Martínez-Cáceres E, Jaleco A C, Res P, Noteboom E, Weijer K, Spits H
Division of Immunology, The Netherlands Cancer Institute, Amsterdam.
Exp Hematol. 1998 Jul;26(7):588-96.
In this paper we report that suspensions of human fetal thymocytes contain cells that express high levels of CD34 and Thy-1. These cells were characterized with regard to location within the thymus, phenotype, and function. Confocal laser scan analysis of frozen sections of fetal thymus with anti-CD34 and Thy-1 antibodies revealed that the double-labeled cells were located in the pericortical area. In addition, it was found that the CD34+Thy-1+ cells lacked CD45 and CD50, indicating that these cells are not of hematopoietic origin; this was confirmed by the finding that these cells could be cultured as adherent cells in a medium with cholera toxin and dexamethasone, but failed to grow in mixtures of hematopoietic growth factors. Further analysis indicated that most cultured CD34+Thy-1+ cells expressed cytokeratin (CK) 14 but lacked CK 13, suggesting that these cells are immature epithelial cells. Cultured CD34+Thy-1+ cells were able to induce differentiation of CD1-CD34+CD3-CD4-CD8- thymic precursors into CD4+CD8+ cells in a reaggregate culture in the absence of exogenous cytokines. The CD4+CD8+ cells that developed in these cultures did not express CD3, indicating that CD34+Thy-1+ thymic stromal cells are not capable of completing full T cell differentiation of thymic hematopoietic progenitor cells.
在本文中,我们报告称人胎儿胸腺细胞悬液中含有高表达CD34和Thy-1的细胞。对这些细胞在胸腺内的位置、表型和功能进行了表征。用抗CD34和Thy-1抗体对胎儿胸腺冰冻切片进行共聚焦激光扫描分析,结果显示双标记细胞位于皮质周区域。此外,发现CD34+Thy-1+细胞缺乏CD45和CD50,这表明这些细胞并非造血来源;这一发现得到了进一步证实,即这些细胞可在含有霍乱毒素和地塞米松的培养基中作为贴壁细胞培养,但在造血生长因子混合物中无法生长。进一步分析表明,大多数培养的CD34+Thy-1+细胞表达细胞角蛋白(CK)14但缺乏CK 13,提示这些细胞是未成熟的上皮细胞。在无外源性细胞因子的重聚集培养中,培养的CD34+Thy-1+细胞能够诱导CD1-CD34+CD3-CD4-CD8-胸腺前体细胞分化为CD4+CD8+细胞。在这些培养物中产生的CD4+CD8+细胞不表达CD3,这表明CD34+Thy-1+胸腺基质细胞无法使胸腺造血祖细胞完成完全的T细胞分化。