Alveolar macrophage subtypes express cholesterol and inflammation genes in cystic fibrosis

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Authors: Xin Li, Fred W Kolling, Daniel Aridgides, Lorraine L. Gwilt, Diane Mellinger, Claudia Jakubzick, Alix Ashare
Cited by: 1
References: 52

Abstract

Cystic fibrosis (CF) is a genetic disease that causes lung inflammation. Although new treatments have improved the quality of life of people with CF, inflammation remains a problem. Alveolar macrophages have been shown to be important mediators of CF lung inflammation although the interactions between macrophages and other immune cells in CF are poorly understood. To identify and compare the cellular composition between CF and healthy airspace macrophages and monocytes, healthy control and CF subjects underwent bronchoscopy and single-cell RNA sequencing was performed on the BAL fluid. Unbiased clustering identified 12 macrophage subtypes. We found up-regulation of macrophages expressing CDKN1A and LDLR, both of which are known to alter cholesterol metabolism and promote inflammation. Pathway analysis revealed important interactions between macrophages and monocytes in CF that likely contribute to overall inflammation and adaptation of recruited monocytes to the CF lung. Some of the top pathways identified were related to inflammation and lipid metabolism, which may contribute to persistent inflammation in CF. Our results may identify novel potential therapeutic targets to treat CF lung inflammation.

Fields of Study & Subjects

Cystic Fibrosis Research Advances Inflammation biomarkers and pathways Biological Research and Disease Studies

Publication details

Journal / source
Life Science Alliance
Publisher
Life Science Alliance, LLC
Volume
9
Issue
7
Pages
e202503482–e202503482
Publication date
16 April 2026
Language
EN