A Novel Magnetic Responsive miR‐26a@SPIONs‐OECs for Spinal Cord Injury: Triggering Neural Regeneration Program and Orienting Axon Guidance in Inhibitory Astrocytic Environment

Author:

Gao Xue1,Li Shengyou1,Yang Yujie1,Yang Shijie2,Yu Beibei2,Zhu Zhijie1,Ma Teng1,Zheng Yi1,Wei Bin1,Hao Yiming1,Wu Haining1,Zhang Yongfeng2,Guo Lingli1,Gao Xueli3,Wei Yitao1,Xue Borui1,Li Jianzhong4,Feng Xue5,Lu Lei6,Xia Bing1,Huang Jinghui1ORCID

Affiliation:

1. Department of Orthopaedics Xijing Hospital Fourth Military Medical University Xi'an 710032 P. R. China

2. Department of Neurosurgery The Second Affiliated Hospital of Xi'an Jiao Tong University Xi'an 710032 P. R. China

3. School of Ecology and Environment Northwestern Polytechnical University Xi'an 710072 P. R. China

4. Department of Thoracic Surgery The Second Affiliated Hospital of Xi'an Jiao Tong University Xi'an 710032 P. R. China

5. Department of Cell Biology School of Medicine Northwest University Xi'an 710032 P. R. China

6. State Key Laboratory of Military Stomatology National Clinical Research Center for Oral Diseases Shaanxi International Joint Research Center for Oral Diseases Department of Oral Anatomy and Physiology and TMD School of Stomatology the Fourth Military Medical University Xi'an 710032 P. R. China

Abstract

AbstractAddressing the challenge of promoting directional axonal regeneration in a hostile astrocytic scar, which often impedes recovery following spinal cord injury (SCI), remains a daunting task. Cell transplantation is a promising strategy to facilitate nerve restoration in SCI. In this research, a pro‐regeneration system is developed, namely miR‐26a@SPIONs‐OECs, for olfactory ensheathing cells (OECs), a preferred choice for promoting nerve regeneration in SCI patients. These entities show high responsiveness to external magnetic fields (MF), leading to synergistic multimodal cues to enhance nerve regeneration. First, an MF stimulates miR‐26a@SPIONs‐OECs to release extracellular vesicles (EVs) rich in miR‐26a. This encourages axon growth by inhibiting PTEN and GSK‐3β signaling pathways in neurons. Second, miR‐26a@SPIONs‐OECs exhibit a tendency to migrate and orientate along the direction of the MF, thereby potentially facilitating neuronal reconnection through directional neurite elongation. Third, miR‐26a‐enriched EVs from miR‐26a@SPIONs‐OECs can interact with host astrocytes, thereby diminishing inhibitory cues for neurite growth. In a rat model of SCI, the miR‐26a@SPIONs‐OECs system led to significantly improved morphological and motor function recovery. In summary, the miR‐26a@SPIONS‐OECs pro‐regeneration system offers innovative insights into engineering exogenous cells with multiple additional cues, augmenting their efficacy for stimulating and guiding nerve regeneration within a hostile astrocytic scar in SCI.

Funder

National Key Research and Development Program of China

Postdoctoral Research Foundation of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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