Stress, Inflammation, and Defense of Homeostasis
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Inflammation is traditionally considered a defense response induced by infection or injury. However, inflammation can also be induced by tissue stress and malfunction in the absence of infection or overt tissue damage. Here we discuss the relationship between homeostasis, stress responses, and inflammation. Stress responses have cell-autonomous and cell-extrinsic components, the latter contributing to tissue level adaptation to stress conditions. Inflammation can be thought of as the extreme end of a spectrum that ranges from homeostasis to stress response to bona fide inflammatory response. Inflammation can be triggered by two types of stimuli: extreme deviations of homeostasis or challenges that cause a disruption of homeostasis. This perspective may help to explain qualitative differences and functional outcomes of diverse inflammatory responses.
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Inflammation is theorized to be a unifying feature of homeostatic perturbation, providing a protective response to extreme deviations from the homeostatic set point.
“Inflammation is theorized to be a unifying feature of homeostatic perturbation: providing a protective response to extreme deviations from the homeostatic set point174,175.”
From Neural mechanisms of social homeostasis (2019) · cites this paper as [174]
Several studies found that sleep reduces neutrophil counts, although some studies did not find any changes.
“In contrast, several studies found that sleep reduces neutrophil counts (69, 112, 178, 287, 326, 338, 480, 580), although again some studies did not find any changes (67, 103, 122, 469).”
From The Sleep-Immune Crosstalk in Health and Disease (2019) · cites this paper as [112]
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Cites
Inflammation and metabolic disorders
Hotamisligil, G. S. (2006) · Nature · doi:10.1038/nature05485 · Cited by 9,199 · see citing works
Exploring the full spectrum of macrophage activation
Mosser, D. M., & Edwards, J. P. (2008) · Nature Reviews Immunology · doi:10.1038/nri2448 · Cited by 9,144 · see citing works
Pattern Recognition Receptors and Inflammation
Takeuchi, O., & Akira, S. (2010) · Cell · doi:10.1016/j.cell.2010.01.022 · Cited by 8,895 · see citing works
Origin and physiological roles of inflammation
Medzhitov, R. (2008) · Nature · doi:10.1038/nature07201 · Cited by 6,618 · see citing works
Self-citationVascular endothelial growth factor induced by hypoxia may mediate hypoxia-initiated angiogenesis
Shweiki, D., Itin, A., Soffer, D., & Keshet, E. (1992) · Nature · doi:10.1038/359843a0 · Cited by 4,617 · see citing works
Cellular and Molecular Mechanisms of Pain
Basbaum, A. I., Bautista, D. M., Scherrer, G., & Julius, D. (2009) · Cell · doi:10.1016/j.cell.2009.09.028 · Cited by 4,344 · see citing works
Inflammatory Mechanisms in Obesity
Gregor, M. F., & Hotamisligil, G. S. (2011) · Annual Review of Immunology · doi:10.1146/annurev-immunol-031210-101322 · Cited by 3,754 · see citing works
Autophagy and the Integrated Stress Response
Kroemer, G., Mariño, G., & Levine, B. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.023 · Cited by 3,506 · see citing works
CCL2 recruits inflammatory monocytes to facilitate breast-tumour metastasis
Qian, B.-Z., Li, J., Zhang, H., Kitamura, T., Zhang, J., Campion, L. R., Kaiser, E. A., Snyder, L. A., & Pollard, J. W. (2011) · Nature · doi:10.1038/nature10138 · Cited by 2,874 · see citing works
Endoplasmic reticulum stress and the inflammatory basis of metabolic disease
Hotamisligil, G. S. (2010) · Cell · doi:10.1016/j.cell.2010.02.034 · Cited by 2,802 · see citing works
Molecular mechanisms of nociception
Julius, D., & Basbaum, A. I. (2001) · Nature · doi:10.1038/35093019 · Cited by 2,685 · cited 1× · see citing works
“C-fiber nociceptors locally produce CGRP and Substance P upon activation by these stressors, and these neuropeptides coordinate local stress adaptations known as neuro-inflammation (Julius and Basbaum, 2001).”
BackgroundKanda, H. (2006) · Journal of Clinical Investigation · doi:10.1172/jci26498 · Cited by 2,682 · see citing works
The Nrf2-antioxidant response element signaling pathway and its activation by oxidative stress
Nguyen, T., Nioi, P., & Pickett, C. B. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.r900010200 · Cited by 2,655 · see citing works
Signal integration by JNK and p38 MAPK pathways in cancer development
Wagner, E. F., & Nebreda, Á. R. (2009) · Nature reviews. Cancer · doi:10.1038/nrc2694 · Cited by 2,583 · see citing works
Venkatachalam, K., & Montell, C. (2007) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.75.103004.142819 · Cited by 1,915 · see citing works
Inflammation 2010: New Adventures of an Old Flame
Medzhitov, R. M. (2010) · Cell · doi:10.1016/j.cell.2010.03.006 · Cited by 1,854 · see citing works
Self-citationHonda, K., & Taniguchi, T. (2006) · Nature reviews. Immunology · doi:10.1038/nri1900 · Cited by 1,676 · see citing works
Regulation of the mTOR Complex 1 Pathway by Nutrients, Growth Factors, and Stress
Sengupta, S., Peterson, T. R., & Sabatini, D. M. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.026 · Cited by 1,234 · see citing works
Trophic macrophages in development and disease
Pollard, J. W. (2009) · Nature Reviews Immunology · doi:10.1038/nri2528 · Cited by 1,178 · see citing works
Tracey, K. J. (2009) · Nature Reviews Immunology · doi:10.1038/nri2566 · Cited by 1,154 · cited 2× · see citing works
“…nociceptors may monitor and control tissue homeostasis not only at the extremes of infection and injury, but also duringmore common and less dramatic alterations of normal tissue states (Ahern, 2013; Basbaum et al., 2009;Mosser and Edwards, 2008; Nguyen et al., 2011; Pollard, 2009; Tracey, 2009).”
