Shi Enyi, Kazui Teruhisa, Jiang Xiaojing, Washiyama Naoki, Yamashita Katsushi, Terada Hitoshi, Bashar Abul Hasan Muhammad
Department of Cardiac Surgery, First Affiliated Hospital, China Medical University, Shenyang, China.
Ann Thorac Surg. 2007 Apr;83(4):1484-90. doi: 10.1016/j.athoracsur.2006.11.048.
Prophylactic transplantation of marrow stromal cells (MSCs) before spinal cord ischemia has been shown to attenuate neurologic injures. We sought to investigate the therapeutic effect of MSCs on ischemia-injured spinal cord.
Marrow stromal cells were expanded in vitro and prelabeled with bromodeoxyuridine. Spinal cord ischemia was induced in rabbits by infrarenal aortic occlusion for 30 minutes. Four groups were enrolled. About 1 x 10(8) MSCs were intrathecally injected 2 hours (group MSC-2h), 24 hours (group MSC-24h), or 48 hours (group MSC-48h) after spinal cord ischemia, respectively. The control group received intrathecal injection of medium alone. Hind-limb motor function was assessed during a 28-day recovery period with Tarlov criteria, and then histologic examination was performed.
Marrow stromal cells still could be found in the spinal cord 4 weeks after transplantation. The capillary density in the ventral gray matter was significantly increased in the three MSC-treated groups (p < 0.01 versus control group, respectively). After a 28-day recovery, marked functional improvement was detected in group MSC-2h (from day 1 to 28, p < 0.05, versus control group, respectively) and group MSC-24h (from day 14 to 28, p < 0.05, versus control group, respectively), but not in group MSC-48h. The number of intact motor neurons was much greater in group MSC-2h (p < 0.05, versus control group).
Intrathecal injection of MSCs enhances angiogenesis in the host spinal cord and improves the motor functional recovery after spinal cord ischemia. The therapeutic time window is critical for the therapeutic effect of MSCs.
脊髓缺血前预防性移植骨髓基质细胞(MSCs)已被证明可减轻神经损伤。我们旨在研究MSCs对缺血性损伤脊髓的治疗作用。
体外扩增骨髓基质细胞并用溴脱氧尿苷进行预标记。通过肾下腹主动脉阻断30分钟诱导兔脊髓缺血。共纳入四组。分别在脊髓缺血后2小时(MSC-2h组)、24小时(MSC-24h组)或48小时(MSC-48h组)鞘内注射约1×10⁸个MSCs。对照组仅鞘内注射培养基。在28天的恢复期内用塔尔洛夫标准评估后肢运动功能,然后进行组织学检查。
移植后4周仍可在脊髓中发现骨髓基质细胞。三个MSC治疗组腹侧灰质中的毛细血管密度显著增加(分别与对照组相比,p<0.01)。经过28天的恢复,MSC-2h组(从第1天到28天,分别与对照组相比,p<0.05)和MSC-24h组(从第14天到28天,分别与对照组相比,p<0.05)检测到明显的功能改善,但MSC-48h组未出现。MSC-2h组完整运动神经元的数量明显更多(与对照组相比,p<0.05)。
鞘内注射MSCs可增强宿主脊髓中的血管生成并改善脊髓缺血后的运动功能恢复。治疗时间窗对MSCs的治疗效果至关重要。