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The role of inducible nitric oxide synthase for interstitial remodeling of alveolar septa in surfactant protein D-deficient mice

机译:诱导型一氧化氮合酶在表面活性剂蛋白D缺陷小鼠中肺泡隔膜间质重塑的作用

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Surfactant protein D (SP-D) modulates the lung's immune system. Its absence leads to NOS2-independent alveolar lipoproteinosis and NOS2-dependent chronic inflammation, which is critical for early emphysematous remodeling. With aging, SP-D knockout mice develop an additional interstitial fibrotic component. We hypothesize that this age-related interstitial septal wall remodeling is mediated by NOS2. Using invasive pulmonary function testing such as the forced oscillation technique and quasistatic pressure-volume perturbation and design-based stereology, we compared 29-wk-old SP-D knockout (Sftpd~(-/-)) mice, SP-D/ NOS2 double-knockout (DiNOS) mice, and wild-type mice (WT). Structural changes, including alveolar epithelial surface area, distribution of septal wall thickness, and volumes of septal wall components (alveolar epithelium, interstitial tissue, and endothelium) were quantified. Twenty-nine-week-old Sftpd~(-/-) mice had preserved lung mechanics at the organ level, whereas elastance was increased in DiNOS. Airspace enlargement and loss of surface area of alveolar epithelium coexist with increased septal wall thickness in Sftpd~(-/-) mice. These changes were reduced in DiNOS, and compared with Sftpd~(-/-) mice a decrease in volumes of interstitial tissue and alveolar epithelium was found. To understand the effects of lung pathology on measured lung mechanics, structural data were used to inform a computational model, simulating lung mechanics as a function of airspace derecruitment, septal wall destruction (loss of surface area), and septal wall thickening. In conclusion, NOS2 mediates remodeling of septal walls, resulting in deposition of interstitial tissue in Sftpd~(-/-). Forward modeling linking structure and lung mechanics describes the complex mechanical properties by parenchymatous destruction (emphysema), interstitial remodeling (septal wall thickening), and altered recruitability of acinar airspaces.
机译:表面活性剂蛋白D(SP-D)调节肺的免疫系统。它的缺失导致NOS2独立的肺泡脂蛋白和NOS2依赖性慢性炎症,这对于早期催育重塑至关重要。随着衰老,SP-D敲除小鼠产生额外的间质纤维化组分。我们假设这种与年龄相关的间质隔膜重塑是由NOS2介导的。采用侵入式肺功能测试,如强制振荡技术和Quasistatic压力扰动和基于设计的立体术,我们将29-WK-Old SP-D敲除(SFTPD〜( - / - ))小鼠,SP-D / NOS2相比双敲除(Dinos)小鼠和野生型小鼠(WT)。定量变化,包括肺泡上皮表面积,隔膜壁厚度分布,以及隔膜壁组分(肺泡上皮,间质组织和内皮)的体积。二十九周的SFTPD〜( - / - )小鼠在器官水平处保存了肺部力学,而恐龙则会增加。 SFTPD〜(/ - / - )小鼠中的隔膜壁厚度增加的肺泡上皮共存的空域扩大和丧失肺泡上皮共存。这些变化在DINOS中减少,并与SFTPD〜( - / - )小鼠进行比较,发现间质组织和肺泡上皮的减少。要了解肺部病理对测量肺部机械的影响,结构数据用于通知计算模型,模拟肺部力学作为空域DASCRIULENT,隔膜壁破坏(表面积丧失)和隔膜壁增厚。总之,NOS2介导隔膜壁的重塑,导致SFTPD〜( - / - )中的间质组织沉积。前进建模连接结构和肺力学描述了通过实质破坏(肺气肿),间质重塑(隔膜壁增厚)的复杂机械性能,并改变了缩醛空腹的征收性。

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