BackgroundAnti-Inflammatory Therapy in Chronic Disease: Challenges and Opportunities
Tabas, I., & Glass, C. K. (2013) · Science · doi:10.1126/science.1230720 · Cited by 1,093 · see citing works
The Cell Non-Autonomous Nature of Electron Transport Chain-Mediated Longevity
Durieux, J., Wolff, S., & Dillin, A. (2011) · Cell · doi:10.1016/j.cell.2010.12.016 · Cited by 1,059 · see citing works
The inflammatory micro-environment in tumor progression: the role of tumor-associated macrophages.
Allavena, P., Sica, A., Solinas, G., Porta, C., & Mantovani, A. (2008) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2007.07.004 · Cited by 1,044 · see citing works
Alternatively activated macrophages produce catecholamines to sustain adaptive thermogenesis
Nguyen, K. D., Qiu, Y., Cui, X., Goh, Y. P. S., Mwangi, J., David, T., Mukundan, L., Brombacher, F., Locksley, R. M., & Chawla, A. (2011) · Nature · doi:10.1038/nature10653 · Cited by 1,038 · see citing works
Weidemann, A., & Johnson, R. S. (2008) · Cell Death & Differentiation · doi:10.1038/cdd.2008.12 · Cited by 941 · see citing works
Regulation of inflammasome signaling
Rathinam, V. A. K., Vanaja, S. K., & Fitzgerald, K. A. (2012) · Nature Immunology · doi:10.1038/ni.2237 · Cited by 929 · see citing works
Homeostasis and Inflammation in the Intestine
Garrett, W. S., Gordon, J. I., & Glimcher, L. H. (2010) · Cell · doi:10.1016/j.cell.2010.01.023 · Cited by 784 · see citing works
The macrophage: Past, present and future
Gordon, S. (2007) · European Journal of Immunology · doi:10.1002/eji.200737638 · Cited by 625 · see citing works
Radiation-induced bystander effects — implications for cancer
Seymour, C. B., & Mothersill, C. E. (2004) · Nature reviews. Cancer · doi:10.1038/nrc1277 · Cited by 478 · see citing works
The p53 network: cellular and systemic DNA damage responses in aging and Cancer
Reinhardt, H. C., & Schumacher, B. (2012) · Trends in Genetics · doi:10.1016/j.tig.2011.12.002 · Cited by 458 · see citing works
TRPA1: A Gatekeeper for Inflammation
Bautista, D. M., Pellegrino, M., & Tsunozaki, M. (2012) · Annual Review of Physiology · doi:10.1146/annurev-physiol-030212-183811 · Cited by 411 · see citing works
Palm, N. W., Rosenstein, R. K., & Medzhitov, R. M. (2012) · Nature · doi:10.1038/nature11047 · Cited by 393 · see citing works
Self-citationEvolution of concepts of stress
Goldstein, D. S., & Kopin, I. J. (2007) · Stress · doi:10.1080/10253890701288935 · Cited by 391 · see citing works
Cao, S. S., & Kaufman, R. J. (2012) · Current Biology · doi:10.1016/j.cub.2012.07.004 · Cited by 365 · see citing works
Regulation of the Cellular Heat Shock Response in Caenorhabditis elegans by Thermosensory Neurons
Prahlad, V., Cornelius, T., & Morimoto, R. I. (2008) · Science · doi:10.1126/science.1156093 · Cited by 359 · see citing works
Induction and function of type I and III interferon in response to viral infection
Levy, D. E., Marié, I. J., & Durbin, J. E. (2011) · Current Opinion in Virology · doi:10.1016/j.coviro.2011.11.001 · Cited by 316 · see citing works
Diverse and Specific Gene Expression Responses to Stresses in Cultured Human Cells
Murray, J. I., Whitfield, M. L., Trinklein, N. D., Myers, R. M., Brown, P. O., & Botstein, D. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-11-0799 · Cited by 300 · see citing works
Pascussi, J., Gerbal‐Chaloin, S., Duret, C., Daujat‐Chavanieu, M., Vilarem, M., & Maurel, P. (2007) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.47.120505.105349 · Cited by 298 · see citing works
ChREBP, a Transcriptional Regulator of Glucose and Lipid Metabolism
