HE staining, and BBB scoring. Subsequently, electrophysiological tests (MEPs and SEPs) and ultrasonography were conducted.

resultsSSCs were transdifferentiated into functional spinal cord neurons. The expression of glial cell-specific genes significantly increased after differentiation, suggesting the existence of an intermediate cell state during this process. SSC-CM markedly promoted HUVEC migration and increased the expression of angiogenic factors. Transdifferentiated neurons survived and maintained neuronal function after transplantation into SCI rats. Neuron transplantation improved spinal cord damage and motor function in SCI rats. Moreover, neuron transplantation improved the MEP and SEP parameters and promoted vascular regeneration in SCI rats.

conclusionsThe intermediate cell state existing during SSC differentiation improves SCI by promoting neurogenesis and angiogenesis, offering a promising approach for spinal cord repair.

Indexed as

Neovascularization, PhysiologicNeurogenesisSpermatogoniaSpinal Cord InjuriesAngiogenesisAnimalsCell DifferentiationCell MovementHumansHuman Umbilical Vein Endothelial CellsMaleNeuronsRatsRats, Sprague-DawleySpinal CordIntermediate statesNeural repairSpermatogonial stem cellsSpinal cord injuryVascular regeneration

Identifiers

PMID40604953
PMCPMC12218824

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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.