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Genomic and nongenomic effects of glucocorticoids
Abstract
The strong anti-inflammatory and immunosuppressive effects of glucocorticoids are mediated primarily by the cytosolic glucocorticoid receptors. These receptors are members of the steroid hormone receptor family, a superfamily of ligand-inducible transcription factors, and exert genomic effects that can result in increased expression of regulatory-including anti-inflammatory-proteins (transactivation), or decreased production of proinflammatory proteins (transrepression). Transactivation is thought to be responsible for numerous adverse effects of glucocorticoids; transrepression is thought to be responsible for many of the clinically desirable anti-inflammatory and immunosuppressive effects of glucocorticoids. Optimized glucocorticoids, such as selective glucocorticoid receptor agonists, are being developed to try to minimize the adverse effects many patients experience. Glucocorticoids also exert their effects via rapid, nongenomic mechanisms that can be classified as involving nonspecific interactions of glucocorticoids with cellular membranes, nongenomic effects that are mediated by cytosolic glucocorticoid receptors, or specific interactions with membrane-bound glucocorticoid receptors. Increased understanding of these mechanisms of glucocorticoid action could enable the development of novel drugs with which to treat patients with inflammatory and autoimmune disease.
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“In contrast, GR-β permanently resides in the nucleus where it selectively acts as a dominant negative inhibitor of GR-α (75). The relative abundance of the inhibitor GR-β, which normally represents only 1% of GR-α in the brain, is thus a key parameter in dictating GC responsiveness (76).”
From The HPA – Immune Axis and the Immunomodulatory Actions of Glucocorticoids in the Brain (2014) · cites this paper as [76]
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“…corticosteroid receptors (mCR) have been detected in human peripheral blood mononuclear cells (Tryc et al., 2006), T cells (Löwenberg et al., 2008), and murine lymphoma cells (Gametchu, 1987; Gametchu et al., 1999) and may mediate GC-induced apoptosis (Stahn and Buttgereit, 2008).”
InfluentialThe Endocrine System and Alcohol Drinking in Females
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“GCs exert their anti-inflammatory and immunosuppressive roles by two different mechanisms: the genomic pathway and the non-genomic pathway [4].”
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“This negative feedback occurs when GCs penetrate the blood–brain barrier and exert rapid (non-genomic) and slower (genomic) effects on the various neural regions that regulate ACTH release [ 24 , 38 , 101 ].”
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“GCs exert their anti-inflammatory and immunosuppressive effects on immune cells, tissues and organs via different genomic and non-genomic mechanisms [6].”
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“Finally, the accumulation of highly lipophilic GC molecules in plasma membrane was postulated, which alters the function of membrane integral proteins such as ion channels or receptors (65).”
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“intensified (and partly different) mechanisms of GC action [12,13].”
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“It is important to note that GR activation by glucocorticoids has been shown to suppress the migration of immune cells, highlighting the tissue- and cell-specific roles of GR/phospho-GR (Stahn & Buttgereit 2008) and underscoring the need to select patients using appropriate biomarkers of phospho-GR signaling in GR+ TN…”
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“The GR can increase the expression of anti-inflammatory proteins (transactivation) or decrease the production of pro-inflammatory proteins (transrepression).(38) The”
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“These effects are mediated by the activation of glucocorticoid receptors (GR) and may involve both genomic and non-genomic mechanisms (Stahn and Buttgereit, 2008).”
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“level of GC that occurs under chronic stress conditions has a strong immunomodulating effect that is mediated primarily by cytosolic GC receptors (see [13] for review).”
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“Nongenomic GR signaling may be initiated by membrane-bound GRs, rather than those found within the cytoplasm (Stahn and Buttgereit, 2008).”
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“Furthermore, GC/cGCR monomers are able to negatively interfere with transcription factors (termed transrepression) such as NF-kB, activator protein-1 (AP-1) and nuclear factor for activated T cells (NFAT), subsequently reducing the expression of proinflammatory proteins like IL-1, IL-6 or TNFa [30,31].”
