GATA1-defective immune-megakaryocytes as possible drivers of idiopathic pulmonary fibrosis.

bioRxiv : the preprint server for biology(2023)

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摘要
Lungs from IPF patients contain many GATA1 negative immune MK mice are the first genetic model with a pathophysiology similar to IPF lungs mice contain defective immune MK with high P-sel, TGF-β and CXCL1 ablation or P-sel/TGF-β/CXCL1 inhibition rescues fibrosis in lung.
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关键词
idiopathic pulmonary fibrosis,immune-megakaryocytes
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