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A mitochondrial specific stress response in mammalian cells
Open accessAbstract
Cells respond to a wide variety of stresses through the transcriptional activation of genes that harbour stress elements within their promoters. While many of these elements are shared by genes encoding proteins representative of all subcellular compartments, cells can also respond to stresses that are specific to individual organelles, such as the endoplasmic reticulum un folded protein response. Here we report on the discovery and characterization of a mitochondrial stress response in mammalian cells. We find that the accumulation of unfolded protein within the mitochondrial matrix results in the transcriptional upregulation of nuclear genes encoding mitochondrial stress proteins such as chaperonin 60, chaperonin 10, mtDnaJ and ClpP, but not those encoding stress proteins of the endoplasmic reticulum. Analysis of the chaperonin 60/10 bidirectional promoter identified a CHOP element as the mitochondrial stress response element. Dominant-negative mutant forms of CHOP and overexpression of CHOP revealed that this transcription factor, in association with C/EBPbeta, regulates expression of mitochondrial stress genes in response to the accumulation of unfolded proteins.
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“Under stress conditions, when the degradation pathways are insufficient to repair the consequences of the alteration in mitochondrial translation [52] or the accumulation of oxidatively damaged or misfolded proteins, a retrograde signal is activated which coordinates nuclear gene expression. This mitochondria-to- nucleus response is named mitochondrial unfolding protein response (UPRmt) [53].”
From The connection between the dynamic remodeling of the mitochondrial network and the regulation of muscle mass (2021) · cites this paper as [53]
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“Under stress conditions, UPRmt occurs in an attempt to maintain mitochondrial proteostasis by upregulating the expression of mitochondrial chaperones and m-AAA proteases (e.g., chaperonin 10, chaperonin 60, and CLPP) (69).”
From From mitochondria to sarcopenia: role of 17β-estradiol and testosterone (2023) · cites this paper as [69]
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“a known protein degraded by LONP1 and an established model for studying mitochondrial proteostasis imbalance38–40”
From Disuse-associated loss of the protease Lonp1 in muscle impairs mitochondrial function and causes reduced skeletal muscle mass and strength (2022) · cites this paper as [38]
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Cites
Site-directed mutagenesis by overlap extension using the polymerase chain reaction
Ho, S. N., Hunt, H. D., Horton, R. M., Pullen, J. K., & Pease, L. R. (1989) · Gene · doi:10.1016/0378-1119(89)90358-2 · Cited by 7,414
Efficient selection for high-expression transfectants with a novel eukaryotic vector
Niwa, H., Yamamura, K., & Miyazaki, J. (1991) · Gene · doi:10.1016/0378-1119(91)90434-d · Cited by 5,149
Control of inositol 1,4,5-trisphosphate-induced Ca2+ release by cytosolic Ca2+
Bootman, M. D., Missiaen, L., Parys, J. B., SMEDT, H. D., & Casteels, R. (1995) · Biochemical Journal · doi:10.1042/bj3060445 · Cited by 5,131
Prevention of Apoptosis by Bcl-2: Release of Cytochrome c from Mitochondria Blocked
Yang, J., Liu, X., Bhalla, K. N., Kim, C. N., Ibrado, A. M., Cai, J., Peng, T.-I., Jones, D. P., & Wang, X. (1997) · Science · doi:10.1126/science.275.5303.1129 · Cited by 4,913
