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人胸腺瘤的肿瘤性胸腺上皮细胞在体外支持T细胞从CD4-CD8-细胞发育为CD4+CD8+细胞。

Neoplastic thymic epithelial cells of human thymoma support T cell development from CD4-CD8- cells to CD4+CD8+ cells in vitro.

作者信息

Inoue M, Fujii Y, Okumura M, Takeuchi Y, Shiono H, Miyoshi S, Matsuda H, Shirakura R

机构信息

First Department of Surgery, Osaka University Medical School, Suita, Japan.

出版信息

Clin Exp Immunol. 1998 Jun;112(3):419-26. doi: 10.1046/j.1365-2249.1998.00606.x.

Abstract

Human thymoma is a thymic epithelial cell tumour which often contains a large number of immature T cells and is frequently associated with autoimmune diseases. Since thymic epithelial cells play key roles in the development and selection of T cells in the normal thymus, we hypothesized that the neoplastic thymic epithelial cells of thymoma may support T cell differentiation in the tumour. We characterized CD4-CD8- cells in thymoma and applied an in vitro reconstitution culture system using the CD4-CD8- cells and the neoplastic epithelial cells isolated from thymoma. CD34, a stem cell marker, was expressed on 29.9 +/- 12.2% of CD4-CD8- cells in thymoma. TCRgammadelta was expressed on 27.4 +/- 15.1% of CD4-CD8- cells and CD19, a B cell marker, was expressed on 14.1 +/- 23.1% of CD4-CD8- cells. CD4-CD8- cells expressed both IL-7R alpha-chain and common gamma-chain. Purified CD4-CD8- cells from thymomas were cultured with the neoplastic epithelial cells, and their differentiation into CD4+CD8+ cells via CD4 single-positive intermediates was observed within 9 days' co-culture in the presence of recombinant IL-7. Furthermore, we examined the reconstitution culture using CD34+CD4-CD8- cells purified from normal infant thymus. The CD34+CD4-CD8- cells in normal thymus also differentiated to CD4+CD8+ cells in the allogeneic co-culture with the neoplastic epithelial cells of thymoma. These results indicate that the tumour cells of thymoma retain the function of thymic epithelial cells and can induce differentiation of T cells in thymoma.

摘要

人类胸腺瘤是一种胸腺上皮细胞肿瘤,通常含有大量未成熟T细胞,且常与自身免疫性疾病相关。由于胸腺上皮细胞在正常胸腺中T细胞的发育和选择过程中发挥关键作用,我们推测胸腺瘤的肿瘤性胸腺上皮细胞可能支持肿瘤内T细胞的分化。我们对胸腺瘤中的CD4-CD8-细胞进行了表征,并应用了一种体外重建培养系统,该系统使用从胸腺瘤中分离出的CD4-CD8-细胞和肿瘤上皮细胞。干细胞标志物CD34在胸腺瘤中29.9±12.2%的CD4-CD8-细胞上表达。TCRγδ在27.4±15.1%的CD4-CD8-细胞上表达,B细胞标志物CD19在14.1±23.1%的CD4-CD8-细胞上表达。CD4-CD8-细胞同时表达IL-7Rα链和共同γ链。将胸腺瘤中纯化的CD4-CD8-细胞与肿瘤上皮细胞一起培养,在重组IL-7存在的情况下,共培养9天内观察到它们通过CD4单阳性中间体分化为CD4+CD8+细胞。此外,我们使用从正常婴儿胸腺中纯化的CD34+CD4-CD8-细胞进行了重建培养。正常胸腺中的CD34+CD4-CD8-细胞在与胸腺瘤的肿瘤上皮细胞进行异基因共培养时也分化为CD4+CD8+细胞。这些结果表明,胸腺瘤的肿瘤细胞保留了胸腺上皮细胞的功能,并且能够诱导胸腺瘤中T细胞的分化。

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