The role of Notch-dependent differentiation of resident fibroblasts in the development of pulmonary fibrosis

I. Chistyakova, N. Bakalenko, A. Malashicheva, M. Atyukov, A. Petrov
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Abstract

Background. Molecular mechanisms of the development of pulmonary fibrosis are poorly understood. It is known that differentiation of resident lung cells into myofibroblasts plays a key role in this disease. The search for factors capable of regulating such differentiation is an urgent task. Objective. To evaluate the effect of Notch signaling pathway activation on resident lung fibroblasts by introducing the intracellular domains of each of the 4 Notch receptors (N1-4ICD). Design and methods. Primary cultures of pulmonary fibroblasts from donors (n = 4) were used. Notch-dependent activation of fibroblasts was carried out by introducing lentiviral vectors with/ without sequences of N1-4ICD domains. After 8 days, immunocytochemical staining was performed and the relative expression levels of the PDPN, HOPX, SLUG, SNAIL and ACTA2 genes were evaluated by qPCR. Results. Activation of the Notch signaling pathway by N1-4CD resulted in increased expression of SLUG, SNAIL and ACTA2. The most pronounced effect was observed with the introduction of Notch4-activating sequence. Induction of signaling by the introduction of N1-3ICD activating components contributed to an increase in PDPN expression, with the introduction of N4ICD, an increase in the level of HOPX expression was noted. Conclusion. Activation of each of the 4 intracellular Notch receptor domains is able to trigger the differentiation of resident alveolar fibroblasts into myofibroblasts, which are key players in the development of pulmonary fibrosis.
原位成纤维细胞Notch依赖性分化在肺纤维化发展中的作用
背景肺纤维化发生的分子机制尚不清楚。众所周知,固有肺细胞分化为肌成纤维细胞在这种疾病中起着关键作用。寻找能够调节这种分化的因素是一项紧迫的任务。客观的通过引入4种Notch受体(N1-4ICD)的细胞内结构域,评估Notch信号通路激活对常驻肺成纤维细胞的影响。设计和方法。使用来自供体(n=4)的肺成纤维细胞的原代培养物。成纤维细胞的Notch依赖性激活是通过引入具有/不具有N1-4ICD结构域序列的慢病毒载体来进行的。8天后,进行免疫细胞化学染色,并通过qPCR评估PDPN、HOPX、SLUG、SNAIL和ACTA2基因的相对表达水平。后果N1-4CD对Notch信号通路的激活导致SLUG、SNAIL和ACTA2的表达增加。通过引入Notch4激活序列观察到最显著的效果。通过引入N1-3ICD激活成分诱导信号传导有助于PDPN表达的增加,随着N4ICD的引入,HOPX表达水平增加。结论激活4个细胞内Notch受体结构域中的每一个都能够触发固有肺泡成纤维细胞分化为肌成纤维细胞,肌成纤维纤维细胞是肺纤维化发展的关键参与者。
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