{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,28]],"date-time":"2026-10-28T22:01:46Z","timestamp":1793224906024,"version":"4.5.0"},"reference-count":102,"publisher":"American Association for the Advancement of Science (AAAS)","issue":"699","content-domain":{"domain":["www.science.org"],"crossmark-restriction":true},"short-container-title":["Sci. Transl. Med."],"published-print":{"date-parts":[[2023,6,7]]},"abstract":"<jats:p>\n                    Unlike solid organs, human airway epithelia derive their oxygen from inspired air rather than the vasculature. Many pulmonary diseases are associated with intraluminal airway obstruction caused by aspirated foreign bodies, virus infection, tumors, or mucus plugs intrinsic to airway disease, including cystic fibrosis (CF). Consistent with requirements for luminal O\n                    <jats:sub>2<\/jats:sub>\n                    , airway epithelia surrounding mucus plugs in chronic obstructive pulmonary disease (COPD) lungs are hypoxic. Despite these observations, the effects of chronic hypoxia (CH) on airway epithelial host defense functions relevant to pulmonary disease have not been investigated. Molecular characterization of resected human lungs from individuals with a spectrum of muco-obstructive lung diseases (MOLDs) or COVID-19 identified molecular features of chronic hypoxia, including increased\n                    <jats:italic>EGLN3<\/jats:italic>\n                    expression, in epithelia lining mucus-obstructed airways. In vitro experiments using cultured chronically hypoxic airway epithelia revealed conversion to a glycolytic metabolic state with maintenance of cellular architecture. Chronically hypoxic airway epithelia unexpectedly exhibited increased MUC5B mucin production and increased transepithelial Na\n                    <jats:sup>+<\/jats:sup>\n                    and fluid absorption mediated by HIF1\u03b1\/HIF2\u03b1-dependent up-regulation of \u03b2 and \u03b3ENaC (epithelial Na\n                    <jats:sup>+<\/jats:sup>\n                    channel) subunit expression. The combination of increased Na\n                    <jats:sup>+<\/jats:sup>\n                    absorption and MUC5B production generated hyperconcentrated mucus predicted to perpetuate obstruction. Single-cell and bulk RNA sequencing analyses of chronically hypoxic cultured airway epithelia revealed transcriptional changes involved in airway wall remodeling, destruction, and angiogenesis. These results were confirmed by RNA\u2013in situ hybridization studies of lungs from individuals with MOLD. Our data suggest that chronic airway epithelial hypoxia may be central to the pathogenesis of persistent mucus accumulation in MOLDs and associated airway wall damage.\n                  <\/jats:p>","DOI":"10.1126\/scitranslmed.abo7728","type":"journal-article","created":{"date-parts":[[2023,6,7]],"date-time":"2023-06-07T13:58:12Z","timestamp":1686146292000},"update-policy":"https:\/\/doi.org\/10.34133\/aaas_crossmark","source":"Crossref","is-referenced-by-count":82,"title":["Chronic airway epithelial hypoxia exacerbates injury in muco-obstructive lung disease through mucus hyperconcentration"],"prefix":"10.1126","volume":"15","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-3262-2958","authenticated-orcid":true,"given":"Yu","family":"Mikami","sequence":"first","affiliation":[{"name":"Marsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599, 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