Lee Seung-Hoon, Chung You-Nam, Kim Yoon-Ha, Kim Young-Ju, Park Jong-Pil, Kwon Dae-Kee, Kwon Oh-Seo, Heo Jae-Hyeok, Kim Yoon-Hee, Ryu Sun, Kang Hyo-Jin, Paek Sun Ha, Wang Kyu-Chang, Kim Seung U, Yoon Byung-Woo
Department of Neurology, Seoul National University and Seoul National University Hospital, Seoul, Korea.
Neurol Res. 2009 Nov;31(9):996-1002. doi: 10.1179/174313209X385626. Epub 2009 Jan 9.
Previous works have reported that the transplantation of neural stem cells (NSCs) may improve functional recovery after spinal cord injury (SCI), but these results have been mainly obtained in rat models. In the present work, the authors sought to determine whether the transplantation of human NSCs improves functional outcome in a canine SCI model and whether transplanted NSCs survive and differentiate.
Human NSCs (HB1. F3 clone) were used in this work. Lateral hemisection at the L2 level was performed in dogs and either (1) Matrigel (200 microl) alone as a growth-promoting matrix or (2) Matrigel seeded with human NSCs (10(7) cells/200 microl) were transplanted into hemisected gaps. Using a canine hind limb locomotor scale, functional outcomes were assessed over 12 weeks. Immunofluorescence staining was performed to examine cell survival, differentiation and axonal regeneration.
Compared with dogs treated with Matrigel alone, dogs treated with Matrigel + human NSCs showed significantly better functional recovery (10.3 +/- 0.7 versus 15.6 +/- 0.7, respectively, at 12 weeks; p<0.05). Human nuclei-positive cells were found mainly near hemisected areas in dogs treated with Matrigel + NSCs. In addition, colocalization of human nuclei and neuronal nuclei or myelin basic protein was clearly observed. Moreover, the Matrigel + NSC group showed more ascending sensory axon regeneration.
The transplantation of human NSCs has beneficial effects on functional recovery after SCI, and these NSCs were found to differentiate into mature neurons and/or oligodendrocytes. These results provide baseline data for future clinical applications.
以往研究报道,神经干细胞(NSCs)移植可能改善脊髓损伤(SCI)后的功能恢复,但这些结果主要是在大鼠模型中获得的。在本研究中,作者试图确定人神经干细胞移植是否能改善犬SCI模型的功能结局,以及移植的神经干细胞是否存活并分化。
本研究使用人神经干细胞(HB1.F3克隆)。对犬进行L2水平的侧半横断,然后将(1)单独的基质胶(200微升)作为促生长基质或(2)接种有人神经干细胞(10⁷个细胞/200微升)的基质胶移植到半横断间隙中。使用犬后肢运动评分量表,在12周内评估功能结局。进行免疫荧光染色以检查细胞存活、分化和轴突再生情况。
与单独接受基质胶治疗的犬相比,接受基质胶+人神经干细胞治疗的犬功能恢复明显更好(12周时分别为10.3±0.7和15.6±0.7;p<0.05)。在接受基质胶+神经干细胞治疗的犬中,人核阳性细胞主要在半横断区域附近发现。此外,清楚地观察到了人核与神经元核或髓鞘碱性蛋白的共定位。而且,基质胶+神经干细胞组显示出更多的上行感觉轴突再生。
人神经干细胞移植对SCI后的功能恢复有有益作用,并且发现这些神经干细胞可分化为成熟神经元和/或少突胶质细胞。这些结果为未来的临床应用提供了基线数据。