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Mitochondrial DNA induces inflammation and increases TLR9/NF-κB expression in lung tissue
Open accessAbstract
Mitochondrial DNA (mtDNA) contains unmethylated CpG motifs that exhibit immune stimulatory capacities. The aim of this study was to investigate whether mtDNA activates the Toll-like receptor 9 (TLR9)/nuclear factor-κB (NF-κB) pathway, thereby contributing to post-traumatic systemic inflammatory response syndrome (SIRS) and lung injury in rats. The effects of mtDNA on macrophage culture were examined in order to elucidate the putative cellular mechanisms. Rats and macrophage cultures were treated with phosphate-buffered saline, nuclear DNA, or mtDNA for 2, 4, 8 and 24 h. Histological analysis of lung tissue was undertaken following hematoxylin and eosin staining, and cytokine levels were assessed by ELISA. NF-κB and IκB-α phosphorylation levels, as well as TLR9 protein expression were determined by western blot analysis; NF-κB, IκB-α and TLR9 mRNA levels were analyzed by RT-PCR. A greater degree of inflammation and lung injury was observed in response to mtDNA. In addition, mtDNA increased serum tumor necrosis factor-α, interleukin (IL)-6 and IL-10 levels in vivo and increased their secretion by cultured macrophages (p<0.05). In lung tissue, mtDNA increased NF-κB, IκB-α and TLR9 mRNA levels (p<0.05); it also increased phosphorylated NF-κB p65 and TLR9 protein levels in the macrophage cultures. Thus, mtDNA may be part of the danger-associated molecular patterns, contributing to the initiation of sterile SIRS through the activation of the TLR9/NF-κB pathway and the induction of pro-inflammatory cytokine production.
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“Interaction of TLR9 with mtDNA activates the nuclear factor kappa B (NF-jB) signaling and increases the expression of other pro-inflammatory cytokines such as tumor necrosis factor-a (TNF-a), interleukin (IL)-6, IL-1b (Julian et al, 2013;Yu & Bennett, 2014;Zhang et al, 2014).”
From Mitochondrial DNA and TLR9 drive muscle inflammation upon Opa1 deficiency (2018) · cites this paper as Zhang et al, 2014
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Cites
Mizgerd, J. P., Kubo, H., Kutkoski, G. J., Bhagwan, S. D., Scharffetter-Kochanek, K., Beaudet, A. L., & Doerschuk, C. M. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.186.8.1357 · Cited by 7,332
MANTOVANI, A., SOZZANI, S., LOCATI, M., ALLAVENA, P., & SICA, A. (2002) · Trends in Immunology · doi:10.1016/s1471-4906(02)02302-5 · Cited by 5,528
NF-κB: a key role in inflammatory diseases
Tak, P. P., & Firestein, G. S. (2001) · Journal of Clinical Investigation · doi:10.1172/jci11830 · Cited by 3,918
Circulating mitochondrial DAMPs cause inflammatory responses to injury
Zhang, Q., Raoof, M., Chen, Y., Sumi, Y., Sursal, T., Junger, W., Brohi, K., Itagaki, K., & Hauser, C. J. (2010) · Nature · doi:10.1038/nature08780 · Cited by 3,812
Yang, Y., Li, S., Yang, Q., Shi, Y., Zheng, M., Liu, Y., Chen, F., Song, G., Xu, H., Wan, T., et al. (2014) · Cellular Physiology and Biochemistry · doi:10.1159/000358696 · Cited by 3,263
DAMPs, PAMPs and alarmins: all we need to know about danger
Bianchi, M. E. (2007) · Journal of Leukocyte Biology · doi:10.1189/jlb.0306164 · Cited by 2,794
Gogos, C. A., Drosou, E., Bassaris, H. P., & Skoutelis, A. (2000) · The Journal of Infectious Diseases · doi:10.1086/315214 · Cited by 883
Goerdt, S., & Orfanos, C. E. (1999) · Immunity · doi:10.1016/s1074-7613(00)80014-x · Cited by 678
Systemic inflammation after trauma
Lenz, A. M., Franklin, G. A., & Cheadle, W. G. (2007) · Injury · doi:10.1016/j.injury.2007.10.003 · Cited by 617
Patterns of mortality and causes of death in polytrauma patients—Has anything changed?
