Totoiu Minodora O, Nistor Gabriel I, Lane Thomas E, Keirstead Hans S
Reeve-Irvine Research Center, Department of Anatomy and Neurobiology, College of Medicine, University of California at Irvine, 2111 Gillespie Neuroscience Research Facility, Irvine, CA 92697-4292, USA.
Exp Neurol. 2004 Jun;187(2):254-65. doi: 10.1016/j.expneurol.2004.01.028.
The behavior and myelinogenic properties of glial cells have been well documented following transplantation into regions of focal experimental demyelination in animal models. However, the ability of glial cell preparations to remyelinate in such models does not necessarily indicate that their transplantation into demyelinated lesions in clinical disease will be successful. One of the precluding factors in this regard is a greater understanding of the environmental conditions that will support transplant-mediated remyelination. In this study, we determined whether the complex and reactive CNS environment of the mouse hepatitis virus (MHV) model of multiple sclerosis (MS) could support transplant-mediated remyelination. Striatal neural precursors derived from postnatal day 1 mice were committed to a glial cell lineage and labeled. Immunohistochemical staining indicated that this population generated >93% glial cells following differentiation in vitro. Transplantation of glial-committed progenitor cells into the T8 spinal cord of MHV-infected mice demonstrating complete hindlimb paralysis resulted in migration of cells up to 12 mm from the implantation site and remyelination of up to 67% of axons. Transplanted-remyelinated animals contained approximately 2x the number of axons within sampled regions of the ventral and lateral columns as compared to non-transplanted animals, suggesting that remyelination is associated with axonal sparing. Furthermore, transplantation resulted in behavioral improvement. This study demonstrates for the first time that transplant-mediated remyelination is possible in the pathogenic environment of the MHV demyelination model and that it is associated with locomotor improvement.
在动物模型中,将神经胶质细胞移植到局灶性实验性脱髓鞘区域后,其行为和髓鞘形成特性已有充分记录。然而,在这类模型中神经胶质细胞制剂进行髓鞘再生的能力并不一定表明将其移植到临床疾病的脱髓鞘病变中会取得成功。在这方面的一个阻碍因素是对支持移植介导的髓鞘再生的环境条件有更深入的了解。在本研究中,我们确定了多发性硬化症(MS)小鼠肝炎病毒(MHV)模型复杂且具有反应性的中枢神经系统环境是否能够支持移植介导的髓鞘再生。从出生后第1天的小鼠中分离出的纹状体神经前体细胞定向分化为神经胶质细胞系并进行标记。免疫组织化学染色表明,该群体在体外分化后产生了>93%的神经胶质细胞。将神经胶质定向祖细胞移植到表现出完全后肢麻痹的MHV感染小鼠的T8脊髓中,结果细胞从植入部位向上迁移了12毫米,并且高达67%的轴突实现了髓鞘再生。与未移植的动物相比,移植后实现髓鞘再生的动物在腹侧和外侧柱的采样区域内轴突数量大约是其两倍,这表明髓鞘再生与轴突保留有关。此外,移植还带来了行为改善。这项研究首次证明,在MHV脱髓鞘模型的致病环境中移植介导的髓鞘再生是可行的,并且与运动功能改善有关。