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Nucleus pulposus degeneration alters properties of resident progenitor cells
Authors:Olga Mizrahi  Dmitriy Sheyn  Wafa Tawackoli  Shiran Ben-David  Susan Su  Ning Li  Anthony Oh  Hyun Bae  Dan Gazit  Zulma Gazit
Institution:1. Department of Molecular Pharmacology, Medical Research Institute, Tokyo Medical and Dental University, Japan;2. Global Center of Excellence (GCOE) Program, Tokyo Medical and Dental University, Japan;3. Department of Periodontology, Tokyo Medical and Dental University, Japan;4. Department of Pharmacology, Division of Molecular Pharmacology, Jichi Medical School, Tochigi, Japan;1. Department of Human Physiology, University of Oregon, Eugene, OR, USA;2. Department of Physical Therapy, University of Evansville, Evansville, IN, USA;3. Liberty Mutual Research Institute for Safety, Hopkinton, MA, USA;1. Department of Sports Medicine, Shanghai Jiaotong University Affiliated Sixth People''s Hospital, No. 600 Yishan Road, Shanghai 200233, China;2. Engineering Research Center for Biomedical Materials of Ministry of Education, East China University of Science and Technology, Shanghai 200237, China;3. Department of Joint Surgery, Shanghai Jiaotong University Affiliated Sixth People''s Hospital, No. 600 Yishan Road, Shanghai 200233, China
Abstract:Background contextThe intervertebral disc (IVD) possesses a minimal capability for self-repair and regeneration. Changes in the differentiation of resident progenitor cells can represent diminished tissue regeneration and a loss of homeostasis. We previously showed that progenitor cells reside in the nucleus pulposus (NP). The effect of the degenerative process on these cells remains unclear.PurposeWe sought to explore the effect of IVD degeneration on the abundance of resident progenitor cells in the NP, their differentiation potential, and their ability to give rise to NP-like cells. We hypothesize that disc degeneration affects those properties.Study designNucleus pulposus cells derived from healthy and degenerated discs were methodically compared for proliferation, differentiation potential, and ability to generate NP-like cells.MethodsIntervertebral disc degeneration was induced in 10 skeletally, mature mini pigs using annular injury approach. Degeneration was induced in three target discs, whereas intact adjacent discs served as controls. The disc degeneration was monitored using magnetic resonance imaging for 6 to 8 weeks. After there was a clear evidence of degeneration, we isolated and compared cells from degenerated discs (D-NP cells NP-derived cells from porcine degenerated discs]) with cells isolated from healthy discs (H-NP cells) obtained from the same animal.ResultsThe comparison showed that D-NP cells had a significantly higher colony-forming unit rate and a higher proliferation rate in vitro. Our data also indicate that although both cell types are able to differentiate into mesenchymal lineages, H-NP cells exhibit significantly greater differentiation toward the chondrogenic lineage and NP-like cells than D-NP cells, displaying greater production of glycosaminoglycans and higher gene expression of aggrecan and collagen IIa.ConclusionsBased on these findings, we conclude that IVD degeneration has a meaningful effect on the cells in the NP. D-NP cells clearly go through the regenerative process; however, this process is not powerful enough to facilitate full regeneration of the disc and reverse the degenerative course. These findings facilitate deeper understanding of the IVD degeneration process and trigger further studies that will contribute to development of novel therapies for IVD degeneration.
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