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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Publication Details

Journal
Molecular Medicine
Published
2024-11-23
DOI
https://doi.org/10.1186/s10020-024-00990-w
Citations
8
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
3.35

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article

Co-culture of human AT2 cells with fibroblasts reveals a MUC5B phenotype: insights from an organoid model

Christoph Beißwenger, Michelle Brand, Frank Langer, Andreas Kamyschnikow et al.
8 citations
Molecular Medicine
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
3.35
article

Co-culture of human AT2 cells with fibroblasts reveals a MUC5B phenotype: insights from an organoid model

Christoph Beißwenger, Michelle Brand, Frank Langer, Andreas Kamyschnikow, Felix Ritzmann, Robert Bals, Yiwen Yao, Holger Garn, Christian Herr, Daniela Yildiz, Sarah Miethe, Betül Colakoglu, Kathrin Kattler‐Lackes
article en
8 citations

Abstract

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.

Molecular MedicineVol. 30(1)
Tongji University (CN), Philipps University of Marburg (DE), Helmholtz Centre for Infection Research (DE), German Center for Lung Research (DE), Universities of Giessen and Marburg Lung Center (DE), Helmholtz Institute for Pharmaceutical Research Saarland (DE), Tongji Hospital (CN), Saarland University (DE)
Bundesministerium für Bildung und Forschung, Universität des Saarlandes, Dr. Rolf M. Schwiete Stiftung
Good health and well-being
Openalex Percentile: Top 7%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
3.35
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