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小鼠T细胞的碳水化合物分化抗原:在肠道淋巴细胞和肠上皮中的表达。

Carbohydrate differentiation antigens of murine T cells: expression on intestinal lymphocytes and intestinal epithelium.

作者信息

Lefrancois L

出版信息

J Immunol. 1987 May 15;138(10):3375-84.

PMID:2437191
Abstract

Carbohydrate differentiation antigens (CT antigens) which previously had been shown to be associated with cytotoxic T cells were found at high levels on intestinal intraepithelial lymphocytes (IEL) and on the intestinal epithelium. Histological examination of intestinal sections demonstrated that the CT1 MAb defined epitopes on IEL and on epithelial cells located in the base of the villi crypts. The CT2 MAb reacted with IEL but also bound to the majority of cells in the intestinal epithelium. When isolated intestinal cell populations were analyzed by flow cytometry, two major size classes of cells were evident. The smaller cells, corresponding to lymphocytes, were primarily Lyt-2+, with a high proportion expressing CT antigens. Another differentiation antigen defined by the MAb J11d was absent from IEL, indicating that those IEL of T cell origin are likely to be mature because thymocytes, but not peripheral T cells, express the J11d antigen. Two-color fluorescence analysis indicated that the CT determinants were present on the Thy-1+, Lyt-2+, and the Thy-1-, Lyt-2+ subsets of IEL. However, the small percentage of L3T4+ IEL were CT-, further supporting our previous demonstration of a correlation between CT expression and Lyt-2 expression. Interesting phenotypic characteristics of IEL other than CT antigen expression were also detected. IEL did not express the MEL-14 lymphocyte homing receptor, and the cell surface level of LFA-1 was significantly lower than that of other peripheral lymphocytes. It was also shown that a small percentage of IEL express a T cell receptor allotypic marker, indicating that at least some of the cells are mature in terms of T cell receptor gene rearrangements. The large intestinal cells, although CT+, were not hematopoietic in origin because they were T200- and were shown by using chimeric mice not to be bone marrow-derived. In contrast to previously reported results, the cytotoxic activity of IEL was negligible with detectable lysis against NK-sensitive cells and other tumor cells, being observed in only one of seven experiments. Thus, the expression of the CT determinants was not indicative of cytotoxic ability, as previously suggested. The presence of specific carbohydrate residues on the cell surface of a subset of lymphocytes in an anatomically distinct immune compartment suggests that a unique differentiation pathway is followed by these cells.

摘要

碳水化合物分化抗原(CT抗原)先前已被证明与细胞毒性T细胞相关,在肠道上皮内淋巴细胞(IEL)和肠道上皮细胞上大量存在。肠道切片的组织学检查表明,CT1单克隆抗体确定了IEL和位于绒毛隐窝底部的上皮细胞上的表位。CT2单克隆抗体与IEL反应,但也与肠道上皮中的大多数细胞结合。当通过流式细胞术分析分离的肠道细胞群体时,明显有两种主要大小类别的细胞。较小的细胞对应于淋巴细胞,主要是Lyt-2 +,其中很大比例表达CT抗原。IEL中不存在由单克隆抗体J11d定义的另一种分化抗原,这表明那些T细胞来源的IEL可能是成熟的,因为胸腺细胞而非外周T细胞表达J11d抗原。双色荧光分析表明,CT决定簇存在于IEL的Thy-1 +、Lyt-2 +以及Thy-1 -、Lyt-2 +亚群上。然而,一小部分L3T4 + IEL是CT -,这进一步支持了我们先前关于CT表达与Lyt-2表达之间相关性的证明。除了CT抗原表达外,还检测到了IEL有趣的表型特征。IEL不表达MEL-14淋巴细胞归巢受体,并且LFA-1的细胞表面水平明显低于其他外周淋巴细胞。还表明一小部分IEL表达T细胞受体同种异型标志物,这表明至少一些细胞在T细胞受体基因重排方面是成熟的。大肠细胞虽然是CT +,但并非造血来源,因为它们是T200 -,并且通过使用嵌合小鼠表明不是骨髓来源的。与先前报道的结果相反,IEL的细胞毒性活性可忽略不计,仅在七个实验中的一个实验中观察到对NK敏感细胞和其他肿瘤细胞的可检测裂解。因此,CT决定簇的表达并不像先前所暗示的那样表明细胞毒性能力。在解剖学上不同的免疫区室中,淋巴细胞亚群的细胞表面存在特定的碳水化合物残基,这表明这些细胞遵循独特的分化途径。

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