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辐射骨髓嵌合体中TCR-αβ⁺ CD4⁻CD8⁻皮肤上皮内淋巴细胞的出现情况。

Appearance of TCR-alpha beta+ CD4-CD8- skin intraepithelial lymphocytes in radiation bone marrow chimeras.

作者信息

Ogimoto M, Matsuzaki G, Yoshikai Y, Tauchi Y, Nomoto K

机构信息

Department of Immunology, Kyushu University, Fukuoka, Japan.

出版信息

J Immunol. 1993 Sep 15;151(6):3000-6.

PMID:8376765
Abstract

Thymocytes expressing homogeneous TCR V gamma 5/V delta 1 gene without N nucleotide addition (canonical sequence) have been reported to be positively selected in fetal thymus. Because skin intraepithelial lymphocytes (s-IEL) also express canonical sequence, it is proposed that s-IEL are generated by an epidermis-specific homing of these positive selected fetal V gamma 5/V delta 1-bearing thymocytes. We have reported that positive selection of V gamma 5+ thymocytes is not seen in AKR/J-->C3H/He bone marrow chimeras. In this report, we analyzed the phenotype of donor-derived s-IEL from AKR/J-->C3H/He bone marrow chimeras that appeared in the absence of positive selection of V gamma 5-bearing thymocytes. We found interestingly that almost all donor-derived s-IEL in the bone marrow chimeras expressed TCR-alpha beta lack expression of both CD4 and CD8. Furthermore, TCR-alpha beta+ s-IEL were detected in adult-thymectomized bone marrow chimeras, indicating that the TCR-alpha beta+ s-IEL are extrathymically derived. All these results suggest that the s-IEL expressing TCR-alpha beta appear extrathymically in the absence of positive selection of V gamma 5/V delta 1-bearing thymocytes. Our results may also explain the contradicting result between human s-IEL, which are TCR-alpha beta+ CD4- CD8- and murine s-IEL, and suggest the importance of extrathymic T cell differentiation pathway of the TCR-alpha beta lineage in immune surveillance.

摘要

据报道,在胎儿胸腺中,表达均一的TCR Vγ5/Vδ1基因且未添加N核苷酸(典型序列)的胸腺细胞会被阳性选择。由于皮肤上皮内淋巴细胞(s-IEL)也表达典型序列,因此有人提出,s-IEL是由这些被阳性选择的携带胎儿Vγ5/Vδ1的胸腺细胞向表皮特异性归巢产生的。我们曾报道,在AKR/J→C3H/He骨髓嵌合体中未观察到Vγ5+胸腺细胞的阳性选择。在本报告中,我们分析了来自AKR/J→C3H/He骨髓嵌合体的供体来源的s-IEL的表型,这些嵌合体在未对携带Vγ5的胸腺细胞进行阳性选择的情况下出现。我们有趣地发现,骨髓嵌合体中几乎所有供体来源的s-IEL都表达TCR-αβ,且CD4和CD8均不表达。此外,在成年胸腺切除的骨髓嵌合体中检测到了TCR-αβ+s-IEL,这表明TCR-αβ+s-IEL是胸腺外来源的。所有这些结果表明,在未对携带Vγ5/Vδ1的胸腺细胞进行阳性选择的情况下,表达TCR-αβ的s-IEL在胸腺外出现。我们的结果也可能解释了人类s-IEL(TCR-αβ+CD4-CD8-)和小鼠s-IEL之间相互矛盾的结果,并提示了TCR-αβ谱系的胸腺外T细胞分化途径在免疫监视中的重要性。

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