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将具有潜在抗病毒作用的胰蛋白酶样丝氨酸蛋白酶抑制剂暴露于人肠上皮细胞和原代人肝细胞中。

Exposure of human intestinal epithelial cells and primary human hepatocytes to trypsin-like serine protease inhibitors with potential antiviral effect.

机构信息

Department of Pharmacology and Toxicology, University of Veterinary Medicine, Budapest, Hungary.

Faculty of Pharmacy, Institute of Pharmaceutical Chemistry, Philipps University Marburg, Marburg, Germany.

出版信息

J Enzyme Inhib Med Chem. 2021 Dec;36(1):659-668. doi: 10.1080/14756366.2021.1886093.

Abstract

Human intestinal epithelial cell line-6 (HIEC-6) cells and primary human hepatocytes (PHHs) were treated with 3-amidinophenylalanine-derived inhibitors of trypsin-like serine proteases for 24 hours. It was proven that treatment with MI-1900 and MI-1907 was tolerated up to 50 μM in HIEC-6. These inhibitors did not cause elevations in extracellular HO levels and in the concentrations of interleukin (IL)-6 and IL-8 and did not alter occludin distribution in HIEC-6. It was also found that MI-1900 and MI-1907 up to 50 μM did not affect cell viability, IL-6 and IL-8 and occludin levels of PHH. Based on our findings, these inhibitors could be safely applicable at 50 μM in HIEC-6 and in PHH; however, redox status was disturbed in case of PHH. Moreover, it has recently been demonstrated that MI-1900 prevents the replication and spread of the new SARS-CoV-2 in infected Calu-3 cells, most-likely via an inhibition of the membrane-bound host protease TMPRSS2.

摘要

人肠道上皮细胞系-6(HIEC-6)细胞和原代人肝细胞(PHH)用胰蛋白酶样丝氨酸蛋白酶的 3-脒基苯丙氨酸衍生抑制剂处理 24 小时。已证明在 HIEC-6 中,MI-1900 和 MI-1907 的处理耐受度高达 50μM。这些抑制剂不会引起细胞外 HO 水平、白细胞介素 (IL)-6 和 IL-8 浓度升高,也不会改变 HIEC-6 中的闭合蛋白分布。还发现,MI-1900 和 MI-1907 高达 50μM 不会影响 PHH 的细胞活力、IL-6 和 IL-8 以及闭合蛋白水平。基于我们的发现,这些抑制剂在 HIEC-6 和 PHH 中可以安全地以 50μM 的浓度应用;然而,在 PHH 的情况下,氧化还原状态被扰乱。此外,最近已经证明 MI-1900 通过抑制膜结合的宿主蛋白酶 TMPRSS2 来阻止感染的 Calu-3 细胞中新型 SARS-CoV-2 的复制和传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b8c/7928042/29a0fa640d40/IENZ_A_1886093_F0001_B.jpg

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