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Perfluorocarbon induces alveolar epithelial cell response through structural and mechanical remodeling

机译:全氟化碳通过结构和机械重塑诱导肺泡上皮细胞响应

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摘要

During total liquid ventilation, lung cells are exposed to perfluorocarbon (PFC) whose chemophysical properties highly differ from standard aqueous cell feeding medium (DMEM). We herein perform a systematic study of structural and mechanical properties of A549 alveolar epithelial cells in order to characterize their response to PFC exposure, using DMEM as control condition. Changes in F-actin structure, focal adhesion density and glycocalyx distribution are evaluated by confocal fluorescent microscopy. Changes in cell mechanics and adhesion are measured by multiscale magnetic twisting cytometry (MTC). Two different microrheological models (single Voigt and power law) are used to analyze the cell mechanics characterized by cytoskeleton (CSK) stiffness and characteristic relaxation times. Cell-matrix adhesion is analyzed using a stochastic multibond deadhesion model taking into account the non-reversible character of the cell response, allowing us to quantify the adhesion weakness and the number of associated bonds. The roles of F-actin structure and glycocalyx layer are evaluated by depolymerizing F-actin and degrading glycocalyx, respectively. Results show that PFC exposure consistently induces F-actin remodeling, CSK softening and adhesion weakening. These results demonstrate that PFC triggers an alveolar epithelial cell response herein evidenced by a decay in intracellular CSK tension, an adhesion weakening and a glycocalyx layer redistribution. These PFC-induced cell adjustments are consistent with the hypothesis that cells respond to a decrease in adhesion energy at cell surface. This adhesion energy can be even further reduced in the presence of surfactant adsorbed at the cell surface.
机译:在总液体通气过程中,肺细胞暴露于全氟化物(PFC),其化学物理学与标准含水细胞喂养介质(DMEM)高度不同。我们在本文中对A549肺泡上皮细胞的结构和机械性能进行了系统研究,以表征其对PFC暴露的响应,使用DMEM作为控制条件。通过共聚焦荧光显微镜评估F-actin结构的变化,焦粘性密度和糖钙分布。通过多尺度磁性扭曲细胞术(MTC)测量细胞力学和粘附性的变化。两种不同的微流学模型(单型voigt和电力法)用于分析特征的细胞力学(Csk)刚度和特征松弛时间。使用随机多元叶状模型进行分析细胞 - 基质粘附,考虑到电池响应的不可逆转特性,允许我们量化粘附弱点和相关键的数量。通过分别解聚的F-肌动蛋白和降解的甘油蛋白和降解甘油蛋白和降解甘油糖蛋白结构和糖粉结构的作用。结果表明,PFC曝光一致地诱导F-actin重塑,CSK软化和粘合削弱。这些结果表明,PFC触发本文的肺泡上皮细胞反应在细胞内CSK张力中的衰减证明,粘附削弱和糖钙层的再分配。这些PFC诱导的细胞调节与细胞响应细胞表面粘附能量的减少的假设一致。在吸附在细胞表面的表面活性剂存在下,这种粘合能甚至可以进一步减少。

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  • 作者单位

    Univ Paris Est UPEC CNRS Equipe 13 UMR S955 ERL 7000 INSERM IMRB U955 Biomecan &

    Appareil Resp 8 Rue Gen Sarrail F-94010 Creteil France;

    Univ Grenoble Alpes Ctr Rech INSERM U1209 CNRS 5309 Grenoble France;

    Univ Paris Est UPEC CNRS Equipe 13 UMR S955 ERL 7000 INSERM IMRB U955 Biomecan &

    Appareil Resp 8 Rue Gen Sarrail F-94010 Creteil France;

    Bertin Technol F-78180 Montigny Le Bretonneux France;

    Univ Paris Est Ecole Natl Vet Alfort INSERM IMRB U955 Equipe 03 UMRS955 UPEC 7 Ave Gen Gaulle F-94700 Maisons Alfort France;

    Univ Paris Est UPEC CNRS Equipe 13 UMR S955 ERL 7000 INSERM IMRB U955 Biomecan &

    Appareil Resp 8 Rue Gen Sarrail F-94010 Creteil France;

    Univ Paris Est UPEC CNRS Equipe 13 UMR S955 ERL 7000 INSERM IMRB U955 Biomecan &

    Appareil Resp 8 Rue Gen Sarrail F-94010 Creteil France;

    Univ Paris Est UPEC CNRS Equipe 13 UMR S955 ERL 7000 INSERM IMRB U955 Biomecan &

    Appareil Resp 8 Rue Gen Sarrail F-94010 Creteil France;

    Univ Paris Est UPEC CNRS Equipe 13 UMR S955 ERL 7000 INSERM IMRB U955 Biomecan &

    Appareil Resp 8 Rue Gen Sarrail F-94010 Creteil France;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物力学;
  • 关键词

    Mechanotransduction; Cytoskeleton; Glycocalyx; Prestress; Surfactant;

    机译:机械手术;细胞骨架;甘油癌;预应力;表面活性剂;

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