人类t细胞白血病病毒的转化模式。

Molecular biology & medicine Pub Date : 1990-02-01
M T Yip, I S Chen
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引用次数: 0

摘要

已经分离出两种致病性人类逆转录病毒,并显示它们引起以t细胞恶性增殖为特征的疾病。人t细胞白血病病毒I型(HTLV-I)是成人t细胞白血病的病毒病原,而人t细胞白血病病毒II型(HTLV-II)很少与毛细胞白血病相关的某些形式的白血病相关。了解这些逆转录病毒的发病机制需要阐明HTLV使细胞不朽的机制。本文讨论了htlv诱导转化的两种假设模式。在细胞表面,HTLV颗粒通过未知受体对t细胞生长有丝分裂作用。一旦HTLV有效地感染细胞,它也可以启动分子变化。HTLV基因组编码一种病毒调控蛋白Tax,该蛋白不仅激活HTLV基因表达,还可能诱导参与细胞增殖的细胞基因的不适当表达。提出了HTLV介导的这些事件如何促进t细胞转化并最终导致白血病的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modes of transformation by the human T-cell leukemia viruses.

Two pathogenic human retroviruses have been isolated and shown to cause diseases characterized by malignant proliferation of T-cells. Human T-cell leukemia virus type I (HTLV-I) is the virus etiologic agent of adult T-cell leukemia, and human T-cell leukemia virus type II (HTLV-II) has been rarely associated with some forms of leukemia related to hairy-cell leukemia. Understanding the pathogenesis of these retroviruses requires elucidating the mechanism by which HTLV immortalizes cells. Two hypothetical modes of HTLV-induced transformation are discussed in this review. At the cell surface, HTLV particles via as yet unknown receptors have mitogenic effects on T-cell growth. Once HTLV productively infects the cell, it can initiate molecular changes as well. The HTLV genome encodes a viral regulatory protein, Tax, which not only activates HTLV gene expression, but may also induce inappropriate expression of cellular genes involved in cell proliferation. Models are proposed for how these events mediated by HTLV may contribute to T-cell transformation and ultimately, leukemia.

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