Comparison of nucleus pulposus stem/progenitor cells isolated from degenerated intervertebral discs with umbilical cord derived mesenchymal stem cells.

Exp Cell Res

Department of Biochemistry and Molecular Biology, School of Preclinical Medicine, Jinan University, Guangzhou 510632, China. Electronic address:

Published: December 2017

AI Article Synopsis

  • Mesenchymal stem-cell therapies are being explored as potential treatments for intervertebral disc (IVD) degeneration, but research is limited due to insufficient knowledge about the characteristics of nucleus pulposus-derived stem cells.* -
  • This study specifically examines stem/progenitor cells from degenerated IVDs (D-NPMSCs) to assess their immune properties, ability to proliferate, and differentiation potential, comparing them to human umbilical cord mesenchymal stem cells (UCMSCs).* -
  • Findings show that D-NPMSCs have notable differences in marker expression and biological functions compared to UCMSCs, suggesting a compromised ability for regeneration in the NP microenvironment, which is crucial for advancing stem

Article Abstract

Mesenchymal stem-cell based therapies have been proposed as novel treatments for intervertebral disc (IVD) degeneration. The development of these treatment strategies, however, has been hindered by the incomplete understanding of the origin, biological properties of nucleus pulposus (NP) derived stem/progenitor cells and their effects on the IVD degeneration. The goal of this study is to explore the biological properties of NP stem/progenitor cells isolated from degenerated IVD (D-NPMSCs) regarding immunotype, proliferative capacity, multi-lineage differentiation abilities, and the expression of NP specific cell surface markers compared to human umbilical cord mesenchymal stem cells (UCMSCs). Our results indicate that although D-NPMSCs shared the mesenchymal stromal cells (MSCs) characteristics with UCMSCs, significant differences exist in phenotype signatures and biological capacities between D-NPMSCs and UCMSCs. D-NPMSCs expressed lower expression levels of CD29 and CD105, the phenotype markers of MSCs, and exhibited reduced proliferation capability and differentiation potentials, which might account for the distinct NP microenvironment and the poor capacity for disc regeneration. This study will lay a foundation for further understanding the mechanism of stem cell-based therapy for IVD degeneration.

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Source
http://dx.doi.org/10.1016/j.yexcr.2017.10.034DOI Listing

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