Effect of coculturing canine notochordal, nucleus pulposus and mesenchymal stromal cells for intervertebral disc regeneration

• Published in: Arthritis research & therapy 2015-03, Vol.17 (1), p.60-60, Article 60
• Main Authors: Arkesteijn, Irene T M, Smolders, Lucas A, Spillekom, Sandra, Riemers, Frank M, Potier, Esther, Meij, Björn P, Ito, Keita, Tryfonidou, Marianna A
• Format: Article
• Language: English
• Subjects: Analysis; Animals; Bioengineering; Biomaterials; Biotechnology; Cell Differentiation; Cell Survival; Cells, Cultured; Cervical Vertebrae; Coculture Techniques; Culture Media, Conditioned - pharmacology; Disease Models, Animal; Dogs; Gene expression; Genetic aspects; Health aspects; Human health and pathology; Intervertebral Disc - pathology; Intervertebral Disc Degeneration - pathology; Life Sciences; Lumbar Vertebrae; Mesenchymal Stromal Cells - pathology; Notochord - pathology; Pharmaceutical industry; Rhumatology and musculoskeletal system; Stem cells; Thoracic Vertebrae
• ISSN: 1478-6354; 1478-6362; 1478-6354
• DOI: 10.1186/s13075-015-0569-6

Early degenerative changes in the nucleus pulposus (NP) are observed after the disappearance of notochordal cells (NCs). Thus, it has been suggested that NCs play an important role in maintaining the NP and may have a regenerative potential on other cells of the NP. As the number of resident NP cells (NPCs) decreases in a degenerating disc, mesenchymal stromal (stem) cells (MSCs) may be used for cell supplementation. In this study, using cells of one species, the regenerative potential of canine NCs was assessed in long-term three-dimensional coculture with canine NPCs or MSCs. Canine NCs and canine NPCs or MSCs were cocultured in alginate beads for 28 days under hypoxic and high-osmolarity conditions. Cell viability, cell morphology and DNA content, extracellular matrix production and expression of genes related to NC markers (Brachyury, KRT18) and NP matrix production (ACAN, COL2A1, COL1A1) were assessed after 1, 15 and 28 days of culture. NCs did not completely maintain their phenotype (morphology, matrix production, gene expression) during 28 days of culture. In cocultures of NPCs and NCs, both extracellular matrix content and anabolic gene expression remained unchanged compared with monoculture groups, whereas cocultures of MSCs and NCs showed increased glycosaminoglycan/DNA. However, the deposition of these proteoglycans was observed near the NCs and not the MSCs. Brachyury expression in the MSC and NC coculture group increased in time. The latter two findings indicate a trophic effect of MSCs on NCs rather than vice versa. No regenerative potential of canine NCs on canine NPCs or MSCs was observed in this study. However, significant changes in NC phenotype in long-term culture may have resulted in a suboptimal regenerative potential of these NCs. In this respect, NC-conditioned medium may be better than coculture for future studies of the regenerative potential of NCs.