Postic, C., Dentin, R., Denechaud, P., & Girard, J. R. (2007) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.27.061406.093618 · Cited by 283 · see citing works
Hitchon, C. A., Wong, K., Ma, G., Reed, J., Lyttle, D., & El-Gabalawy, H. S. (2002) · Arthritis & Rheumatism · doi:10.1002/art.10520 · Cited by 247 · see citing works
DNA damage in germ cells induces an innate immune response that triggers systemic stress resistance
Ermolaeva, M. A., Segref, A., Dakhovnik, A., Ou, H.-L., Schneider, J. I., Utermöhlen, O., Hoppe, T., & Schumacher, B. (2013) · Nature · doi:10.1038/nature12452 · Cited by 221 · see citing works
The Immune System as a Sensor of the Metabolic State
Odegaard, J. I., & Chawla, A. (2013) · Immunity · doi:10.1016/j.immuni.2013.04.001 · Cited by 215 · see citing works
Buchman, T. G. (2002) · Nature · doi:10.1038/nature01260 · Cited by 207 · see citing works
Rutkowski, D. T., & Kaufman, R. J. (2003) · Developmental Cell · doi:10.1016/s1534-5807(03)00100-x · Cited by 192 · see citing works
Heat Shock Factor 1 as a Coordinator of Stress and Developmental Pathways
Anckar, J., & Sistonen, L. (2007) · Springer eBooks · doi:10.1007/978-0-387-39975-1_8 · Cited by 181 · see citing works
Saito, S., Furuno, A., Sakurai, J., Sakamoto, A., Park, H.-R., Shin‐ya, K., Tsuruo, T., & Tomida, A. (2009) · Cancer Research · doi:10.1158/0008-5472.can-08-2689 · Cited by 160 · see citing works
Goto, M. (2008) · PubMed · Cited by 154 · see citing works
Mechanism of Inflammation in Age-Related Macular Degeneration
Parmeggiani, F., Romano, M., Costagliola, C., Semeraro, F., Incorvaia, C., D’Angelo, S., Perri, P., Palma, P. D., Nadai, K. D., & Sebastiani, A. (2012) · Mediators of Inflammation · doi:10.1155/2012/546786 · Cited by 135 · see citing works
Page, T. J., Sikder, D. S., Yang, L., Pluta, L., Wolfinger, R. D., Kodadek, T. J., & Thomas, R. S. (2006) · Molecular BioSystems · doi:10.1039/b606129j · Cited by 124 · see citing works
CELL SURVIVAL IN THE HOSTILE ENVIRONMENT OF THE RENAL MEDULLA
Neuhofer, W., & Beck, F.-X. (2004) · Annual Review of Physiology · doi:10.1146/annurev.physiol.67.031103.154456 · Cited by 121 · see citing works
Aramburu, J. F., Drews‐Elger, K., Estrada-Gelonch, A., Minguillón, J., Morancho, B., Santiago, V., & López‐Rodríguez, C. (2006) · Biochemical Pharmacology · doi:10.1016/j.bcp.2006.07.002 · Cited by 121 · see citing works
Mense, S. M., Sengupta, A., Zhou, M., Lan, C., Bentsman, G., Volsky, D. J., & Li, Z. (2006) · Physiological Genomics · doi:10.1152/physiolgenomics.00315.2005 · Cited by 120 · see citing works
DNA recognition in immunity and disease
Holm, C. K., Paludan, S. R., & Fitzgerald, K. A. (2013) · Current Opinion in Immunology · doi:10.1016/j.coi.2012.12.006 · Cited by 57 · see citing works
Transient receptor potential channels and energy homeostasis
Ahern, G. P. (2013) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2013.06.005 · Cited by 48 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- Costanzo LS 2010 Physiology Philadelphia, PA Saunders/Elsevier 1 online resource xi 493
Cited by
Sorted by citations
Control of adaptive immunity by the innate immune system
Iwasaki, A., & Medzhitov, R. (2015) · Nature Immunology · doi:10.1038/ni.3123 · Cited by 2,160 · see citing works
Self-citationThe Sleep-Immune Crosstalk in Health and Disease
Besedovsky, L., Lange, T., & Haack, M. (2019) · Physiological Reviews · doi:10.1152/physrev.00010.2018 · Cited by 1,479 · see citing works
“The typical inflammatory response is triggered by a local infection or tissue injury, involving PAMPs and DAMPs, and is traditionally thought of as a protective reaction that defends and restores physiological functions (111, 296).”
