主动脉夹层中 LPS-LBP 复合物诱导的内皮细胞脓毒症与肠道菌群失调有关

IF 2.6 4区 医学 Q3 IMMUNOLOGY
Gulinazi Yesitayi, Qi Wang, Mengmeng Wang, Mierxiati Ainiwan, Kaisaierjiang Kadier, Aliya Aizitiaili, Yitong Ma, Xiang Ma
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引用次数: 0

摘要

急性主动脉夹层(AAD)是影响主动脉的最严重创伤性疾病。热蛋白沉积介导的血管壁炎症是诱发急性主动脉夹层的关键因素,其确切机制有待进一步研究。本研究的蛋白质组分析显示,AAD 患者血浆和主动脉组织中的脂多糖(LPS)结合蛋白(LBP)明显上调。此外,粪便样本的 16S rRNA 测序表明,AAD 患者的肠道菌群失调可能导致肠道屏障受损和 LPS 泄漏。通过与对照组小鼠进行比较,我们发现枸杞多糖(包括 Pyrin Domain Containing Protein3,NLRP3)、含 CARD 的适配器凋亡相关斑点样蛋白(apoptosis-associated speck-like protein,ASC)和裂解的 caspase-1 在 AAD 主动脉中上调,而肠道屏障相关蛋白下调。此外,与 AAD 小鼠相比,用 LBPK95A(一种 LBP 抑制剂)治疗可减轻 AAD 的发病率、热噬相关因子的表达水平以及血管病理变化的程度。此外,LPS和LBP处理人脐静脉内皮细胞(HUVECs)激活了TLR4信号传导和细胞内活性氧(ROS)的产生,从而刺激了NLRP3炎性体的形成并介导了内皮细胞的热蛋白沉积。我们的研究结果表明,肠道菌群失调通过 LPS-LBP 复合物介导了热蛋白沉积,从而为 AAD 的发展提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
LPS-LBP complex induced endothelial cell pyroptosis in aortic dissection is associated with gut dysbiosis.

Acute aortic dissection (AAD) is the most severe traumatic disease affecting the aorta. Pyroptosis-mediated vascular wall inflammation is a crucial trigger for AAD, and the exact mechanism requires further investigation. In this study, our proteomic analysis showed that Lipopolysaccharide (LPS)-binding protein (LBP) was significantly upregulated in the plasma and aortic tissue of patients with AAD. Further, 16S rRNA sequencing of stool samples suggested that patients with AAD exhibit gut dysbiosis, which may lead to an impaired intestinal barrier and LPS leakage. By comparing with control mice, we found that LBP, including Pyrin Domain Containing Protein3 (NLRP3), the CARD-containing adapter apoptosis-associated speck-like protein (ASC), and Cleaved caspase-1, were upregulated in the AAD aorta, whereas gut intestinal barrier-related proteins were downregulated. Moreover, treated with LBPK95A (an LBP inhibitor) attenuated the incidence of AAD, the expression levels of pyroptosis-related factors, and the extent of vascular pathological changes compared to those in AAD mice. In addition, LPS and LBP treatment of human umbilical vein endothelial cells (HUVECs) activated TLR4 signaling and intracellular reactive oxygen species (ROS) production, which stimulated NLRP3 inflammasome formation and mediated pyroptosis in endothelial cells. Our findings showed that gut dysbiosis mediates pyroptosis by the LPS-LBP complex, thus providing new insights into developing AAD.

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来源期刊
Microbes and Infection
Microbes and Infection 医学-病毒学
CiteScore
12.60
自引率
1.70%
发文量
90
审稿时长
40 days
期刊介绍: Microbes and Infection publishes 10 peer-reviewed issues per year in all fields of infection and immunity, covering the different levels of host-microbe interactions, and in particular: the molecular biology and cell biology of the crosstalk between hosts (human and model organisms) and microbes (viruses, bacteria, parasites and fungi), including molecular virulence and evasion mechanisms. the immune response to infection, including pathogenesis and host susceptibility. emerging human infectious diseases. systems immunology. molecular epidemiology/genetics of host pathogen interactions. microbiota and host "interactions". vaccine development, including novel strategies and adjuvants. Clinical studies, accounts of clinical trials and biomarker studies in infectious diseases are within the scope of the journal. Microbes and Infection publishes articles on human pathogens or pathogens of model systems. However, articles on other microbes can be published if they contribute to our understanding of basic mechanisms of host-pathogen interactions. Purely descriptive and preliminary studies are discouraged.
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