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远志皂苷 D 是桔梗的一种天然成分,可通过阻碍膜融合来阻止溶酶体和 TMPRSS2 驱动的 SARS-CoV-2 感染。

Platycodin D, a natural component of Platycodon grandiflorum, prevents both lysosome- and TMPRSS2-driven SARS-CoV-2 infection by hindering membrane fusion.

机构信息

Center for Cognition and Sociality, Cognitive Glioscience Group, Institute for Basic Science, Daejeon, 34126, Republic of Korea.

Zoonotic Virus Laboratory, Institut Pasteur Korea, Seongnam, Republic of Korea.

出版信息

Exp Mol Med. 2021 May;53(5):956-972. doi: 10.1038/s12276-021-00624-9. Epub 2021 May 25.

DOI:10.1038/s12276-021-00624-9
PMID:34035463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8143993/
Abstract

An ongoing pandemic of coronavirus disease 2019 (COVID-19) is now the greatest threat to global public health. Herbal medicines and their derived natural products have drawn much attention in the treatment of COVID-19, but the detailed mechanisms by which natural products inhibit SARS-CoV-2 have not been elucidated. Here, we show that platycodin D (PD), a triterpenoid saponin abundant in Platycodon grandiflorum (PG), a dietary and medicinal herb commonly used in East Asia, effectively blocks the two main SARS-CoV-2 infection routes via lysosome- and transmembrane protease serine 2 (TMPRSS2)-driven entry. Mechanistically, PD prevents host entry of SARS-CoV-2 by redistributing membrane cholesterol to prevent membrane fusion, which can be reinstated by treatment with a PD-encapsulating agent. Furthermore, the inhibitory effects of PD are recapitulated by the pharmacological inhibition or gene silencing of NPC1, which is mutated in patients with Niemann-Pick type C (NPC) displaying disrupted membrane cholesterol distribution. Finally, readily available local foods or herbal medicines containing PG root show similar inhibitory effects against SARS-CoV-2 infection. Our study proposes that PD is a potent natural product for preventing or treating COVID-19 and that briefly disrupting the distribution of membrane cholesterol is a potential novel therapeutic strategy for SARS-CoV-2 infection.

摘要

目前,2019 年冠状病毒病(COVID-19)的持续流行是对全球公共卫生的最大威胁。草药及其衍生的天然产物在 COVID-19 的治疗中引起了广泛关注,但天然产物抑制 SARS-CoV-2 的详细机制尚未阐明。在这里,我们表明,源自桔梗(PG)的三萜皂苷桔梗皂苷 D(PD)有效阻断了通过溶酶体和跨膜丝氨酸蛋白酶 2(TMPRSS2)驱动进入的两种主要 SARS-CoV-2 感染途径。在机制上,PD 通过重新分配膜胆固醇来阻止 SARS-CoV-2 的宿主进入,从而阻止膜融合,而用 PD 包封剂处理可恢复这种作用。此外,NPC1 的药理抑制或基因沉默可再现 PD 的抑制作用,NPC1 在 NPC 型患者中发生突变,表现出膜胆固醇分布紊乱。最后,含有 PG 根的现成当地食品或草药也显示出对 SARS-CoV-2 感染的类似抑制作用。我们的研究表明 PD 是预防或治疗 COVID-19 的有效天然产物,而短暂破坏膜胆固醇的分布可能是 SARS-CoV-2 感染的一种潜在新型治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81fb/8178399/a6e2a42d19b7/12276_2021_624_Fig7_HTML.jpg
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