Pfeifer, R., Tarkin, I. S., Rocos, B., & Pape, H. (2009) · Injury · doi:10.1016/j.injury.2009.05.006 · Cited by 459
MITOCHONDRIAL DNA IS RELEASED BY SHOCK AND ACTIVATES NEUTROPHILS VIA P38 MAP KINASE
Zhang, Q., Itagaki, K., & Hauser, C. J. (2010) · Shock · doi:10.1097/shk.0b013e3181cd8c08 · Cited by 361
Pittet, D., Rangel-Frausto, S., Li, N., Tarara, D. T., Costigan, M., Rempe, L., JEBSON, P. J. R., & Wenzel, R. P. (1995) · Intensive Care Medicine · doi:10.1007/bf01705408 · Cited by 330
Christman, J. W., LANCASTER, L. H., & Blackwell, T. S. (1998) · Intensive Care Medicine · doi:10.1007/s001340050735 · Cited by 299
Postinjury multiple organ failure
Dewar, D., Moore, F. A., Moore, E. E., & Balogh, Z. J. (2009) · Injury · doi:10.1016/j.injury.2009.05.024 · Cited by 286
Role of Chemokines in the Pathogenesis of Acute Lung Injury
Bhatia, M., Zemans, R. L., & Jeyaseelan, S. (2012) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2011-0392tr · Cited by 274
Edwin, A. D. (2006) · Frontiers in bioscience · doi:10.2741/1816 · Cited by 242
Sun, S., Sursal, T., Adibnia, Y., Zhao, C., Zheng, Y. Z., Li, H., Otterbein, L. E., Hauser, C. J., & Itagaki, K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0059989 · Cited by 220
Klune, J. R., & Tsung, A. (2010) · Surgical Clinics of North America · doi:10.1016/j.suc.2010.04.003 · Cited by 209
Epidemiology of Injuries: Current Trends and Future Challenges
MacKenzie, E. J. (2000) · Epidemiologic Reviews · doi:10.1093/oxfordjournals.epirev.a018006 · Cited by 204
Cytokines in the systemic inflammatory response syndrome: a review.
Jaffer, U., Wade, R. G., & Gourlay, T. (2010) · Europe PMC (PubMed Central) · Cited by 187
Current theories on the pathophysiology of multiple organ failure after trauma
Tsukamoto, T., Chanthaphavong, R. S., & Pape, H. (2009) · Injury · doi:10.1016/j.injury.2009.07.010 · Cited by 181
Mitochondrial Peptides Are Potent Immune Activators That Activate Human Neutrophils Via FPR-1
Raoof, M., Zhang, Q., Itagaki, K., & Hauser, C. J. (2010) · The Journal of Trauma: Injury, Infection, and Critical Care · doi:10.1097/ta.0b013e3181dcd28d · Cited by 124
Early events in the recognition of danger signals after tissue injury
Kaczorowski, D. J., Mollen, K. P., Edmonds, R. D., & Billiar, T. R. (2007) · Journal of Leukocyte Biology · doi:10.1189/jlb.0607374 · Cited by 121
How tissue injury alarms the immune system and causes a systemic inflammatory response syndrome
Pugin, J. (2012) · Annals of Intensive Care · doi:10.1186/2110-5820-2-27 · Cited by 112
Hauser, C. J., Sursal, T., Rodriguez, E. K., Appleton, P. T., Zhang, Q., & Itagaki, K. (2010) · Journal of Orthopaedic Trauma · doi:10.1097/bot.0b013e3181ec4991 · Cited by 107
Pattern Recognition Receptor-Dependent Mechanisms of Acute Lung Injury
Xiang, M., & Fan, J. (2009) · Molecular Medicine · doi:10.2119/molmed.2009.00097 · Cited by 105
Zhou, H., Zheng, J., Liangxi, W., Ding, G., Luo, P., Lu, Y., Wendong, P., & Ming-hai, W. (2004) · International Immunopharmacology · doi:10.1016/j.intimp.2003.12.006 · Cited by 105
PROGNOSTIC VALUE OF CYTOKINES IN SIRS GENERAL MEDICAL PATIENTS
Rodrı́guez-Gaspar, M., Santolaria, F., Jarque-López, A., González‐Reimers, E., Milena, A., de la Vega, M.-J., Rodríguez-Rodríguez, E., & Gómez-Sirvent, J. L. (2001) · Cytokine · doi:10.1006/cyto.2001.0932 · Cited by 100
Matsuda, N., Hattori, Y., Jesmin, S., & Gando, S. (2004) · Molecular Pharmacology · doi:10.1124/mol.104.005926 · Cited by 97
