Oh Ju Hee, Park Sunyou, Hong Eunmi, Choi Myeong A, Kwon Ye-Mi, Park Jin-Wan, Lee A Hyeon, Park Gye Ryeol, Kim Hye Young, Lee Seung Min, Lee Ju Yeon, Bae Sang Hyun, Lee Ji Hoon, Lee Jung Yeol, Jun Dae Won
Department of Obstetrics and Gynecology, Institute of Women's Medical Life Science, Yonsei Cancer Center, Severance Hospital, Yonsei University College of Medicine, Seoul 03722, Korea.
New Drug Development Center, Daegu-Gyeongbuk Medical Innovation Foundation (DGMIF), Daegu 41061, Korea.
ACS Pharmacol Transl Sci. 2023 Sep 11;6(10):1471-1479. doi: 10.1021/acsptsci.3c00131. eCollection 2023 Oct 13.
The pseudokinase mixed-lineage kinase domain-like protein plays a crucial role in programmed cell death via necroptosis. We developed a novel mixed-lineage kinase domain-like inhibitor, P28, which demonstrated potent necroptosis inhibition and antifibrotic effects. P28 treatment directly inhibited mixed-lineage kinase domain-like phosphorylation and oligomerization after necroptosis induction, inhibited immune cell death after necroptosis, and reduced the expression of adhesion molecules. Additionally, P28 treatment reduced the level of activation of hepatic stellate cells and the expression of hepatic fibrosis markers induced by necroptosis stimulation. Unlike the necrosulfonamide treatment, the P28 treatment did not induce cytotoxicity. Finally, the cysteine covalent bonding of P28 was confirmed by liquid chromatography-tandem mass spectrometry.
假激酶混合谱系激酶结构域样蛋白在程序性坏死性细胞死亡中起关键作用。我们开发了一种新型的混合谱系激酶结构域样抑制剂P28,它具有强大的坏死性凋亡抑制作用和抗纤维化作用。P28处理在坏死性凋亡诱导后直接抑制混合谱系激酶结构域样的磷酸化和寡聚化,抑制坏死性凋亡后的免疫细胞死亡,并降低黏附分子的表达。此外,P28处理降低了肝星状细胞的激活水平以及坏死性凋亡刺激诱导的肝纤维化标志物的表达。与坏死磺酰胺处理不同,P28处理未诱导细胞毒性。最后,通过液相色谱-串联质谱法证实了P28的半胱氨酸共价键合。