UMMS Affiliation
Department of Medicine, Division of Pulmonary, Allergy and Critical Care Medicine
Publication Date
2018-08-09
Document Type
Article
Disciplines
Hemic and Immune Systems | Immune System Diseases | Immunopathology | Pathological Conditions, Signs and Symptoms | Pulmonology | Respiratory System | Respiratory Tract Diseases | Skin and Connective Tissue Diseases
Abstract
Severe lung inflammation and alveolar hemorrhage can be life-threatening in systemic lupus erythematosus (SLE) patients if not treated early and aggressively. Neutrophil influx is the driver key of this pathology, but little is known regarding the molecular events regulating this recruitment. Here, we uncover a role for IL-16/mir-125a in this pathology and show not only that IL-16 is a target for miR-125a but that reduced miR-125a expression in SLE patients associates with lung involvement. Furthermore, in the pristane model of acute "SLE-like" lung inflammation and alveolar hemorrhage, we observed reduced pulmonary miR-125a and enhanced IL-16 expression. Neutrophil infiltration was markedly reduced in the peritoneal lavage of pristane-treated IL-16-deficient mice and elevated following i.n. delivery of IL-16. Moreover, a miR-125a mimic reduced pristane-induced IL-16 expression and neutrophil recruitment and rescued lung pathology. Mechanistically, IL-16 acts directly on the pulmonary epithelium and markedly enhances neutrophil chemoattractant expression both in vitro and in vivo, while the miR-125a mimic can prevent this. Our results reveal a role for miR-125a/IL-16 in regulating lung inflammation and suggest this axis may be a therapeutic target for management of acute lung injury in SLE.
Keywords
Autoimmunity, Chemokines, Immunology, Lupus, Neutrophils
Rights and Permissions
Copyright © 2018, American Society for Clinical Investigation. Publisher pdf posted as allowed by the publisher's open access policy at https://insight.jci.org/kiosks/terms.
DOI of Published Version
10.1172/jci.insight.120798
Source
JCI Insight. 2018 Aug 9;3(15). pii: 120798. doi: 10.1172/jci.insight.120798. Link to article on publisher's site
Journal/Book/Conference Title
JCI insight
Related Resources
PubMed ID
30089723
Repository Citation
Smith S, Kornfeld H, Jefferies CA. (2018). IL-16/miR-125a axis controls neutrophil recruitment in pristane-induced lung inflammation. Open Access Articles. https://doi.org/10.1172/jci.insight.120798. Retrieved from https://escholarship.umassmed.edu/oapubs/3557
Included in
Hemic and Immune Systems Commons, Immune System Diseases Commons, Immunopathology Commons, Pathological Conditions, Signs and Symptoms Commons, Pulmonology Commons, Respiratory System Commons, Respiratory Tract Diseases Commons, Skin and Connective Tissue Diseases Commons
Comments
Full author list omitted for brevity. For the full list of authors, see article.