Yoshida, H., Matsui, T., Yamamoto, A., Okada, T., & Mori, K. (2001) · Cell · doi:10.1016/s0092-8674(01)00611-0 · Cited by 4,054
Mutation of the mouse klotho gene leads to a syndrome resembling ageing
Kuro-o, M., Matsumura, Y., Aizawa, H., Kawaguchi, H., Suga, T., Utsugi, T., Ohyama, Y., Kurabayashi, M., Kaname, T., Kume, E., et al. (1997) · Nature · doi:10.1038/36285 · Cited by 3,837
Molecular chaperones in cellular protein folding
Hartl, F. U. (1996) · Nature · doi:10.1038/381571a0 · Cited by 3,584
Regulated Translation Initiation Controls Stress-Induced Gene Expression in Mammalian Cells
Harding, H. P., Novoa, I., Zhang, Y., Zeng, H., Wek, R. C., Schapira, M., & Ron, D. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)00108-8 · Cited by 3,344
IRE1 couples endoplasmic reticulum load to secretory capacity by processing the XBP-1 mRNA
Calfon, M. A., Zeng, H., Urano, F., Till, J. H., Hubbard, S. R., Harding, H. P., Clark, S. G., & Ron, D. (2002) · Nature · doi:10.1038/415092a · Cited by 2,907
Andrews, N. C., & Faller, D. V. (1991) · Nucleic Acids Research · doi:10.1093/nar/19.9.2499 · Cited by 2,337
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 999
Protein Misfolding, Aggregation, and Degradation in Disease
Gregersen, N., Bolund, L., & Bross, P. (2005) · Molecular Biotechnology · doi:10.1385/mb:31:2:141 · Cited by 70
Jacques, S., van der Sloot, A. M., Huard, C., Coulombe‐Huntington, J., Tsao, S., Tollis, S., Bertomeu, T., Culp, E. J., Pallant, D., Cook, M. A., et al. (2020) · Genetics · doi:10.1534/genetics.119.302851 · Cited by 70
Straub, I. R., Weraarpachai, W., & Shoubridge, E. A. (2021) · Human Molecular Genetics · doi:10.1093/hmg/ddab078 · Cited by 67
Mitochondrial maintenance failure in aging and role of sexual dimorphism
Tower, J. (2014) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2014.10.008 · Cited by 68
The mitochondrial unfolded protein response in mammalian physiology
Mottis, A., Jovaisaite, V., & Auwerx, J. H. (2014) · Mammalian Genome · doi:10.1007/s00335-014-9525-z · Cited by 70
The transcription factor ATF5: role in cellular differentiation, stress responses, and cancer
Sears, T. K., & Angelastro, J. M. (2017) · Oncotarget · doi:10.18632/oncotarget.21102 · Cited by 68
Jazwinski, S. M. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-394625-6.00005-2 · Cited by 67
Chemical Modulation of Human Mitochondrial ClpP: Potential Application in Cancer Therapeutics
Wong, K. S., & Houry, W. A. (2019) · ACS Chemical Biology · doi:10.1021/acschembio.9b00347 · Cited by 67
Organismal Protein Homeostasis Mechanisms
Hoppe, T., & Cohen, E. (2020) · Genetics · doi:10.1534/genetics.120.301283 · Cited by 68
The use of stress‐70 proteins in physiology: a re‐appraisal
Morris, J. P., Thatje, S., & Hauton, C. (2013) · Molecular Ecology · doi:10.1111/mec.12216 · Cited by 67
Why genes persist in organelle genomes
Daley, D. O., & Whelan, J. (2005) · Genome Biology · doi:10.1186/gb-2005-6-5-110 · Cited by 66
Integrating the UPRmtinto the mitochondrial maintenance network
Fiorese, C. J., & Haynes, C. M. (2017) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2017.1291577 · Cited by 68
Unveiling “Musica Universalis” of the Cell: A Brief History of Biological 12-Hour Rhythms
Zhu, B., Dacso, C. C., & O’Malley, B. W. (2018) · Journal of the Endocrine Society · doi:10.1210/js.2018-00113 · Cited by 64
Wardelmann, K., Blümel, S., Rath, M., Alfine, E., Chudoba, C., Schell, M., Cai, W., Hauffe, R., Warnke, K., Flore, T., et al. (2019) · Molecular Metabolism · doi:10.1016/j.molmet.2019.01.001 · Cited by 69
Ramachandran, A., CEASER, E. K., & Darley-Usmar, V. M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0304653101 · Cited by 67
