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人胎肝和胸腺中T细胞前体的表型与功能分析:T细胞和髓细胞发育早期的CD7表达

Phenotypic and functional analysis of T-cell precursors in the human fetal liver and thymus: CD7 expression in the early stages of T- and myeloid-cell development.

作者信息

Bárcena A, Muench M O, Galy A H, Cupp J, Roncarolo M G, Phillips J H, Spits H

机构信息

Human Immunology Department, DNAX Research Institute, Palo Alto, CA 94304-1104.

出版信息

Blood. 1993 Dec 1;82(11):3401-14.

PMID:7694684
Abstract

It has been proposed that the CD7 molecule is the first antigen expressed on the membrane of cells committed to the T-cell lineage during human fetal T-cell ontogeny. To further identify the pre-T cell subpopulation that migrates to the thymus early in ontogeny, we analyzed the phenotypic and functional characteristics of the fetal liver populations separated on the basis of CD7 expression. Three populations expressing different levels of CD7 were observed: CD7bright, CD7dull, and CD7-. A CD7bright population depleted of mature T, B, and myeloid cells (lineage negative, lin-) and mostly composed of CD56+ CD34- natural killer cells did not mature into T cells in a fetal thymic organ culture (FTOC) assay and was devoid of myeloid progenitors in a clonal colony-forming cell assay. In contrast, the CD7-/dull CD34+ lin- populations were capable of differentiating into phenotypically mature T cells after injection into FTOC and contained early myeloid progenitors. Here we phenotypically compared the fetal liver CD7 populations with the most immature fetal thymic subset that differentiated in the FTOC assay, namely the triple negative (TN, CD3-CD4-CD8-) thymocytes. Fetal TN lin- expressed high levels of CD34 marker and were further subdivided by their expression of CD1 antigen, because CD1- TN thymocytes express higher levels of CD34 antigen compared with CD1+ TN cells. CD1- lin -TN thymocytes are characterized by expressing high levels of CD2, CD7, and CD34 markers and dull levels of CD5, CD10, and CD28 molecules. We could not find fetal liver pre-T cells with a phenotype equivalent to that of TN thymocytes. Our data show that CD7 does not necessarily identify T-cell precursors during fetal T-cell development and strongly support the hypothesis that the acquisition of early T-cell markers as CD2, CD28, and CD5 molecules on the cell surface of T-cell progenitors takes place intrathymically.

摘要

有人提出,CD7分子是人类胎儿T细胞个体发育过程中,在T细胞谱系的细胞表面表达的首个抗原。为了进一步鉴定在个体发育早期迁移至胸腺的前T细胞亚群,我们分析了基于CD7表达分离出的胎儿肝脏群体的表型和功能特征。观察到三个表达不同水平CD7的群体:CD7明亮型、CD7暗淡型和CD7阴性型。一个CD7明亮型群体,缺乏成熟的T细胞、B细胞和髓样细胞(谱系阴性,lin-),主要由CD56+ CD34-自然杀伤细胞组成,在胎儿胸腺器官培养(FTOC)试验中不会成熟为T细胞,并且在克隆集落形成细胞试验中没有髓样祖细胞。相比之下,CD7阴性/暗淡型CD34+ lin-群体在注入FTOC后能够分化为表型成熟的T细胞,并且含有早期髓样祖细胞。在这里,我们对胎儿肝脏CD7群体与在FTOC试验中分化的最不成熟的胎儿胸腺亚群,即三阴性(TN,CD3-CD4-CD8-)胸腺细胞进行了表型比较。胎儿TN lin-表达高水平的CD34标志物,并根据其CD1抗原的表达进一步细分,因为与CD1+ TN细胞相比,CD1- TN胸腺细胞表达更高水平的CD34抗原。CD1- lin -TN胸腺细胞的特征是表达高水平的CD2、CD7和CD34标志物以及低水平的CD5、CD10和CD28分子。我们未能找到具有与TN胸腺细胞相当表型的胎儿肝脏前T细胞。我们的数据表明CD7在胎儿T细胞发育过程中不一定能识别T细胞前体,并有力支持了T细胞祖细胞细胞表面上早期T细胞标志物如CD2、CD28和CD5分子是在胸腺内获得的这一假说。

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