Magnetic Nanoparticles and Methylprednisolone Based Physico-Chemical Bifunctional Neural Stem Cells Delivery System for Spinal Cord Injury Repair.

Adv Sci (Weinh)

Department of Orthopaedics, Qilu Hospital of Shandong University, Shandong University Centre for Orthopaedics, Advanced Medical Research Institute, Shandong University, No. 107 Wenhua West Road, Lixia District, Jinan, 250012, China.

Published: June 2024

AI Article Synopsis

  • Neural stem cells (NSCs) transplantation offers a promising method for treating spinal cord injuries (SCI), but challenges like inflammation and NSC differentiation hinder its effectiveness.
  • A novel delivery system combining magnetic nanoparticles and methylprednisolone is designed to enhance NSC function by managing inflammation and promoting neuron formation.
  • Experiments show that this system improves recovery in SCI mice, leading to reduced inflammation and increased functional neurons, paving the way for better clinical applications in SCI treatment.*

Article Abstract

Neural stem cells (NSCs) transplantation is an attractive and promising treatment strategy for spinal cord injury (SCI). Various pathological processes including the severe inflammatory cascade and difficulty in stable proliferation and differentiation of NSCs limit its application and translation. Here, a novel physico-chemical bifunctional neural stem cells delivery system containing magnetic nanoparticles (MNPs and methylprednisolone (MP) is designed to repair SCI, the former regulates NSCs differentiation through magnetic mechanical stimulation in the chronic phase, while the latter alleviates inflammatory response in the acute phase. The delivery system releases MP to promote microglial M2 polarization, inhibit M1 polarization, and reduce neuronal apoptosis. Meanwhile, NSCs tend to differentiate into functional neurons with magnetic mechanical stimulation generated by MNPs in the static magnetic field, which is related to the activation of the PI3K/AKT/mTOR pathway. SCI mice achieve better functional recovery after receiving NSCs transplantation via physico-chemical bifunctional delivery system, which has milder inflammation, higher number of M2 microglia, more functional neurons, and axonal regeneration. Together, this bifunctional NSCs delivery system combined physical mechanical stimulation and chemical drug therapy is demonstrated to be effective, which provides new treatment insights into clinical transformation of SCI repair.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11151057PMC
http://dx.doi.org/10.1002/advs.202308993DOI Listing

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