Departments of Stem Cell Biology and Histology, Tohoku University Graduate School of Medicine, Aoba-ku, Sendai, Japan.
J Neuropathol Exp Neurol. 2010 Sep;69(9):973-85. doi: 10.1097/NEN.0b013e3181eff6dc.
Human umbilical cord-derived mesenchymal stromal cells (UC-MSCs) that are available from cell banks can be induced to differentiate into various cell types, thereby making them practical potential sources for cell-based therapies. In injured peripheral nerves, Schwann cells (SCs) contribute to functional recovery by supporting axonal regeneration and myelin reconstruction. Here, we first demonstrate a system to induce UC-MSCs to differentiate into cells with SC properties (UC-SCs) by treatment with β-mercaptoethanol followed by retinoic acid and a set of specific cytokines. The UC-SCs are morphologically similar to SCs and express SC markers, including P0, as assessed by immunocytochemistry and reverse transcription polymerase chain reaction. Transplantation of UC-SCs into transected sciatic nerves in adult rats enhanced nerve regeneration. The effectiveness of UC-SCs for axonal regeneration was comparable to that of authentic human SCs based on histological criteria and functional recovery. Immunohistochemistry and immunoelectron microscopy also demonstrated myelination of regenerated axons by UC-SCs. These findings indicate that cells with SC properties and with the ability to support axonal regeneration and reconstruct myelin can be successfully induced from UC-MSCs to promote functional recovery after peripheral nerve injury. This system may be applicable for the development of cell-based therapies.
人脐带间充质干细胞(UC-MSCs)可从细胞库中获得,经过诱导可分化为多种细胞类型,因此成为细胞治疗的潜在实用来源。在受损的周围神经中,施万细胞(SCs)通过支持轴突再生和髓鞘重建有助于功能恢复。在这里,我们首先通过用β-巯基乙醇处理,然后用维甲酸和一组特定的细胞因子处理,证明了一种诱导 UC-MSCs 分化为具有 SC 特性的细胞(UC-SCs)的系统。通过免疫细胞化学和逆转录聚合酶链反应评估,UC-SCs 在形态上类似于 SCs,并表达 SC 标志物,包括 P0。将 UC-SCs 移植到成年大鼠横断的坐骨神经中可增强神经再生。根据组织学标准和功能恢复,UC-SCs 促进轴突再生的效果可与真实的人 SCs 相媲美。免疫组织化学和免疫电镜还表明 UC-SCs 可对再生轴突进行髓鞘形成。这些发现表明,可以成功地从 UC-MSCs 中诱导出具有 SC 特性和支持轴突再生和重建髓鞘能力的细胞,以促进周围神经损伤后的功能恢复。该系统可能适用于细胞治疗的开发。