PRECLINICAL MODELS OF TRAUMATIC, HEMORRHAGIC SHOCK
Hauser, C. J. (2005) · Shock · doi:10.1097/01.shk.0000191387.18818.43 · Cited by 93
Early events in innate immunity in the recognition of microbial pathogens
Kapétanovic, R., & Cavaillon, J. (2007) · Expert Opinion on Biological Therapy · doi:10.1517/14712598.7.6.907 · Cited by 85
Li, B., Zhang, R., Li, J., Zhang, L., Ding, G., Luo, P., He, S., Dong, Y., Jiang, W., Lu, Y., et al. (2008) · International Immunopharmacology · doi:10.1016/j.intimp.2007.10.024 · Cited by 75
Mitochondrial transcription factor A is a proinflammatory mediator in hemorrhagic shock
Wang, P. (2012) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2012.959 · Cited by 73
Tarlowe, M. H., Kannan, K. B., Itagaki, K., Adams, J. M., Livingston, D. H., & Hauser, C. J. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.4.2066 · Cited by 60
Tschaikowsky, K., Sittl, R., Braun, G. G., Hering, W., & R�gheimer, E. (1993) · Journal of Molecular Medicine · doi:10.1007/bf00231111 · Cited by 44
Maggi, L. B., Moran, J. M., Scarim, A. L., Ford, D. A., Yoon, J., McHowat, J., Buller, R. M. L., & Corbett, J. A. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m206247200 · Cited by 42
A Review of metabolic staging in severely injured patients
Aller, M., Arias, J. I., Alonso-Poza, A., & Árias, J. (2010) · Scandinavian Journal of Trauma Resuscitation and Emergency Medicine · doi:10.1186/1757-7241-18-27 · Cited by 42
Evolution of the mitochondrial protein synthetic machinery
Benne, R., & Sloof, P. (1987) · Biosystems · doi:10.1016/0303-2647(87)90006-2 · Cited by 38
The actions of bacterial DNA on murine macrophages
Sester, D. P., Stacey, K. J., Sweet, M. J., Beasley, S. J., Cronau, S. L., & Hume, D. A. (1999) · Journal of Leukocyte Biology · doi:10.1002/jlb.66.4.542 · Cited by 36
Hypothermia in multisystem trauma
Fukudome, E. Y., & Alam, H. B. (2009) · Critical Care Medicine · doi:10.1097/ccm.0b013e3181aa60ac · Cited by 33
CpG DNA-mediated Induction of Acute Liver Injury in d-Galactosamine-sensitized Mice
Yi, A., Yoon, H., Park, J. J., Kim, B., Kim, H. J., & Martínez‐Hernández, A. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m601337200 · Cited by 32
Systemic nf-κB activation in a transgenic mouse model of acute pancreatitis
Gray, K. D., Simovic, M. O., Chapman, W. C., Blackwell, T. S., Christman, J. W., Washington, M. K., Yull, F. E., Jaffal, N., Jansen, D., Gautman, S., et al. (2003) · Journal of Surgical Research · doi:10.1016/s0022-4804(03)00024-6 · Cited by 31
Femoral Shaft Fracture Fixation and Chest Injury After Polytrauma
Bone, L. B., & Giannoudis, P. V. (2011) · Journal of Bone and Joint Surgery · doi:10.2106/jbjs.j.00334 · Cited by 31
Réponse inflammatoire et anti-inflammatoire de l’hôte au cours du sepsis
Adib‐Conquy, M., & Cavaillon, J. (2012) · Pathologie Biologie · doi:10.1016/j.patbio.2012.03.011 · Cited by 30
Williams, D. L., Ha, T., Li, C., Laffan, J. J., Kalbfleisch, J. M., & Browder, W. (2000) · Shock · doi:10.1097/00024382-200006000-00005 · Cited by 26
Sugishita, Y., Shimizu, T., Yao, A., Kinugawa, K., Nojiri, T., Harada, K., Matsui, H., Nagai, R., & Takahashi, T. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.2165 · Cited by 20
Sun, T., Wang, X., Liu, Z., Liu, S., & Zhang, J. (2011) · Injury · doi:10.1016/j.injury.2011.03.040 · Cited by 12
Self-citationHypoadrenalism following trauma: is sepsis always necessary?
