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从海洋天然产物文库中鉴定新型 HIV-1 潜伏逆转剂。

Identification of Novel HIV-1 Latency-Reversing Agents from a Library of Marine Natural Products.

机构信息

Faculty of Health Sciences, Simon Fraser University, Burnaby, BC V5A 1S6, Canada.

Departments of Chemistry and Earth, Ocean & Atmospheric Sciences, University of British Columbia, Vancouver, BC V6T 1Z4, Canada.

出版信息

Viruses. 2018 Jun 27;10(7):348. doi: 10.3390/v10070348.

Abstract

Natural products originating from marine and plant materials are a rich source of chemical diversity and unique antimicrobials. Using an established model of HIV-1 latency, we screened 257 pure compounds from a marine natural product library and identified 4 (psammaplin A, aplysiatoxin, debromoaplysiatoxin, and previously-described alotaketal C) that induced expression of latent HIV-1 provirus in both cell line and primary cell models. Notably, aplysiatoxin induced similar levels of HIV-1 expression as prostratin but at up to 900-fold lower concentrations and without substantial effects on cell viability. Psammaplin A enhanced HIV-1 expression synergistically when treated in combination with the protein kinase C (PKC) activator prostratin, but not the histone deacetylase inhibitor (HDACi) panobinostat, suggesting that psammaplin A functions as a latency-reversing agent (LRA) of the HDACi class. Conversely, aplysiatoxin and debromoaplysiatoxin synergized with panobinostat but not prostratin, suggesting that they function as PKC activators. Our study identifies new compounds from previously untested marine natural products and adds to the repertoire of LRAs that can inform therapeutic “shock-and-kill”-based strategies to eliminate latent HIV-infected reservoirs.

摘要

天然产物来源于海洋和植物材料,是化学多样性和独特抗菌剂的丰富来源。我们使用已建立的 HIV-1 潜伏期模型,从海洋天然产物文库中筛选了 257 种纯化合物,并鉴定出 4 种(沙玛林 A、海兔毒素、去溴海兔毒素和先前描述的阿托卡酮 C)可诱导细胞系和原代细胞模型中潜伏 HIV-1 前病毒的表达。值得注意的是,海兔毒素诱导 HIV-1 表达的水平与 prostratin 相似,但浓度低至 900 倍,且对细胞活力无明显影响。当与蛋白激酶 C(PKC)激活剂 prostratin 联合处理时,Psammaplin A 增强 HIV-1 的表达具有协同作用,但与组蛋白去乙酰化酶抑制剂(HDACi)panobinostat 没有协同作用,这表明 Psammaplin A 作为 HDACi 类别的潜伏逆转剂(LRA)发挥作用。相反,海兔毒素和去溴海兔毒素与 panobinostat 协同作用,但与 prostratin 没有协同作用,表明它们作为 PKC 激活剂发挥作用。我们的研究从以前未经测试的海洋天然产物中鉴定出了新的化合物,并增加了可用于治疗“休克和杀伤”策略的 LRA repertoire,以消除潜伏的 HIV 感染库。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b93/6071113/c9ba62a71ae4/viruses-10-00348-g001.jpg

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