高氧
支气管肺发育不良
肺
肺泡巨噬细胞
巨噬细胞
生物
转录组
免疫学
病理
男科
医学
生理学
内科学
基因表达
体外
基因
怀孕
遗传学
胎龄
作者
Connor C. Leek,Abiud Cantu,Shilpa Sonti,Manuel Cantu Gutierrez,Laurie C. Eldredge,Enikö Sajti,He N. Xu,Krithika Lingappan
出处
期刊:Redox biology
[Elsevier BV]
日期:2024-08-02
卷期号:75: 103296-103296
被引量:1
标识
DOI:10.1016/j.redox.2024.103296
摘要
The lung macrophages play a crucial role in health and disease. Sexual dimorphism significantly impacts the phenotype and function of tissue-resident macrophages. The primary mechanisms responsible for sexually dimorphic outcomes in bronchopulmonary dysplasia (BPD) remain unidentified. We tested the hypothesis that biological sex plays a crucial role in the transcriptional state of alveolar macrophages, using neonatal murine hyperoxia-induced lung injury as a relevant model for human BPD. The effects of neonatal hyperoxia exposure (95 % FiO
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