AI Article Synopsis

  • Traditional meniscectomy or suture techniques often lead to unsuccessful self-healing of meniscal tears and can worsen cartilage degeneration and osteoarthritis.
  • A new therapeutic approach using CD56 umbilical cord mesenchymal stem cells encapsulated in a modified decellularized Wharton's Jelly hydrogel (DWJH/CD56Exos) has shown promising potential for enhancing meniscal tear healing.
  • In both in vitro and in vivo studies, the DWJH/CD56Exos demonstrated excellent biocompatibility, supported chondrogenesis, promoted meniscal tissue regeneration, and helped prevent further cartilage degeneration in the knee.

Article Abstract

Traditional meniscectomy or suture for meniscal tear usually leads to failed self-healing, cartilage degeneration and worse osteoarthritis. The strategies that facilitate the healing process of torn meniscus and safeguard knee cartilage against degeneration will be promising for clinical therapy. The CD56 umbilical cord mesenchymal stem cells (UCSCs) (CD56UCSCs) were sorted from Wharton's jelly using flow cytometer. Then, the modified decellularized Wharton's Jelly hydrogel (DWJH) was combined with isolated CD56Exos from CD56UCSCs to fabricate DWJH/CD56Exos. The in vitro studies were performed to characterize the DWJ (decellularized Wharton's Jelly). The injectability and rheological properties were assessed by shear rate and frequency sweep analysis. The biocompatibility and chondrogenic differentiation inducibility of DWJH/CD56Exos were performed on human bone marrow mesenchymal stem cells (hBMSCs) and RAW 264.7 cells. The release dynamics was evaluated in vitro and in vivo experiments. As for the in vivo experiments, the operated rats that subjected to a 2 mm full-thickness longitudinal tear in right medial anterior meniscus were injected a single dose of DWJH/CD56Exos. At 4 and 8 weeks postoperatively, torn meniscus healing and articular cartilage degeneration were evaluated by hematoxylin and eosin (H&E), safranin O/fast green (SO&FG), and Sirius red staining. In in vitro experiments, the injectable DWJH/CD56Exos demonstrated excellent biocompatibility, exosome releasing efficiency, injectable property and chondrogenic inducibility. The results of in vivo experiments revealed that DWJH/CD56Exos degraded over time, promoted meniscal chondrogenesis, organized meniscal extracellular matrix remodeling, safeguard articular cartilage and inhibited secondary cartilage degeneration, which accelerated further facilitated torn meniscus healing. The novel injectable DWJH/CD56Exos promoted meniscal tear healing by promoting meniscal chondrogenesis, safeguarding articular cartilage, and inhibiting secondary cartilage degeneration.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11437876PMC
http://dx.doi.org/10.1016/j.mtbio.2024.101258DOI Listing

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