Evidence map›Paper›PMID 42486482›Full record

ArticleStem cells translational medicine2026

A human iPSC-derived 3D spinal cord organoid model to study radiation-induced neural injury.

Yifei Jiang, Xubo Li, Jingguang Zeng, Shiju Chen, Runtao Zhou, Yixun Wu, Ganggang Kong, Fawei Liao, Bo Wang, Fangze Qi and 6 more

Abstract read
In one paragraph

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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Yifei JiangDepartment of Microsurgery, Orthopedic Trauma and Hand Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Xubo LiDepartment of Microsurgery, Orthopedic Trauma and Hand Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Jingguang ZengDepartment of Microsurgery, Orthopedic Trauma and Hand Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Shiju ChenDepartment of Microsurgery, Orthopedic Trauma and Hand Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Runtao ZhouDepartment of Microsurgery, Orthopedic Trauma and Hand Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Yixun WuDepartment of Microsurgery, Orthopedic Trauma and Hand Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Ganggang KongGuangdong Provincial Key Laboratory of Orthopedics and Traumatology, Sun Yat-sen University, Guangzhou, 510080, China.
Fawei LiaoDepartment of Microsurgery, Orthopedic Trauma and Hand Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Bo WangDepartment of Microsurgery, Orthopedic Trauma and Hand Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Fangze QiDepartment of Microsurgery, Orthopedic Trauma and Hand Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Cheng GuGuangdong Provincial Key Laboratory of Orthopedics and Traumatology, Sun Yat-sen University, Guangzhou, 510080, China.
Shiyi YinDepartment of Microsurgery, Orthopedic Trauma and Hand Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Qiguang PangDepartment of Microsurgery, Orthopedic Trauma and Hand Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Weidong MuDepartment of Orthopedics, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, 250021,China.
Qingtang ZhuDepartment of Microsurgery, Orthopedic Trauma and Hand Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Canbin ZhengDepartment of Microsurgery, Orthopedic Trauma and Hand Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.ORCID 0000-0002-4560-8242

Funding

Guangdong Basic and Applied Basic Research Foundation 2023A1515011443Guangdong Basic and Applied Basic Research Foundation 2024A1515010373Guangdong Basic and Applied Basic Research Foundation 2024A1515013183Guangdong Basic and Applied Basic Research Foundation 2026A1515011596Guangdong Basic and Applied Basic Research Foundation 2026B0303000013National Key Research and Development Program of China 2024YFA1107900National Natural Science Foundation of China 82171650National Natural Science Foundation of China 82222045
6 · The paper itself

Abstract

backgroundRadiation therapy remains a cornerstone in the treatment of primary and metastatic tumors; however, its efficacy is limited by the spinal cord's high sensitivity to radiation-induced injury. To better understand the mechanisms underlying spinal cord radiosensitivity, we developed a three-dimensional human spinal cord organoid model derived from human-induced pluripotent stem cells using a neuroectodermal differentiation protocol that closely mimics embryonic spinal cord development.

methodsMature spinal cord organoids were exposed to a clinically relevant 2 Gy dose of ionizing radiation, and subsequent assessments included evaluation of DNA damage, astrocytic response, and neuronal functionality.

resultsThe organoids successfully recapitulated key features of spinal cord development, including neural differentiation, spontaneous electrophysiological activity, and functional maturation. Radiation exposure led to pronounced DNA double-strand breaks, particularly in SOX2-expressing progenitor cells. Astrocyte hyperplasia was evident through increased GFAP expression, indicating a reactive gliosis response. Electrophysiological analysis revealed a marked reduction in spike frequency and burst activity, indicative of impaired neuronal function. Although partial recovery was observed over time, functional deficits persisted, suggesting sustained damage.

conclusionThis human spinal cord organoid model offers a physiologically relevant platform for studying radiation-induced spinal cord injury and provides valuable insights into the cellular and functional consequences of radiation exposure. It holds significant potential for advancing neuroprotective strategies and therapeutic interventions targeting radiation-induced damage in the central nervous system.

Indexed as

Induced Pluripotent Stem CellsOrganoidsRadiation InjuriesSpinal CordSpinal Cord InjuriesCell DifferentiationHumansNeuronsDNA damage responseDNA-double strand breakhuman pluripotent stem cellsradiation-induced damagespinal cord organoids

Identifiers

PMID42486482
PMCPMC13391157

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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.