Chan, J. Y. H., Cheng, H., Chou, J. L., Li, F. C. H., Dai, K., Chan, S. H. H., & Chang, A. Y. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m603394200 · Cited by 67
Mammalian integrated stress responses in stressed organelles and their functions
Lu, H.-J., Koju, N., & Sheng, R. (2024) · Acta Pharmacologica Sinica · doi:10.1038/s41401-023-01225-0 · Cited by 73
Luckhart, S., Giulivi, C., Drexler, A., Antonova‐Koch, Y., Sakaguchi, D., Napoli, E., Wong, S., Price, M. S., Eigenheer, R. A., Phinney, B. S., et al. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003180 · Cited by 68
Mitochondrially-targeted treatment strategies
Bozi, L. H. M., Campos, J. C., Zambelli, V. O., Ferreira, N. D., & Ferreira, J. C. B. (2019) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2019.100836 · Cited by 67
Mitochondrial unfolded protein response (UPRmt): what we know thus far
Torres, A. K., Fleischhart, V., & Inestrosa, N. C. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1405393 · Cited by 65
Mitochondrial dysfunction in Alzheimer's disease: Guiding the path to targeted therapies
Percy, K. C. M., Liu, Z., & Qi, X. (2025) · Neurotherapeutics · doi:10.1016/j.neurot.2025.e00525 · Cited by 70
Moisoi, N., Fedele, V., Edwards, J., & Martins, L. M. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.10.009 · Cited by 68
Designed hybrid TPR peptide targeting Hsp90 as a novel anticancer agent
Horibe, T., Kohno, M., Haramoto, M., Ohara, K., & Kawakami, K. (2011) · Journal of Translational Medicine · doi:10.1186/1479-5876-9-8 · Cited by 64
Sirtuins in mitochondrial stress: Indispensable helpers behind the scenes
Lin, S., Xing, H., Zang, T., Ruan, X., Wo, L., & He, M. (2018) · Ageing Research Reviews · doi:10.1016/j.arr.2018.03.006 · Cited by 65
Cilleros-Holgado, P., Gómez-Fernández, D., Piñero-Pérez, R., Romero-Domínguez, J. M., Reche-López, D., López-Cabrera, A., Álvarez-Córdoba, M., Munuera-Cabeza, M., Talaverón-Rey, M., Suárez-Carrillo, A., et al. (2023) · Biomolecules · doi:10.3390/biom13121789 · Cited by 68
Bennett, C. F., & Kaeberlein, M. R. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.02.002 · Cited by 61
Mitochondrial Quality Control Governed by Ubiquitin
Ravanelli, S., den Brave, F., & Hoppe, T. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00270 · Cited by 66
Mitochondrial stress-dependent regulation of cellular protein synthesis
Topf, U., Uszczynska-Ratajczak, B., & Chacinska, A. (2019) · Journal of Cell Science · doi:10.1242/jcs.226258 · Cited by 52
Bai, Y., Wu, J., Yang, Z., Wang, X., Zhang, D., & Ma, J. (2022) · Cell Biology and Toxicology · doi:10.1007/s10565-022-09716-2 · Cited by 64
Stress responsive mitochondrial proteins in Arabidopsis thaliana
Wang, Y., Berkowitz, O., Selinski, J., Xu, Y., Hartmann, A., & Whelan, J. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.03.031 · Cited by 62
Martínez‐Klimova, E., Aparicio‐Trejo, O. E., Gómez‐Sierra, T., Jiménez‐Uribe, A. P., Bellido, B., & Pedraza‐Chaverrí, J. (2020) · BioFactors · doi:10.1002/biof.1673 · Cited by 62
Manipulation of Host Cell Organelles by Intracellular Pathogens
Kellermann, M., Scharte, F., & Hensel, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126484 · Cited by 63
Control of mitochondrial integrity in ageing and disease
Szklarczyk, R., Nooteboom, M., & Osiewacz, H. D. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0439 · Cited by 66
Cortopassi, G. A., Danielson, S. R., Alemi, M., Zhan, S. S., Tong, W., Carelli, V., Martinuzzi, A., Marzuki, S., Majamaa, K., & Wong, A. (2006) · Mitochondrion · doi:10.1016/j.mito.2006.05.002 · Cited by 60
