Olfactory ensheathing cells seeded decellularized scaffold promotes axonal regeneration in spinal cord injury rats. Issue 5 (22nd August 2020)

• Record Type: Journal Article
• Authors: Yu, Fangzheng; Li, Peifeng; Du, Shenghu; Lui, KoonHei W.; Lin, Yutian; Chen, Lumin; Ren, Qi; Wang, Jian; Mei, Jin; Xiao, Jian; Zhu, Junyi
• Is Part Of: Journal of biomedical materials research. Volume 109:Issue 5(2021)
• Page Start: 779
• Page End: 787
• Publication Date: 2020-08-22
• Subjects: decellularized spinal scaffolds -- axonal regeneration -- olfactory ensheathing cells -- scaffold -- spinal cord injury; Biomedical materials -- Periodicals; 610.28
• DOI: 10.1002/jbm.a.37066
• Languages: English
• ISSNs: 1549-3296

Abstract

Abstract: Spinal cord decellularized (DC) scaffolds can promote axonal regeneration and restore hindlimb motor function of spinal cord defect rats. However, scarring caused by damage to the astrocytes at the margin of injury can hinder axon regeneration. Olfactory ensheathing cells (OECs) integrate and migrate with astrocytes at the site of spinal cord injury, providing a bridge for axons to penetrate the scars and grow into lesion cores. The purpose of this study was to evaluate whether DC scaffolds carrying OECs could better promote axon growth. For these studies, DC scaffolds were cocultured with primary extracted and purified OECs. Immunofluorescence and electron microscopy were used for verification of cells adhere and growth on the scaffold. Scaffolds with OECs were transplanted into rat spinal cord defects to evaluate axon regeneration and functional recovery of hind limbs. Basso, Beattie, and Bresnahan (BBB) scoring was used to assess motor function recovery, and glial fibrillary acidic protein (GFAP) and NF200‐stained tissue sections were used to evaluate axonal regeneration and astrological scar distribution. Our results indicated that spinal cord DC scaffolds have good histocompatibility and spatial structure, and can promote the proliferation of adherent OECs. In animal experiments, scaffolds carrying OECs have better axon regeneration promoting protein expression than the SCI model, and improve the proliferation and distribution of astrocytes at the site of injury. These results proved that the spinal cord DC scaffold with OECs can promote axon regeneration at the site of injury, providing a new basis for clinical application.