Optical imaging detection of extracellular vesicles of miR-146 modified bone marrow mesenchymal stem cells promoting spinal cord injury repair

• DOI: 10.1016/j.slast.2024.100172
• Publication Date: 2024-07-26T18:37:03Z
• Authors: Qianli Tang; Wu Chen; Huang Ke; Changgong Lan
• Keywords: TNF Receptor-Associated Factor 6; Functional recovery; Mesenchymal Stem Cells; Bone Marrow Cells; Rats; miR-146a; Rats, Sprague-Dawley; MicroRNAs; Extracellular Vesicles; Disease Models, Animal; Interleukin-1 Receptor-Associated Kinases; Oxidative stress; Medical technology; Animals; Optical imaging detection; BMSCs; R855-855.5; TP248.13-248.65; Spinal Cord Injuries; Biotechnology; Signal Transduction

Bone Marrow mesenchymal Stem Cells (BMSCs) are considered as an important source of cells for regenerative medicine, In particular, Bone Marrow mesenchymal Stem Cells Exosomes (BMSCs-EXO) have the most significant effect in the treatment of Spinal Cord Injury (SCI), but the mechanism of action is still unknown. This study found that compared with other SCI groups, BMSCs-EXO loaded with miR-146a could significantly improve the functional recovery of the hind limbs of SCI rats. Hematoxylin and eosin (H&E) indicated that the lesion area of spinal cord injury was less, nissl staining indicated that the number of nissl bodies remained more; the mechanism may be through inhibiting the expression of IRAK1 and TRAF6, blocking the activation of NF-κB p65, reducing the expression of TNF-α, IL-1β and IL-6 inflammatory factors and oxidative stress, improving the SCI microenvironment, and promoting the repair of neural function. In general, we found that BMSCs-EXO loaded with miR-146a could reduce the inflammatory response and oxidative stress in SCI by inhibiting the activation of IRAK1/TRAF6/NF-κB p65 signaling pathway, and promote the recovery of neurological function in SCI rats.