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体外胸腺上皮。V. 胸腺细胞与培养的胸腺上皮细胞的结合。

Thymic epithelium in vitro. V. Binding of thymocytes to cultured thymic epithelial cells.

作者信息

Muñoz-Blay T, Nieburgs A C, Cohen S

机构信息

Department of Pathology, University of Connecticut Health Center, Farmington 06032.

出版信息

Cell Immunol. 1987 Oct 15;109(2):371-83. doi: 10.1016/0008-8749(87)90320-0.

Abstract

Direct contact between thymocytes and thymic stromal elements may be one of the mechanisms involved in thymocyte differentiation. Thymic lymphoepithelial complexes have been isolated in which thymocytes appear to be in direct association with cortical epithelial cells. We have previously reported the isolation and successful culture of two morphologically distinct types of murine thymic epithelial cells. We have utilized these to study the interactions of lymphoid and epithelial cells by means of an in vitro assay of the binding of radiolabeled thymocytes to monolayers of these cultured thymic epithelial cells. The percentage of bound cells increased rapidly during the first hour of incubation, reaching approximately 40% binding. Binding continued to increase slowly until plateau levels were reached at approximately 5 hr. Thymocyte binding to thymic epithelium, but not fibroblast monolayers, was trypsin-sensitive, suggesting that specific protein interactions may be involved. Binding of thymocytes to epithelium was temperature-dependent, involved formation of cytoplasmic projections, and was inhibited by cytochalasin B. We also found that cortical thymocytes (peanut agglutinin-positive (PNA+)cells) bound to cultured epithelium to a greater degree than medullary thymocytes (PNA- cells). This correlates with in vivo studies by others in which thymocytes associated with lymphoepithelial complexes have been found to have immature phenotypes. This system provides a means for a quantitative study of the role of cell to cell contact in the process of thymocyte selection and differentiation.

摘要

胸腺细胞与胸腺基质成分之间的直接接触可能是参与胸腺细胞分化的机制之一。已分离出胸腺淋巴上皮复合体,其中胸腺细胞似乎与皮质上皮细胞直接相关。我们之前报道过两种形态不同的小鼠胸腺上皮细胞的分离和成功培养。我们利用这些细胞,通过放射性标记的胸腺细胞与这些培养的胸腺上皮细胞单层结合的体外试验,来研究淋巴细胞与上皮细胞之间的相互作用。在孵育的第一个小时内,结合细胞的百分比迅速增加,达到约40%的结合率。结合率继续缓慢增加,直到大约5小时达到平台期。胸腺细胞与胸腺上皮而非成纤维细胞单层的结合对胰蛋白酶敏感,这表明可能涉及特定的蛋白质相互作用。胸腺细胞与上皮的结合是温度依赖性的,涉及细胞质突起的形成,并被细胞松弛素B抑制。我们还发现,皮质胸腺细胞(花生凝集素阳性(PNA+)细胞)比髓质胸腺细胞(PNA-细胞)与培养的上皮结合程度更高。这与其他人的体内研究结果相关,在这些研究中,已发现与淋巴上皮复合体相关的胸腺细胞具有未成熟的表型。该系统为定量研究细胞间接触在胸腺细胞选择和分化过程中的作用提供了一种方法。

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