Tufekci Kemal Ugur, Ercan Ilkcan, Isci Kamer Burak, Olcum Melis, Tastan Bora, Gonul Ceren Perihan, Genc Kursad, Genc Sermin
Izmir Biomedicine and Genome Center (IBG), Izmir, Turkey; Vocational School of Health Services, Izmir Democracy University, Izmir, Turkey.
Izmir Biomedicine and Genome Center (IBG), Izmir, Turkey; Izmir International Biomedicine and Genome Institute, Dokuz Eylul University, Izmir, Turkey.
Immunol Lett. 2021 May;233:20-30. doi: 10.1016/j.imlet.2021.03.004. Epub 2021 Mar 9.
The NLRP3 inflammasome is a multiprotein complex that activates caspase-1 and triggers the release of the proinflammatory cytokines IL-1β and IL-18 in response to diverse signals. Although inflammasome activation plays critical roles against various pathogens in host defense, overactivation of inflammasome contributes to the pathogenesis of inflammatory diseases, including acute CNS injuries and chronic neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease. In the current study, we demonstrated that Sulforaphane (SFN), a dietary natural product, inhibits NLRP3 inflammasome mediated IL-1β and IL-18 secretion and pyroptosis in murine microglial cells. SFN decreased the secretion of IL-1β and IL-18, and their mRNA levels in LPS primed microglia triggered by ATP. SFN suppressed the overexpression of cleaved caspase-1 and NLRP3 protein expressions as measured by caspase activity assay and western blot, respectively. SFN also prevented caspase-1 dependent pyroptotic cell death in microglia. Our data indicate that SFN suppresses NLRP3 inflammasome via the inhibition of NF-κB nuclear translocation and Nrf2 mediated miRNAs expression modulation in murine microglia.
NLRP3炎性小体是一种多蛋白复合物,可激活半胱天冬酶-1,并响应多种信号触发促炎细胞因子IL-1β和IL-18的释放。尽管炎性小体激活在宿主防御中对各种病原体起着关键作用,但炎性小体的过度激活会导致包括急性中枢神经系统损伤以及阿尔茨海默病和帕金森病等慢性神经退行性疾病在内的炎症性疾病的发病机制。在本研究中,我们证明了膳食天然产物萝卜硫素(SFN)可抑制小鼠小胶质细胞中NLRP3炎性小体介导的IL-1β和IL-18分泌以及细胞焦亡。SFN降低了由ATP触发的LPS预处理小胶质细胞中IL-1β和IL-18的分泌及其mRNA水平。通过半胱天冬酶活性测定和蛋白质印迹分别测量,SFN抑制了裂解的半胱天冬酶-1的过表达和NLRP3蛋白表达。SFN还可预防小胶质细胞中半胱天冬酶-1依赖性的细胞焦亡性细胞死亡。我们的数据表明,SFN通过抑制小鼠小胶质细胞中NF-κB的核转位和Nrf2介导的miRNA表达调节来抑制NLRP3炎性小体。