Wictorin K, Brundin P, Gustavii B, Lindvall O, Björklund A
Department of Medical Cell Research, University of Lund, Sweden.
Nature. 1990 Oct 11;347(6293):556-8. doi: 10.1038/347556a0.
The failure of lesioned axons to regenerate over long distances in the mammalian central nervous system (CNS) is not due to an inability of central neurons to regenerate, but rather to the non-permissive nature of the CNS tissue environment. Regenerating CNS axons, which grow well within a peripheral nerve, for example, fail to penetrate mature CNS tissue by more than about 1 mm. Recent evidence indicates that this may be due to inhibitory membrane proteins associated with CNS oligodendrocytes and myelin. We report here that human telencephalic neuroblasts implanted into the excitotoxically lesioned striatum of adult rats can escape or neutralize this inhibitory influence of the adult CNS environment and extend axons along major myelinated fibre tracts for distances of up to approximately 20 mm. The axons were seen to elongate along the paths of the striato-nigral and cortico-spinal tracts to reach the substantia nigra, the pontine nuclei and the cervical spinal cord, which are the normal targets for the striatal and cortical projection neurons likely to be present in these implants.
在哺乳动物中枢神经系统(CNS)中,受损轴突无法进行长距离再生,这并非是由于中枢神经元缺乏再生能力,而是由于CNS组织环境具有非许可性。例如,在周围神经中能良好生长的再生CNS轴突,在成熟的CNS组织中却无法穿透超过约1毫米的距离。最近的证据表明,这可能是由于与CNS少突胶质细胞和髓磷脂相关的抑制性膜蛋白所致。我们在此报告,植入成年大鼠经兴奋性毒素损伤的纹状体中的人端脑神经母细胞能够逃避或中和成年CNS环境的这种抑制性影响,并沿着主要的有髓纤维束延伸轴突,延伸距离可达约20毫米。可以看到轴突沿着纹状体 - 黑质束和皮质 - 脊髓束的路径伸长,到达黑质、脑桥核和颈脊髓,这些是这些植入物中可能存在的纹状体和皮质投射神经元的正常靶标。