Spatially distinct molecular patterns of gene expression in idiopathic pulmonary fibrosis
Abstract
Idiopathic pulmonary fibrosis (IPF) is a heterogeneous disease that is pathologically characterized by areas of normal-appearing lung parenchyma, active fibrosis (transition zones including fibroblastic foci) and dense fibrosis. Defining transcriptional differences between these pathologically heterogeneous regions of the IPF lung is critical to understanding the distribution and extent of fibrotic lung disease and identifying potential therapeutic targets. Application of a spatial transcriptomics platform would provide more detailed spatial resolution of transcriptional signals compared to previous single cell or bulk RNA-Seq studies.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Nov 17, 2023
- Source ID
- 10.1186/s12931-023-02572-6
Entities
People
- Avram D. Walts
- Carlyne D. Cool
- David A Schwartz
- David Heinz
- Ivana V. Yang
- Jonathan S Kurche
- Rachel Z. Blumhagen
- Tasha E. Fingerlin
Organizations
- National Heart, Lung, and Blood Institute
- United States Department of Defense