Advancing Recovery Post‐Spinal Cord Injury: Nanoparticle‐Mediated Reprogramming of Peripheral Macrophages

Author:

Liu Jingsong1234ORCID,Liu Daqian5,Ma Rui6,Ma Zhengang6,Peng Zhibin278,Wang Yangyang123,Liu Yishu123,Zhang Yubo123,Li Pengfei123,Li Mi123,Luan Zhiwei123,Zhao Yutong5,Xu Fangxing5,Wang Yansong1234ORCID

Affiliation:

1. Department of Orthopedic Surgery The First Affiliated Hospital of Harbin Medical University Harbin Medical University Harbin 150000 P. R. China

2. The Key Laboratory of Myocardial Ischemia Ministry of Education Harbin Medical University Harbin 150000 P. R. China

3. NHC Key Laboratory of Cell Transplantation Harbin Medical University Harbin 150000 P. R. China

4. State Key Laboratory of Frigid Zone Cardiovascular Diseases Harbin Medical University Harbin China

5. The Second Affiliated Hospital of Harbin Medical University Harbin Medical University Harbin 150000 P. R. China

6. School of Pharmacy Yancheng Teachers University Yancheng 224051 P. R. China

7. Center for Endemic Disease Control Chinese Center for Disease Control and Prevention Harbin Medical University Harbin 150000 P. R. China

8. Key Lab of Etiology and Epidemiology Education Bureau of Heilongjiang Province & Ministry of Health (23618504) Harbin Medical University Harbin Heilongjiang 150000 P. R. China

Abstract

AbstractSpinal cord injuries (SCIs) often result in secondary damage; therefore, interventions beyond current cell transplantation methods must be explored. The innate phagocytic propensity of macrophages are exploited for artificially aged erythrocytes and developed a delivery system fusing erythrocytes with reactive oxygen species (ROS)‐reactive nanoparticles prepared from a diselenide‐bond cross‐linked organic compound. The system targets peripheral blood macrophages, delivering anti‐glutamate drug‐loaded nanoparticles to the SCI site, releasing the drug upon ROS stimulation. This efficiently enables targeted drug delivery and reprograms peripheral macrophages through synergistic action with erythrocytes and encapsulated nucleic acids, effectively modulating the immune microenvironment in the SCI zone (significantly reduces neuronal apoptosis and alters the macrophage phenotype in the SCI region). The approach effectively addresses glutamate toxicity and immune inflammation by effectively regulating the lesion microenvironment, providing protection to neurons and creating favorable conditions for regeneration. Departing from the conventional “red blood cell backpack” model, the “chocolate chip cookie” concept is paradigm‐altering, enabling multifaceted erythrocyte functions. Collectively, the system comprehensively enhances the post‐SCI microenvironment. Its efficacy in SCI treatment and innovative drug delivery approach open new possibilities for neural function recovery. By laying the groundwork for future clinical applications, the research pioneers a transformative path toward advancing SCI therapeutics.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Heilongjiang Province

Publisher

Wiley

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