Evidence map›Paper›PMID 40734274›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2025

Fetal rat neural progenitor cell transplantation after spinal cord injury improves motor recovery following optogenetic stimulation.

María Del Mar Sánchez-Martín, Esther Giraldo, Ana Alastrue-Agudo, Eric López-Mocholi, Samuel Martín-Pérez, Loris Maninno, Guillem Paniagua Soriano, Ana Isabel Fraga Sánchez, Javier Monreal-Trigo, José Manuel Terrés-Haro and 5 more

Abstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
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

15 authors.

María Del Mar Sánchez-MartínNeuronal and Tissue Regeneration Laboratory, Principe Felipe Research Center (CIPF), 46012 Valencia, Spain.
Esther GiraldoNeuronal and Tissue Regeneration Laboratory, Principe Felipe Research Center (CIPF), 46012 Valencia, Spain; Department of Biotechnology, within the Interuniversity Research Institute for Molecular Recognition and Technology Development (idm UPV-UV), Universitat Politècnica de València, 46022 Valencia, Spain; UPV-CIPF Joint Research Unit Disease Mechanisms and Nanomedicine, CIPF, 46012 Valencia, Spain. Electronic address: egiraldo@cipf.es.
Ana Alastrue-AgudoNeuronal and Tissue Regeneration Laboratory, Principe Felipe Research Center (CIPF), 46012 Valencia, Spain.
Eric López-MocholiNeuronal and Tissue Regeneration Laboratory, Principe Felipe Research Center (CIPF), 46012 Valencia, Spain.
Samuel Martín-PérezNeuronal and Tissue Regeneration Laboratory, Principe Felipe Research Center (CIPF), 46012 Valencia, Spain.
Loris ManinnoNeuronal and Tissue Regeneration Laboratory, Principe Felipe Research Center (CIPF), 46012 Valencia, Spain.
Guillem Paniagua SorianoNeuronal and Tissue Regeneration Laboratory, Principe Felipe Research Center (CIPF), 46012 Valencia, Spain.
Ana Isabel Fraga SánchezNeuronal and Tissue Regeneration Laboratory, Principe Felipe Research Center (CIPF), 46012 Valencia, Spain.
Javier Monreal-TrigoElectronic Development and Printed Sensors (ged+ps), within the Interuniversity Research Institute for Molecular Recognition and Technology Development (idm UPV-UV), in Universitat Politècnica de València (UPV), 46021 València, Spain.
José Manuel Terrés-HaroElectronic Development and Printed Sensors (ged+ps), within the Interuniversity Research Institute for Molecular Recognition and Technology Development (idm UPV-UV), in Universitat Politècnica de València (UPV), 46021 València, Spain.
Quique Vidal BeneytoInstitute for Integrative Systems Biology, Spanish National Research Council, Paterna, Valencia, Spain.
Ana ConesaInstitute for Integrative Systems Biology, Spanish National Research Council, Paterna, Valencia, Spain.
Erna van NiekerkDepartment of Neurosciences, University of California, San Diego, La Jolla, CA, USA.
Mark TuszynskiDepartment of Neurosciences, University of California, San Diego, La Jolla, CA, USA.
Victoria Moreno-ManzanoNeuronal and Tissue Regeneration Laboratory, Principe Felipe Research Center (CIPF), 46012 Valencia, Spain. Electronic address: vmorenom@cipf.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinal cord injury (SCI) disrupts communication between the brain and the spinal circuits, resulting in severe motor, sensory, and autonomic dysfunctions. Transplantation of neural progenitor cells (NPCs) has been demonstrated to provide multiple benefits; however, limited graft survival and neuronal differentiation must be overcome to achieve improved results. Here, we explore the optogenetic modulation of rat spinal cord-derived NPC expressing channelrhodopsin-2 (ChR2) through adeno-associated virus serotype 9-mediated transduction, transplanted into the sub-acute stage after SCI. Daily blue-light stimulation and ChR2-dependent activation control of the modified NPC significantly enhanced locomotor skills, run speed, sustained walking coordination, and body stability in a rat SCI model. Engrafted rat NPC-ChR2 reduces astrocytic reactivity and the injured area volume, preserves a higher number of descending propriospinal neurons above the injury and a higher innervation of 5-hydroxytryptamine fibers to choline acetyltransferase-positive motoneurons below the injury, and the increased vesicular glutamate transporter expression suggests an enhanced excitatory synaptic activity. Overall, sustained activation of rat NPC post-transplantation offers a promising strategy for improved locomotor recovery following SCI.

Indexed as

Neural Stem CellsOptogeneticsRecovery of FunctionSpinal Cord InjuriesStem Cell TransplantationAnimalsChannelrhodopsinsDependovirusDisease Models, AnimalFemaleGenetic VectorsLocomotionMotor NeuronsRatsRats, Sprague-DawleyChannelrhodopsinschannelrhodopsin-2human neural stem cellsmotor recoveryoptogeneticsrat neural progenitors cellspinal cord injury

Identifiers

PMID40734274
PMCPMC12848215

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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 OpenQuestion graph.