BackgroundRole of tumor microenvironment in tumorigenesis
Wang, M., Zhao, J., Zhang, L., Wei, F., Lian, Y., Wu, Y., Gong, Z., Zhang, S., Zhou, J., Cao, K., et al. (2017) · Journal of Cancer · doi:10.7150/jca.17648 · Cited by 1,404 · see citing works
Homeostasis, Inflammation, and Disease Susceptibility
Kotas, M. E., & Medzhitov, R. (2015) · Cell · doi:10.1016/j.cell.2015.02.010 · Cited by 1,213 · see citing works
Self-citationSarin, S. K., Choudhury, A. K., Sharma, M. K., Maiwall, R., Mahtab, M. A., Rahman, S., Saigal, S., Saraf, N., Soin, A. S., Devarbhavi, H. C., et al. (2019) · Hepatology International · doi:10.1007/s12072-019-09946-3 · Cited by 904 · see citing works
Clària, J., Stauber, R. E., Coenraad, M. J., Moreau, R., Jalan, R., Pavesi, M., Amorós, À., Titos, E., Alcaraz‐Quiles, J., Oettl, K., et al. (2016) · Hepatology · doi:10.1002/hep.28740 · Cited by 774 · see citing works
Engineering T Cells with Customized Therapeutic Response Programs Using Synthetic Notch Receptors
Roybal, K. T., Williams, J. Z., Morsut, L., Rupp, L. J., Kolinko, I., Choe, J. H., Walker, W. J., McNally, K. A., & Lim, W. A. (2016) · Cell · doi:10.1016/j.cell.2016.09.011 · Cited by 723 · see citing works
Vainchtein, I. D., Chin, G., Cho, F. S., Kelley, K. W., Miller, J. G., Chien, E. C., Liddelow, S. A., Nguyen, P. T., Nakao-Inoue, H., Dorman, L. C., et al. (2018) · Science · doi:10.1126/science.aal3589 · Cited by 657 · see citing works
Tissue biology perspective on macrophages
Okabe, Y., & Medzhitov, R. M. (2015) · Nature Immunology · doi:10.1038/ni.3320 · Cited by 633 · see citing works
Self-citationThe role of interleukin-1 in general pathology
Kaneko, N., Kurata, M., Yamamoto, T., Morikawa, S., & Masumoto, J. (2019) · Inflammation and Regeneration · doi:10.1186/s41232-019-0101-5 · Cited by 616 · see citing works
Panduro, M., Benoist, C., & Mathis, D. (2016) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032712-095948 · Cited by 536 · see citing works
Banales, J. M., Huebert, R. C., Karlsen, T., Strazzabosco, M., LaRusso, N. F., & Gores, G. J. (2019) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0125-y · Cited by 517 · see citing works
Endoplasmic Reticulum Stress in Immunity
Bettigole, S. E., & Glimcher, L. H. (2014) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032414-112116 · Cited by 508 · see citing works
Astrocytes and microglia: In sickness and in health
Vainchtein, I. D., & Molofsky, A. V. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.01.003 · Cited by 450 · see citing works
Acute-on-chronic liver failure in cirrhosis
Arroyo, V., Moreau, R., Kamath, P. S., Jalan, R., Ginès, P., Nevens, F., Fernández, J., To, U. K., García–Tsao, G., & Schnabl, B. (2016) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2016.41 · Cited by 442 · see citing works
Redox homeostasis maintained by GPX4 facilitates STING activation
Jia, M., Qin, D., Zhao, C., Chai, L., Yu, Z., Wang, W., Li, T., Lv, L., Wang, Y., Rehwinkel, J., et al. (2020) · Nature Immunology · doi:10.1038/s41590-020-0699-0 · Cited by 426 · see citing works
Macrophages and Iron Metabolism
Soares, M. P., & Hamza, I. (2016) · Immunity · doi:10.1016/j.immuni.2016.02.016 · Cited by 401 · see citing works
Mino, T., Murakawa, Y., Fukao, A., Vandenbon, A., Wessels, H.-H., Ori, D., Uehata, T., Tartey, S., Akira, S., Suzuki, Y., et al. (2015) · Cell · doi:10.1016/j.cell.2015.04.029 · Cited by 390 · see citing works
Therapy resistance: opportunities created by adaptive responses to targeted therapies in cancer
Labrie, M., Brugge, J. S., Mills, G. B., & Zervantonakis, I. K. (2022) · Nature reviews. Cancer · doi:10.1038/s41568-022-00454-5 · Cited by 388 · see citing works
TLR4 Cross-Talk With NLRP3 Inflammasome and Complement Signaling Pathways in Alzheimer's Disease
Yang, J., Wise, L., & Fukuchi, K.-I. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00724 · Cited by 387 · see citing works
Disease tolerance and immunity in host protection against infection
Soares, M. P., Teixeira, L., & Moita, L. F. (2017) · Nature reviews. Immunology · doi:10.1038/nri.2016.136 · Cited by 376 · see citing works
Tissue homeostasis and inflammation
Meizlish, M. L., Franklin, R. A., Zhou, X., & Medzhitov, R. (2021) · Annual Review of Immunology · doi:10.1146/annurev-immunol-061020-053734 · Cited by 364 · see citing works
Self-citationAcute-on-chronic liver failure: terminology, mechanisms and management
Sarin, S. K., & Choudhury, A. K. (2016) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2015.219 · Cited by 347 · see citing works
Health benefits of dietary marine DHA/EPA-enriched glycerophospholipids
