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Histone deacetylase inhibitors suppress natural killer cell cytolytic activity.

机译:组蛋白脱乙酰基酶抑制剂抑制自然杀伤细胞的细胞溶解活性。

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摘要

Treatment of transformed cells from leukemia or solid tumors with histone deacetylase inhibitors (HDACi) was shown to increase their sensitivity to NK cell lysis. In this study, treatment of IL-2-activated NK cells with HDACi including suberoylanilide hydroxamic acid and valproic acid was studied. Both drugs at therapeutic concentrations inhibited NK cell cytotoxicity on human leukemic cells. This inhibition was associated with decreased expression and function of NK cell activating receptors NKp46 and NKp30 as well as impaired granule exocytosis. NFkappaB activation in IL-2-activated NK cells was inhibited by both HDACi. Pharmacologic inhibition of NFkappaB activity resulted in similar effects on NK cell activity like those observed for HDACi. These results demonstrate for the first time that HDACi prevent NK cytotoxicity by downregulation of NK cell activating receptors probably through the inhibition of NFkappaB activation.
机译:用组蛋白脱乙酰基酶抑制剂(HDACi)处理来自白血病或实体瘤的转化细胞,可提高其对NK细胞裂解的敏感性。在这项研究中,研究了包括辛二酰苯胺异羟肟酸和丙戊酸在内的HDACi对IL-2活化的NK细胞的处理。两种药物均具有治疗浓度,可抑制NK细胞对人类白血病细胞的细胞毒性。这种抑制作用与NK细胞活化受体NKp46和NKp30的表达和功能降低以及颗粒胞吐功能受损有关。两个HDACi均抑制IL-2激活的NK细胞中的NFkappaB激活。药理抑制NFkappaB活性对NK细胞活性的影响与HDACi观察到的相似。这些结果首次证明,HDACi可能通过抑制NKkappaB激活而通过下调NK细胞激活受体来预防NK细胞毒性。

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