Centers of Cardiovascular Research, Inflammation Lung Research, USA.
Metabolic Disease Research, Thrombosis Research, Departments of Cardiovascular Sciences, USA.
Redox Biol. 2021 Nov;47:102142. doi: 10.1016/j.redox.2021.102142. Epub 2021 Sep 27.
To determine the roles of nuclear localization of pro-caspase-1 in human aortic endothelial cells (HAECs) activated by proatherogenic lipid lysophosphatidylcholine (LPC), we examined cytosolic and nuclear localization of pro-caspase-1, identified nuclear export signal (NES) in pro-caspase-1 and sequenced RNAs. We made the following findings: 1) LPC increases nuclear localization of procaspase-1 in HAECs. 2) Nuclear pro-caspase-1 exports back to the cytosol, which is facilitated by a leptomycin B-inhibited mechanism. 3) Increased nuclear localization of pro-caspase-1 by a new NES peptide inhibitor upregulates inflammatory genes in oxidative stress and Th17 pathways; and SUMO activator N106 enhances nuclear localization of pro-caspase-1 and caspase-1 activation (p20) in the nucleus. 4) LPC plus caspase-1 enzymatic inhibitor upregulates inflammatory genes with hypercytokinemia/hyperchemokinemia and interferon pathways, suggesting a novel capsase-1 enzyme-independent inflammatory mechanism. 5) LPC in combination with NES inhibitor and caspase-1 inhibitor upregulate inflammatory gene expression that regulate Th17 activation, endotheli-1 signaling, p38-, and ERK- MAPK pathways. To examine two hallmarks of endothelial activation such as secretomes and membrane protein signaling, LPC plus NES inhibitor upregulate 57 canonical secretomic genes and 76 exosome secretomic genes, respectively, promoting four pathways including Th17, IL-17 promoted cytokines, interferon signaling and cholesterol biosynthesis. LPC with NES inhibitor also promote inflammation via upregulating ROS promoter CYP1B1 and 11 clusters of differentiation (CD) membrane protein pathways. Mechanistically, all the LPC plus NES inhibitor-induced genes are significantly downregulated in CYP1B1-deficient microarray, suggesting that nuclear caspase-1-induced CYP1B1 promotes strong inflammation. These transcriptomic results provide novel insights on the roles of nuclear caspase-1 in sensing DAMPs, inducing ROS promoter CYP1B1 and in regulating a large number of genes that mediate HAEC activation and inflammation. These findings will lead to future development of novel therapeutics for cardiovascular diseases (CVD), inflammations, infections, transplantation, autoimmune disease and cancers. (total words: 284).
为了确定在促动脉粥样硬化脂质溶血磷脂酰胆碱(LPC)激活的人主动脉内皮细胞(HAEC)中,前胱冬酶-1 的核定位的作用,我们检查了前胱冬酶-1 的胞质和核定位,鉴定了前胱冬酶-1 中的核输出信号(NES)并对 RNA 进行了测序。我们发现:1)LPC 增加 HAEC 中前胱冬酶-1 的核定位。2)核前胱冬酶-1 通过莱普霉素 B 抑制机制输出回胞质。3)新型 NES 肽抑制剂增加核前胱冬酶-1 的核定位,上调氧化应激和 Th17 途径中的炎症基因;SUMO 激活剂 N106 增强核内前胱冬酶-1 的核定位和 caspase-1 的激活(p20)。4)LPC 加 caspase-1 酶抑制剂上调炎症基因,伴有细胞因子血症/趋化因子血症和干扰素途径,提示一种新的 caspase-1 酶非依赖性炎症机制。5)LPC 与 NES 抑制剂和 caspase-1 抑制剂联合使用可上调调节 Th17 激活、内皮-1 信号、p38-和 ERK-MAPK 途径的炎症基因表达。为了研究内皮细胞激活的两个特征,如分泌组和膜蛋白信号,LPC 加 NES 抑制剂分别上调 57 个经典分泌组基因和 76 个外泌体分泌组基因,分别促进包括 Th17、IL-17 促进细胞因子、干扰素信号和胆固醇生物合成在内的四个途径。LPC 加 NES 抑制剂还通过上调炎症的 ROS 启动子 CYP1B1 和 11 个分化簇(CD)膜蛋白途径来促进炎症。从机制上讲,LPC 加 NES 抑制剂诱导的所有基因在 CYP1B1 缺陷的微阵列中显著下调,表明核 caspase-1 诱导的 CYP1B1 促进了强烈的炎症。这些转录组结果提供了核 caspase-1 在感知 DAMPs、诱导 ROS 启动子 CYP1B1 和调节介导 HAEC 激活和炎症的大量基因方面的作用的新见解。这些发现将为心血管疾病(CVD)、炎症、感染、移植、自身免疫性疾病和癌症的新型治疗方法的发展提供依据。(总字数:284)