The DOI matches its Crossref record; 12 of the 12 references it cites were found in a registry or an index.
Mitochondrial control of the NLRP3 inflammasome
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“In humans, IL-18 blood levels increase with ageing, and strong evidence from mouse studies indicates that blockade of the NLRP3 inflammasome extends healthspan, attenuating multiple age-related degenerative changes that have been linked to inflammageing, including insulin resistance, thymic involution, T cell senescence, and bone loss as well as physical and cognitive function decline114,117,118.”
From Inflammageing: chronic inflammation in ageing, cardiovascular disease, and frailty (2018) · cites this paper as [117]
Citations
Cites
A role for mitochondria in nlrp3 inflammasome activation
Zhou, R., Yazdi, A. S., Menu, P., & Tschopp, J. (2011) · Nature · doi:10.1038/nature09663 · Cited by 5,602
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
Mitochondrial membrane permeabilization in cell death
Kroemer, G., Galluzzi, L., & Brenner, C. (2007) · Physiological Reviews · doi:10.1152/physrev.00013.2006 · Cited by 3,598
Self-citationSeth, R. B., Sun, L., Ea, C.-K., & Chen, Z. J. (2005) · Cell · doi:10.1016/j.cell.2005.08.012 · Cited by 3,329
Nakahira, K., Haspel, J. A., Rathinam, V. A. K., Lee, S.-J., Dolinay, T., Lam, H. C., Englert, J. A., Rabinovitch, M., Cernadas, M., Kim, H. P., et al. (2011) · Nature Immunology · doi:10.1038/ni.1980 · Cited by 3,049
Innate Immune Activation Through Nalp3 Inflammasome Sensing of Asbestos and Silica
Dostert, C., Pétrilli, V., Van Bruggen, R., Steele, C., Mossman, B. T., & Tschopp, J. (2008) · Science · doi:10.1126/science.1156995 · Cited by 2,658
Molecular mechanisms of necroptosis: an ordered cellular explosion
Vandenabeele, P., Galluzzi, L., Vanden Berghe, T., & Kroemer, G. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2970 · Cited by 2,382
Self-citationLoss of the autophagy protein Atg16L1 enhances endotoxin-induced IL-1β production
Saitoh, T., Fujita, N., Jang, M. H., Uematsu, S., Yang, B., Satoh, T., Omori, H., Noda, T., Yamamoto, N., Komatsu, M., et al. (2008) · Nature · doi:10.1038/nature07383 · Cited by 2,064
The roles of TLRs, RLRs and NLRs in pathogen recognition
Kawai, T., & Akira, S. (2009) · International Immunology · doi:10.1093/intimm/dxp017 · Cited by 1,725
Travassos, L. H., Carneiro, L. A. M., Ramjeet, M., Hussey, S., Kim, Y.-G., Magalhães, J. G., Yuan, L., Soares, F., Chea, E., Le Bourhis, L., et al. (2010) · Nature Immunology · doi:10.1038/ni.1823 · Cited by 1,306
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BackgroundEmerging Role of Mitophagy in Inflammatory Diseases: Cellular and Molecular Episodes
Adil, A. M., Ameenudeen, S., Kumar, A., Hemalatha, S., Ahmed, N., Ali, N., Alasmari, A. F., Aashique, M., & Waseem, M. (2020) · Current Pharmaceutical Design · doi:10.2174/1381612826666200107144810 · Cited by 17
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McCoy, S. S., Stannard, J. N., & Kahlenberg, J. M. (2015) · Translational research · doi:10.1016/j.trsl.2015.06.006 · Cited by 16
Xie, Q., Wei, T., Huang, C., Liu, P., Sun, M., Shen, W., & Gao, P. (2016) · Scientific Reports · doi:10.1038/srep34326 · Cited by 16
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Seo, Y., Shin, T., Ahn, J., Oh, S., Shin, Y. Y., Yang, J. W., Park, H., Shin, S., Kwon, H., Kim, J. M., et al. (2020) · Cells · doi:10.3390/cells9030636 · Cited by 16
“Mitochondrial ROS has been reported to be one of the important upstream signals for NLRP3 inflammasome activation and a number of studies have demonstrated that ROS scavengers can suppress NLRP3 inflammasome activation [55,56].”
