Evidence map›Paper›PMID 41267687›Full record

ArticleJournal of tissue engineering

Controlled spatial and temporal release of neurotrophic growth factor from genetically modified tissue engineering living scaffolds.

Hannah H Lee, Sam E Lien, Viviana Alpizar Vargas, Robert B Shultz, Franco A Laimo, Kritika S Katiyar, D Kacy Cullen

Abstract read
In one paragraph

Article in Journal of tissue engineering. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

7 authors.

Hannah H LeeDepartment of Research, Center for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA, USA.ORCID https://orcid.org/0000-0003-4942-9580
Sam E LienDepartment of Research, Center for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA, USA.
Viviana Alpizar VargasDepartment of Research, Center for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA, USA.ORCID https://orcid.org/0009-0002-8718-9725
Robert B ShultzAxonova Medical, Inc., Philadelphia, PA, USA.
Franco A LaimoDepartment of Research, Center for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA, USA.
Kritika S KatiyarAxonova Medical, Inc., Philadelphia, PA, USA.
D Kacy CullenDepartment of Research, Center for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA, USA.

Funding

Development of Tissue Engineered Neuromuscular Interfaces from GalSafe NeuronsR44NS125892 · NINDS · AXONOVA MEDICAL, LLC · PI Kritika Katiyar · 2024 to 2026
$2.8M
Tissue Engineered Motor Units for Neuromuscular Modeling and RepairR01AR083489 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Daniel Kacy Cullen · 2024 to 2026
$1.7M
NIAMS NIH HHS R01 AR083489NINDS NIH HHS R44 NS125892RRD VA IK2 RX003947
6 · The paper itself

Abstract

Peripheral nerve injuries (PNIs) affect thousands of patients yearly, often resulting in loss of function, sensation, and chronic pain. In critical-size defects, advanced surgical repair strategies often fail to restore full function. A key limitation is the lack of sustained, localized delivery of biological cues for axonal regeneration, such as growth factors. Glial-cell line-derived neurotrophic factor (GDNF) is known to promote axonal growth, Schwann cell migration, and neuronal survival, but uncontrolled release may cause axonal entrapment. We previously developed tissue-engineered nerve grafts (TENGs) composed of two neuronal populations connected by stretch-grown axons. In this study, we genetically modified the distal population to express human GDNF under a Tet-on inducible promoter, temporally controlling GDNF release through doxycycline administration. Modified TENGs survived implantation in a 1.5-cm rat sciatic nerve defect, supporting future studies. This approach offers a promising platform for spatially and temporally controlled neurotrophic factor delivery from tissue-engineered living scaffolds.

Indexed as

axonscell engineeringcontrolled releaseGDNFgenetic modificationgrowth factorsliving scaffoldperipheral nerve injurytissue engineering

Identifiers

PMID41267687
PMCPMC12627380

What OpenQuestion holds

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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.