肥胖会损害小鼠气道上皮细胞的纤毛功能和粘液纤毛清除能力。

IF 3.6 2区 医学 Q1 PHYSIOLOGY
Yuko Tanaka, Tomoyuki Fujisawa, Shusuke Yazawa, Isao Ohta, Yasuharu Takaku, Masahiko Ito, Yusuke Inoue, Hideki Yasui, Hironao Hozumi, Masato Karayama, Yuzo Suzuki, Kazuki Furuhashi, Noriyuki Enomoto, Mitsutoshi Setou, Naoki Inui, Tetsuro Suzuki, Takafumi Suda
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引用次数: 0

摘要

肥胖是增加病毒性呼吸道感染发病率和死亡率的一个风险因素。气道黏膜纤毛清除(MCC)是宿主抵御病毒感染的主要防御手段。然而,肥胖对MCC的影响尚不清楚,因此促成了这项研究。我们利用小鼠气管组织培养和体外甲型流感病毒(IAV)感染模型,分析了气道上皮细胞中纤毛驱动的气流和纤毛跳动频率(CBF),以评估MCC。短期 IAV 感染会增加对照组小鼠的纤毛驱动流量和 CBF,但不会增加高脂饮食诱导的肥胖小鼠的纤毛驱动流量和 CBF。肥胖小鼠的基础纤毛驱动血流和 CBF 也低于对照组小鼠。从机理上讲,在对照组小鼠中观察到的 IAV 感染期间细胞外三磷酸腺苷(ATP)释放的增加在肥胖小鼠中被取消了,尽管 ATP 的添加能使对照组和肥胖小鼠的纤毛驱动血流和 CBF 增加到相似的程度。此外,RNA 测序和反转录聚合酶链反应显示,几个纤毛相关基因下调,包括 Dnah1、Dnal1、Armc4 和 Ttc12(动力蛋白相关基因);Ulk4(多毛体分化基因);与对照组相比,肥胖小鼠气管组织中的 Cep164(纤毛发生和囊内转运基因)、Rsph4a、Cfap206 和 Ppil6(径向辐条结构和组装基因)以及 Drc3(nexin-dynein 调控复合物基因)的含量均有所下降。总之,我们的研究表明,肥胖会通过下调纤毛相关基因的表达和抑制细胞外 ATP 的释放,在基础条件下和 IAV 感染期间减弱 MCC,从而增加 IAV 感染的易感性和严重程度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Obesity impairs ciliary function and mucociliary clearance in the murine airway epithelium.

Obesity is a risk factor for increased morbidity and mortality in viral respiratory infection. Mucociliary clearance (MCC) in the airway is the primary host defense against viral infections. However, the impact of obesity on MCC is unclear, prompting this study. Using murine tracheal tissue culture and in vitro influenza A virus (IAV) infection models, we analyzed cilia-driven flow and ciliary beat frequency (CBF) in the airway epithelium to evaluate MCC. Short-term IAV infection increased cilia-driven flow and CBF in control mice, but not in high-fat diet-induced obese mice. Basal cilia-driven flow and CBF were also lower in obese mice than in control mice. Mechanistically, the increase of extracellular adenosine triphosphate (ATP) release during IAV infection, which was observed in the control mice, was abolished in the obese mice; however, the addition of ATP increased cilia-driven flow and CBF both in control and obese mice to a similar extent. In addition, RNA sequencing and reverse transcription-polymerase chain reaction revealed the downregulation of several cilia-related genes, including Dnah1, Dnal1, Armc4, and Ttc12 (the dynein-related genes); Ulk4 (the polychaete differentiation gene); Cep164 (the ciliogenesis and intraflagellar transport gene); Rsph4a, Cfap206, and Ppil6 (the radial spoke structure and assembly gene); and Drc3(the nexin-dynein regulatory complex genes) in obese murine tracheal tissues compared with their control levels. In conclusion, our studies demonstrate that obesity attenuates MCC under basal conditions and during IAV infection by downregulating the expression of cilia-related genes and suppressing the release of extracellular ATP, thereby increasing the susceptibility and severity of IAV infection.NEW & NOTEWORTHY Our study shows that obesity impairs airway mucociliary clearance (MCC), an essential physical innate defense mechanism for viral infection. Mechanically, this is likely due to the obesity-induced downregulation of cilia-related genes and attenuation of extracellular ATP release. This study provides novel insights into the mechanisms driving the higher susceptibility and severity of viral respiratory infections in individuals with obesity.

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来源期刊
CiteScore
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.
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