Department of Orthopaedic Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan; Department of Physiology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.
Department of Orthopaedic Surgery, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.
Stem Cell Reports. 2018 Dec 11;11(6):1416-1432. doi: 10.1016/j.stemcr.2018.10.022. Epub 2018 Nov 29.
Treatment involving regenerative medicine for chronic spinal cord injury (SCI) is difficult due to phase-dependent changes in the intraspinal environment. We previously reported that treatment with a gamma-secretase inhibitor (GSI), which inhibits Notch signaling, promotes the differentiation into mature neurons in human induced pluripotent stem cell-derived neural stem/progenitor cell (hiPSC-NS/PC) transplantation for subacute SCI. Here, we evaluated the efficacy of GSI-treated hiPSC-NS/PC transplantation in treating chronic SCI, which resulted in significantly enhanced axonal regrowth, remyelination, inhibitory synapse formation with the host neural circuitry, and reticulo spinal tract fiber formation. Interestingly, inhibiting Notch signaling with GSI caused phosphorylation of p38 MAPK, which is a key molecule required to promote axonal regeneration. These favorable outcomes contributed to motor function improvement. Therefore, treating cells with GSI provides a beneficial effect after transplantation, even in the chronic phase following SCI.
由于脊髓内环境的时相依赖性变化,涉及再生医学的慢性脊髓损伤 (SCI) 治疗较为困难。我们之前报道过,用γ-分泌酶抑制剂(GSI)治疗可促进 Notch 信号转导抑制,从而促进人诱导多能干细胞源性神经干细胞/祖细胞(hiPSC-NS/PC)移植治疗亚急性 SCI 后向成熟神经元分化。在此,我们评估了 GSI 处理的 hiPSC-NS/PC 移植治疗慢性 SCI 的疗效,结果表明其明显促进了轴突再生、髓鞘再生、与宿主神经回路的抑制性突触形成以及网状脊髓束纤维形成。有趣的是,GSI 抑制 Notch 信号转导会导致 p38 MAPK 磷酸化,这是促进轴突再生所必需的关键分子。这些有利的结果有助于运动功能的改善。因此,GSI 处理细胞在移植后甚至在 SCI 后的慢性期也会产生有益的效果。