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“The corticosteroid-GR complex also elicits non-genomic effects, such as inhibition of vasodilation, vascular permeability, and migration of leukocytes.(2,4) In addition, corticosteroids mediate non-genomic anti-inflammatory effects by binding to membrane-bound GRs and through direct nonspecific interactions with cellu…”
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“A detailed explanation of the currently available data on immune mechanisms of GC is beyond the scope of this article and discussed thoroughly elsewhere (14).”
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“In addition to the genomic pathway, glucocorticoid can also mediate acute physiological effect without the genomic pathway (Croxtall et al., 2002; Tasker et al., 2006; Stahn and Buttgereit, 2008).”
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“High concentrations of steroids intercalate into the plasma and mitochondrial membranes of immune cells, thereby altering their physicochemical properties and the activities of membrane- associated proteins (25), which are believed to contribute to rapid immunosuppression.”
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“44 Corticosteroids also have rapid direct non-genomic mechanisms likely through heterogeneous receptors and pathways with similarly diverse impacts.”
Miljković, Ž., Momčilović, M., Miljković, D., & Mostarica-Stojković, M. (2009) · Journal of Neuroinflammation · doi:10.1186/1742-2094-6-37 · Cited by 35
“Recently, a new concept of non-genomic actions of glucocorticoids emerged which assumes that activated glucocorticoid receptor may produce effects without an action on gene transcription [reviewed in [18]].”
BackgroundGlucocorticoid-Induced Osteoporosis: A Review
Bouvard, B., Legrand, É., Audran, M., & Chappard, D. (2009) · Clinical Reviews in Bone and Mineral Metabolism · doi:10.1007/s12018-009-9051-9 · Cited by 37
“The human cGCR gene, located at chromosome 5q31.”
BackgroundInfluentialDahabiyeh, L. A., Malkawi, A. K., Wang, X., Çolak, D., Mujamammi, A. H., Sabi, E. M., Li, L., Dasouki, M., & Rahman, A. M. A. (2020) · Metabolites · doi:10.3390/metabo10020042 · Cited by 35
“GCs exert their biological effects by binding with GC receptors (GCRs) and activating genomic and non‐genomic pathways [3].”
BackgroundManagement of Lupus Nephritis: New Treatments and Updated Guidelines
Avasare, R. S., Drexler, Y. R., Caster, D. J., Mitrofanova, A. V., & Jefferson, J. A. (2023) · Kidney360 · doi:10.34067/kid.0000000000000230 · Cited by 34
“46 Thus, IV methylprednisolone pulses (up to a cumulative dose of 1 – 1.5 g) can rapidly induce both anti-in fl ammatory and immune effects, followed by reduced dose GCs to maintain immunosuppression.”
BackgroundInfluentialPharmacological therapies for acute respiratory distress syndrome
Spieth, P. M., & Zhang, H. (2013) · Current Opinion in Critical Care · doi:10.1097/mcc.0000000000000056 · Cited by 33
Localization and Dynamics of Glucocorticoid Receptor at the Plasma Membrane of Activated Mast Cells
Oppong, E. K., Hedde, P. N., Sekula‐Neuner, S., Yang, L., Brinkmann, F., Dörlich, R. M., Hirtz, M., Fuchs, H., Nienhaus, G. U., & Cato, A. C. B. (2014) · Small · doi:10.1002/smll.201303677 · Cited by 34
Transcriptional Regulation of Human Transforming Growth Factor-α in Astrocytes
Karki, P., Johnson, J., Son, D., Aschner, M., & Lee, E.-S. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-9705-9 · Cited by 34
“plex, followed by the complex’s binding to the promoter region where the GRE cis-element is located, resulting in modulation of gene transcriptions of interest [65].”
Lehloenya, R. J., Isaacs, T., Nyika, D. T., Dhana, A. V., Knight, L., Veenstra, S. H., & Peter, J. (2020) · The Journal of Allergy and Clinical Immunology In Practice · doi:10.1016/j.jaip.2020.08.012 · Cited by 34
Kuperminc, E., Heming, N., Carlos, M., & Annane, D. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12093340 · Cited by 40
“Cellular effects of corticosteroids are mediated by both genomic and non-genomic signaling pathways [34].”
