The DOI matches its Crossref record; 107 of the 107 references it cites were found in a registry or an index.
Mitochondrial dysfunction and damage associated molecular patterns (DAMPs) in chronic inflammatory diseases
Open accessAbstract
Inflammation represents a comprehensive host response to external stimuli for the purpose of eliminating the offending agent, minimizing injury to host tissues and fostering repair of damaged tissues back to homeostatic levels. In normal physiologic context, inflammatory response culminates with the resolution of infection and tissue damage response. However, in a pathologic context, persistent or inappropriately regulated inflammation occurs that can lead to chronic inflammatory diseases. Recent scientific advances have integrated the role of innate immune response to be an important arm of the inflammatory process. Accordingly, the dysregulation of innate immunity has been increasingly recognized as a driving force of chronic inflammatory diseases. Mitochondria have recently emerged as organelles which govern fundamental cellular functions including cell proliferation or differentiation, cell death, metabolism and cellular signaling that are important in innate immunity and inflammation-mediated diseases. As a natural consequence, mitochondrial dysfunction has been highlighted in a myriad of chronic inflammatory diseases. Moreover, the similarities between mitochondrial and bacterial constituents highlight the intrinsic links in the innate immune mechanisms that control chronic inflammation in diseases where mitochondrial damage associated molecular patterns (DAMPs) have been involved. Here in this review, the role of mitochondria in innate immune responses is discussed and how it pertains to the mitochondrial dysfunction or DAMPs seen in chronic inflammatory diseases is reviewed.
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“in AD, the chronic release of DAMPs, mitochondrial-released DAMPs and pro-inflammatory molecules contributes to the onset and progression of neurodegeneration [57, 76, 97, 149, 194, 270, 304, 333, 345]”
From Microglia and monocytes in inflammatory CNS disease: integrating phenotype and function (2022) · cites this paper as [76]
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“Mitochondrial dysfunction is a hallmark of many chronic inflammatory diseases193, including those caused by the innate immune response194.”
From Mitochondrial and metabolic dysfunction in ageing and age-related diseases (2022) · cites this paper as [193]
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Cited by
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Mitochondrial and metabolic dysfunction in ageing and age-related diseases
Amorim, J. A., Coppotelli, G., Rolo, A. P., Palmeira, C. M., Ross, J. M., & Sinclair, D. A. (2022) · Nature Reviews Endocrinology · doi:10.1038/s41574-021-00626-7 · Cited by 990
Mitochondrial dysfunction in pathophysiology of heart failure
Zhou, B., & Tian, R. (2018) · Journal of Clinical Investigation · doi:10.1172/jci120849 · Cited by 973
The role of mitochondria in aging
Jang, J. Y., Blum, A., Liu, J., & Finkel, T. (2018) · Journal of Clinical Investigation · doi:10.1172/jci120842 · Cited by 358
Mitochondria as a Cellular Hub in Infection and Inflammation
Andrieux, P., Chevillard, C., Cunha-Neto, E., & Nunes, J. P. S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111338 · Cited by 346
Microglia Phenotypes in Aging and Neurodegenerative Diseases
Wendimu, M. Y., & Hooks, S. B. (2022) · Cells · doi:10.3390/cells11132091 · Cited by 336
Metadata
- Authors
- Dela Cruz, C. S., & Kang, M.-J.
- Affiliations
- Yale University (US)
- Corresponding author
- Kang, Min-Jong
- ORCID
- Kang, Min-Jong
- Venue
- Mitochondrion
- Publisher
- Elsevier BV
- Published
- 2018-07
- Volume
- 41
- Pages
- 37-44
- ISSN
- 1567-7249 (ISSN-L)
- PMC
- PMC5988941
- OpenAlex
- W2771620838
- Cited by
- 255
- References
- 107
- Citations by year
- 2026: 34 · 2025: 28 · 2024: 45 · 2023: 37 · 2022: 23 · 2021: 43 · 2020: 22 · 2019: 19 · 2018: 4
- FWCI
- 1.27
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Mitochondrion (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NHLBI (R01HL130283, R01HL126094)
- NIA (R01AG053495)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Keywords
- mitochondrial dysfunction, damage-associated molecular patterns, chronic inflammatory diseases, innate immunity, mitochondrial DAMPs, mitochondrial signaling, mitochondrial metabolism, mitochondrial cell death
- MeSH terms
- Alarmins, Animals, Chronic Disease, Humans, Inflammation, Mitochondria, Mitochondrial Proteins, Mitochondrial Diseases
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