Human Lung Tissue Implanted on the Chick Chorioallantoic Membrane
Current antifibrotic agents are not curative for idiopathic pulmonary fibrosis (IPF). Moreover, existing preclinical models do not fully replicate the human pathophysiology for IPF. In a new study, researchers have developed a robust model by implanting IPF lung-tissue derived cells into the chorioallantoic membrane (CAM) of chick embryos. This model can be used for the screening of novel antifibrotic drugs in an effective and cost-efficient manner.
Видео Human Lung Tissue Implanted on the Chick Chorioallantoic Membrane канала American Thoracic Society
Видео Human Lung Tissue Implanted on the Chick Chorioallantoic Membrane канала American Thoracic Society
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