SDH-derived ROS开车增加巨噬细胞的炎症Bmal1的删除。Bmal1 + / +和Bmal1 - / - BMDMs孵化等渗压的,与洋地黄皂苷permeabilized ADP-supplemented线粒体分析解决方案。(A)海马XF分析用于分析OCR的变化以应对注射琥珀酸(1.25毫米)。琥珀酸(B)响应测量的变化百分比OCR直接注射琥珀酸。试验结果提出了+ / - SEM和n = 3代表独立的实验。BMDMs与LPS刺激(100 ng / ml)和(C)沾CellROX测量的活性氧水平通过流式细胞术或(D)分析细胞溶解的pro IL-1β蛋白表达的免疫印迹使用β-Actin作为加载控制。(E)和活性氧(F) pro IL-1β蛋白表达测量与数字预处理后与LPS刺激之前。西方免疫印迹资料代表n = 3独立的实验。箴IL-1β时间测密度术是相对于Bmal1 + / +控制乐队。微Bmal1 + / +和Bmal1 - /数字/有限合伙人乐队是相对的有限合伙人的乐队。 These bands are indicated by * symbols. Flow cytometry data presented is at least n=3 independent experiments +/- SEM with each data point representative of at least 5,000 events from one sample. Statistical analysis was performed for Seahorse XF data by unpaired student’s t test and for flow cytometry data by two-way ANOVA with Tukey’s multiple comparisons test (*p < 0.05, ****p < 0.0001). Credit: DOI: 10.3389/fimmu.2021.700431