Molecular mechanisms underlying hyperoxia-induced lung fibrosis

I. Ting Chen, Liang Ti Huang, Chih Cheng Chen, Chung Ming Chen

研究成果: 雜誌貢獻回顧型文獻同行評審

摘要

Supplemental oxygen is often used to treat newborns with respiratory disorders. Exposure to high concentration of oxygen and long-term oxygen causes inflammation and acute lung injury. The acute inflammatory phase is followed by a fibroproliferative repair phase, leading to lung fibrosis. Many infants with lung fibrosis develop significant respiratory morbidities including reactive airways dysfunction and obstructive lung disease during childhood. Despite the absence of effective treatments and the incomplete understanding regarding mechanisms underlying fibrosis, extensive literature regarding lung fibrosis from in vitro and in vivo hyperoxia-exposed models is available. In this review, we discuss molecular mediators and signaling pathways responsible for increased fibroblast proliferation and collagen production, excessive extracellular matrix accumulation, and eventually, lung fibrosis. We discuss each of these mediators separately to facilitate clear understanding as well as significant interactions occurring among these molecular mediators and signaling pathways.
原文英語
頁(從 - 到)109-116
頁數8
期刊Pediatrics and Neonatology
63
發行號2
DOIs
出版狀態已發佈 - 3月 2022

ASJC Scopus subject areas

  • 兒科、圍產兒和兒童健康

指紋

深入研究「Molecular mechanisms underlying hyperoxia-induced lung fibrosis」主題。共同形成了獨特的指紋。

引用此