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CD8(+) T 淋巴细胞介导的 HIV-1 复制抑制的表观遗传调控。

Epigenetic regulation of CD8(+) T-lymphocyte mediated suppression of HIV-1 replication.

机构信息

Duke Human Vaccine Institute, Duke University Medical Center, Durham, NC, 27710, USA.

出版信息

Virology. 2010 Sep 15;405(1):234-42. doi: 10.1016/j.virol.2010.06.001. Epub 2010 Jul 1.

Abstract

CD8(+) T-lymphocytes from HIV-1 infected individuals express unidentified factors that suppress viral replication by inhibiting HIV-1 gene expression. We examined the role of epigenetics in modulating the HIV-1 suppressive factors expressed by primary CD8(+) T cells from subjects naturally controlling virus replication. HIV-1 suppression by CD8(+) T-lymphocytes was reversed up to 40% by the addition of a histone deacetylase (HDAC) inhibitor. Noncytolytic suppression was not dependent on epigenetic changes within the target cells, as HDAC1 within the target cell was dispensable, and HIV-1 LTR histone acetylation remained unchanged in the presence of CD8(+) T-lymphocytes. Histone deacetylation within CD8(+) T-lymphocytes was necessary for potent HIV-1 suppression. Blocking HDACs impairs the ability of CD8(+) T-lymphocytes to repress HIV-1 transcription, demonstrating that expression of a portion of the suppressive factors is regulated by epigenetics. These data provide a way to focus the search for the suppressive factors and to potentially modulate their expression.

摘要

来自 HIV-1 感染者的 CD8(+) T 淋巴细胞表达不明因素,通过抑制 HIV-1 基因表达来抑制病毒复制。我们研究了表观遗传学在调节自然控制病毒复制的主体原代 CD8(+) T 细胞中表达的 HIV-1 抑制因子中的作用。通过添加组蛋白去乙酰化酶 (HDAC) 抑制剂,CD8(+) T 淋巴细胞对 HIV-1 的抑制作用可逆转高达 40%。非细胞溶解抑制作用不依赖于靶细胞内的表观遗传变化,因为靶细胞内的 HDAC1 是可有可无的,并且在 CD8(+) T 淋巴细胞存在的情况下 HIV-1 LTR 组蛋白乙酰化保持不变。CD8(+) T 淋巴细胞内的组蛋白去乙酰化对于有效的 HIV-1 抑制是必要的。阻断 HDAC 会损害 CD8(+) T 淋巴细胞抑制 HIV-1 转录的能力,表明部分抑制因子的表达受表观遗传调控。这些数据为寻找抑制因子并可能调节其表达提供了一种方法。

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