Yamada M, Zurbriggen A, Fujinami R S
Department of Pathology, University of California, San Diego, La Jolla.
Am J Pathol. 1990 Dec;137(6):1467-79.
The DA strain of Theiler's murine encephalomyelitis virus (DAV) causes a chronic demyelinating disease in susceptible mouse strains. To elucidate the pathogenesis of DAV-induced demyelination, the authors investigated the spatial and chronologic relationship between virus (antigen and RNA), myelin-specific mRNAs, and demyelination in DAV-infected mice using immunohistochemistry, in situ hybridization, and slot blot hybridization analyses. In spinal cord white matter, viral RNA was detected easily in ventral root entry zones 1 to 2 weeks after infection. Viral RNA increased to maximum levels by 4 weeks after infection, which was associated with inflammation and mild demyelination. At 8 to 12 weeks after infection, when demyelination became most extensive, viral RNA was significantly decreased. Demyelination did not chronologically or spatially parallel the presence of viral RNA within the spinal cord. Decrease of myelin-specific mRNAs, including myelin-basic protein and proteolipid protein mRNAs, was observed within the demyelinating lesions with or without detectable viral RNA. These results indicate that a viral infection of white matter in the early phase of the infection initiates spinal cord disease leading to demyelination, but later an ongoing immunopathologic process contributes to the presence of extensive demyelination.
泰勒氏鼠脑脊髓炎病毒(DAV)的DA株可在易感小鼠品系中引发慢性脱髓鞘疾病。为阐明DAV诱导脱髓鞘的发病机制,作者利用免疫组织化学、原位杂交和狭缝印迹杂交分析,研究了DAV感染小鼠中病毒(抗原和RNA)、髓鞘特异性mRNA与脱髓鞘之间的空间和时间关系。在脊髓白质中,感染后1至2周在腹根进入区很容易检测到病毒RNA。感染后4周病毒RNA增加到最高水平,这与炎症和轻度脱髓鞘有关。感染后8至12周,当脱髓鞘最为广泛时,病毒RNA显著减少。脱髓鞘在时间或空间上与脊髓内病毒RNA的存在并不平行。在有或没有可检测到病毒RNA的脱髓鞘病变中,均观察到髓鞘特异性mRNA(包括髓鞘碱性蛋白和蛋白脂蛋白mRNA)减少。这些结果表明,感染早期白质的病毒感染引发导致脱髓鞘的脊髓疾病,但后期持续的免疫病理过程导致广泛脱髓鞘的出现。