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髓质胸腺上皮细胞诱导对细胞内蛋白质的耐受性。

Medullary thymic epithelial cells induce tolerance to intracellular proteins.

作者信息

Oukka M, Cohen-Tannoudji M, Tanaka Y, Babinet C, Kosmatopoulos K

机构信息

INSERM Unit 267, Paul Brousse Hospital, Villejuif, France.

出版信息

J Immunol. 1996 Feb 1;156(3):968-75.

PMID:8558024
Abstract

The role of the medullary thymic epithelial cells in tolerance induction to MHC class I restricted self peptides has been analyzed by studying the beta-galactosidase (beta-gal)-specific cytotoxic T cell response of a transgenic mouse expressing beta-gal in the thymus, skin, and central nervous system (Tg beta-gal mouse). Our results showed that: 1) beta-gal expression in the thymus was limited in a subpopulation of medullary epithelial cells, and bone marrow-derived thymic cells were beta-gal-1; 2) Tg beta-gal mice did not mount an anti-beta-gal CTL response even in the presence of exogenous IL-2, while Tg beta-gal-->B6 chimeras responded to beta-gal as strongly as NTg beta-gal mice; 3) Tg beta-gal mice did not generate CTL against the immunodominant Kb-restricted beta-gal 497-504 peptide; 4) tolerance was due to the thymic epithelial cells that expressed beta-gal because nude mice grafted with thymus from Tg beta-gal mice were also unable to respond to beta-gal; 5) the Tg beta-gal mouse-derived beta-gal+ medullary epithelial TEC.X10 line presented the Kb-restricted beta-gal 497-504 epitope. In conclusion, these results demonstrate that medullary thymic epithelial cells induce a complete tolerance towards class I-restricted self peptides presented on their own surface.

摘要

通过研究在胸腺、皮肤和中枢神经系统中表达β-半乳糖苷酶(β-gal)的转基因小鼠(Tgβ-gal小鼠)对β-半乳糖苷酶特异性细胞毒性T细胞的反应,分析了髓质胸腺上皮细胞在诱导对MHC I类限制性自身肽耐受中的作用。我们的结果表明:1)胸腺中β-gal的表达局限于髓质上皮细胞的一个亚群,而骨髓来源的胸腺细胞不表达β-gal;2)即使存在外源性白细胞介素-2,Tgβ-gal小鼠也不会产生抗β-gal细胞毒性T淋巴细胞(CTL)反应,而Tgβ-gal→B6嵌合体对β-gal的反应与非转基因Tgβ-gal小鼠一样强烈;3)Tgβ-gal小鼠不会产生针对免疫显性的Kb限制性β-gal 497-504肽的CTL;4)耐受性归因于表达β-gal的胸腺上皮细胞,因为移植了Tgβ-gal小鼠胸腺的裸鼠也无法对β-gal产生反应;5)Tgβ-gal小鼠来源的β-gal+髓质上皮TEC.X10系呈递Kb限制性β-gal 497-504表位。总之,这些结果表明,髓质胸腺上皮细胞可诱导对其自身表面呈递的I类限制性自身肽产生完全耐受。

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