Local delivery of EGFR+NSCs-derived exosomes promotes neural regeneration post spinal cord injury via miR-34a-5p/HDAC6 pathway

Tian Qin; Chengjun Li; Yan Xu; Yiming Qin; Yuxin Jin; Rundong He; Zixiang Luo; Jinyun Zhao; Chunyue Duan; Hongbin Lu; Yong Cao; Jianzhong Hu

doi:10.1016/j.bioactmat.2023.11.013

Local delivery of EGFR⁺NSCs-derived exosomes promotes neural regeneration post spinal cord injury via miR-34a-5p/HDAC6 pathway

Bioact Mater. 2023 Nov 28:33:424-443. doi: 10.1016/j.bioactmat.2023.11.013. eCollection 2024 Mar.

Authors

Tian Qin^{1

2

3}, Chengjun Li^{2

3

4}, Yan Xu^{2

3

4}, Yiming Qin^{1

2

3}, Yuxin Jin^{1

2

3}, Rundong He^{1

2

3}, Zixiang Luo^{1

2

3}, Jinyun Zhao^{1

2

3}, Chunyue Duan^{1

2

3}, Hongbin Lu^{2

3

4}, Yong Cao^{1

2

3}, Jianzhong Hu^{1

2

3}

Affiliations

¹ Department of Spine Surgery and Orthopaedics, Xiangya Hospital, Central South University, Xiangya Road 87, Changsha, 410008, China.
² Key Laboratory of Organ Injury, Aging and Regenerative Medicine of Hunan Province, Xiangya Road 87, Changsha, 410008, China.
³ National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Xiangya Road 87, Changsha, 410008, China.
⁴ Department of Sports Medicine, Xiangya Hospital, Central South University, Xiangya Road 87, Changsha, 410008, China.

Abstract

Spinal cord injury (SCI) causes severe axon damage, usually leading to permanent paraparesis, which still lacks effective regenerative therapy. Recent studies have suggested that exosomes derived from neural stem cells (NSCs) may hold promise as attractive candidates for SCI treatment. Epidermal Growth Factor Receptor positive NSC (EGFR⁺NSC) is a subpopulation of endogenous NSCs, showing strong regenerative capability in central nervous system disease. In the current study, we isolated exosomes from the EGFR⁺NSCs (EGFR⁺NSCs-Exos) and discovered that local delivery of EGFR⁺NSCs-Exos can effectively promote neurite regrowth in the injury site of spinal cord-injured mice and improve their neurological function recovery. Using the miRNA-seq, we firstly characterized the microRNAs (miRNAs) cargo of EGFR⁺NSCs-Exos and identified miR-34a-5p which was highly enriched in EGFR⁺NSCs derived exosomes. We further interpreted that exosomal miR-34a-5p could be transferred to neurons and inhibit the HDAC6 expression by directly binding to its mRNA, contributing to microtubule stabilization and autophagy induction for aiding SCI repair. Overall, our research demonstrated a novel therapeutic approach to improving neurological functional recovery by using exosomes secreted from a subpopulation of endogenous NSCs and providing a precise cell-free treatment strategy for SCI repair.

Keywords: Exosomes; HDAC6; Neural regeneration; Spinal cord injury; miR-34a-5p.