Department of Immunobiology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.
Department of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.
Acta Biochim Biophys Sin (Shanghai). 2022 Jan 25;54(1):64-76. doi: 10.3724/abbs.2021004.
Macrophages are critical sentinel cells armed with multiple regulated necrosis pathways, including pyroptosis, apoptosis followed by secondary necrosis, and necroptosis, and are poised to undergo distinct form(s) of necrosis for tackling dangers of pathogenic infection or toxic exposure. The natural BH3-mimetic gossypol is a toxic phytochemical that can induce apoptosis and/or pyroptotic-like cell death, but what exact forms of regulated necrosis are induced remains largely unknown. Here we demonstrated that gossypol induces pyroptotic-like cell death in both unprimed and lipopolysaccharide-primed mouse bone marrow-derived macrophages (BMDMs), as evidenced by membrane swelling and ballooning accompanied by propidium iodide incorporation and lactic acid dehydrogenase release. Notably, gossypol simultaneously induces the activation of both pyroptotic and apoptotic (followed by secondary necrosis) pathways but only weakly activates the necroptosis pathway. Unexpectedly, gossypol-induced necrosis is independent of nucleotide-binding oligomerization domain-like receptor family pyrin domain containing 3 (NLRP3) inflammasome, as neither inhibitor for the NLRP3 pathway nor NLRP3 deficiency protects the macrophages from the necrosis. Furthermore, necrotic inhibitors or even pan-caspase inhibitor alone does not or only partly inhibit such necrosis. Instead, a combination of inhibitors composed of pan-caspase inhibitor IDN-6556, RIPK3 inhibitor GSK'872 and NADPH oxidase inhibitor GKT137831 not only markedly inhibits the necrosis, with all apoptotic and pyroptotic pathways being blocked, but also attenuates gossypol-induced peritonitis in mice. Lastly, the activation of the NLRP3 pathway and apoptotic caspase-3 appears to be independent of each other. Collectively, gossypol simultaneously induces the activation of multiple subroutines of regulated necrosis in macrophages depending on both apoptotic and inflammatory caspases.
巨噬细胞是具有多种调控性细胞坏死途径的关键哨兵细胞,包括细胞焦亡、凋亡后继发坏死和坏死性凋亡,并且能够针对病原体感染或毒性暴露的危险,经历不同形式的细胞坏死。天然 BH3 模拟物棉酚是一种有毒的植物化学物质,可诱导细胞凋亡和/或细胞焦亡样死亡,但确切的调控性细胞坏死形式仍知之甚少。本研究表明,棉酚在未被激活和脂多糖激活的小鼠骨髓来源巨噬细胞(BMDM)中均可诱导细胞焦亡样死亡,表现为细胞膜肿胀和气球样变,同时伴随碘化丙啶掺入和乳酸脱氢酶释放。值得注意的是,棉酚同时激活细胞焦亡和凋亡(继发坏死)途径,但仅弱激活坏死性凋亡途径。出乎意料的是,棉酚诱导的坏死不依赖于核苷酸结合寡聚化结构域样受体家族富含半胱氨酸的蛋白 3(NLRP3)炎症小体,因为 NLRP3 通路抑制剂或 NLRP3 缺乏均不能保护巨噬细胞免于坏死。此外,坏死抑制剂甚至单独的全胱天冬酶抑制剂不能或仅部分抑制这种坏死。相反,由全胱天冬酶抑制剂 IDN-6556、RIPK3 抑制剂 GSK'872 和 NADPH 氧化酶抑制剂 GKT137831 组成的抑制剂组合不仅显著抑制坏死,同时阻断所有的凋亡和细胞焦亡途径,还能减轻棉酚诱导的小鼠腹膜炎。最后,NLRP3 通路的激活和凋亡 caspase-3 似乎彼此独立。总之,棉酚可根据凋亡和炎症半胱天冬酶同时诱导巨噬细胞中多种调控性细胞坏死亚程序的激活。