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佛波酯激活的CD4+8+ T细胞上淋巴细胞分化抗原的表达改变。

Altered expression of lymphocyte differentiation antigens on phorbol ester-activated CD4+8+ T cells.

作者信息

Richie E R, McEntire B, Phillips J, Allison J P

机构信息

University of Texas System Cancer Center, Science Park-Research Division, Smithville 78957.

出版信息

J Immunol. 1988 Jun 15;140(12):4115-22.

PMID:3259607
Abstract

Altered expression of cell surface Ag is an early event accompanying Ag-, mitogen-, or phorbol ester-induced activation of mature T cells. In this report, phorbol ester-induced changes in the expression of several functionally significant cell surface molecules are explored on immature thymocytes and lymphoma cells presenting a cortical CD4+8+ double-positive (DP) phenotype. Both CD4 and CD8 expressions are down-modulated on DP cells incubated with PMA. Cell-surface expression of CD4 and CD8 remains depressed for 72 h in the presence of PMA, but is restored after removal of PMA from the culture medium. The PMA-mediated loss of Ag expression is associated with a rapid down-regulation of steady state CD4 and CD8 mRNA transcript levels in treated cells. The sustained loss of CD4 and CD8 surface expression on DP cells is a selective event because CD5 expression is enhanced, H-2 expression is unchanged, and CD3 expression is only transiently diminished by PMA stimulation. Other T cell-activating agents, including Con A, ionomycin, and anti-CD3 mAb, induce selected surface antigenic changes on DP cells, but do not mimic the pattern of altered Ag expression observed after PMA stimulation. These data demonstrate that, similar to mature subsets, T cells in the DP nonmature compartment undergo alterations in expression of functionally important cell-surface molecules in response to activating agents. Nevertheless, distinctions between mature and nonmature T cells regarding specific alterations in differentiation Ag phenotype suggest that the effect of PMA on expression of these molecules depends, in part, on the maturation stage of the target cell population.

摘要

细胞表面抗原表达的改变是伴随抗原、丝裂原或佛波酯诱导成熟T细胞活化的早期事件。在本报告中,研究了佛波酯诱导的几种功能重要的细胞表面分子在呈现皮质CD4 + 8 +双阳性(DP)表型的未成熟胸腺细胞和淋巴瘤细胞上的表达变化。在用佛波酯处理的DP细胞上,CD4和CD8的表达均下调。在存在佛波酯的情况下,CD4和CD8的细胞表面表达在72小时内持续降低,但从培养基中去除佛波酯后可恢复。佛波酯介导的抗原表达丧失与处理细胞中稳态CD4和CD8 mRNA转录水平的快速下调有关。DP细胞上CD4和CD8表面表达的持续丧失是一个选择性事件,因为CD5表达增强,H-2表达不变,并且CD3表达仅被佛波酯刺激短暂降低。其他T细胞激活剂,包括刀豆蛋白A、离子霉素和抗CD3单克隆抗体,可诱导DP细胞上选定的表面抗原变化,但不能模拟佛波酯刺激后观察到的抗原表达改变模式。这些数据表明,与成熟亚群类似,DP未成熟区室中的T细胞在激活剂作用下会发生功能重要的细胞表面分子表达的改变。然而,成熟和未成熟T细胞在分化抗原表型的特定改变方面的差异表明,佛波酯对这些分子表达的影响部分取决于靶细胞群体的成熟阶段。

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