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在LEC突变大鼠中,从CD4+8+胸腺细胞到CD4+8-胸腺细胞的成熟停滞是由骨髓来源的细胞引起的。

Maturational arrest from CD4+8+ to CD4+8- thymocytes is caused by the bone marrow-derived cells in LEC mutant rats.

作者信息

Sakai T, Agui T, Matsumoto K

机构信息

Institute for Animal Experimentation, University of Tokushima School of Medicine, Japan.

出版信息

Immunol Lett. 1993 Oct;38(2):145-52. doi: 10.1016/0165-2478(93)90180-a.

Abstract

LEC rats exhibit a congenital maturational arrest from CD4+8+ to CD4+8- but not to CD4-8+ cells in the thymus. To elucidate a cause of this mutation, bone marrow (BM) chimera rats were made between LEC and normal (WKAH) rats. In (WKAH-->LEC) BM chimera rats, donor-derived T cells matured normally, suggesting that LEC rat thymic stroma has a normal ability in supporting thymocyte differentiation. On the other hand in (LEC-->WKAH) BM chimera rats, LEC rat BM-derived T cells showed the arrest of maturation from CD4+8+ to CD4+8- cells in spite of having normal functions of WKAH rat-derived thymic stroma. In these chimeric rats, even though the maturational arrest from CD4+8+ to CD4+8- cells occurred in the thymus, CD4+ cells were found in peripheral lymph nodes (LNs), suggesting that these CD4+ cells differentiated extrathymically. These results suggest that the maturational arrest from CD4+8+ to CD+8- thymocytes is caused by BM-derived cells but not by thymic stroma.

摘要

LEC大鼠在胸腺中表现出从CD4⁺8⁺细胞到CD4⁺8⁻细胞的先天性成熟停滞,但不存在到CD4⁻8⁺细胞的成熟停滞。为了阐明这种突变的原因,构建了LEC大鼠与正常(WKAH)大鼠之间的骨髓(BM)嵌合大鼠。在(WKAH→LEC)BM嵌合大鼠中,供体来源的T细胞正常成熟,这表明LEC大鼠胸腺基质在支持胸腺细胞分化方面具有正常能力。另一方面,在(LEC→WKAH)BM嵌合大鼠中,尽管具有WKAH大鼠来源胸腺基质的正常功能,但LEC大鼠BM来源的T细胞仍表现出从CD4⁺8⁺细胞到CD4⁺8⁻细胞的成熟停滞。在这些嵌合大鼠中,尽管胸腺中发生了从CD4⁺8⁺细胞到CD4⁺8⁻细胞的成熟停滞,但在外周淋巴结(LN)中发现了CD4⁺细胞,这表明这些CD4⁺细胞是在胸腺外分化的。这些结果表明,从CD4⁺8⁺胸腺细胞到CD4⁺8⁻胸腺细胞的成熟停滞是由BM来源的细胞引起的,而不是由胸腺基质引起的。

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