已发表论文

PLA/GO/抗 TNF-α 复合物对脊髓损伤后神经免疫微环境的调节以促进神经修复

 

Authors Liu Y , Liu J, Wang Y, Zhang Y , Peng Z, Li P, Li M, Xue B, Wang Y

Received 17 December 2024

Accepted for publication 14 April 2025

Published 17 April 2025 Volume 2025:20 Pages 4919—4942

DOI https://doi.org/10.2147/IJN.S509954

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 4

Editor who approved publication: Prof. Dr. RDK Misra

Yishu Liu,1– 3 Jingsong Liu,1– 3 Yangyang Wang,1– 3 Yubo Zhang,1– 3 Zhibin Peng,1– 3 Pengfei Li,1– 3 Mi Li,1– 3 Bing Xue,4 Yansong Wang1– 3,5 

1Department of Orthopedics, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People’s Republic of China; 2The Key Laboratory of Myocardial Ischemia, Ministry of Education, Harbin Medical University, Harbin, Heilongjiang, People’s Republic of China; 3State Key Laboratory of Frigid Zone Cardiovascular Diseases, Harbin Medical University, Harbin, Heilongjiang, People’s Republic of China; 4Department of Orthopedics, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People’s Republic of China; 5NHC Key Laboratory of Cell Transplantation, Harbin Medical University, Harbin, Heilongjiang, People’s Republic of China

Correspondence: Yansong Wang, Email wyshmu1975@163.com

Introduction: Spinal cord injury (SCI) is a severe neurological condition with limited treatment options. Polylactic acid (PLA)+graphene oxide (GO)+anti-TNF-α (Ab) composites have shown potential in regulating immune responses and promoting neural repair.
Methods: Electrospinning PLA+GO+Ab materials were characterized using scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and X-ray diffraction (XRD). Their effects on neural stem cells (NSCs) and macrophage polarization were evaluated through in vitro assays, including proliferation, migration, differentiation, and flow cytometry. A rat SCI model was used to assess motor function recovery and histological changes.
Results: PLA+GO+Ab promoted NSC proliferation, migration, and differentiation while inducing macrophage polarization toward the M2 phenotype, reducing inflammation. In the SCI model, PLA+GO+Ab treatment enhanced motor function recovery, reduced spinal cord damage, and promoted axonal regeneration and oligodendrocyte maturation. RNA sequencing identified activation of the Rap1 signaling pathway, contributing to these effects.
Discussion: PLA+GO+Ab composites effectively modulate the neuroimmune microenvironment, supporting SCI recovery by promoting neural repair and immune regulation. These findings suggest its potential as a therapeutic biomaterial for SCI treatment.

Keywords: spinal cord injury, nerve regeneration, graphene, polylactic acid, anti-tumor necrosis factor α, neuroimmunomodulation