利用培养的人肺泡基底细胞模拟特发性肺纤维化中蜂窝的形成

IF 4.7 2区 医学 Q1 RESPIRATORY SYSTEM Respiratory Research Pub Date : 2024-01-10 DOI:10.1186/s12931-024-02666-9
Sabrina Blumer, Petra Khan, Nataliia Artysh, Linda Plappert, Spasenija Savic, Lars Knudsen, Danny Jonigk, Mark P. Kuehnel, Antje  Prasse, Katrin E. Hostettler
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引用次数: 0

摘要

肺泡内的蜂窝状囊肿(HC)是特发性肺纤维化(IPF)患者肺部明显的组织病理学特征。蜂窝状囊肿内衬为单层或分层基底细胞(BC),或由基底、纤毛和分泌上皮细胞组成的支气管样上皮。通过使用培养自 IPF 患者的肺泡 BC,我们旨在建立一个体外和体内模型来模拟 IPF 中 HC 的形成。我们:(1)优化了培养和繁殖 IPF 患者肺泡 BC 的条件;(2)在气液界面(ALI)或三维(3D)类器官模型中培养细胞;(3)研究了细胞灌注到博莱霉素挑战小鼠体内后的行为。从外周 IPF 肺组织中培养肺泡 BC,并在组织培养处理过的塑料、ALI 或三维类器官模型中生长。此外,还将细胞灌注到博莱霉素致病的 NRG 小鼠体内。样本通过 TaqMan RT-PCR、免疫印迹、免疫细胞化学/免疫荧光(ICC/IF)或免疫组织化学(IHC)/IF 进行分析。使用 GraphPad Prism 软件进行 Mann-Whitney 检验。培养的肺泡BC显示了典型基底细胞标志物(TP63、角蛋白(KRT)5、KRT14、KRT17)的高表达、旺盛的增殖和伤口闭合能力。这些细胞可低温保存并繁殖四次,而基底细胞标志物不会明显丢失。在ALI或三维类器官模型中培养时,肺泡BC分化为纤毛上皮细胞和分泌上皮细胞。当把人肺泡BC细胞灌注到博莱霉素感染的小鼠体内时,小鼠实质内的人肺泡BC细胞形成了由人基底细胞和分泌上皮细胞组成的HC样结构。IPF患者衍生的肺泡BC细胞在ALI、三维有机体或注入博莱霉素挑战小鼠体内后形成HC样结构,与IPF肺内的HC非常相似。因此,这些模型是研究蜂窝状结构及其在 IPF 中的潜在治疗抑制作用的有力工具。
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The use of cultured human alveolar basal cells to mimic honeycomb formation in idiopathic pulmonary fibrosis
Honeycomb cysts (HC) within the alveolar region are distinct histopathological features in the lungs of idiopathic pulmonary fibrosis (IPF) patients. HC are lined with a single-or stratified layer of basal cells (BC), or with a bronchiolar-like epithelium composed of basal-, ciliated- and secretory epithelial cells. By using cultured IPF patient-derived alveolar BC, we aimed to establish an in vitro- and in vivo model to mimic HC formation in IPF. We (1) optimized conditions to culture and propagate IPF patient-derived alveolar BC, (2) cultured the cells on an air liquid interface (ALI) or in a three dimensional (3D) organoid model, and (3) investigated the cells` behavior after instillation into bleomycin-challenged mice. Alveolar BC were cultured from peripheral IPF lung tissue and grown on tissue-culture treated plastic, an ALI, or in a 3D organoid model. Furthermore, cells were instilled into bleomycin-challenged NRG mice. Samples were analyzed by TaqMan RT-PCR, immunoblotting, immunocytochemistry/immunofluorescence (ICC/IF), or immunohistochemistry (IHC)/IF. Mann–Whitney tests were performed using GraphPad Prism software. Cultured alveolar BC showed high expression of canonical basal cell markers (TP63, keratin (KRT)5, KRT14, KRT17), robust proliferation, and wound closure capacity. The cells could be cryopreserved and propagated for up to four passages without a significant loss of basal cell markers. When cultured on an ALI or in a 3D organoid model, alveolar BC differentiated to ciliated- and secretory epithelial cells. When instilled into bleomycin-challenged mice, human alveolar BC cells formed HC-like structures composed of human basal-, and secretory epithelial cells within the mouse parenchyma. IPF patient-derived alveolar BC on an ALI, in 3D organoids or after instillation into bleomycin-challenged mice form HC-like structures that closely resemble HC within the IPF lung. These models therefore represent powerful tools to study honeycomb formation, and its potential therapeutic inhibition in IPF.
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Respiratory Research
Respiratory Research 医学-呼吸系统
自引率
1.70%
发文量
314
期刊介绍: Respiratory Research publishes high-quality clinical and basic research, review and commentary articles on all aspects of respiratory medicine and related diseases. As the leading fully open access journal in the field, Respiratory Research provides an essential resource for pulmonologists, allergists, immunologists and other physicians, researchers, healthcare workers and medical students with worldwide dissemination of articles resulting in high visibility and generating international discussion. Topics of specific interest include asthma, chronic obstructive pulmonary disease, cystic fibrosis, genetics, infectious diseases, interstitial lung diseases, lung development, lung tumors, occupational and environmental factors, pulmonary circulation, pulmonary pharmacology and therapeutics, respiratory immunology, respiratory physiology, and sleep-related respiratory problems.
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