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T细胞受体Vβ基因在泰勒氏病毒诱导的小鼠脱髓鞘中的作用。

Role of T cell receptor V beta genes in Theiler's virus-induced demyelination of mice.

作者信息

Rodriguez M, Patick A K, Pease L R, David C S

机构信息

Department of Neurology, Mayo Clinic, Rochester, MN 55905.

出版信息

J Immunol. 1992 Feb 1;148(3):921-7.

PMID:1309845
Abstract

Intracerebral infection of certain strains of mice with Theiler's virus results in chronic immune-mediated demyelination in spinal cord. We used mouse mutants with deletion of the V beta class of TCR genes to examine the role of TCR genes in this demyelinating disease which is similar to multiple sclerosis. Quantitative analysis of spinal cord lesions demonstrated a markedly increased number and extent of demyelinated lesions in persistently infected RIII S/J mice which have a massive deletion of the TCR V beta-chain (V beta 5.2, V beta 8.3, V beta 5.1, V beta 8.2, V beta 5.3, V beta 8.1, V beta 13, V beta 12, V beta 11, V beta 9, V beta 6, V beta 15, V beta 17) compared with B10.RIII mice which are of identical MHC haplotype (H-2r) but have normal complement of V beta TCR genes. In contrast, infection of C57L (H-2b) or C57BR (H-2k) mice which have deletion of the V beta TCR genes (V beta 5.2, V beta 8.3, V beta 5.1, V beta 8.2, V beta 5.3, V beta 8.1, V beta 13, V beta 12, V beta 11, and V beta 9) resulted in few demyelinating lesions. Genetic segregation analysis of (B10.RIII x RIII S/J) x RIII S/J backcrossed mice and (B10.RIII x RIII S/J) F2 mice demonstrated correlation of increased susceptibility to demyelination with deletion of TCR V beta genes. The increase in number of demyelinating lesions correlated with increase in number of virus-Ag+ cells in spinal cord. These experiments provide strong evidence that the structural diversity at the TCR beta-complex can influence susceptibility to virus-induced demyelination.

摘要

用泰勒氏病毒感染某些品系的小鼠会导致脊髓出现慢性免疫介导的脱髓鞘病变。我们利用TCR基因Vβ类缺失的小鼠突变体,来研究TCR基因在这种类似于多发性硬化症的脱髓鞘疾病中的作用。对脊髓病变的定量分析表明,持续感染的RIII S/J小鼠(其TCR Vβ链有大量缺失,缺失的Vβ链包括Vβ5.2、Vβ8.3、Vβ5.1、Vβ8.2、Vβ5.3、Vβ8.1、Vβ13、Vβ12、Vβ11、Vβ9、Vβ6、Vβ15、Vβ17)与具有相同MHC单倍型(H-2r)但Vβ TCR基因互补正常的B10.RIII小鼠相比,脱髓鞘病变的数量和范围显著增加。相比之下,Vβ TCR基因(Vβ5.2、Vβ8.3、Vβ5.1、Vβ8.2、Vβ5.3、Vβ8.1、Vβ13、Vβ12、Vβ11和Vβ9)缺失的C57L(H-2b)或C57BR(H-2k)小鼠感染后,脱髓鞘病变较少。对(B10.RIII×RIII S/J)×RIII S/J回交小鼠和(B10.RIII×RIII S/J)F2小鼠的遗传分离分析表明,脱髓鞘易感性增加与TCR Vβ基因缺失相关。脱髓鞘病变数量的增加与脊髓中病毒-Ag+细胞数量的增加相关。这些实验提供了有力证据,证明TCRβ复合体的结构多样性会影响对病毒诱导脱髓鞘的易感性。

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