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人类1型T细胞白血病病毒编码的p40x诱导白细胞介素2受体基因表达。

Induction of interleukin 2 receptor gene expression by p40x encoded by human T-cell leukemia virus type 1.

作者信息

Inoue J, Seiki M, Taniguchi T, Tsuru S, Yoshida M

出版信息

EMBO J. 1986 Nov;5(11):2883-8. doi: 10.1002/j.1460-2075.1986.tb04583.x.

DOI:10.1002/j.1460-2075.1986.tb04583.x
PMID:3024966
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1167238/
Abstract

Human T-cell leukemia virus type 1 (HTLV-1) is an etiologic agent of adult T-cell leukemia (ATL). A viral product, p40x, encoded by the pX sequence of HTLV-1 is a trans-acting transcriptional activator of the long terminal repeat (LTR) and has been suspected of involvement in leukemogenesis, activating the cellular genes. The cellular interleukin-2 (IL-2) and its receptor (IL-2R), the latter of which is expressed on ATL leukemic cells, were shown to be transiently induced by transfection of plasmid pMTPX expressing pX in two T-cell lines, Jurkat and HSB-2, but not in other human T- or B-cell lines. The cell type specificity of IL-2R induction by pX expression was the same as that by phytohaemagglutinin/phorbol ester activation, indicating the requirement for some specific cellular factors or a certain state of cellular differentiation. Induction of IL-2 and IL-2R at mRNA level was also demonstrated in transfected cells. Transfections with mutants of pMTPX in which the open reading frames for p40x, p27x-III and p21x-III were inactivated indicated that p40x alone was sufficient for induction of the IL-2R in inducible cells. This induction of the IL-2R by p40x of HTLV-1 may contribute to preferential proliferation of HTLV-1 infected cells at an early stage of ATL development and eventually increase the number of putative target cells for malignant transformation.

摘要

人类T细胞白血病病毒1型(HTLV-1)是成人T细胞白血病(ATL)的病原体。由HTLV-1的pX序列编码的一种病毒产物p40x是长末端重复序列(LTR)的反式作用转录激活因子,并且一直被怀疑参与白血病发生过程,激活细胞基因。细胞白细胞介素-2(IL-2)及其受体(IL-2R),后者在ATL白血病细胞上表达,在两种T细胞系Jurkat和HSB-2中,通过转染表达pX的质粒pMTPX可短暂诱导它们表达,但在其他人类T细胞或B细胞系中则不能。pX表达诱导IL-2R的细胞类型特异性与植物血凝素/佛波酯激活诱导的特异性相同,表明需要一些特定的细胞因子或特定的细胞分化状态。在转染细胞中也证实了在mRNA水平上诱导IL-2和IL-2R。用pMTPX的突变体进行转染,其中p40x、p27x-III和p21x-III的开放阅读框被灭活,结果表明单独的p40x就足以在可诱导细胞中诱导IL-2R。HTLV-1的p40x对IL-2R的这种诱导可能有助于在ATL发展的早期阶段HTLV-1感染细胞的优先增殖,并最终增加假定的恶性转化靶细胞的数量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f55/1167238/41f712cef946/emboj00174-0147-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f55/1167238/d78e218175b0/emboj00174-0146-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f55/1167238/41f712cef946/emboj00174-0147-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f55/1167238/d78e218175b0/emboj00174-0146-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f55/1167238/41f712cef946/emboj00174-0147-a.jpg

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