Woodruff R H, Franklin R J
MRC Cambridge Centre for Brain Repair, Department of Clinical Veterinary Medicine, University of Cambridge, Cambridge, UK.
Neuropathol Appl Neurobiol. 1999 Jun;25(3):226-35. doi: 10.1046/j.1365-2990.1999.00172.x.
To gain insights into the mechanisms of myelin repair in the CNS and to establish the extent to which this process resembles myelination in development we have examined the patterns of expression of transcripts of the major myelin proteins, myelin basic protein (MBP) and proteolipid protein (PLP) during remyelination of lysolecithin-induced demyelination in the adult rat spinal cord. Injection of 1 microliter 1% lysolecithin into the dorsal funiculus caused a dramatic decrease in levels of MBP exon 1 and MBP exon 2-containing transcripts and PLP/DM20 transcripts. Between 10 and 21 days post-lesion induction there was a gradual increase in levels of expression of all transcripts, which had returned to levels associated with normally myelinated spinal cord white matter at 21 days. These increases in levels of expression corresponded to the appearance of remyelinated axons, detected on toluidine blue-stained resin sections. Foci of high levels of expression occurred in regions of the lesion in which new myelin sheath formation was occurring, although the level of expression throughout the lesion never exceeded levels associated with myelin sheath maintenance in normal white matter due to the asynchronous pattern of remyelination. The changes in levels of expression of MBP exon 2 closely followed those of MBP exon 1. Our results indicate that (i) myelin protein gene expression associated with myelinogenesis during remyelination follows a similar pattern to that of myelinogenesis during development and that (ii) in rat models of demyelination changes of expression of MBP exon 1 and exon 2-containing transcripts are of equal value, an observation relevant to quantifying the effects of putative remyelination-enhancing strategies using the lysolecithin model.
为深入了解中枢神经系统中髓鞘修复的机制,并确定该过程与发育过程中髓鞘形成的相似程度,我们研究了成年大鼠脊髓中溶血卵磷脂诱导的脱髓鞘再髓鞘化过程中主要髓鞘蛋白——髓鞘碱性蛋白(MBP)和蛋白脂蛋白(PLP)转录本的表达模式。将1微升1%的溶血卵磷脂注射到背侧索中,导致含MBP外显子1和MBP外显子2的转录本以及PLP/DM20转录本的水平急剧下降。在损伤诱导后的10至21天之间,所有转录本的表达水平逐渐升高,在21天时已恢复到与正常髓鞘化脊髓白质相关的水平。这些表达水平的升高与在甲苯胺蓝染色的树脂切片上检测到的再髓鞘化轴突的出现相对应。尽管由于再髓鞘化的异步模式,整个损伤区域的表达水平从未超过正常白质中与髓鞘维持相关的水平,但高水平表达的病灶出现在正在形成新髓鞘的损伤区域。MBP外显子2表达水平的变化与MBP外显子1的变化密切相关。我们的结果表明:(i)再髓鞘化过程中与髓鞘形成相关的髓鞘蛋白基因表达模式与发育过程中的髓鞘形成模式相似;(ii)在脱髓鞘大鼠模型中,含MBP外显子1和外显子2的转录本表达变化具有同等价值,这一观察结果与使用溶血卵磷脂模型量化假定的再髓鞘化增强策略的效果相关。