期刊
ACS NANO
卷 17, 期 8, 页码 7562-7575出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsnano.2c12722
关键词
extracellular vesicles; severe acute pancreatitis; acute lung injury; integrin ? M; integrin? 2; pulmonary microvascular endothelial cells
Integrins expressed on SAP-EVs mediate ALI through their accumulation in the lung. Preincubation of SAP-EVs with HYD-1 attenuates pulmonary inflammation and disruption of the PMVEC barrier. Injections of EVs overexpressing ITGAM and ITGB2 also attenuate pulmonary accumulation of pancreas-derived EVs, as well as decrease pulmonary inflammation and disruption of the endothelial cell barrier.
Integrins expressed on extracellular vesicles (EVs) secreted by various cancers are reported to mediate the organotropism of these EVs. Our previous experiment found that pancreatic tissue of mice with severe cases of acute pancreatitis (SAP) overexpresses several integrins and that serum EVs of these mice (SAP-EVs) can mediate acute lung injury (ALI). It is unclear if SAP-EV express integrins that can promote their accumulation in the lung to promote ALI. Here, we report that SAP-EV overexpress several integrins and that preincubation of SAP-EV with the integrin antagonist peptide HYD-1 markedly attenuates their pulmonary inflammation and disrupt the pulmonary microvascular endothelial cell (PMVEC) barrier. Further, we report that injecting SAP mice with EVs engineered to overexpress two of these integrins (ITGAM and ITGB2) can attenuate the pulmonary accumulation of pancreas-derived EVs and similarly decrease pulmonary inflammation and disruption of the endothelial cell barrier. Based on these findings, we propose that pancreatic EVs can mediate ALI in SAP patients and that this injury response could be attenuated by administering EVs that overexpress ITGAM and/or ITGB2, which is worthy of further study due to the lack of effective therapies for SAP-induced ALI.
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