Zhang, T.-T., Xu, J., Wang, Y.-M., & Xue, C.-H. (2019) · Progress in Lipid Research · doi:10.1016/j.plipres.2019.100997 · Cited by 339 · see citing works
Insular cortex neurons encode and retrieve specific immune responses
Koren, T., Yifa, R., Amer, M., Krot, M., Boshnak, N., Ben-Shaanan, T. L., Azulay-Debby, H., Zalayat, I., Avishai, E., Hajjo, H., et al. (2021) · Cell · doi:10.1016/j.cell.2021.10.013 · Cited by 334 · see citing works
Crosstalk between ER stress, NLRP3 inflammasome, and inflammation
Li, W., Cao, T., Luo, C., Cai, J., Zhou, X., Xiao, X., & Liu, S. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-10614-y · Cited by 308 · see citing works
Dzutsev, A., Badger, J. H., Perez-Chanona, E., Roy, S., Salcedo, R., Smith, C. K., & Trinchieri, G. (2017) · Annual Review of Immunology · doi:10.1146/annurev-immunol-051116-052133 · Cited by 302 · see citing works
Abt, M. C., Lewis, B. B., Caballero, S., Xiong, H., Carter, R. A., Sušac, B., Ling, L., Leiner, I. M., & Pamer, E. G. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.06.011 · Cited by 293 · see citing works
Contribution of metabolic reprogramming to macrophage plasticity and function
Kasmi, K. C. E., & Stenmark, K. R. (2015) · Seminars in Immunology · doi:10.1016/j.smim.2015.09.001 · Cited by 276 · see citing works
Neural mechanisms of social homeostasis
Matthews, G. A., & Tye, K. M. (2019) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14016 · Cited by 273 · see citing works
The complex aetiology of cerebral palsy
Korzeniewski, S. J., Slaughter‐Acey, J., Lenski, M., Haak, P., & Paneth, N. (2018) · Nature Reviews Neurology · doi:10.1038/s41582-018-0043-6 · Cited by 272 · see citing works
How biological sex of the host shapes its gut microbiota
Valeri, F., & Endres, K. (2021) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2021.100912 · Cited by 267 · see citing works
Selective Autophagy and Xenophagy in Infection and Disease
Sharma, V., Verma, S., Seranova, E., Sarkar, S., & Kumar, D. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00147 · Cited by 248 · see citing works
Linking the Microbiota, Chronic Disease, and the Immune System
Hand, T. W., Vujkovic-Cvijin, I., Ridaura, V. K., & Belkaid, Y. (2016) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2016.08.003 · Cited by 247 · see citing works
Hajishengallis, G., & Korostoff, J. M. (2017) · Periodontology 2000 · doi:10.1111/prd.12181 · Cited by 245 · see citing works
Advanced nanomedicines for the treatment of inflammatory diseases
Brusini, R., Varna, M., & Couvreur, P. (2020) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2020.07.010 · Cited by 244 · see citing works
Periprosthetic Osteolysis: Mechanisms, Prevention and Treatment
Goodman, S. B., & Gallo, J. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8122091 · Cited by 243 · see citing works
Neuroimmunity: Physiology and Pathology
Talbot, S., Foster, S. L., & Woolf, C. J. (2016) · Annual Review of Immunology · doi:10.1146/annurev-immunol-041015-055340 · Cited by 239 · see citing works
Interleukin-17 governs hypoxic adaptation of injured epithelium
Konieczny, P., Xing, Y., Sidhu, I., Subudhi, I., Mansfield, K. P., Hsieh, B., Biancur, D. E., Larsen, S. B., Cammer, M., Li, D., et al. (2022) · Science · doi:10.1126/science.abg9302 · Cited by 230 · see citing works
Magnesium and inflammation: Advances and perspectives
Maier, J. A. M., Castiglioni, S., Locatelli, L., Zocchi, M., & Mazur, A. (2020) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2020.11.002 · Cited by 225 · see citing works
The mechanism of ferroptosis and its related diseases
Feng, S., Tang, D., Wang, Y., Li, X., Bao, H., Tang, C., Dong, X., Li, X., Yang, Q., Yan, Y., et al. (2023) · Molecular Biomedicine · doi:10.1186/s43556-023-00142-2 · Cited by 224 · see citing works
Barrera, M.-J., Aguilera, S., Castro, I., Carvajal, P., Jara, D., Molina, C., González, S., & González, M.-J. (2021) · Autoimmunity Reviews · doi:10.1016/j.autrev.2021.102867 · Cited by 213 · see citing works
The lymph node microenvironment and its role in the progression of metastatic cancer
Pereira, E. R., Jones, D., Jung, K., & Padera, T. P. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.01.008 · Cited by 210 · see citing works
UPFront and center in RNA decay: UPF1 in nonsense-mediated mRNA decay and beyond
Kim, Y. K., & Maquat, L. E. (2019) · RNA · doi:10.1261/rna.070136.118 · Cited by 210 · see citing works
Rahbardar, M. G., & Hosseinzadeh, H. (2020) · PubMed Central · doi:10.22038/ijbms.2020.45269.10541 · Cited by 202 · see citing works
Kasembeli, M. M., Bharadwaj, U., Robinson, P., & Tweardy, D. J. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19082299 · Cited by 199 · see citing works
Mechanisms of Vascular Remodeling in Hypertension.
