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Research Article | Open Access

Electrospun nanofiber scaffolds loaded with copper oxide for repairing traumatic brain injury through restoring copper homeostasis and regulating pyroptosis pathway

Yumei An1,‡, Sunao Li1,‡, Xinqi Huang1,‡, Xueshi Chen1, Mingyuan Xu1, Chen Chen2, Xuefeng Zhou3, Haiyan Shan4 ( ), Luyang Tao1( ), Mingyang Zhang1,5 ( )
Department of Forensic Sciences, The Affiliated Guangji Hospital, School of Basic Medical Sciences, Suzhou Medical College of Soochow University, No. 178 Ganjiang East Road, Gusu District, Suzhou, Jiangsu, 215123, China
Department of Orthopedics, Dongtai People’s Hospital, No. 2 Kangfu West Road, Dongtai District, Dongtai, Jiangsu, 224200, China
School of Biological Science and Medical Engineering, Southeast University, No. 399 Linquan Road, Suzhou Industrial Park, Suzhou, Jiangsu, 215123, China
Department of Obstetrics and Gynecology, The Affiliated Suzhou Hospital of Nanjing Medical University, No. 66 Huangli Road, Xiangcheng District, Suzhou, Jiangsu, 215131, China
Jiangsu Key Laboratory of Drug Discovery and Translational Research for Brain Diseases, School of Basic Medical Sciences, Soochow University, No. 199 Renai Road, Suzhou Industrial Park, Suzhou, Jiangsu, 215123, China

‡Yumei An, Sunao Li and Xinqi Huang contributed equally.

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Highlights

• Electrostatically spun scaffolds loaded with copper oxide enable a slow, continuous, and low-dose supply of copper.

• Electrospun nanofiber scaffolds with sustained copper delivery are an effective strategy for brain tissue engineering to attenuate brain injury.

• Therapeutic effect of copper-loaded electrospun nanofiber scaffolds may be suppressing TBI-induced pyroptosis in brain regions.

Abstract

Background

Traumatic brain injury (TBI) is one of the leading causes of injury and disability worldwide. Pyroptosis, a specific type of programmed cell death (PCD) triggered by inflammatory signals, plays a significant part in the pathological process after TBI. Copper ions play an important role in anti-inflammation and anti-oxidative stress. There is a more active copper metabolism in neurons after injury, and that neurons may require more copper ions and downstream copper-based enzymes to maintain normal physiological functions. Given these understandings of the roles of pyroptosis and copper ions in TBI pathology, this study aims to elucidate the interplay between copper ions and pyroptosis following TBI, with the goal of identifying novel therapeutic targets for TBI management.

Methods

We developed an electrostatic spinning scaffold loaded with copper oxide (CuO@PCL/gelatiin, CuO@PG) to achieve small-dose local administration and avoid toxic side effects. The membranes underwent preparation and characterization through various techniques including Fourier transform infrared spectroscopy, measurement of water contact angle, antibacterial experiment, scanning electron microscopy, and assessment of in vitro release of copper. In addition, we used a controlled cortical impact to establish a TBI model in mice to examine the effect of CuO@PG on TBI-induced pyroptosis and the ability of the membranes to heal brain injury.

Results

CuO@PG inhibited TBI-induced neuronal pyroptosis. CuO@PG can inhibit the expression of the pyroptosis-related proteins. Moreover, CuO@PG also alleviates brain edema and the degree of neurodegeneration in the acute phase of TBI. The neuroprotective effect of CuO@PG was further confirmed by wire-grip test, open field test, Morris water maze test. Lastly, the beneficial results were significantly inhibited by the use of the copper chelator tetrathiomolybdate.

Conclusions

In this study, we successfully constructed electrostatically spun scaffolds loaded with copper oxide to achieve slow, continuous and low-dose copper supply to the local brain, which provides a new theoretical basis for the imbalance of copper homeostasis in the brain after TBI.

Graphical Abstract

References

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Burns & Trauma
Article number: tkaf030

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Cite this article:
An Y, Li S, Huang X, et al. Electrospun nanofiber scaffolds loaded with copper oxide for repairing traumatic brain injury through restoring copper homeostasis and regulating pyroptosis pathway. Burns & Trauma, 2025, 13(8): tkaf030. https://doi.org/10.1093/burnst/tkaf030

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Received: 17 June 2024
Revised: 02 May 2025
Accepted: 06 May 2025
Published: 09 May 2025
© The Author(s) 2025. Published by Oxford University Press.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.