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II类阳性造血细胞无法在II类缺陷小鼠中介导CD4 + T淋巴细胞的阳性选择。

Class II-positive hematopoietic cells cannot mediate positive selection of CD4+ T lymphocytes in class II-deficient mice.

作者信息

Markowitz J S, Auchincloss H, Grusby M J, Glimcher L H

机构信息

Department of Cancer Biology, Harvard School of Public Health, Boston, MA 02115.

出版信息

Proc Natl Acad Sci U S A. 1993 Apr 1;90(7):2779-83. doi: 10.1073/pnas.90.7.2779.

Abstract

Generation of immunocompetent alpha/beta T-cell receptor-positive T cells from CD4+CD8+ thymocytes depends upon their interaction with thymic major histocompatibility complex (MHC) molecules. This process of positive selection provides mature T cells that can recognize antigens in the context of self-MHC proteins. Previous studies investigating haplotype restriction in thymic and bone-marrow chimeras concluded that radioresistant thymic cortical epithelium directs the positive selection of thymocytes. There is controversy, however, as to whether intra- or extrathymic radiosensitive bone marrow-derived macrophage and dendritic cells also can mediate positive selection. To determine whether CD4+ T cells can be positively selected by hematopoietic cells, we generated chimeric animals expressing MHC class II molecules on either bone marrow-derived or thymic stromal cells by using a recently produced strain of MHC class II-deficient mice. CD4+ T cells developed only when class II MHC molecules were expressed on radioresistant thymic cells. In contrast to what recently has been observed for the selection of CD8+ T lymphocytes, MHC class II-positive bone marrow-derived cells were unable to mediate the selection of CD4+ T cells when the thymic epithelium lacked MHC class II expression. These data suggest that CD4+ and CD8+ T cells may be generated by overlapping, but not identical, mechanisms.

摘要

从CD4⁺CD8⁺胸腺细胞生成具有免疫活性的α/βT细胞受体阳性T细胞,取决于它们与胸腺主要组织相容性复合体(MHC)分子的相互作用。这种阳性选择过程产生了能够在自身MHC蛋白背景下识别抗原的成熟T细胞。先前对胸腺和骨髓嵌合体中单体型限制的研究得出结论,放射抗性胸腺皮质上皮引导胸腺细胞的阳性选择。然而,关于胸腺内或胸腺外放射敏感的骨髓来源巨噬细胞和树突状细胞是否也能介导阳性选择,存在争议。为了确定造血细胞是否能对CD4⁺T细胞进行阳性选择,我们通过使用最近培育出的II类MHC缺陷小鼠品系,培育了在骨髓来源细胞或胸腺基质细胞上表达II类MHC分子的嵌合动物。只有当II类MHC分子在放射抗性胸腺细胞上表达时,CD4⁺T细胞才会发育。与最近观察到的CD8⁺T淋巴细胞选择情况相反,当胸腺上皮缺乏II类MHC表达时,II类MHC阳性骨髓来源细胞无法介导CD4⁺T细胞的选择。这些数据表明,CD4⁺和CD8⁺T细胞可能通过重叠但不相同的机制产生。

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