Humphrey, J. (2020) · American Journal of Hypertension · doi:10.1093/ajh/hpaa195 · Cited by 168 · see citing works
It's time to redefine inflammation
Antonelli, M. J., & Kushner, I. (2017) · The FASEB Journal · doi:10.1096/fj.201601326r · Cited by 188 · see citing works
Tissue damage control in disease tolerance
Soares, M. P., Gozzelino, R., & Weis, S. (2014) · Trends in Immunology · doi:10.1016/j.it.2014.08.001 · Cited by 187 · see citing works
Type-I-interferon-responsive microglia shape cortical development and behavior
Escoubas, C. C., Dorman, L. C., Nguyen, P. T., Lagares-Linares, C., Nakajo, H., Anderson, S. R., Barron, J. J., Wade, S. D., Cuevas, B., Vainchtein, I. D., et al. (2024) · Cell · doi:10.1016/j.cell.2024.02.020 · Cited by 179 · see citing works
Integration of Innate Immune Signaling
Thaiss, C. A., Levy, M., Itav, S., & Elinav, E. (2016) · Trends in Immunology · doi:10.1016/j.it.2015.12.003 · Cited by 182 · see citing works
Programmed Necrosis and Disease:We interrupt your regular programming to bring you necroinflammation
Kim, E. H., Wong, S., & Martinez, J. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-018-0179-3 · Cited by 176 · see citing works
Reactive Glia Inflammatory Signaling Pathways and Epilepsy
Sanz, P., & García-Gimeno, M. A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21114096 · Cited by 176 · see citing works
Metabolic and Innate Immune Cues Merge into a Specific Inflammatory Response via the UPR
Mogilenko, D. A., Haas, J. T., L’homme, L., Fleury, S., Quemener, S., Levavasseur, M., Becquart, C., Wartelle, J., Bogomolova, A., Pineau, L., et al. (2019) · Cell · doi:10.1016/j.cell.2019.03.018 · Cited by 171 · see citing works
Immune Dysregulation in Autism Spectrum Disorder: What Do We Know about It?
Robinson-Agramonte, M. D. L. A., Noris García, E., Fraga Guerra, J., Vega Hurtado, Y., Antonucci, N., Semprún-Hernández, N., Schultz, S., & Siniscalco, D. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23063033 · Cited by 168 · see citing works
Neuron–Microglia Interactions in Mental Health Disorders: “For Better, and For Worse”
Wohleb, E. S. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00544 · Cited by 164 · see citing works
Distinct Oral Neutrophil Subsets Define Health and Periodontal Disease States
Fine, N., Hassanpour, S., Borenstein, A., Sima, C., Oveisi, M., Scholey, J., Cherney, D., & Glogauer, M. (2016) · Journal of Dental Research · doi:10.1177/0022034516645564 · Cited by 163 · see citing works
Targeting the complement system for the management of retinal inflammatory and degenerative diseases
Xu, H., & Chen, M. (2016) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2016.03.001 · Cited by 162 · see citing works
Martins, S. G., Zilhão, R., Þorsteinsdóttir, S., & Carlos, A. R. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.673002 · Cited by 160 · see citing works
Shen-Orr, S. S., Furman, D., Kidd, B. A., Hadad, F., Lovelace, P., Huang, Y.-W., Rosenberg-Hasson, Y., Mackey, S., Grisar, F. A. G., Pickman, Y., et al. (2016) · Cell Systems · doi:10.1016/j.cels.2016.09.009 · Cited by 154 · see citing works
Disease Tolerance as an Inherent Component of Immunity
Martins, R., Carlos, A. R., Braza, F., Thompson, J. A., Bastos-Amador, P., Ramos, S., & Soares, M. P. (2019) · Annual Review of Immunology · doi:10.1146/annurev-immunol-042718-041739 · Cited by 149 · see citing works
Red alert: labile heme is an alarmin
Soares, M. P., & Bozza, M. T. (2016) · Current Opinion in Immunology · doi:10.1016/j.coi.2015.11.006 · Cited by 148 · see citing works
Physiologic disruption and metabolic reprogramming in infection and sepsis
Willmann, K. L., & Moita, L. F. (2024) · Cell Metabolism · doi:10.1016/j.cmet.2024.02.013 · Cited by 145 · see citing works
Picca, A., Lezza, A. M. S., Leeuwenburgh, C., Pesce, V., Calvani, R., Bossola, M., Manes-Gravina, E., Landi, F., Bernabei, R., & Marzetti, E. (2018) · Rejuvenation Research · doi:10.1089/rej.2017.1989 · Cited by 144 · see citing works
Inflammation: A New Look at an Old Problem
Gusev, E., & Zhuravleva, Y. A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094596 · Cited by 142 · see citing works
Brain-spleen axis in health and diseases: A review and future perspective
Wei, Y., Wang, T., Liao, L., Fan, X., Chang, L., & Hashimoto, K. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2022.02.008 · Cited by 134 · see citing works
