细支气管
内质网
特发性肺纤维化
未折叠蛋白反应
XBP1型
肺
表型
生物
肺纤维化
发病机制
病理
表面活性蛋白C
细胞生物学
纤维化
免疫学
医学
内科学
基因
遗传学
核糖核酸
RNA剪接
作者
Rachel Z. Blumhagen,Jonathan S. Kurche,Carlyne D. Cool,David Heinz,Xiaoqian Ma,Elizabeth Davidson,Tasha E. Fingerlin,Jonathan Huber,Evgenia Dobrinskikh,David A. Schwartz,Ivana V. Yang
标识
DOI:10.1165/rcmb.2025-0261oc
摘要
We used spatial transcriptomics from idiopathic pulmonary fibrosis (IPF) and unaffected control lung tissue to further understand the pathogenesis of MUC5B-driven lung fibrosis. We captured 43 fields of view in 15 IPF and 13 controls with and without the MUC5B promoter variant using the CosMx® platform and identified 19 cell types via semi-supervised clustering. MUC5B was ectopically expressed in AT2 cells in controls with the risk variant. We observed a decreased proportion of AT2 cells in controls and an increased proportion of aberrant basaloid cells in IPF associated with the MUC5B risk variant. We identified co-localized expression of MUC5B in respiratory bronchioles with 13 genes including the endoplasmic reticulum (ER) stress marker XBP1 and distal secretory markers SCGB3A1 and SCGB1A1. Experimentally, we demonstrated a direct relationship between MUC5B expression and ER stress in bronchiolar epithelia in vitro and validated the co-expression of MUC5B and XBP1 in the IPF lung. Based on our results, we conclude that MUC5B injures alveolar and bronchiolar epithelia that results in loss of AT2 cells and an increase in aberrant basaloid cells which initiates ER stress and a secretory phenotype in the terminal respiratory bronchiole, establishing a persistently injured distal airspace.
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