Kang, S.-M., Kim, S.-J., Kim, J. H., Lee, W., Kim, G., Lee, K.-H., Choi, K., & Oh, J. (2009) · Cancer Letters · doi:10.1016/j.canlet.2009.02.003 · Cited by 60
Regulation of the H+-ATP synthase by IF1: a role in mitohormesis
Esparza‐Moltó, P. B., Nuevo‐Tapioles, C., & Cuezva, J. M. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2462-8 · Cited by 64
Chemical Profiling of the Endoplasmic Reticulum Proteome Using Designer Labeling Reagents
Fujisawa, A., Tamura, T., Yasueda, Y., Kuwata, K., & Hamachi, I. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b08606 · Cited by 59
Mitochondrial Quality Control in Sarcopenia: Updated Overview of Mechanisms and Interventions
Liu, D., Fan, Y., Tao, X., Pan, W., Wu, Y., Wang, X., He, Y., Xiao, W., & Li, Y. (2021) · Aging and Disease · doi:10.14336/ad.2021.0427 · Cited by 62
Guo, Q., Xu, Z., Zhou, D., Fu, T., Wang, W., Sun, W., Xiao, L., Liu, L., Ding, C., Yin, Y., et al. (2022) · Science Advances · doi:10.1126/sciadv.abo0340 · Cited by 59
Jensen, M. B., Qi, Y., Riley, R. R., Rabkina, L., & Jasper, H. (2017) · eLife · doi:10.7554/elife.26952 · Cited by 63
Mitochondrial Dysfunction and Stress Responses in Alzheimer’s Disease
Weidling, I. W., & Swerdlow, R. H. (2019) · Biology · doi:10.3390/biology8020039 · Cited by 59
The Mitochondrial Unfolded Protein Response: A Hinge Between Healthy and Pathological Aging
Muñoz-Carvajal, F., & Sanhueza, M. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.581849 · Cited by 61
Cellular Stress and General Pathological Processes
Gusev, E. Y., & Zotova, N. V. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666190319114641 · Cited by 64
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Trempe, J., & Gehring, K. (2023) · Journal of Molecular Biology · doi:10.1016/j.jmb.2023.168090 · Cited by 63
Mitochondrial stress: Balancing friend and foe
Runkel, E. D., Baumeister, R., & Schulze, E. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.02.013 · Cited by 59
Fan, D., Yang, X., Li, Y., & Guo, L. (2018) · Medical Science Monitor · doi:10.12659/msm.909365 · Cited by 59
The Unfolded Protein Response in Protein Aggregating Diseases
Gow, A., & Sharma, R. (2003) · NeuroMolecular Medicine · doi:10.1385/nmm:4:1-2:73 · Cited by 58
Insight into the mitochondrial unfolded protein response and cancer: opportunities and challenges
Wang, G., Fan, Y., Cao, P., & Tan, K. (2022) · Cell & Bioscience · doi:10.1186/s13578-022-00747-0 · Cited by 58
NAD+ dependent UPRmt activation underlies intestinal aging caused by mitochondrial DNA mutations
Yang, L., Ruan, Z., Lin, X., Wang, H., Xin, Y., Tang, H., Hu, Z., Zhou, Y., Wu, Y., Wang, J., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-44808-z · Cited by 61
Self-citationThe integrated stress response in neurodegenerative diseases
Bravo-Jimenez, M. A., Sharma, S., & Karimi‐Abdolrezaee, S. (2025) · Molecular Neurodegeneration · doi:10.1186/s13024-025-00811-6 · Cited by 67
Erlich, A. T., Tryon, L. D., Crilly, M. J., Memme, J. M., Moosavi, Z. S. M., Oliveira, A. N., Beyfuss, K. A., & Hood, D. A. (2016) · Integrative Medicine Research · doi:10.1016/j.imr.2016.05.003 · Cited by 59
The role of mitochondria in mTOR‐regulated longevity
Wei, Y., Zhang, Y., Cai, Y., & Xu, M. (2015) · Biological Reviews · doi:10.1111/brv.12103 · Cited by 56
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Li, J., Zhang, D., Brundel, B. J. J. M., & Wiersma, M. (2019) · Cells · doi:10.3390/cells8121617 · Cited by 55
Lee, H., Ha, T. Y., Jung, C. H., Nirmala, F. S., Park, S., Huh, Y. H., & Ahn, J. (2021) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12794 · Cited by 56