The immune system and psychiatric disease: a basic science perspective
Bennett, F. C., & Molofsky, A. V. (2019) · Clinical & Experimental Immunology · doi:10.1111/cei.13334 · Cited by 133 · see citing works
Inflammatory phenotypes in the intestine of poultry: not all inflammation is created equal
Kogut, M. H., Genovese, K. J., Swaggerty, C. L., He, H., & Broom, L. J. (2018) · Poultry Science · doi:10.3382/ps/pey087 · Cited by 132 · see citing works
Impacts of marine heat extremes on bivalves
Masanja, F., Yang, K., Xu, Y., He, G., Liu, X., Xu, X., Xiaoyan, J., Xin, L., Mkuye, R., Deng, Y., et al. (2023) · Frontiers in Marine Science · doi:10.3389/fmars.2023.1159261 · Cited by 132 · see citing works
Kulkarni, N., Jain, P., Shindikar, A., Suryawanshi, P., & Thorat, N. D. (2022) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2022.119351 · Cited by 126 · see citing works
Synthetic Immunology: Hacking Immune Cells to Expand Their Therapeutic Capabilities
Roybal, K. T., & Lim, W. A. (2017) · Annual Review of Immunology · doi:10.1146/annurev-immunol-051116-052302 · Cited by 124 · see citing works
Phull, A. R., Ahmed, M., & Park, H.-J. (2022) · Microorganisms · doi:10.3390/microorganisms10020405 · Cited by 124 · see citing works
Batistel, F., Arroyo, J. M., Garcés, C., Trevisi, E., Parys, C., Ballou, M., Cardoso, F. C., & Loor, J. J. (2017) · Journal of Dairy Science · doi:10.3168/jds.2017-13185 · Cited by 122 · see citing works
Maekawa, T., Hosur, K. B., Abe, T., Kantarcı, A., Ziogas, A., Wang, B., Dyke, T. E. V., Chavakis, T., & Hajishengallis, G. (2015) · Nature Communications · doi:10.1038/ncomms9272 · Cited by 121 · see citing works
Inflammatory and Immune Responses in the Arterial Media
Tellides, G., & Pober, J. S. (2015) · Circulation Research · doi:10.1161/circresaha.116.301312 · Cited by 117 · see citing works
Kerr, N. A., Vaccari, J. P. D. R., Abbassi, S., Kaur, H., Zambrano, R. A. P., WU, S. M., Dietrich, W. D., & Keane, R. W. (2018) · Journal of Neurotrauma · doi:10.1089/neu.2017.5430 · Cited by 116 · see citing works
The innate immune system in diabetic retinopathy
Pan, W. W., Lin, F., & Fort, P. E. (2021) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2021.100940 · Cited by 115 · see citing works
The challenges of primary biliary cholangitis: What is new and what needs to be done
Terziroli Beretta-Piccoli, B., Mieli-Vergani, G., Vergani, D., Vierling, J. M., Adams, D., Alpini, G., Banales, J. M., Beuers, U., Björnsson, E., Bowlus, C., et al. (2019) · Journal of Autoimmunity · doi:10.1016/j.jaut.2019.102328 · Cited by 114 · see citing works
Currais, A. J. M., Fischer, W. H., Maher, P. A., & Schubert, D. A. (2016) · The FASEB Journal · doi:10.1096/fj.201601184 · Cited by 114 · see citing works
Functional roles and mechanisms of ginsenosides from Panax ginseng in atherosclerosis
Xue, Q., He, N., Wang, Z., Fu, X., Aung, L. H. H., Liu, Y., Li, M., Cho, J. Y., Yang, Y., & Yu, T. (2020) · Journal of Ginseng Research · doi:10.1016/j.jgr.2020.07.002 · Cited by 112 · see citing works
Jang, W. Y., Hwang, J. Y., & Cho, J. Y. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076119 · Cited by 113 · see citing works
The Acute-on-Chronic Liver Failure Syndrome, or When the Innate Immune System Goes Astray
Clària, J., Arroyo, V., & Moreau, R. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1600818 · Cited by 111 · see citing works
Mouse pancreatic islet macrophages use locally released ATP to monitor beta cell activity
Weitz, J., Makhmutova, M., Almaça, J., Stertmann, J., Aamodt, K. I., Briššová, M., Speier, S., Rodriguez‐Diaz, R., & Caicedo, A. (2017) · Diabetologia · doi:10.1007/s00125-017-4416-y · Cited by 111 · see citing works
Li, J., Yao, Y.-M., & Tian, Y. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.701163 · Cited by 109 · see citing works
The discontinuity theory of immunity
Pradeu, T., & Vivier, É. (2016) · Science Immunology · doi:10.1126/sciimmunol.aag0479 · Cited by 108 · see citing works
Role of Inflammatory Cells in Fibroblast Activation
Hartupee, J., & Mann, D. (2015) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2015.11.016 · Cited by 97 · see citing works
Inflammation and its resolution and the musculoskeletal system
Gallo, J., Raška, M., Kriegová, E., & Goodman, S. B. (2017) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2017.05.007 · Cited by 107 · see citing works
