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小鼠小肠上皮内淋巴细胞的功能特性。IV. 使用佛波酯和钙离子载体研究上皮内淋巴细胞的增殖能力。

Functional properties of intra-epithelial lymphocytes from mouse small intestine. IV. Investigation of the proliferative capacity of IEL using phorbol ester and calcium ionophore.

作者信息

Mowat A M, McInnes I B, Parrott D M

机构信息

Department of Bacteriology and Immunology, Western Infirmary, Glasgow.

出版信息

Immunology. 1989 Mar;66(3):398-403.

Abstract

Intra-epithelial lymphocytes (IEL) from mouse small intestine normally show very poor proliferative responses to mitogens or antigens in vitro. In this report, we show that purified IEL give a moderate proliferative response when stimulated with a combination of phorbol myristate acetate (PMA) and the calcium ionophore, A23187. Nevertheless, the response of IEL to these agents was much less than that of other lymphoid cells, even when stimulated additionally with concanavalin A (Con A). Furthermore, in comparison with spleen cells, the optimal response of IEL to PMA required higher concentrations of A23187. Optimally stimulated IEL made significant amounts of T-cell growth factor and addition of rIL-2 to the cultures did not enhance the optimal response of IEL to PMA + A23187. Subsequent studies showed that the majority of IEL which respond to PMA + A23187 are L3T4+ Lyt-2-, despite the fact that Lyt-2+ cells from the spleen and thymus responded well to these agents. Our study indicates that the majority of IEL have a very low proliferative potential in vitro and this may reflect a large population of IL-2-unresponsive Lyt-2+ IEL.

摘要

来自小鼠小肠的上皮内淋巴细胞(IEL)在体外对丝裂原或抗原通常表现出非常弱的增殖反应。在本报告中,我们表明,用佛波醇肉豆蔻酸酯乙酸酯(PMA)和钙离子载体A23187联合刺激时,纯化的IEL会产生适度的增殖反应。然而,即使额外用刀豆球蛋白A(Con A)刺激,IEL对这些试剂的反应也远低于其他淋巴细胞。此外,与脾细胞相比,IEL对PMA的最佳反应需要更高浓度的A23187。最佳刺激的IEL产生大量的T细胞生长因子,并且向培养物中添加重组白细胞介素-2(rIL-2)并不能增强IEL对PMA + A23187的最佳反应。随后的研究表明,尽管来自脾脏和胸腺的Lyt-2 +细胞对这些试剂反应良好,但对PMA + A23187有反应的大多数IEL是L3T4 + Lyt-2-。我们的研究表明,大多数IEL在体外具有非常低的增殖潜力,这可能反映了大量对白细胞介素-2无反应的Lyt-2 + IEL。

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Human intraepithelial lymphocytes.人上皮内淋巴细胞
Springer Semin Immunopathol. 1990;12(2-3):165-90. doi: 10.1007/BF00197504.

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