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Thermosensitive hydrogel-based GPR124 delivery strategy for rebuilding blood-spinal cord barrier.
Shu, Jiawei; Wang, Chenggui; Tao, Yiqing; Wang, Shaoke; Cheng, Feng; Zhang, Yuang; Shi, Kesi; Xia, Kaishun; Wang, Ronghao; Wang, Jingkai; Yu, Chao; Chen, Jiangjie; Huang, Xianpeng; Xu, Haibin; Zhou, Xiaopeng; Wu, Haobo; Liang, Chengzhen; Chen, Qixin; Yan, Shigui; Li, Fangcai.
Afiliación
  • Shu J; International Institutes of Medicine The Fourth Affiliated Hospital, Zhejiang University School of Medicine Yiwu Zhejiang People's Republic of China.
  • Wang C; Department of Orthopedics Surgery The Second Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang People's Republic of China.
  • Tao Y; Orthopedics Research Institute of Zhejiang University, Zhejiang University Hangzhou Zhejiang People's Republic of China.
  • Wang S; Key Laboratory of Motor System Disease Research and Precision Therapy of Zhejiang Province Hangzhou Zhejiang People's Republic of China.
  • Cheng F; The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University Wenzhou Zhejiang People's Republic of China.
  • Zhang Y; Department of Orthopedics Surgery The Second Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang People's Republic of China.
  • Shi K; Orthopedics Research Institute of Zhejiang University, Zhejiang University Hangzhou Zhejiang People's Republic of China.
  • Xia K; Key Laboratory of Motor System Disease Research and Precision Therapy of Zhejiang Province Hangzhou Zhejiang People's Republic of China.
  • Wang R; Department of Orthopedics Surgery The Second Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang People's Republic of China.
  • Wang J; Orthopedics Research Institute of Zhejiang University, Zhejiang University Hangzhou Zhejiang People's Republic of China.
  • Yu C; Key Laboratory of Motor System Disease Research and Precision Therapy of Zhejiang Province Hangzhou Zhejiang People's Republic of China.
  • Chen J; Department of Orthopedics Surgery The Second Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang People's Republic of China.
  • Huang X; Orthopedics Research Institute of Zhejiang University, Zhejiang University Hangzhou Zhejiang People's Republic of China.
  • Xu H; Key Laboratory of Motor System Disease Research and Precision Therapy of Zhejiang Province Hangzhou Zhejiang People's Republic of China.
  • Zhou X; Department of Orthopedics Surgery The Second Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang People's Republic of China.
  • Wu H; Orthopedics Research Institute of Zhejiang University, Zhejiang University Hangzhou Zhejiang People's Republic of China.
  • Liang C; Key Laboratory of Motor System Disease Research and Precision Therapy of Zhejiang Province Hangzhou Zhejiang People's Republic of China.
  • Chen Q; Department of Orthopedics Surgery The Second Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou Zhejiang People's Republic of China.
  • Yan S; Orthopedics Research Institute of Zhejiang University, Zhejiang University Hangzhou Zhejiang People's Republic of China.
  • Li F; Key Laboratory of Motor System Disease Research and Precision Therapy of Zhejiang Province Hangzhou Zhejiang People's Republic of China.
Bioeng Transl Med ; 8(5): e10561, 2023 Sep.
Article en En | MEDLINE | ID: mdl-37693060
ABSTRACT
Spinal cord injury (SCI) causes blood-spinal cord barrier (BSCB) disruption, leading to secondary damage, such as hemorrhagic infiltration, inflammatory response, and neuronal cell death. It is of great significance to rebuild the BSCB at the early stage of SCI to alleviate the secondary injury for better prognosis. Yet, current research involved in the reconstruction of BSCB is insufficient. Accordingly, we provide a thermosensitive hydrogel-based G protein-coupled receptor 124 (GPR124) delivery strategy for rebuilding BSCB. Herein, we firstly found that the expression of GPR124 decreased post-SCI and demonstrated that treatment with recombinant GPR124 could partially alleviate the disruption of BSCB post-SCI by restoring tight junctions (TJs) and promoting migration and tube formation of endothelial cells. Interestingly, GPR124 could also boost the energy metabolism of endothelial cells. However, the absence of physicochemical stability restricted the wide usage of GPR124. Hence, we fabricated a thermosensitive heparin-poloxamer (HP) hydrogel that demonstrated sustained GPR124 production and maintained the bioactivity of GPR124 (HP@124) for rebuilding the BSCB and eventually enhancing functional motor recovery post-SCI. HP@124 hydrogel can encapsulate GPR124 at the lesion site by injection, providing prolonged release, preserving wounded tissues, and filling injured tissue cavities. Consequently, it induces synergistically efficient integrated regulation by blocking BSCB rupture, decreasing fibrotic scar formation, minimizing inflammatory response, boosting remyelination, and regenerating axons. Mechanistically, giving GPR124 activates energy metabolism via elevating the expression of phosphoenolpyruvate carboxykinase 2 (PCK2), and eventually restores the poor state of endothelial cells. This research demonstrated that early intervention by combining GPR124 with bioactive multifunctional hydrogel may have tremendous promise for restoring locomotor recovery in patients with central nervous system disorders, in addition to a translational approach for the medical therapy of SCI.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Bioeng Transl Med Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Bioeng Transl Med Año: 2023 Tipo del documento: Article