AI Article Synopsis

  • Researchers are addressing spinal cord injury (SCI) by exploring the use of menstrual blood-derived mesenchymal stem cells (MenSCs) to promote axon regeneration in rats, but face challenges with the harsh microenvironment post-injury.
  • A new composite scaffold made from decellularized spinal cord extracellular matrix-gel (DSCG) and GelMA hydrogel was developed to create a supportive environment for MenSCs, enhancing their survival and function.
  • The combined approach of using MenSC-encapsulated scaffolds led to improved motor function, reduced inflammation, and better neuronal differentiation in SCI rat models, highlighting the potential of bioactive materials in stem cell therapy for SCI treatment.

Article Abstract

Spinal cord injury (SCI), as a serious disabling disease, is still haunted by lacking of effective treatments. We previously found that transplantation of menstrual blood-derived mesenchymal stem cells (MenSCs) promoted axon regeneration in rats with SCI, while the abominable microenvironment after the SCI inhibited the survival of stem cells after transplantation. Biomaterials can support the activity of stem cells and accelerate the functional reconstruction of the injured spinal cord. In this study, we constructed a novel composite scaffold consisting of the decellularized spinal cord extracellular matrix-gel (DSCG) and the GelMA hydrogel, which harbored high water retention, wettability, degradability and soft mechanical property. , the DSCG/GelMA composite scaffold provided a dual bionic microenvironment with optimized bioactive components and favorable microstructures for the adhesion, proliferation and differentiation of MenSCs. After that, we prepared MenSC-encapsulated DSCG/GelMA composite scaffolds to bridge the 2 mm gap in rats with completely transected SCI. The results showed that the combined use of the DSCG/GelMA composite scaffold with MenSCs improved the motor function, reduced the inflammatory response, promoted neuronal differentiation, and inhibited the proliferation of reactive astrocytes after spinal cord injury. Altogether, our study provided a promising novel therapeutic option of using bioactive materials synergistic with stem cells for the treatment of SCI.

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Source
http://dx.doi.org/10.1039/d2tb00792dDOI Listing

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