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非肥胖糖尿病小鼠自身免疫性甲状腺炎中T细胞受体V区β链基因的表达

T-cell receptor V region beta-chain gene expression in the autoimmune thyroiditis of non-obese diabetic mice.

作者信息

Matsuoka N, Bernard N, Concepcion E S, Graves P N, Ben-Nun A, Davies T F

机构信息

Department of Medicine, Mount Sinai School of Medicine, New York, New York.

出版信息

J Immunol. 1993 Aug 1;151(3):1691-701.

PMID:8393051
Abstract

The non-obese diabetic (NOD) mouse develops both a spontaneous T-cell-mediated autoimmune insulitis and, in addition, a well characterized thyroiditis. We have examined the repertoire of murine T-cell receptor (TCR) variable (V) beta-chain genes used by intrathyroidal T cells with specific oligonucleotides that amplified 17 murine V beta gene families in cDNA samples prepared from intact NOD thyroid tissues. Normal NOD thyroid tissue contained only low levels of TCR V gene mRNA. In contrast, NOD mice with histologic thyroiditis showed the marked expression of up to 3 TCR V beta genes consistent with a restricted T-cell invasion. Sequencing of amplified TCR V beta cDNA showed that within each NOD thyroid sample at least one of the overexpressed V beta gene families was clonally expanded. However, the clonally expanded T-cell V gene family was not consistent in all animals. Even within the same TCR V beta gene families, various D and J segments had been rearranged with open reading frames and together with insertions and deletions gave no significant homology at the nucleotide or amino acid level. In summary, these data showed that the intrathyroidal T-cell infiltrate in NOD mice was markedly biased towards the use of a single, but variable, TCR V gene family within each animal. It also appeared that the choice of the TCR V beta chain determined the intrathyroidal infiltrative process rather than the choice of D and/or J regions. However, there was no consistent use of a single TCR V beta chain. As thyroiditis does not occur uniformly in apparently genetically homogeneous animals, reared under similar environmental conditions, it may not be surprising that different TCR V genes are involved in different animals.

摘要

非肥胖型糖尿病(NOD)小鼠不仅会自发发生T细胞介导的自身免疫性胰岛炎,还会发生特征明确的甲状腺炎。我们使用特异性寡核苷酸检测了甲状腺内T细胞所使用的小鼠T细胞受体(TCR)可变(V)β链基因库,这些寡核苷酸可扩增从完整的NOD甲状腺组织制备的cDNA样本中的17个小鼠Vβ基因家族。正常NOD甲状腺组织仅含有低水平的TCR V基因mRNA。相比之下,患有组织学甲状腺炎的NOD小鼠显示出高达3个TCR Vβ基因的显著表达,这与有限的T细胞浸润一致。扩增的TCR Vβ cDNA测序表明,在每个NOD甲状腺样本中,至少有一个过表达的Vβ基因家族发生了克隆性扩增。然而,克隆性扩增的T细胞V基因家族在所有动物中并不一致。即使在相同的TCR Vβ基因家族内,各种D和J片段也已与开放阅读框重排,并且连同插入和缺失在核苷酸或氨基酸水平上没有显著的同源性。总之,这些数据表明,NOD小鼠甲状腺内的T细胞浸润明显偏向于在每只动物中使用单个但可变的TCR V基因家族。似乎TCR Vβ链的选择决定了甲状腺内的浸润过程,而不是D和/或J区域的选择。然而,并没有一致地使用单个TCR Vβ链。由于甲状腺炎在明显基因同质、在相似环境条件下饲养的动物中并非均匀发生,不同的TCR V基因参与不同动物的情况可能并不奇怪。

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