4.8 Article

Core-shell oxygen-releasing fibers for annulus fibrosus repair in the intervertebral disc of rats

Journal

MATERIALS TODAY BIO
Volume 18, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.mtbio.2022.100535

Keywords

Perfluorotributylamine; Coaxial electrospinning; Annulus fibrosus defect; Intervertebral disc degeneration; Hypoxia

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The repair of annulus fibrosus (AF) defect after discectomy in the intervertebral disc (IVD) has been a challenge due to hostile microenvironments, particularly compression and hypoxia. This study developed a oxygen-releasing scaffold using perfluorotributylamine (PFTBA) core-shell fibers to promote endogenous repair in the AF. The oxygen released from the PFTBA fibers protected annulus fibrosus stem cells (AFSCs) from hypoxia-induced apoptosis and promoted proliferation, migration, and extracellular matrix (ECM) production in AFSCs. In vivo studies showed that the oxygen-supplying fibers improved disc degeneration after discectomy by enhancing disc height and morphological integrity.
The repair of annulus fibrosus (AF) defect after discectomy in the intervertebral disc (IVD) has presented a challenge over the past decade. Hostile microenvironments in the IVD, including, compression and hypoxia, are critical issues that require special attention. Till date, little information is available on potential strategies to cope with the hypoxia dilemma in AF defect sites. In this study, perfluorotributylamine (PFTBA) core-shell fibers were fabricated by coaxial electrospinning to construct oxygen-releasing scaffold for promoting endogenous repair in the AF after discectomy. We demonstrated that PFTBA fibers (10% chitosan, chitosan: PCL, 1:6) could release oxygen for up to 144 h. The oxygen released from PFTBA fibers was found to protect annulus fibrosus stem cells (AFSCs) from hypoxia-induced apoptosis. In addition, the PFTBA fibers were able to promote proliferation, migration and extracellular matrix (ECM) production in AFSCs under hypoxia, highlighting their therapeutic potential in AF defect repair. Subsequent in vivo studies demonstrated that oxygen-supplying fibers were capable of ameliorating disc degeneration after discectomy, which was evidenced by improved disc height and morphological integrity in rats with the oxygen-releasing scaffolds. Further transcriptome analysis indicated that differential expression genes (DEGs) were enriched in oxygen transport and angiogenesis, which likely contributed to their beneficial effect on endogenous AF regeneration. In summary, the oxygen-releasing scaffold provides novel insights into the oxygen regulation by bioactive materials and raises the therapeutic possibility of oxygen supply strategies for defect repair in AF, as well as other aerobic tissues.

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