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Injectable conductive hydrogel remodeling microenvironment and mimicking neuroelectric signal transmission after spinal cord injury.
Ye, Jingjia; Pan, Xihao; Wen, Zhengfa; Wu, Tianxin; Jin, Yuting; Ji, Shunxian; Zhang, Xianzhu; Ma, Yuanzhu; Liu, Wei; Teng, Chong; Tang, Longguang; Wei, Wei.
Afiliación
  • Ye J; Center for Regenerative Medicine, the Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, Zhejiang 322000, China.
  • Pan X; Dr. Li Dak Sum & Yip Yio Chin Center for Stem Cells and Regenerative Medicine, and Department of Orthopedic Surgery of the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang 310000, China; Zhejiang University-University of Edinburgh Institute, Zhejiang Univers
  • Wen Z; Center for Regenerative Medicine, the Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, Zhejiang 322000, China.
  • Wu T; Center for Regenerative Medicine, the Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, Zhejiang 322000, China.
  • Jin Y; Center for Regenerative Medicine, the Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, Zhejiang 322000, China.
  • Ji S; Center for Regenerative Medicine, the Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, Zhejiang 322000, China.
  • Zhang X; Department of Orthopedics, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
  • Ma Y; Department of Automation, Tsinghua University, Beijing 100084, China.
  • Liu W; Center for Regenerative Medicine, the Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, Zhejiang 322000, China.
  • Teng C; Center for Regenerative Medicine, the Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, Zhejiang 322000, China. Electronic address: tengchong1984@zju.edu.cn.
  • Tang L; Center for Regenerative Medicine, the Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, Zhejiang 322000, China. Electronic address: tanglongguang@zju.edu.cn.
  • Wei W; Center for Regenerative Medicine, the Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, Zhejiang 322000, China. Electronic address: zjewwei@zju.edu.
J Colloid Interface Sci ; 668: 646-657, 2024 Aug 15.
Article en En | MEDLINE | ID: mdl-38696992
ABSTRACT
Severe spinal cord injury (SCI) leads to dysregulated neuroinflammation and cell apoptosis, resulting in axonal die-back and the loss of neuroelectric signal transmission. While biocompatible hydrogels are commonly used in SCI repair, they lack the capacity to support neuroelectric transmission. To overcome this limitation, we developed an injectable silk fibroin/ionic liquid (SFMA@IL) conductive hydrogel to assist neuroelectric signal transmission after SCI in this study. The hydrogel can form rapidly in situ under ultraviolet (UV) light. The mechanical supporting and neuro-regenerating properties are provided by silk fibroin (SF), while the conductive capability is provided by the designed ionic liquid (IL). SFMA@IL showed attractive features for SCI repair, such as anti-swelling, conductivity, and injectability. In vivo, SFMA@IL hydrogel used in rats with complete transection injuries was found to remodel the microenvironment, reduce inflammation, and facilitate neuro-fiber outgrowth. The hydrogel also led to a notable decrease in cell apoptosis and the achievement of scar-free wound healing, which saved 45.6 ± 10.8 % of spinal cord tissue in SFMA@IL grafting. Electrophysiological studies in rats with complete transection SCI confirmed SFMA@IL's ability to support sensory neuroelectric transmission, providing strong evidence for its signal transmission function. These findings provide new insights for the development of effective SCI treatments.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Traumatismos de la Médula Espinal / Transmisión Sináptica / Hidrogeles / Líquidos Iónicos / Fibroínas Idioma: En Revista: J Colloid Interface Sci / J. colloid interface sci / Journal of colloid and interface science Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Traumatismos de la Médula Espinal / Transmisión Sináptica / Hidrogeles / Líquidos Iónicos / Fibroínas Idioma: En Revista: J Colloid Interface Sci / J. colloid interface sci / Journal of colloid and interface science Año: 2024 Tipo del documento: Article