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短期胸腺基质细胞培养中CD3-4-8-胸腺细胞的分化

Differentiation of CD3-4-8- thymocytes in short-term thymic stromal cell culture.

作者信息

Sen-Majumdar A, Lieberman M, Alpert S, Wiessman I L, Small M

机构信息

Department of Radiation Oncology, Howard Hughes Medical Institute, Stanford University School of Medicine, California 94305.

出版信息

J Exp Med. 1992 Aug 1;176(2):543-51. doi: 10.1084/jem.176.2.543.

Abstract

We have investigated the ability of a heterogeneous thymic stromal cell (HTSC) culture system to promote in vitro differentiation of CD3-4-8- thymocytes. Culture of purified murine CD3-4-8- thymocytes on HTSC for 1 d resulted in the appearance of CD4+8+ cells, which did not occur when the sorted cells were maintained in medium alone. It is remarkable that when the culture period was extended to 2 d, CD3-4-8- progenitors differentiated further to CD4+8- and CD4-8+ cells, which also expressed high levels of TCR-CD3. This rapid differentiation on stroma in vitro appears to outpace parallel development in vivo. The differentiation potential of a subset of CD3-4-8- thymocytes that express high levels of a marker of normal and neoplastic thymic progenitors, the 1C11 antigen, was examined next. 1C11hiCD3-4-8- cells also gave rise to CD4-8+ and CD4+8+ populations after 1 d of culture on HTSC. Extending the culture period to 2 d resulted in a significant percentage of CD3-expressing cells that were CD4+8+, CD4+8- and CD4-8+ cells. These results suggest that in the in vitro HTSC culture system, various subsets of immature thymocytes can differentiate into all the mature phenotypes of cells normally found in the adult mouse thymus. This may provide a novel and rapid assay for thymic progenitors.

摘要

我们研究了异质性胸腺基质细胞(HTSC)培养系统促进CD3 - 4 - 8 - 胸腺细胞体外分化的能力。将纯化的小鼠CD3 - 4 - 8 - 胸腺细胞在HTSC上培养1天,导致出现CD4 + 8 + 细胞,而当分选的细胞单独维持在培养基中时则不会出现这种情况。值得注意的是,当培养期延长至2天时,CD3 - 4 - 8 - 祖细胞进一步分化为CD4 + 8 - 和CD4 - 8 + 细胞,这些细胞也表达高水平的TCR - CD3。体外基质上的这种快速分化似乎超过了体内的平行发育。接下来研究了表达高水平正常和肿瘤性胸腺祖细胞标志物1C11抗原的CD3 - 4 - 8 - 胸腺细胞亚群的分化潜能。1C11hiCD3 - 4 - 8 - 细胞在HTSC上培养1天后也产生了CD4 - 8 + 和CD4 + 8 + 群体。将培养期延长至2天导致出现相当比例的表达CD3的细胞,这些细胞为CD4 + 8 + 、CD4 + 8 - 和CD4 - 8 + 细胞。这些结果表明,在体外HTSC培养系统中,未成熟胸腺细胞的各种亚群可以分化为成年小鼠胸腺中正常发现的所有成熟细胞表型。这可能为胸腺祖细胞提供一种新颖且快速的检测方法。

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