BackgroundLin, W., Li, L., Hsiao, Y.-Y., Wong, W.-T., Chiu, H., Hsu, H.-T., Peng, Y., Ho, C., Chernikov, O. V., Cheng, S., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.870627 · Cited by 15
“CS Inhibits the Activation Signal by Reducing Mitochondrial Dysfunction NLRP3 activator-induced K efflux activates downstream signalling pathways leading to mitochondrial damage and NLRP3 inflammasome activation (21, 22).”
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“Dysfunctional aged mitochondria release mitochondrial DAMPs, reactive oxygen species (ROS), and ATP, which can induce inflammasome activation [48, 49].”
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“Localization of the NLRP3 inflammasome at the mitochondria has also been reported to be a key event leading to its activation [7, 8].”
BackgroundFan, Y., Wang, J., Feng, Z., Cao, K. J., Liu, J., & Xu, H. (2022) · Environmental Toxicology · doi:10.1002/tox.23507 · Cited by 12
“have suggested that the dysfunctional mitochondria generate ROS, which is the main source of ROS required for NLRP3 inflammasome activation.(10) Iyer et al.”
BackgroundLiu, M.-L., Wong, W.-T., Weng, Y., Ho, C., Hsu, H.-T., Hua, K., Wu, C., & Li, L.-H. (2024) · Journal of physiological investigation. · doi:10.4103/ejpi.ejpi-d-24-00017 · Cited by 11
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Yang, S., Hua, K., Takahata, A., Wu, C.-Y., Hsieh, C., Chiu, H., Chen, C., Mukhopadhyay, D., Suzuki, Y., Ka, S., et al. (2020) · The Journal of Pathology · doi:10.1002/path.5609 · Cited by 11
“Mitochondrial damage is one of the downstream signalling events of K+ efflux, which is characterised by mitochondrial ROS production and the loss of the mitochondrial membrane integrity [63].”
BackgroundMonteiro, J., Morais, C. M., Oliveira, P. J., & Jurado, A. S. (2014) · Current Drug Targets · doi:10.2174/1389450115666140623115315 · Cited by 10
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BackgroundChen, Y., Zhang, G., Cao, D., Wang, F., Zhang, F., Shao, H., & Jiao, W. (2023) · Molecules · doi:10.3390/molecules28196922 · Cited by 6
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Lin, W.-Y., Tsui, J.-L., Chiu, H., Wong, W.-T., Wu, C., Hsu, H.-T., Ho, C., Yeh, S.-P., Rao, Y. K., Chen, A., et al. (2024) · BMC Infectious Diseases · doi:10.1186/s12879-024-10208-3 · Cited by 4
“The ROS generated by damaged mitochondria can exacerbate further mitochondrial impairment, including the loss of mitochondrial membrane integrity and membrane potential [13].”
Liu, M., Deng, M., Luo, Q., Sun, P., Liang, A., Li, X., Luo, X., Pan, J., Zhang, W., Mo, M., et al. (2023) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2023.166765 · Cited by 4
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Land, W. G. (2020) · Springer eBooks · doi:10.1007/978-3-030-53868-2_8 · Cited by 2
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Chakraborty, S., Khanna, K., & Agrawal, A. (2019) · Springer eBooks · doi:10.1007/978-981-32-9366-3_6 · Cited by 2
Bushen Zhuyun Decoction Improves Endometrial Receptivity by Inhibiting NF-κB/NLRP3 Signaling Pathway
Wang, X., Tong, Y., Zhang, H., Zou, Y., Ding, Y., Liu, B., Zhou, W., Shan, J., Ji, J., Su, W., et al. (2024) · Combinatorial Chemistry & High Throughput Screening · doi:10.2174/0113862073309790240711110744 · Cited by 2
Kwon, M., Su-jin, Y. O. O., In Seol, Y. O. O., Jinhyun, K. I. M., Seong Wook, K. A. N. G., In Ah, C. H. O. I., Mi-kyoung, L. I. M., & JOUNG, C.-I. (2019) · Archives of Rheumatology · doi:10.5606/archrheumatol.2019.7113 · Cited by 2
Zhong, Z. (2013) · Loyola eCommons (Loyola University of Chicago) · Cited by 1
Immune Senescence and Inflammaging in Neurological Diseases
Baden, P., Cicco, S. D., Yu, C., & Deleidi, M. (2019) · Springer eBooks · doi:10.1007/978-3-319-99375-1_143 · Cited by 1
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Horn, R. C., Mayer, M. S., Wolkmer, P., Tissiani, A. C., Cunha, A., Bonfanti, G., Moreira, P. R., Golle, D. P., Heringer, T. A., Alegransi, C., et al. (2022) · Ciência e Natura · doi:10.5902/2179460x44026 · Cited by 1
Mitochondrial Biology in Hepatobiliary Tumors: Changes of the Cellular Energy Factory
Zimmermann, A. (2016) · Springer eBooks · doi:10.1007/978-3-319-26587-2_171-1 · Cited by 1
Tabeeva, G. I., Равилевна, Д. М., Asaturova, A. V., Богданова, И. М., Sanaya, S. Z., & Tregubova, A. (2020) · CLINICAL AND EXPERIMENTAL MORPHOLOGY · doi:10.31088/cem2020.9.3.12-20 · Cited by 1
Mitochondrial Biology in Hepatobiliary Tumors: Changes of the Cellular Energy Factory
Zimmermann, A. (2016) · Springer eBooks · doi:10.1007/978-3-319-26956-6_171 · Cited by 1
[Autoinflammatory diseases: a glimpse at the innate immunity and its pathology].
