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Phenotypic drug screening for novel antifibrotic therapeutics in lung health.
In: Phenotypic Screening. Berlin [u.a.]: Springer, 2026. 227-240 (Methods Mol. Biol. ; 2989)
Lung diseases are among the leading causes of death worldwide. Still, noncommunicable pulmonary diseases, such as chronic obstructive pulmonary disease (COPD), and interstitial lung disease (ILD), are lacking curative pharmacotherapies. Either degradation or excessive production of altered pulmonary extracellular matrix (ECM) is a common key feature of those devastating diseases, respectively. Recapitulating those pathological changes in miniaturized cell culture models is key for phenotypic drug discovery approaches targeting the ECM for novel pharmacotherapies in pulmonary disease. We describe here a phenotypic immunofluorescence-based high-content/high-throughput assay in 384-well plate format to measure ECM deposition activity by primary human lung fibroblasts (phLFs) in a pulmonary fibrosis disease context.
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Publication type
Article: Periodical or book chapter
Keywords
Ecm Deposition ; Fibroblast ; High-throughput Screening ; Lung Fibrosis ; Phenotypic Drug Screening
ISSN (print) / ISBN
1064-3745
e-ISSN
1940-6029
Book Volume Title
Phenotypic Screening
Journal
Methods in Molecular Biology
Quellenangaben
Volume: 2989,
Pages: 227-240
Publisher
Springer
Publishing Place
Berlin [u.a.]
Reviewing status
Peer reviewed
Institute(s)
Institute of Lung Health and Immunity (LHI)