柚皮素对脂多糖诱导的软骨细胞焦亡抑制作用及其机制OACSTPCD
Inhibition of naringenin on lipopolysaccharide-induced pyroptosis of chondrocytes and its mechanism
目的 观察柚皮素(NAR)对脂多糖(LPS)诱导的软骨细胞焦亡的抑制作用,并探讨其可能的机制.方法 将对数生长期的C28/I2细胞分为LPS组(用含100 ng/mL LPS的DMEM培养基培养)、LPS+NAR组(用含100 ng/mL LPS+100 μmol/L NAR的培养基培养)、LPS+NAR+DORS组(用含100 ng/mL LPS+100 μmol/L NAR+50 μmol/L腺苷—磷酸激活蛋白激酶α(AMPKα)抑制剂DORS的培养基培养)、Control组(普通培养基培养),均培养8 h.取各组细胞,采用CCK-8法检测细胞增殖光密度(OD)值,TUNEL法检测细胞凋亡率,Western blotting法检测焦亡标志物[白细胞介素18(IL-18)、消皮素D(GSDMD)]、AMPKα、磷酸化AMPKα(p-AMPKα)、NLRP3炎症小体标志蛋白[凋亡相关的半胱氨酸蛋白酶激活和召募结构域蛋白(ASC)、半胱氨酸天冬氨酸特异性蛋白酶1(Caspase-1)、核苷酸结合寡聚化域样受体家族带脒基结构域3(NLRP3)、切割模式的Caspase-1(cleaved-Caspase-1)]蛋白相对表达量,ELISA法检测细胞上清液IL-1β、IL-6、肿瘤坏死因子α(TNF-α)水平.结果 Control组、LPS+NAR组、LPS+NAR+DORS组、LPS组细胞增殖OD值依次降低、细胞凋亡率依次升高,细胞IL-18、GSDMD、ASC、Caspase-1、NLRP3、cleaved-Caspase-1蛋白相对表达量依次升高,p-AMPKα蛋白相对表达量依次降低,细胞上清液IL-1β、IL-6、TNF-α水平依次升高而IL-10、IL-13水平依次降低,组间两两比较P均<0.05.LPS组、LPS+NAR+DORS组细胞AMPKα蛋白相对表达量均低于Control组、LPS+NAR组(P均<0.05).结论 NAR可抑制LPS诱导的软骨细胞焦亡,其机制可能与激活AMPKα信号通路、抑制NLRP3炎症小体介导的炎症反应有关.
Objective To observe the inhibitory effect of naringenin(NAR)on lipopolysaccharide(LPS)-induced pyroptosis of chondrocytes and to explore its possible mechanism.Methods C28/I2 cells in the logarithmic growth phase were divided into the LPS group(cultured with DMEM medium containing 100 ng/mL LPS),the LPS+NAR group(cultured with medium containing 100 ng/mL LPS+100 μmol/L NAR),the LPS+NAR+DORS group(cultured with medium containing 100 ng/mL LPS+100 μmol/L NAR+50 μmol/L DORS),and the Control group(cultured with ordi-nary medium),and all groups were cultured for 8 h.Cells in each group were taken.The cell proliferation optical density(OD)value was detected by the CCK-8 method,the apoptosis rate was detected by the TUNEL method,the relative pro-tein expression levels of pyroptosis markers[interleukin(IL)-18,GSDMD],adenosine-monophosphate-activated protein kinase α(AMPKα),phosphorylated AMPKα(p-AMPKα),NLRP3 inflammasome marker proteins[apoptosis-associated speck-like protein containing a CARD(ASC),Caspase-1),nucleotide-binding oligomerization domain-like receptor fami-ly pyrin domain-containing 3(NLRP3),and cleaved-Caspase-1]were detected by Western blotting,and the levels of IL-1β,IL-6,and tumor necrosis factor-α(TNF-α)in the cell supernatant were detected by ELISA.Results In the Control group,LPS+NAR group,LPS+NAR+DORS group,and LPS group,the cell proliferation OD values decreased succes-sively,the apoptosis rates increased successively,the relative protein expression levels of IL-18,GSDMD,ASC,Caspase-1,NLRP3,and cleaved-Caspase-1 in the cells increased successively,the relative protein expression level of p-AMPKα decreased successively,the levels of IL-1β,IL-6,and TNF-α in the cell supernatant increased successively while the lev-els of IL-10 and IL-13 decreased successively,with statistically significant difference between groups(all P<0.05).The relative protein expression levels of AMPKα in the LPS group and LPS+NAR+DORS group were both lower than those in the Control group and LPS+NAR group(all P<0.05).Conclusion NAR can inhibit LPS-induced chondrocyte pyropto-sis,and its mechanism may be related to activating the AMPKα signaling pathway and inhibiting the NLRP3 inflamma-some-mediated inflammatory response.
艾孜热提·阿布都卡地尔;周静;买吾拉尼江·依孜布拉
新疆医科大学第一附属医院药学部,乌鲁木齐 830054新疆医科大学中心实验室
临床医学
柚皮素AMPKα信号通路NLRP3炎症小体软骨细胞细胞焦亡
naringeninAMPKα signal pathwayNLRP3 inflammasomechondrocytepyroptosis
《山东医药》 2024 (035)
26-30 / 5
新疆维吾尔族自治区自然科学基金资助项目(2023D01C318).
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