Card11 在高脂饮食诱导的肥胖小鼠气道高反应性中的重要作用

IF 9.5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hyun-Seung Lee, Byung-Keun Kim, Suh-Young Lee, Hyuktae Kwon, Heung-Woo Park
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引用次数: 0

摘要

高脂肪饮食(HFD)可以诱导肥胖小鼠气道高反应性(AHR),独立于过敏致敏。本研究旨在确定hfd诱导肥胖小鼠AHR相关的关键分子。通过对hfd诱导的肥胖小鼠脂肪和肺组织中基因时间序列表达的聚类分析,我们发现Caspase募集结构域家族成员11 (Card11)基因是一个重要分子。我们测量了肥胖哮喘患者外周血单个核细胞(PBMCs)中CARD11的表达,并通过CARD11 siRNA对hfd诱导的肥胖小鼠进行了CARD11信号抑制。脂肪组织中M1巨噬细胞(IL-1β+CD11c+ CD11b+中的CD206-)和肺组织中ILC3s (Lin-中IL7R+中的rorγ - t+)中Card11的表达显著升高。此外,肥胖哮喘患者PBMCs中ILC3s和lps刺激的IL-1β+CD16+单核细胞中的CARD11+群体显著高于肥胖对照或非肥胖哮喘患者。当我们在13周HFD喂养的前7周或后7周通过给药Card11 siRNA抑制Card11信号通路时,HFD诱导的肥胖小鼠AHR消失。最后,我们在体外证实了Card11 siRNA降低了脂肪组织中M1巨噬细胞的数量和肺组织中ILC3s的数量。Card11通过影响脂肪和肺组织中的免疫细胞,显著促进hfd诱导的肥胖小鼠AHR的发展。HFD饲喂的中期似乎对这些过程至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Essential role of Card11 in airway hyperresponsiveness in high-fat diet-induced obese mice

Essential role of Card11 in airway hyperresponsiveness in high-fat diet-induced obese mice
A high-fat diet (HFD) can induce airway hyperresponsiveness (AHR) in obese mice, independent of allergic sensitization. This study aimed to identify the key molecules related to AHR in HFD-induced obese mice. In a cluster analysis of time series gene expression in the adipose and lung tissues of HFD-induced obese mice, we identified the Caspase Recruitment Domain Family Member 11 (Card11) gene as an essential molecule. We measured CARD11 expression in peripheral blood mononuclear cells (PBMCs) from obese individuals with asthma and performed Card11 signal inhibition in HFD-induced obese mice via Card11 siRNA. Card11 expression was significantly increased in M1 macrophages (IL-1β+CD11c+CD206- in CD11b+) in adipose tissue and in ILC3s (RORγt+ in IL7R+ of Lin-) in lung tissue from HFD-induced obese mice. In addition, CARD11+ populations among ILC3s and LPS-stimulated IL-1β+CD16+ monocytes from the PBMCs of obese individuals with asthma were significantly greater than those from obese controls or nonobese individuals with asthma. AHR in HFD-induced obese mice disappeared when we inhibited the Card11 signaling pathway by administering Card11 siRNA during the first or last seven weeks of the 13-week HFD feeding. Finally, we confirmed that Card11 siRNA decreased the number of M1 macrophages in adipose tissue and the number of ILC3s in lung tissue in vitro. Card11 significantly contributes to the development of AHR in HFD-induced obese mice by affecting immune cells in both adipose and lung tissues. The middle stage of HFD feeding seemed to be critical for these processes. Obesity is a metabolic disease and a major risk factor for several non-communicable diseases. The link between obesity and asthma is not fully understood. The study used a murine model to investigate how obesity affects asthma. Researchers fed mice a high-fat diet and analyzed gene expression in their adipose and lung tissues. They identified the Card11 gene as a key player in airway hyperresponsiveness in obese mice. This was an experimental study involving mice. Results showed that Card11 expression increased in immune cells from both adipose and lung tissues of obese mice. Inhibiting Card11 reduced AHR and inflammation. Researchers concluded that Card11 is crucial in obesity-related asthma. Future studies could explore Card11 as a therapeutic target for asthma in obese individuals. This summary was initially drafted using artificial intelligence, then revised and fact-checked by the author.
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来源期刊
Experimental and Molecular Medicine
Experimental and Molecular Medicine 医学-生化与分子生物学
CiteScore
19.50
自引率
0.80%
发文量
166
审稿时长
3 months
期刊介绍: Experimental & Molecular Medicine (EMM) stands as Korea's pioneering biochemistry journal, established in 1964 and rejuvenated in 1996 as an Open Access, fully peer-reviewed international journal. Dedicated to advancing translational research and showcasing recent breakthroughs in the biomedical realm, EMM invites submissions encompassing genetic, molecular, and cellular studies of human physiology and diseases. Emphasizing the correlation between experimental and translational research and enhanced clinical benefits, the journal actively encourages contributions employing specific molecular tools. Welcoming studies that bridge basic discoveries with clinical relevance, alongside articles demonstrating clear in vivo significance and novelty, Experimental & Molecular Medicine proudly serves as an open-access, online-only repository of cutting-edge medical research.
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