Journal
MUCOSAL IMMUNOLOGY
Volume 9, Issue 1, Pages 240-253Publisher
ELSEVIER SCIENCE INC
DOI: 10.1038/mi.2015.56
Keywords
-
Categories
Funding
- FP7 Marie-Curie Reintegration grant [256311]
- US-Israel Binational Science Foundation [2009222, 2011244]
- Israel Science Foundation [955/11]
- Israel Cancer Research Foundation (ICRF) Research Career Development Award (RCDA)
- Fritz Thyssen Stiftung
- Tel-Aviv University Stolz Award
- U.S. Department of Veterans Affairs
Ask authors/readers for more resources
Molecular mechanisms that regulate lung repair vs. progressive scarring in pulmonary fibrosis remain elusive. Interleukin (IL)-4 and IL-13 are pro-fibrotic cytokines that share common receptor chains including IL-13 receptor (R) alpha 1 and are key pharmacological targets in fibrotic diseases. However, the roles of IL-13R alpha 1 in mediating lung injury/repair are unclear. We report dysregulated levels of IL-13 receptors in the lungs of bleomycin-treated mice and to some extent in idiopathic pulmonary fibrosis patients. Transcriptional profiling demonstrated an epithelial cell-associated gene signature that was homeostatically dependent on IL-13R alpha 1 expression. IL-13R alpha 1 regulated a striking array of genes in the lung following bleomycin administration and Il13ra1 deficiency resulted in exacerbated bleomycin-induced disease. Increased pathology in bleomycin-treated Il13ra1(-/-) mice was due to IL-13R alpha 1 expression in structural and hematopoietic cells but not due to increased responsiveness to IL-17, IL-4, IL-13, increased IL-13R alpha 2 or type 1 IL-4R signaling. These data highlight underappreciated protective roles for IL-13R alpha 1 in lung injury and homeostasis.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available