The role of secretome from mesenchymal stromal cells in promoting nerve regeneration after neurotmesis

[EN] Background: Neurotmesis, remains a significant clinical challenge due to limited intrinsic regenerative capacity and suboptimal outcomes of current therapies. Mesenchymal stromal cells (MSCs) secretome has emerged as a promising cell-free alternative, providing neurotrophic and immunomodulatory...

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Detalhes bibliográficos
Autores: González Rodríguez, Yaiza, Casado Santos, Alejandro, Rodríguez Díaz, María, Nevado Sánchez, Endika, Mesas, Francisco Isidoro, Martín Tamayo, Irene, Martínez Flórez, Susana, González Fernández, María Luisa, Labrador, Jorge, Villar Suárez, María Vega
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2026
País:España
Recursos:Universidad de León
Repositorio:BULERIA. Repositorio Institucional de la Universidad de León
OAI Identifier:oai:dnet:buleria_____::9db7d0f763d8efa2a06a19d5ee761409
Acesso em linha:https://link.springer.com/article/10.1186/s13287-026-04911-y
https://hdl.handle.net/10612/28446
Access Level:acceso abierto
Palavra-chave:Anatomía
Veterinaria
Neurotmesis
Secretome
Mesenchymal stromal cells
Nerve regeneration
3109 Ciencias Veterinarias
3109.01 Anatomía
3109.07 Patología
Descrição
Resumo:[EN] Background: Neurotmesis, remains a significant clinical challenge due to limited intrinsic regenerative capacity and suboptimal outcomes of current therapies. Mesenchymal stromal cells (MSCs) secretome has emerged as a promising cell-free alternative, providing neurotrophic and immunomodulatory factors to support nerve repair. This study aimed to evaluate the regenerative efficacy of primed adipose-derived MSC secretome in a rat model of sciatic nerve neurotmesis. Methods: Human and rat adipose-derived MSCs were cultured and primed under hypoxic and inflammatory conditions. Secretomes were characterized by nanoparticle tracking analysis, proteomics, and total protein quantification. Neurotmesis was induced in Wistar rats, followed by repair with biomaterial alone or combined with human or rat secretome. Functional recovery was assessed by neurophysiological measurements at 6 months. Molecular and morphological regeneration was evaluated. Results: Secretome priming enhanced the secretion of neurotrophic factors and immunomodulatory proteins, as confirmed by transcriptomic and proteomic analyses. In vivo, secretome-treated groups showed significantly improved neurophysiological recovery and increased NGF levels. qPCR revealed upregulation of myelination-associated genes in treated nerves. Histological and TEM analyses demonstrated robust axonal regeneration. Conclusions: Primed MSC secretome markedly enhances structural and functional recovery after sciatic nerve neurotmesis, supporting its potential as a safe, effective, and scalable cell-free therapy for peripheral nerve repair