Mitochondrial stress signaling: a pathway unfolds
Broadley, S. A., & Hartl, F. U. (2007) · Trends in Cell Biology · doi:10.1016/j.tcb.2007.11.003 · Cited by 57
Ogunbileje, J. O., Porter, C. C., Herndon, D. N., Chao, T., Abdelrahman, D. R., Papadimitriou, A., Chondronikola, M., Zimmers, T. A., Reidy, P. T., Rasmussen, B. B., et al. (2016) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00535.2015 · Cited by 55
Bross, P., & Guerra, P. F. (2016) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2016.00049 · Cited by 56
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Levytskyy, R. M., Bohovych, I., & Khalimonchuk, O. (2017) · Biochemistry · doi:10.1021/acs.biochem.7b00663 · Cited by 58
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Tatsuta, T. (2009) · The Journal of Biochemistry · doi:10.1093/jb/mvp122 · Cited by 59
Netherton, C. L., Parsley, J. C., & Wileman, T. E. (2004) · Journal of Virology · doi:10.1128/jvi.78.19.10825-10828.2004 · Cited by 56
Lan, B., He, Y., Sun, H., Zheng, X., Gao, Y., & Li, N. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.116587 · Cited by 58
Zhou, B., Fang, L., Dong, Y., Yang, J., Chen, X., Zhang, N., Zhu, Y., & Huang, T. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03660-5 · Cited by 56
Guha, M., Pan, H., Fang, J.-K., & Avadhani, N. G. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-04-0296 · Cited by 55
Siegelin, M. D. (2013) · Cancer Letters · doi:10.1016/j.canlet.2013.01.045 · Cited by 56
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Soledad, R. B., Charles, S., & Das, S. (2019) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2019.03.019 · Cited by 54
Rath, E., & Haller, D. (2011) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21944 · Cited by 55
Guha, M., Srinivasan, S., Biswas, G., & Avadhani, N. G. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611693200 · Cited by 54
Aras, S., Purandare, N., Gladyck, S., Somayajulu‐Nitu, M., Zhang, K., Wallace, D. C., & Grossman, L. I. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2005877117 · Cited by 52
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Smyrnias, I. (2021) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2021.105934 · Cited by 54
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Ji, C. (2015) · Biomolecules · doi:10.3390/biom5021099 · Cited by 54
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Li, J., Wang, Z., Li, C., Song, Y., Wang, Y., Hai, B., & Zhang, Y. (2022) · Cells · doi:10.3390/cells11132086 · Cited by 56
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Zhou, Z., Lu, J., Yang, M., Cai, J., Fu, Q., Ma, J., & Zhu, L. (2022) · Experimental & Molecular Medicine · doi:10.1038/s12276-022-00885-y · Cited by 52
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Lionaki, E., & Tavernarakis, N. (2013) · Journal of Proteomics · doi:10.1016/j.jprot.2013.03.022 · Cited by 56
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Szabadkai, G., & Duchen, M. R. (2009) · APOPTOSIS · doi:10.1007/s10495-009-0363-5 · Cited by 54
Nutlin-3 enhances the bortezomib sensitivity of p53-defective cancer cells by inducing paraptosis
Lee, D. M., Kim, I. Y., Seo, M. J., Kwon, M. R., & Choi, K. S. (2017) · Experimental & Molecular Medicine · doi:10.1038/emm.2017.112 · Cited by 52
mPOS is a novel mitochondrial trigger of cell death – implications for neurodegeneration
Coyne, L. P., & Chen, X. J. (2017) · FEBS Letters · doi:10.1002/1873-3468.12894 · Cited by 51
Role of the mitochondrial stress response in human cancer progression
Wang, S., Chen, S., Tseng, L., & Lee, H. (2020) · Experimental Biology and Medicine · doi:10.1177/1535370220920558 · Cited by 51
