Evidence map›Paper›PMID 40702833›Full record

ArticleAdvanced healthcare materials2025

3D-Printed Scaffolds Promote Enhanced Spinal Organoid Formation for Use in Spinal Cord Injury.

Guebum Han, Nicolas S Lavoie, Nandadevi Patil, Olivia G Korenfeld, Hyunjun Kim, Manuel Esguerra, Daeha Joung, Michael C McAlpine, Ann M Parr

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
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  7. Article
  8. Organoids for disease modeling and treatment: state-of-the-art.Experimental hematology & oncology · 2026
    Review
  9. 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.

Guebum HanDepartment of Mechanical Engineering, University of Minnesota, Minneapolis, MN, 55455, USA.ORCID https://orcid.org/0000-0001-8808-1607
Nicolas S LavoieDepartment of Neurosurgery, Stem Cell Institute, University of Minnesota, Minneapolis, MN, 55455, USA.
Nandadevi PatilDepartment of Neurosurgery, Stem Cell Institute, University of Minnesota, Minneapolis, MN, 55455, USA.
Olivia G KorenfeldDepartment of Neurosurgery, Stem Cell Institute, University of Minnesota, Minneapolis, MN, 55455, USA.
Hyunjun KimDepartment of Mechanical Engineering, University of Minnesota, Minneapolis, MN, 55455, USA.
Manuel EsguerraDepartment of Neuroscience, University of Minnesota, Minneapolis, MN, 55455, USA.
Daeha JoungDepartment of Physics, Virginia Commonwealth University, Richmond, VA, 23284, USA.
Michael C McAlpineDepartment of Mechanical Engineering, University of Minnesota, Minneapolis, MN, 55455, USA.
Ann M ParrDepartment of Neurosurgery, Stem Cell Institute, University of Minnesota, Minneapolis, MN, 55455, USA.ORCID https://orcid.org/0000-0002-7228-2647

Funding

3D Bioprinted Spinal Cord Organoids as a Relay System for Spinal Cord InjuryR01NS119297 · NINDS · UNIVERSITY OF MINNESOTA · PI PARR, ANN M · 2021 to 2025
$2.4M
NIH HHS R01-NS119297NINDS NIH HHS R01 NS119297Spinal Cord Society UMF 0021424State of Minnesota Spinal Cord Injury and Traumatic Brain Injury Research Grant Program 159877
6 · The paper itself

Abstract

The transplantation of regionally specific spinal neural progenitor cells (sNPCs) has shown promise for functional restoration after spinal cord injury (SCI) by forming connections with host neural circuits. Here, 3D-printed organoid scaffolds for transplantation using clinically relevant human induced pluripotent stem cell-derived regionally specific sNPCs is developed. Scaffolds with microscale channels are printed, and sNPCs are subsequently printed within these channels. The scaffolds direct axonal projections along the channels and guide the cells to simulate in vivo-like conditions, leading to more effective cell maturation and the development of neuronal networks crucial for restoring function after SCI. The scaffolds, with organoids assembled along their lengths, are transplanted into the transected spinal cords of rats. This significantly promotes the functional recovery of the rats. At 12 weeks post-transplantation, the majority of the cells in the scaffolds differentiate into neurons and integrate into the host spinal cord tissue. These results demonstrate their potential to create a relay system along the spinal cord and form synapses in both the rostral and caudal directions relative to the scaffold. It is envisioned that combining sNPCs, organoid assembly, and 3D printing strategies can ultimately lead to a transformative treatment approach for SCI.

Indexed as

OrganoidsPrinting, Three-DimensionalSpinal Cord InjuriesTissue ScaffoldsAnimalsCell DifferentiationFemaleHumansInduced Pluripotent Stem CellsNeural Stem CellsRatsRats, Sprague-DawleySpinal Cord3D‐printed scaffoldfunctional recoveryhuman induced pluripotent stem cellsspinal cord organoidsspinal neural progenitor cells

Identifiers

PMID40702833
PMCPMC12447032

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Registered trials

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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.