
pmid: 28145804
Recent studies suggested that notochordal cells (NCs) and NC-conditioned medium (NCCM) can stimulate cell viability and matrix production of nucleus pulposus cells (NPCs). However, the potential of notochordal cell-rich nucleus pulposus (NRNP) incorporating the native environment of the intervertebral disc (IVD) has not been evaluated. The objective of this study was to develop an optimal NRNP model and test whether it can allow a significant level of NPC activation in vitro. Rabbit NRNP explants were divided into three groups according to different digestion time: digestion NRNP of 8 h, partial digestion NRNP of 2 h, and natural NRNP. Cell viability and NC phenotype were compared between these groups after 14 days of incubation. The products of the selected partial digestion NRNP group were then cocultured with human degenerated NPCs for 14 days. NPC viability, cell proliferation and senescence, the production of glycosaminoglycan (GAG) found in extracellular matrix, and NP matrix production by NPCs were assessed. The results showed that coculturing with partial digestion NRNP significantly improved the cell proliferation, cell senescence, and disc matrix gene expression of NPCs compared with those in the monoculture group. In addition, GAG/DNA ratio in the coculture group increased significantly, while the level of collagen II protein remained unchanged. In this study, we demonstrated that partial digestion NRNP may show a promising potential for NPC regeneration in IVD tissue engineering.
Male, Nucleus Pulposus, Cell Survival, Notochord, Cell Count, DNA, Intervertebral Disc Degeneration, Middle Aged, Coculture Techniques, Extracellular Matrix, Phenotype, Gene Expression Regulation, Animals, Humans, Female, Rabbits, Cells, Cultured, Cellular Senescence, Cell Proliferation, Glycosaminoglycans
Male, Nucleus Pulposus, Cell Survival, Notochord, Cell Count, DNA, Intervertebral Disc Degeneration, Middle Aged, Coculture Techniques, Extracellular Matrix, Phenotype, Gene Expression Regulation, Animals, Humans, Female, Rabbits, Cells, Cultured, Cellular Senescence, Cell Proliferation, Glycosaminoglycans
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