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新型冬凌草甲素衍生物 12-O-二十三烷酰基佛波醇-20-醋酸酯的抗 HIV 活性及作用机制研究。

Anti-HIV Activities and Mechanism of 12-O-Tricosanoylphorbol-20-acetate, a Novel Phorbol Ester from Ostodes katharinae.

机构信息

Key Laboratory of Bioactive Peptides of Yunnan Province/Key Laboratory of Animal Models and Human Disease Mechanisms of the Chinese Academy of Sciences, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, Yunnan, China.

Kunming College of Life Science, University of Chinese Academy of Sciences, Kunming 650204, Yunnan, China.

出版信息

Molecules. 2017 Sep 8;22(9):1498. doi: 10.3390/molecules22091498.

Abstract

APOBEC3G is a member of the human cytidine deaminase family that restricts Vif-deficient viruses by being packaged with progeny virions and inducing the G to A mutation during the synthesis of HIV-1 viral DNA when the progeny virus infects new cells. HIV-1 Vif protein resists the activity of A3G by mediating A3G degradation. Phorbol esters are plant-derived organic compounds belonging to the tigliane family of diterpenes and could activate the PKC pathway. In this study, we identified an inhibitor 12--tricosanoylphorbol-20-acetate (hop-8), a novel ester of phorbol which was isolated from of the family Euphorbiaceae, that inhibited the replication of wild-type HIV-1 and HIV-2 strains and drug-resistant strains broadly both in C8166 cells and PBMCs with low cytotoxicity and the EC values ranged from 0.106 μM to 7.987 μM. One of the main mechanisms of hop-8 is to stimulate A3G expressing in HIV-1 producing cells and upregulate the A3G level in progeny virions, which results in reducing the infectivity of the progeny virus. This novel mechanism of hop-8 inhibition of HIV replication might represents a promising approach for developing new therapeutics for HIV infection.

摘要

APOBEC3G 是人类胞嘧啶脱氨酶家族的一员,它通过与子代病毒颗粒包装在一起,并在子代病毒感染新细胞时诱导 HIV-1 病毒 DNA 的合成过程中的 G 到 A 突变,从而限制了 Vif 缺陷型病毒。HIV-1 Vif 蛋白通过介导 A3G 降解来抵抗 A3G 的活性。佛波醇酯是植物来源的有机化合物,属于二萜类中的瑞香烷家族,可激活 PKC 途径。在本研究中,我们鉴定了一种抑制剂 12--二十三烷酰佛波醇-20-乙酸酯(hop-8),这是一种从大戟科植物中分离得到的新型佛波醇酯,它能够抑制野生型 HIV-1 和 HIV-2 株以及广泛的耐药株在 C8166 细胞和 PBMC 中的复制,具有低细胞毒性,EC 值范围为 0.106 μM 至 7.987 μM。hop-8 的主要机制之一是刺激 HIV-1 产生细胞中 A3G 的表达,并上调子代病毒颗粒中的 A3G 水平,从而降低子代病毒的感染力。hop-8 抑制 HIV 复制的这种新机制可能为开发 HIV 感染的新疗法提供了一种有前途的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dda7/6151696/40faa26c5e38/molecules-22-01498-g001.jpg

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