人 AT2 细胞与成纤维细胞的共培养揭示了 MUC5B 表型:类器官模型的启示。

IF 6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yiwen Yao, Felix Ritzmann, Sarah Miethe, Kathrin Kattler-Lackes, Betül Colakoglu, Christian Herr, Andreas Kamyschnikow, Michelle Brand, Holger Garn, Daniela Yildiz, Frank Langer, Robert Bals, Christoph Beisswenger
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引用次数: 0

摘要

成纤维细胞与肺细胞的相互作用受损是特发性肺纤维化(IPF)等慢性肺病恶化的原因之一。粘蛋白5B(MUC5B)与特发性肺纤维化有关。在这里,我们分析了原代成纤维细胞和肺泡2型(AT2)肺细胞在类器官模型中的相互作用。单细胞分析、组织学和qRT-PCR显示,表达高水平纤维化标志物的成纤维细胞会调节AT2细胞中的STAT3信号,而STAT3信号会伴随囊性类器官生长和MUC5B的表达。囊性生长和 MUC5B 的表达也是由细胞因子 IL-6 引起的。成纤维细胞中的PI3K-Akt信号通路被激活。药物达沙替尼阻止了表达MUC5B的囊性器官组织的形成。在IPF患者的样本中,MUC5B与AT2细胞相关。我们的模型表明,纤维化的原发性成纤维细胞通过STAT3信号通路诱导AT2细胞分化受损,这在IPF患者中也能观察到。该模型可用于机理研究和药物开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Co-culture of human AT2 cells with fibroblasts reveals a MUC5B phenotype: insights from an organoid model.

Impaired interaction of fibroblasts with pneumocytes contributes to the progression of chronic lung disease such as idiopathic pulmonary fibrosis (IPF). Mucin 5B (MUC5B) is associated with IPF. Here we analyzed the interaction of primary fibroblasts and alveolar type 2 (AT2) pneumocytes in the organoid model. Single-cell analysis, histology, and qRT-PCR revealed that fibroblasts expressing high levels of fibrosis markers regulate STAT3 signaling in AT2 cells, which is accompanied by cystic organoid growth and MUC5B expression. Cystic growth and MUC5B expression were also caused by the cytokine IL-6. The PI3K-Akt signaling pathway was activated in fibroblasts. The drug dasatinib prevented the formation of MUC5B-expressing cystic organoids. MUC5B associated with AT2 cells in samples obtained from IPF patients. Our model shows that fibrotic primary fibroblasts induce impaired differentiation of AT2 cells via STAT3 signaling pathways, as observed in IPF patients. It can be used for mechanistic studies and drug development.

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来源期刊
Molecular Medicine
Molecular Medicine 医学-生化与分子生物学
CiteScore
8.60
自引率
0.00%
发文量
137
审稿时长
1 months
期刊介绍: Molecular Medicine is an open access journal that focuses on publishing recent findings related to disease pathogenesis at the molecular or physiological level. These insights can potentially contribute to the development of specific tools for disease diagnosis, treatment, or prevention. The journal considers manuscripts that present material pertinent to the genetic, molecular, or cellular underpinnings of critical physiological or disease processes. Submissions to Molecular Medicine are expected to elucidate the broader implications of the research findings for human disease and medicine in a manner that is accessible to a wide audience.
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