Paquette, I. M., & Burchard, K. W. (2008) · PubMed Central · Cited by 3
[Establishment of the rapid, hypersensitive testing systems for sepsis/SIRS].
Kitajima, I., & Niimi, H. (2012) · PubMed · Cited by 2
Analysis of the rat primary hepatocyte nuclear proteome through sub-cellular fractionation
Goldring, C. E., Rowe, C., Jenkins, R., Kitteringham, N. R., & Park, K. (2012) · Journal of Integrated OMICS · doi:10.5584/jiomics.v2i2.102 · Cited by 1
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Mills, E. L., Kelly, B., & O'Neill, L. A. J. (2017) · Nature Immunology · doi:10.1038/ni.3704 · Cited by 1,161
Hypoxia, oxidative stress and inflammation
McGarry, T., Biniecka, M., Veale, D. J., & Fearon, U. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.03.042 · Cited by 620
Diverse roles of mitochondria in ischemic stroke
Yang, J., Mukda, S., & Chen, S. (2018) · Redox Biology · doi:10.1016/j.redox.2018.03.002 · Cited by 459
Hypoxia, mitochondrial dysfunction and synovial invasiveness in rheumatoid arthritis
Fearon, U., Canavan, M., Biniecka, M., & Veale, D. J. (2016) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2016.69 · Cited by 455
Mitochondrial Damage-Associated Molecular Patterns: From Inflammatory Signaling to Human Diseases
Grazioli, S., & Pugin, J. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00832 · Cited by 429
Metadata
- Authors
- ZHANG, J.-Z., LIU, Z., LIU, J., REN, J.-X., & SUN, T.-S.
- Affiliations
- The Military General Hospital of Beijing PLA (CN)
- Venue
- International Journal of Molecular Medicine
- Publisher
- Spandidos Publications
- Published
- 2014-02-10
- Volume
- 33
- Issue
- 4
- Pages
- 817-824
- ISSN
- 1107-3756 (ISSN-L)
- 1791-244X
- PMC
- PMC3976143
- OpenAlex
- W2165572246
- Cited by
- 194
- References
- 50
- Citations by year
- 2026: 1 · 2025: 6 · 2024: 6 · 2023: 15 · 2022: 21 · 2021: 23 · 2020: 27 · 2019: 24 · 2018: 22 · 2017: 16 · 2016: 16 · 2015: 12 · 2014: 5
- FWCI
- 7.46
- Type
- journal article
- Language
- en
- Status
- Retracted
- Update notices
- retraction (2023-02-17)
- Open access
- hybrid
- doi.org
- Licence
- cc-by-nc
- Locations
- International Journal of Molecular Medicine (publishedVersion, cc-by-nc)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
- Life Sciences › Immunology and Microbiology › Immunology › Inflammation biomarkers and pathways
- Keywords
- mitochondrial DNA, TLR9, NF-κB signaling, systemic inflammatory response syndrome, lung injury, macrophages, damage-associated molecular patterns, sterile inflammation, inflammatory cytokines, TNF-α, interleukin-6, IL-10, IκBα phosphorylation, CpG motifs
- MeSH terms
- NF-KappaB Inhibitor alpha, Animals, Cells, Cultured, DNA, Mitochondrial, Gene Expression Regulation, Inflammation, Lung, Macrophages, Male, Phosphorylation, RNA, Messenger, Cytokines, NF-kappa B, Rats, Sprague-Dawley, I-kappa B Proteins, Toll-Like Receptor 9, Rats, Acute Lung Injury
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