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由HTLV-1编码的p40x和T3/Ti复合物触发导致白细胞介素-2自分泌环异常激活的证据。

Evidence for aberrant activation of the interleukin-2 autocrine loop by HTLV-1-encoded p40x and T3/Ti complex triggering.

作者信息

Maruyama M, Shibuya H, Harada H, Hatakeyama M, Seiki M, Fujita T, Inoue J, Yoshida M, Taniguchi T

出版信息

Cell. 1987 Jan 30;48(2):343-50. doi: 10.1016/0092-8674(87)90437-5.

Abstract

In this study we provide evidence that distinct DNA sequences within the 5'-flanking regions of the genes for interleukin-2 (IL-2) and its receptor (IL-2R) are involved in human T-cell-specific activation of transcription by p40x, a product of human T cell leukemia virus type I (HTLV-1). The same DNA sequences appear to be responsible for induction of the genes in a T cell line, Jurkat, by mitogens. Although the IL-2 gene sequences are activated by p40x with much lower efficiency than the IL-2R gene sequences, they are synergistically activated by the p40x expression and subsequent extracellular stimulation by Concanavalin-A or anti-T3. We propose a model for two-step activation of the IL-2 autocrine loop in ATL development.

摘要

在本研究中,我们提供了证据,即白细胞介素-2(IL-2)及其受体(IL-2R)基因5'-侧翼区域内不同的DNA序列参与了人T细胞特异性的转录激活,该激活由人类I型T细胞白血病病毒(HTLV-1)的产物p40x介导。相同的DNA序列似乎也负责有丝分裂原在T细胞系Jurkat中诱导这些基因。尽管IL-2基因序列被p40x激活的效率远低于IL-2R基因序列,但它们通过p40x表达以及随后伴刀豆球蛋白A或抗T3的细胞外刺激而被协同激活。我们提出了一个在成人T细胞白血病(ATL)发展过程中IL-2自分泌环两步激活的模型。

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