Hinojosa‐Azaola, A., & Alcocer-Varela, J. C. (2012) · PubMed
Fang, Y. (2012) · cIRcle (University of British Columbia) · doi:10.14288/1.0073123
injuryinflammasome activation and renal tubular Mitochondrial dysfunction confers albumin-induced
Wang, R., Jia, Z., Huang, S., Zhang, A., Zhuang, Y., & Hu, C. (2016)
The role of mitochondria in innate immunity and inflammation
Widdrington, J. D. (2016)
Autophagy: A New Therapeutic Target
Ceylan, A. F. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-805253-2.00022-5
Mitochondria-targeted drugs and immune function
Ckless, K., & Sunasee, R. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85666-9.00006-1
Immune Senescence and Inflammaging in Neurological Diseases
Baden, P., Cicco, S. D., Yu, C., & Deleidi, M. (2017) · Springer eBooks · doi:10.1007/978-3-319-64597-1_143-1
Mitochondrial transfer: A novel mechanism and promising therapeutic strategy in ageing kidney
Xu, J., Li, X., Zhang, Z., Wu, J., Yu, H., Wu, Y. C., Wang, D., Bao, R., Wang, T., Zhang, Y., et al. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103051
Inflammation, aging and chronic diseases : implication of inflammasomes
Guerville, F. (2023) · theses.fr (ABES) · doi:10.70675/eac3286czda71z4606z9c90z3d3efeaf1afe
Les mécanismes de microvésiculation des cytokines de la famille de l’IL-1
Cambon, A. (2023) · theses.fr (ABES) · doi:10.70675/159070b7za2b7z411fzb52azb56bb6841949
Zhang, X., Liu, W., Fu, Z., Chen, Z., Chen, Q., Shen, Y., Jin, Y., Xu, D., Wang, Y., Qu, X., et al. (2026) · Metabolites · doi:10.3390/metabo16050340
“Mitochondrial quality control serves as a crucial strategy in the prevention and treat-ment of heart diseases [22].”
Heid, M. E. (2013) · D-Scholarship@Pitt (University of Pittsburgh)
Metadata
- Authors
- Kepp, O., Galluzzi, L., & Kroemer, G.
- Affiliations
- Université Paris-Sud (FR)
- Inserm (FR)
- Corresponding author
- Kroemer, Guido
- Venue
- Nature Immunology
- Published
- 2011-02-15
- Volume
- 12
- Issue
- 3
- Pages
- 199-200
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- OpenAlex
- W1981120301
- Cited by
- 168
- References
- 12
- Citations by year
- 2026: 4 · 2025: 4 · 2024: 10 · 2023: 8 · 2022: 16 · 2021: 9 · 2020: 17 · 2019: 12 · 2018: 8 · 2017: 12 · 2016: 14 · 2015: 10 · 2014: 12 · 2013: 16 · 2012: 11
- FWCI
- 5.72
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Keywords
- mitochondria, NLRP3 inflammasome, innate immunity, inflammatory cytokines, inflammasome regulation, mitochondrial function
- MeSH terms
- NLR Family, Pyrin Domain-Containing 3 Protein, Animals, Carrier Proteins, Humans, Immunity, Innate, Mitochondria, Models, Biological, Signal Transduction, Cytokines, Inflammasomes
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