首页> 外文OA文献 >FTY720, a novel immunosuppressant, induces sequestration of circulating mature lymphocytes by acceleration of lymphocyte homing in rats, III. Increase in frequency of CD62L-positive T cells in Peyer's patches by FTY720-induced lymphocyte homing.
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FTY720, a novel immunosuppressant, induces sequestration of circulating mature lymphocytes by acceleration of lymphocyte homing in rats, III. Increase in frequency of CD62L-positive T cells in Peyer's patches by FTY720-induced lymphocyte homing.

机译:FTY720是一种新型的免疫抑制剂,可通过促进大鼠淋巴细胞归巢来诱导螯合循环中的成熟淋巴细胞。通过FTY720诱导的淋巴细胞归巢增加Peyer斑中CD62L阳性T细胞的频率。

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摘要

FTY720, a novel immunosuppressant, sequesters circulating mature lymphocytes, especially T cells, within lymph nodes and Peyer's patches by accelerating lymphocyte homing, and thereby causes lymphocyte depletion in the blood. The FTY720-induced acceleration of lymphocyte homing appears to be mediated by lymphocyte homing receptors including CD62L, CD49d/beta7, and CD11a/CD18. In this study, expressions of CD62L, CD49d and CD11a on T cells in the peripheral blood, lymph nodes and Peyer's patches were analysed by flow cytometry in rats given FTY720 (1 mg/kg) orally. FTY720 markedly decreased the number of peripheral blood T cells, while not affecting CD62L, CD49d and CD11a expressions at 1-3 hr after administration. In contrast, both the frequency of CD62L-positive T cells and intensity of CD62L expression on T cells were increased in Peyer's patches but not lymph nodes at 3 hr after administration of FTY720. CD49d and CD11a expressions on T cells were unaffected by FTY720 in both Peyer's patches and lymph nodes at the same point in time. On the other hand, analysis of lymphocyte homing with calcein-labelled lymphocytes and anti-CD62L monoclonal antibody (mAb) confirmed that FTY720 predominantly increased CD62L-dependent lymphocyte homing to Peyer's patches. These findings indicate that FTY720 increases the frequency of CD62L-positive T cells by accelerating CD62L-predominant homing in Peyer's patches.
机译:FTY720是一种新型的免疫抑制剂,它通过加速淋巴细胞归巢来隔离淋巴结和Peyer斑块内循环的成熟淋巴细胞,特别是T细胞,从而导致血液中的淋巴细胞耗竭。 FTY720诱导的淋巴细胞归巢加速似乎是由淋巴细胞归巢受体(包括CD62L,CD49d / beta7和CD11a / CD18)介导的。在这项研究中,通过流式细胞术分析了口服FTY720(1 mg / kg)大鼠的外周血,淋巴结和Peyer斑块中T细胞上CD62L,CD49d和CD11a的表达。 FTY720显着减少了外周血T细胞的数量,但在给药后1-3小时不影响CD62L,CD49d和CD11a表达。相反,施用FTY720后3小时,在Peyer斑中CD62L阳性T细胞的频率和CD62L表达在T细胞上的表达强度均增加,但在淋巴结中却没有增加。在同一时间,在淋巴结和淋巴结中,FTY720不会影响T细胞上的CD49d和CD11a表达。另一方面,用钙黄绿素标记的淋巴细胞和抗CD62L单克隆抗体(mAb)对淋巴细胞归巢的分析证实,FTY720主要增加了CD62L依赖性淋巴细胞归巢至Peyer's斑块。这些发现表明FTY720通过加速Peyer斑块中以CD62L为主的归巢而增加了CD62L阳性T细胞的频率。

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