Department of Pharmacology and Toxicology, University of Veterinary Medicine, Budapest, Hungary.
Faculty of Pharmacy, Institute of Pharmaceutical Chemistry, Philipps University Marburg, Marburg, Germany.
J Enzyme Inhib Med Chem. 2021 Dec;36(1):659-668. doi: 10.1080/14756366.2021.1886093.
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.
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。