Chronic Low-grade Inflammatory Phenotype (CLIP) and Senescent Immune Dysregulation
Chen, Y., Liu, S., & Leng, S. X. (2019) · Clinical Therapeutics · doi:10.1016/j.clinthera.2019.02.001 · Cited by 107 · see citing works
Widespread parainflammation in human cancer
Aran, D., Lasry, A., Zinger, A., Biton, M., Pikarsky, E., Hellman, A., Butte, A. J., & Ben‐Neriah, Y. (2016) · Genome biology · doi:10.1186/s13059-016-0995-z · Cited by 104 · see citing works
C/EBPβ: The structure, regulation, and its roles in inflammation-related diseases
Ren, Q., Liu, Z., Wu, L., Yin, G., Xie, X., Kong, W., Zhou, J., & Liu, S. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115938 · Cited by 104 · see citing works
Oxy-nitroso shielding burst model of cold atmospheric plasma therapeutics
Graves, D. B. (2014) · Clinical Plasma Medicine · doi:10.1016/j.cpme.2014.11.001 · Cited by 103 · see citing works
Constrained Mixture Models of Soft Tissue Growth and Remodeling – Twenty Years After
Humphrey, J. D. (2021) · Journal of Elasticity · doi:10.1007/s10659-020-09809-1 · Cited by 103 · see citing works
Electrochromic Sensors Based on Conducting Polymers, Metal Oxides, and Coordination Complexes
Celiešiūtė, R., Ramanavičienė, A., Gicevičius, M., & Ramanavičius, A. (2018) · Critical Reviews in Analytical Chemistry · doi:10.1080/10408347.2018.1499009 · Cited by 102 · see citing works
Ulven, S. M., Holven, K. B., Gil, Á., & Rangel-Huerta, Ó. D. (2018) · Advances in Nutrition · doi:10.1093/advances/nmy072 · Cited by 101 · see citing works
Paraspeckle nuclear condensates: Global sensors of cell stress?
McCluggage, F., & Fox, A. H. (2021) · BioEssays · doi:10.1002/bies.202000245 · Cited by 101 · see citing works
Hyperthermia and protein homeostasis: Cytoprotection and cell death
Ahmed, K., Zaidi, S. F., Mati-ur-Rehman, Rehman, R. A., & Kondo, T. (2020) · Journal of Thermal Biology · doi:10.1016/j.jtherbio.2020.102615 · Cited by 100 · see citing works
PKCα-LSD1-NF-κB-Signaling Cascade Is Crucial for Epigenetic Control of the Inflammatory Response
Kim, D., Nam, H. J., Lee, W., Yim, H. Y., Ahn, J.-Y., Park, S. W., Shin, H. R., Yu, R., Won, K., Bae, J., et al. (2018) · Molecular Cell · doi:10.1016/j.molcel.2018.01.002 · Cited by 99 · see citing works
Impact of obesity and overweight on DNA stability: Few facts and many hypotheses
Setayesh, T., Nersesyan, A., Mišík, M., Ferk, F., Langie, S., Andrade, V. M., Haslberger, A., & Knasmüller, S. (2018) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2018.07.001 · Cited by 98 · see citing works
Kostenko, V. О., Akimov, O. Y., Gutnik, O. M., Kostenko, H., Kostenko, V., Romantseva, T. O., Morhun, Y., Nazarenko, S. M., & Taran, O. V. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e15551 · Cited by 97 · see citing works
Guthrie, L. N., Abiraman, K., Plyler, E. S., Sprenkle, N. T., Gibson, S. A., McFarland, B. C., Rajbhandari, R., Rowse, A. L., Benveniste, E. N., & Meares, G. P. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.738021 · Cited by 97 · see citing works
- Authors
- Chovatiya, R., & Medzhitov, R.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Medzhitov, Ruslan
- Venue
- Molecular Cell
- Publisher
- Elsevier BV
- Published
- 2014-04
- Volume
- 54
- Issue
- 2
- Pages
- 281-288
- ISSN
- 1097-2765 (ISSN-L)
- PMC
- PMC4048989
- OpenAlex
- W1975024842
- Cited by
- 704
- References
- 54
- Citations by year
- 2026: 42 · 2025: 66 · 2024: 60 · 2023: 57 · 2022: 80 · 2021: 72 · 2020: 63 · 2019: 64 · 2018: 54 · 2017: 54 · 2016: 51 · 2015: 31 · 2014: 8 · 2013: 1
- FWCI
- 4.69
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Molecular Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Howard Hughes Medical Institute
- Blavatnik Family Foundation
- National Institutes of Health (AI046688)
- National Institute of General Medical Sciences (T32GM007205)
- National Institute of Allergy and Infectious Diseases (R37AI046688, AI046688)
- 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 › Cancer Research › NF-κB Signaling Pathways
- Keywords
- inflammation, homeostasis, tissue stress, stress response, tissue adaptation
- MeSH terms
- Gene Expression Regulation, HeLa Cells, Homeostasis, Humans, Inflammation, Models, Biological, Stress, Physiological
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