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T细胞对H-2和Ir基因表型的特异性与胸腺抗原呈递细胞的表型相关。

T-cell specificity for H-2 and Ir gene phenotype correlates with the phenotype of thymic antigen-presenting cells.

作者信息

Longo D L, Schwartz R H

出版信息

Nature. 1980 Sep 4;287(5777):44-6. doi: 10.1038/287044a0.

Abstract

Experiments with chimaeric animals have demonstrated that the H-2 restriction specificity and immune response (Ir) gene phenotype of the T cell is acquired during development in the thymus. The mechanism by which this process occurs is unclear. One level of obligate expression of H-2 and Ir gene products is on the surface of antigen-presenting cells (APCs) which come from bone marrow precursors. We have now examined the turnover of APCs in the thymuses of F1 leads to parent (P) radiation-induced bone marrow chimaeras and found that APCs of donor phenotype appear at about 2 months after reconstitution. If the peripheral T-cell population is depleted after this time, new T cells emerging from the parental thymus (containing F1 APCs) behaving like F1 T cells, suggesting that cells from the bone marrow can influence thymic-directed T-cell differentiation. The thymic APC is an attractive condidate to play such a part in the development of the T-cell repertoire.

摘要

对嵌合体动物的实验表明,T细胞的H-2限制特异性和免疫反应(Ir)基因表型是在胸腺发育过程中获得的。这一过程发生的机制尚不清楚。H-2和Ir基因产物的一个必然表达水平是在来自骨髓前体的抗原呈递细胞(APC)表面。我们现在研究了F1与亲代(P)辐射诱导的骨髓嵌合体胸腺中APC的更新情况,发现供体表型的APC在重建后约2个月出现。如果在此之后外周T细胞群体被耗尽,从亲代胸腺(含有F1 APC)中出现的新T细胞表现得像F1 T细胞,这表明来自骨髓的细胞可以影响胸腺定向的T细胞分化。胸腺APC是在T细胞库发育中发挥这一作用的一个有吸引力的候选者。

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