eNAMPT Is a Novel Damage-associated Molecular Pattern Protein That Contributes to the Severity of Radiation-Induced Lung Fibrosis
Open accessAbstract
The paucity of therapeutic strategies to reduce the severity of radiation-induced lung fibrosis (RILF), a life-threatening complication of intended or accidental ionizing radiation exposure, is a serious unmet need. We evaluated the contribution of eNAMPT (extracellular nicotinamide phosphoribosyltransferase), a damage-associated molecular pattern (DAMP) protein and TLR4 (Toll-like receptor 4) ligand, to the severity of whole-thorax lung irradiation (WTLI)-induced RILF. Wild-type (WT) and Nampt +/− heterozygous C57BL6 mice and nonhuman primates (NHPs, Macaca mulatta) were exposed to a single WTLI dose (9.8 or 10.7 Gy for NHPs, 20 Gy for mice). WT mice received IgG1 (control) or an eNAMPT-neutralizing polyclonal or monoclonal antibody (mAb) intraperitoneally 4 hours after WTLI and weekly thereafter. At 8–12 weeks after WTLI, NAMPT expression was assessed by immunohistochemistry, biochemistry, and plasma biomarker studies. RILF severity was determined by BAL protein/cells, hematoxylin and eosin, and trichrome blue staining and soluble collagen assays. RNA sequencing and bioinformatic analyses identified differentially expressed lung tissue genes/pathways. NAMPT lung tissue expression was increased in both WTLI-exposed WT mice and NHPs. Nampt +/− mice and eNAMPT polyclonal antibody/mAb-treated mice exhibited significantly attenuated WTLI-mediated lung fibrosis with reduced: 1) NAMPT and trichrome blue staining; 2) dysregulated lung tissue expression of smooth muscle actin, p-SMAD2/p-SMAD1/5/9, TGF-β, TSP1 (thrombospondin-1), NOX4, IL-1β, and NRF2; 3) plasma eNAMPT and IL-1β concentrations; and 4) soluble collagen. Multiple WTLI-induced dysregulated differentially expressed lung tissue genes/pathways with known tissue fibrosis involvement were each rectified in mice receiving eNAMPT mAbs.The eNAMPT/TLR4 inflammatory network is essentially involved in radiation pathobiology, with eNAMPT neutralization an effective therapeutic strategy to reduce RILF severity.
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NAMPT from damaged lung epithelial cells promotes radiation-induced pulmonary fibrosis.
“It has shown that NAMPT from damaged lung epithelial cells promotes radiation-induced pulmonary fibrosis 50, 51”
From Nicotinamide phosphoribosyltransferase prompts bleomycin-induced pulmonary fibrosis by driving macrophage M2 polarization in mice (2024) · cites this paper as [50]
Many studies choose heterozygous mice (NAMPT+/-) to mimic downregulation of NAMPT systemically.
“many studies have to choose heterozygous mice (NAMPT+/-) to mimic the downregulation of NAMPT systemically 50.”
From Nicotinamide phosphoribosyltransferase prompts bleomycin-induced pulmonary fibrosis by driving macrophage M2 polarization in mice (2024) · cites this paper as [50]
Extracellular NAMPT acts mainly as a damage-associated molecular pattern, mediating and exacerbating liver and heart fibrosis.
“Extracellular NAMPT has been reported to act mainly as a damage-associated molecular pattern, mediating and exacerbating liver and heart fibrosis 50, 54, 55.”
From Nicotinamide phosphoribosyltransferase prompts bleomycin-induced pulmonary fibrosis by driving macrophage M2 polarization in mice (2024) · cites this paper as [50]
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References 82 · Cited by 42
- Authors
- Garcia, A. N., Casanova, N. G., Kempf, C. L., Bermudez, T., Valera, D. G., Song, J. H., Sun, X., Cai, H., Moreno-Vinasco, L., Gregory, T., Oita, R. C., Hernon, V. R., Camp, S. M., Rogers, C., Kyubwa, E. M., Menon, N., Axtelle, J., Rappaport, J., Bime, C., Sammani, S., Cress, A. E., & Garcia, J. G. N.
- Affiliations
- Department of Radiation Oncology
- Department of Medicine, and
- University of California, Los Angeles (US)
- ChromoLogic (United States) (US)
- Tulane University (US)
- University of Arizona (US)
- Corresponding author
- Garcia, Joe G. N.
- ORCID
- Venue
- American Journal of Respiratory Cell and Molecular Biology
- Publisher
- Oxford University Press (OUP)
- Published
- 2022-05-01
- Volume
- 66
- Issue
- 5
- Pages
- 497-509
- ISSN
- 1044-1549 (ISSN-L)
- 1535-4989
- PMC
- PMC9116358
- OpenAlex
- W4212828161
- Cited by
- 42
- References
- 82
- Citations by year
- 2026: 5 · 2025: 8 · 2024: 13 · 2023: 8 · 2022: 8
- FWCI
- 5.26
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- American Journal of Respiratory Cell and Molecular Biology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Heart, Lung, and Blood Institute (R01 HL094394, R42 HL152888, P01 HL134610)
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Effects of Radiation Exposure
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- visfatin, radiation-induced pulmonary fibrosis, TLR4, IL-1β, TGF-beta signaling, thrombospondin-1, NOX4, Nrf2, soluble collagen, non-human primates, mouse model
- MeSH terms
- Alarmins, Animals, Antibodies, Monoclonal, Lung, Mice, Inbred C57BL, Pulmonary Fibrosis, Thorax, Cytokines, Toll-Like Receptor 4, Mice, Nicotinamide Phosphoribosyltransferase, Lung Injury
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