Department of Orthopaedic Surgery, Duke University Medical Center, Durham, North Carolina, United States of America.
PLoS One. 2013 Sep 25;8(9):e75548. doi: 10.1371/journal.pone.0075548. eCollection 2013.
A large percentage of the population may be expected to experience painful symptoms or disability associated with intervertebral disc (IVD) degeneration - a condition characterized by diminished integrity of tissue components. Great interest exists in the use of autologous or allogeneic cells delivered to the degenerated IVD to promote matrix regeneration. Induced pluripotent stem cells (iPSCs), derived from a patient's own somatic cells, have demonstrated their capacity to differentiate into various cell types although their potential to differentiate into an IVD cell has not yet been demonstrated. The overall objective of this study was to assess the possibility of generating iPSC-derived nucleus pulposus (NP) cells in a mouse model, a cell population that is entirely derived from notochord. This study employed magnetic activated cell sorting (MACS) to isolate a CD24(+) iPSC subpopulation. Notochordal cell-related gene expression was analyzed in this CD24(+) cell fraction via real time RT-PCR. CD24(+) iPSCs were then cultured in a laminin-rich culture system for up to 28 days, and the mouse NP phenotype was assessed by immunostaining. This study also focused on producing a more conducive environment for NP differentiation of mouse iPSCs with addition of low oxygen tension and notochordal cell conditioned medium (NCCM) to the culture platform. iPSCs were evaluated for an ability to adopt an NP-like phenotype through a combination of immunostaining and biochemical assays. Results demonstrated that a CD24(+) fraction of mouse iPSCs could be retrieved and differentiated into a population that could synthesize matrix components similar to that in native NP. Likewise, the addition of a hypoxic environment and NCCM induced a similar phenotypic result. In conclusion, this study suggests that mouse iPSCs have the potential to differentiate into NP-like cells and suggests the possibility that they may be used as a novel cell source for cellular therapy in the IVD.
预计很大一部分人群会经历与椎间盘(IVD)退变相关的疼痛症状或残疾-这种情况的特征是组织成分完整性降低。人们对将自体或同种异体细胞递送到退变的 IVD 以促进基质再生的应用非常感兴趣。诱导多能干细胞(iPSCs)源自患者自身的体细胞,已证明其能够分化为各种细胞类型,尽管尚未证明其分化为 IVD 细胞的潜力。本研究的总体目标是评估在小鼠模型中生成 iPSC 衍生的髓核(NP)细胞的可能性,这是一种完全源自脊索的细胞群体。本研究采用磁激活细胞分选(MACS)分离 CD24+ iPSC 亚群。通过实时 RT-PCR 分析该 CD24+细胞群中的脊索细胞相关基因表达。然后将 CD24+ iPSCs 在富含层粘连蛋白的培养系统中培养长达 28 天,并通过免疫染色评估小鼠 NP 表型。本研究还专注于通过向培养平台中添加低氧张力和脊索细胞条件培养基(NCCM)来为小鼠 iPSC 的 NP 分化产生更有利的环境。通过免疫染色和生化测定组合评估 iPSC 采用 NP 样表型的能力。结果表明,可以回收 CD24+的小鼠 iPSC 并分化为能够合成类似于天然 NP 的基质成分的群体。同样,添加低氧环境和 NCCM 诱导了类似的表型结果。总之,本研究表明,小鼠 iPSCs 有可能分化为 NP 样细胞,并表明它们可能被用作 IVD 细胞治疗的新型细胞来源。