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* Coculture with Partial Digestion Notochordal Cell-Rich Nucleus Pulposus Tissue Activates Degenerative Human Nucleus Pulposus Cells.

Authors :
Bai XD
Li XC
Chen JH
Guo ZM
Hou LS
Wang DL
He Q
Ruan DK
Source :
Tissue engineering. Part A [Tissue Eng Part A] 2017 Aug; Vol. 23 (15-16), pp. 837-846. Date of Electronic Publication: 2017 Feb 28.
Publication Year :
2017

Abstract

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.

Details

Language :
English
ISSN :
1937-335X
Volume :
23
Issue :
15-16
Database :
MEDLINE
Journal :
Tissue engineering. Part A
Publication Type :
Academic Journal
Accession number :
28145804
Full Text :
https://doi.org/10.1089/ten.TEA.2016.0428