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Advanced Lung-on-a-Chip Technology: Mimicking the Complex Human Lung Microenvironment. | LitMetric

AI Article Synopsis

  • The study highlights the importance of crosstalk among lung cell types for proper lung function and illustrates the inadequacies of traditional 2D and 3D lung models in mimicking this complexity.
  • An advanced multicellular 3D lung-on-a-chip system was developed using natural polymers and blood coagulation factors to accurately represent the dynamic microenvironment of lung tissue.
  • This new system allows for quick and sensitive toxicity detection in lung cells, identifying SERPINB2 as a key biomarker for lung toxicity while incorporating a fluorescence-based screening platform for evaluating drug candidates.

Article Abstract

Intricate crosstalk among various lung cell types is crucial for orchestrating diverse physiological processes. Traditional two-dimensional and recent three-dimensional (3D) assay platforms fail to precisely replicate these complex communications. Many lung models do not effectively reflect the multicellular complexity of lung tissue. Here, we fabricated an advanced multicellular 3D lung-on-a-chip system that properly replicates the dynamic pulmonary microenvironment and its intricate microarchitecture. Diverse lung cells were incorporated into a microstructure formed from a mixture of natural polymers, including collagen and hyaluronic acid, and blood coagulation factors acting as natural crosslinking agents. The system accurately reflects the complex 3D architecture of the lung. Biomarkers demonstrate more rapid and sensitive responses to toxic substances than functional indicators, such as cell proliferation and apoptosis. SERPINB2 was identified as a biomarker of lung toxicity; it was activated in small airway epithelial cells exposed to various toxic substances. We then developed a fluorescence-linked toxicity biomarker screening platform that enables both intuitive and quantitative evaluation of lung toxicity by measuring the converted fluorescent signal strength. This fluorescent tagging system was incorporated into small airway epithelial cells within a fabricated chip platform; enabling lung-on-a-chip enabled evaluation of the lung toxicity of prospective drug candidates.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11667821PMC
http://dx.doi.org/10.7150/ijbs.105702DOI Listing

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