ACE2-Ang-(1-7)-Mas 轴对 SuHx 小鼠肠道菌群多样性和肠道代谢物的影响。

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2024-08-23 eCollection Date: 2024-01-01 DOI:10.3389/fmicb.2024.1412502
Asimuguli Abudukeremu, Ainiwaer Aikemu, Tao Yang, Lei Fang, Adilai Aihemaitituoheti, Yupeng Zhang, Daliya Shanahaiti, Yiliyaer Nijiati
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引用次数: 0

摘要

目的:肺动脉高压(PAH)是一项重大挑战,因为其治疗方案有限且死亡率高。ACE2-Ang-(1-7)-Mas 轴在调节血压和抑制心肌重塑方面发挥着关键作用。然而,人们对 ACE2-Ang-(1-7)-Mas 轴与 PAH 之间的确切机理联系仍然知之甚少。本研究旨在阐明 ACE2-Ang-(1-7)-Mas 轴参与 PAH 的发生:方法:使用Sugen5416/缺氧诱导小鼠发生PAH,使用心脏超声检测PAAT/PET比值和PA;使用细胞计数珠阵列(CBA)试剂盒检测肠道中的MCP-1、TNF、IL-10和IL-12p70等炎症相关因子;通过HE染色和Masson染色评估肺和肠道组织的组织病理学和形态学变化,以评价PAH的进展。免疫组织化学和 Western 印迹法测定了肠组织中两种紧密连接蛋白(occludin 和 ZO-1)的表达水平。此外,还利用 16rRNA 测序和 LC-MS/MS 非靶向代谢组学技术研究了 ACE2-Ang-(1-7)-Mas 轴对肠道内容物微生物多样性和代谢组学的影响:结果:激活 ACE2-Ang-(1-7)-Mas 轴可改善 SuHx 小鼠的心脏功能、减少肠道炎症因子并改善病理和组织学改变。这种激活明显提高了肠道组织中闭塞素和 ZO-1 蛋白的表达,促进了产生 SCFA 的细菌属(如 g_Candidatus_Saccharimonas)的增殖。此外,它还提高了有益代谢物的丰度,包括色氨酸和丁酸:研究结果表明,调节 ACE2-Ang-(1-7)-Mas 轴可通过调节肠道微生物和代谢物缓解 PAH。这些结果凸显了 ACE2-Ang-(1-7)-Mas 轴作为 PAH 临床治疗靶点的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of the ACE2-Ang-(1-7)-Mas axis on gut flora diversity and intestinal metabolites in SuHx mice.

Objective: Pulmonary artery hypertension (PAH) poses a significant challenge due to its limited therapeutic options and high mortality rates. The ACE2-Ang-(1-7)-Mas axis plays a pivotal role in regulating blood pressure and inhibiting myocardial remodeling. However, the precise mechanistic links between the ACE2-Ang-(1-7)-Mas axis and PAH remain poorly understood. This study aimed to elucidate the involvement of the ACE2-Ang-(1-7)-Mas axis in the development of PAH.

Methods: PAH was induced in mice using Sugen5416/hypoxia, PAAT/PET ratio and PA were detected using cardiac ultrasound; inflammation related factors such as MCP-1, TNF, IL-10and IL-12p70 were detected in intestines using cytometric bead array (CBA) kits; histopathological and morphological changes in lung and intestinal tissues were assessed via HE staining and Masson staining to evaluate the progression of PAH. Immunohistochemistry and western blotting were employed to determine the expression levels of two tight junction proteins, occludin and ZO-1, in intestinal tissues. Additionally, 16rRNA sequencing and non-targeted metabolomics by LC-MS/MS techniques were utilized to investigate the impact of the ACE2-Ang-(1-7)-Mas axis on microbial diversity and metabolomics of intestinal contents.

Results: Activation of the ACE2-Ang-(1-7)-Mas axis improves heart function, reduces intestines inflammatory factors and ameliorates pathological and histological alterations in SuHx mice. This activation notably upregulated the expression of occludin and ZO-1 proteins in intestinal tissues and promoted the proliferation of SCFA-producing bacteria genera, such as g_Candidatus_Saccharimonas. Furthermore, it enhanced the abundance of beneficial metabolites, including tryptophan and butyric acid.

Conclusion: The findings suggest that modulation of the ACE2-Ang-(1-7)-Mas axis can alleviate PAH by regulating intestinal microbes and metabolites. These results highlight the potential of the ACE2-Ang-(1-7)-Mas axis as a promising therapeutic target for clinical management of PAH.

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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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