Smulan, L. J., Martinez, N., Kiritsy, M. C., Kativhu, C. L., Cavallo, K., Sassetti, C. M., Singhal, A., Remold, H. G., & Kornfeld, H. (2021) · mBio · doi:10.1128/mbio.03140-20 · Cited by 52
Angireddy, R., Chowdhury, A. R., Zielonka, J., Ruthel, G. T., Kalyanaraman, B., & Avadhani, N. G. (2020) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2020.06.030 · Cited by 51
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Soo, S. K., Rudich, Z. D., Ko, B., Moldakozhayev, A., AlOkda, A., & Raamsdonk, J. M. V. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101941 · Cited by 58
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Kamimura, D., Katsunuma, K., Arima, Y., Atsumi, T., Jiang, J., Bando, H., Meng, J., Sabharwal, L., Štofková, A., Nishikawa, N., et al. (2015) · Nature Communications · doi:10.1038/ncomms8474 · Cited by 51
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Park, H., Lee, J., Lim, J., & Kang, B. H. (2014) · Molecular Cancer · doi:10.1186/1476-4598-13-148 · Cited by 52
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Tetracycline-induced mitohormesis mediates disease tolerance against influenza
Mottis, A., Li, T. Y., Alam, G. E., Rapin, A., Katsyuba, E., Liaskos, D., D’Amico, D., Harris, N. L., Grier, M. C., Mouchiroud, L., et al. (2022) · Journal of Clinical Investigation · doi:10.1172/jci151540 · Cited by 48
Meister, S., Frey, B., Lang, V. R., Gaipl, U. S., Schett, G. A., Schlötzer-Schrehardt, U. M., & Voll, R. E. (2010) · Neoplasia · doi:10.1593/neo.10228 · Cited by 49
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Metadata
- Authors
- Zhao, Q., Wang, J., Levichkin, I. V., Stasinopoulos, S., Ryan, M. T., & Hoogenraad, N. J.
- Affiliations
- La Trobe University (AU)
- Corresponding author
- Hoogenraad, Nicholas J.
- ORCID
- Zhao, Quan
- Venue
- The EMBO Journal
- Published
- 2002-09-02
- Volume
- 21
- Issue
- 17
- Pages
- 4411-4419
- ISSN
- 0261-4189 (ISSN-L)
- 1460-2075
- PMC
- PMC126185
- OpenAlex
- W2108738634
- Cited by
- 1,026
- References
- 55
- Citations by year
- 2026: 58 · 2025: 64 · 2024: 71 · 2023: 59 · 2022: 71 · 2021: 88 · 2020: 77 · 2019: 60 · 2018: 60 · 2017: 46 · 2016: 50 · 2015: 42 · 2014: 45 · 2013: 38 · 2012: 29
- FWCI
- 4.06
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The EMBO Journal (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Medical Research Council
- Australian Research Council
- National Health and Medical Research Council
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heat shock proteins research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Endoplasmic Reticulum Stress and Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Keywords
- mitochondrial stress response, unfolded protein accumulation, mitochondrial matrix, CHOP, C/EBPβ, transcriptional regulation, chaperonin 60, GroES, ClpP, unfolded protein response, mammalian cells
- MeSH terms
- Adenosine Triphosphatases, Animals, Cell Nucleus, Chlorocebus aethiops, Gene Expression Regulation, Genes, Dominant, Heat-Shock Proteins, Mitochondria, Ornithine Carbamoyltransferase, Promoter Regions, Genetic, Protein Processing, Post-Translational, Recombinant Fusion Proteins, Regulatory Sequences, Nucleic Acid, Serine Endopeptidases, Stress, Physiological, Transcription Factors, Transcription, Genetic, Transfection, Signal Transduction, Sequence Deletion, Protein Folding, Chaperonin 60, Chaperonin 10, COS Cells, Protein Transport, CCAAT-Enhancer-Binding Proteins, Endopeptidase Clp, HSP40 Heat-Shock Proteins, Transcription Factor CHOP
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