Wu Hao, Zeng Xiaoli, Yu Jiayue, Shang Yupan, Tu Mei, Cheang Lek Hang, Zhang Jiaqing
Department of Orthopedic Surgery, The First Affiliated Hospital, Jinan University, Guangzhou 510632, China.
Department of Biochemistry and Molecular Biology, School of Preclinical Medicine, Jinan University, Guangzhou 510632, China.
Exp Cell Res. 2017 Dec 15;361(2):324-332. doi: 10.1016/j.yexcr.2017.10.034. Epub 2017 Oct 31.
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.
基于间充质干细胞的疗法已被提议作为治疗椎间盘(IVD)退变的新方法。然而,由于对源自髓核(NP)的干细胞/祖细胞的起源、生物学特性及其对IVD退变的影响了解不全面,这些治疗策略的发展受到了阻碍。本研究的目的是探讨从退变的IVD中分离出的NP干细胞/祖细胞(D-NPMSCs)的生物学特性,包括免疫表型、增殖能力、多向分化能力,以及与人类脐带间充质干细胞(UCMSCs)相比NP特异性细胞表面标志物的表达情况。我们的结果表明,尽管D-NPMSCs与UCMSCs具有间充质基质细胞(MSCs)的共同特征,但D-NPMSCs与UCMSCs在表型特征和生物学能力方面存在显著差异。D-NPMSCs表达较低水平的MSCs表型标志物CD29和CD105,并且增殖能力和分化潜能降低,这可能解释了独特的NP微环境和椎间盘再生能力差的原因。本研究将为进一步了解基于干细胞治疗IVD退变的机制奠定基础。