<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fang XZ</submitter><funding>National Natural Science Foundation of China</funding><pagination>175-186</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10658225</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>53</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Pulmonary fibrosis is a major cause of the poor prognosis of acute respiratory distress syndrome (ARDS). While mechanical ventilation (MV) is an indispensable life-saving intervention for ARDS, it may cause the remodeling process in lung epithelial cells to become disorganized and exacerbate ARDS-associated pulmonary fibrosis. Piezo1 is a mechanosensitive ion channel that is known to play a role in regulating diverse physiological processes, but whether Piezo1 is necessary for MV-exacerbated ARDS-associated pulmonary fibrosis remains unknown.&lt;h4>Objectives&lt;/h4>This study aimed to explore the role of Piezo1 in MV-exacerbated ARDS-associated pulmonary fibrosis.&lt;h4>Methods&lt;/h4>Human lung epithelial cells were stimulated with hydrochloric acid (HCl) followed by mechanical </pubmed_abstract><journal>Journal of advanced research</journal><pubmed_title>Mechanosensitive ion channel Piezo1 mediates mechanical ventilation-exacerbated ARDS-associated pulmonary fibrosis.</pubmed_title><pmcid>PMC10658225</pmcid><funding_grant_id>81971818</funding_grant_id><funding_grant_id>82002026</funding_grant_id><funding_grant_id>81772047</funding_grant_id><funding_grant_id>82172171</funding_grant_id><funding_grant_id>82272217</funding_grant_id><pubmed_authors>Reng LH</pubmed_authors><pubmed_authors>Yuan SY</pubmed_authors><pubmed_authors>Xu JQ</pubmed_authors><pubmed_authors>Zhou T</pubmed_authors><pubmed_authors>Sun DY</pubmed_authors><pubmed_authors>Li M</pubmed_authors><pubmed_authors>Zhang P</pubmed_authors><pubmed_authors>Sun MM</pubmed_authors><pubmed_authors>Yang YY</pubmed_authors><pubmed_authors>He YJ</pubmed_authors><pubmed_authors>Shu HQ</pubmed_authors><pubmed_authors>Fang XZ</pubmed_authors><pubmed_authors>Shang Y</pubmed_authors><pubmed_authors>Li RT</pubmed_authors><pubmed_authors>Xu JX</pubmed_authors><pubmed_authors>Wang YX</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mechanosensitive ion channel Piezo1 mediates mechanical ventilation-exacerbated ARDS-associated pulmonary fibrosis.</name><description>&lt;h4>Introduction&lt;/h4>Pulmonary fibrosis is a major cause of the poor prognosis of acute respiratory distress syndrome (ARDS). While mechanical ventilation (MV) is an indispensable life-saving intervention for ARDS, it may cause the remodeling process in lung epithelial cells to become disorganized and exacerbate ARDS-associated pulmonary fibrosis. Piezo1 is a mechanosensitive ion channel that is known to play a role in regulating diverse physiological processes, but whether Piezo1 is necessary for MV-exacerbated ARDS-associated pulmonary fibrosis remains unknown.&lt;h4>Objectives&lt;/h4>This study aimed to explore the role of Piezo1 in MV-exacerbated ARDS-associated pulmonary fibrosis.&lt;h4>Methods&lt;/h4>Human lung epithelial cells were stimulated with hydrochloric acid (HCl) followed by mechanical </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2025-04-04T11:35:48.804Z</modification><creation>2025-04-04T11:35:48.804Z</creation></dates><accession>S-EPMC10658225</accession><cross_references><pubmed>36526145</pubmed><doi>10.1016/j.jare.2022.12.006</doi></cross_references></HashMap>