{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Margaroli C"],"funding":["Veterans Administration","Cystic Fibrosis Foundation","NIH"],"pagination":["e153560"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8876451"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["7(4)"],"pubmed_abstract":["Chronic obstructive pulmonary disease (COPD) is a debilitating chronic disease and the third-leading cause of mortality worldwide. It is characterized by airway neutrophilia, promoting tissue injury through release of toxic mediators and proteases. Recently, it has been shown that neutrophil-derived extracellular vesicles (EVs) from lungs of patients with COPD can cause a neutrophil elastase-dependent (NE-dependent) COPD-like disease upon transfer to mouse airways. However, in vivo preclinical models elucidating the impact of EVs on disease are lacking, delaying opportunities for therapeutic testing. Here, we developed an in vivo preclinical mouse model of lung EV-induced COPD. EVs from in vivo LPS-activated mouse neutrophils induced COPD-like disease in naive recipients through an α-1 ant"],"journal":["JCI insight"],"pubmed_title":["An in vivo model for extracellular vesicle-induced emphysema."],"pmcid":["PMC8876451"],"funding_grant_id":["ROWE19R0","HL153113","101CX001969","K12 GM088010","5R35HL135710"],"pubmed_authors":["Gaggar A","Viera L","Margaroli C","Blalock JE","Madison MC","Genschmer KR","Russell DW"],"additional_accession":[]},"is_claimable":false,"name":"An in vivo model for extracellular vesicle-induced emphysema.","description":"Chronic obstructive pulmonary disease (COPD) is a debilitating chronic disease and the third-leading cause of mortality worldwide. It is characterized by airway neutrophilia, promoting tissue injury through release of toxic mediators and proteases. Recently, it has been shown that neutrophil-derived extracellular vesicles (EVs) from lungs of patients with COPD can cause a neutrophil elastase-dependent (NE-dependent) COPD-like disease upon transfer to mouse airways. However, in vivo preclinical models elucidating the impact of EVs on disease are lacking, delaying opportunities for therapeutic testing. Here, we developed an in vivo preclinical mouse model of lung EV-induced COPD. EVs from in vivo LPS-activated mouse neutrophils induced COPD-like disease in naive recipients through an α-1 ant","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Jan","modification":"2025-04-18T20:03:19.972Z","creation":"2025-04-07T07:49:53.065Z"},"accession":"S-EPMC8876451","cross_references":{"pubmed":["35077395"],"doi":["10.1172/jci.insight.153560"]}}