BackgroundPérez, M. H., Cormack, J., Mallinson, D. J., & Mutungi, G. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2013.256586 · Cited by 36
“8; Barnes, 1998; Stahn & Buttgereit, 2008).”
BackgroundInfluentialWehmeyer, L., Toit, A. D., Lang, D. M., & Hapgood, J. P. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.544742 · Cited by 34
de Theije, C. C., Schols, A. M. W. J., Lamers, W. H., Ceelen, J., van Gorp, R. H., Hermans, J. J. R., Köhler, E. S., & LANGEN, R. C. J. (2017) · Endocrinology · doi:10.1210/en.2017-00603 · Cited by 33
Glucocorticoid-Like Activity of Escin: A New Mechanism for an Old Drug
Gallelli, L., Cione, E., Wang, T., & Zhang, L. (2021) · Drug Design Development and Therapy · doi:10.2147/dddt.s297501 · Cited by 33
“cates together with its ligand into the nucleus within 10 to 30 min.(10) In the nucleus, homodimers of the glucocorti-”
BackgroundJurgens, M. S., Jacobs, J. W. G., Geenen, R., Bossema, E. R., Bakker, M. F., Bijlsma, J. W. J., van Albada‐Kuipers, I. A., Ehrlich, J. C., Lafeber, F. P. J. G., Welsing, P. M. J., et al. (2012) · Arthritis Care & Research · doi:10.1002/acr.21797 · Cited by 31
“We cannot distinguish between individual hypothetical effects explaining weight gain, such as GCinduced increase of appetite or metabolic effects, via the genomic mechanism of transactivation (17,18), and diminished cytokine-induced weight loss.”
BackgroundFokidis, H. B., Adomat, H. H., Kharmate, G., Beheshti, E. H., Guns, E. S. T., & Soma, K. K. (2014) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2014.08.005 · Cited by 31
“, 2004), which can require high doses (Stahn and Buttgereit, 2008).”
BackgroundWill we ever have better glucocorticoids?
Buttgereit, F., Bijlsma, J. W. J., & Strehl, C. (2017) · Clinical Immunology · doi:10.1016/j.clim.2017.07.023 · Cited by 31
Murata, I., Ooi, K., Shoji, S., Motohashi, Y., Kan, M., Ohtake, K., Kimura, S., UEDA, H. M. D., Nakano, G., Sonoda, K., et al. (2013) · The Journal of Trauma: Injury, Infection, and Critical Care · doi:10.1097/ta.0b013e3182905f11 · Cited by 31
“In addition to the local nongenomic signaling mediated by DEX (as discussed previously), DEX also exerts its antiinflammatory actions at the transcriptional level via the genomic pathway by either direct or indirect interactions with transcription factors, such as nuclear factor-kappa B and activator protein 1.(24) Wh…”
BackgroundZaydfudim, V. M., Feurer, I. D., Landman, M. P., Moore, D. E., Wright, K. J., & Pinson, W. C. (2011) · Journal of the American College of Surgeons · doi:10.1016/j.jamcollsurg.2011.10.006 · Cited by 30
“These effects are notably dose-dependent and are also influenced by the duration of treatment.(16,17) We aimed to test the association between the dosedependent effects of corticosteroids and health-related quality of life after liver transplantation.”
As-needed ICS-LABA in Mild Asthma: What Does the Evidence Say?
Domingo, C., Rello, J., & Sogo, A. (2019) · Drugs · doi:10.1007/s40265-019-01202-0 · Cited by 30
Diffuse Alveolar Hemorrhage After Pediatric Hematopoietic Stem Cell Transplantation
Fan, K., McArthur, J. A., Morrison, R. R., & Ghafoor, S. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.01757 · Cited by 30
“Glucocorticoids inhibit the cycling of sodium and calcium across the plasma membrane, reducing the availability of intracellular free calcium, which inhibits neutrophil degranulation (58, 60, 66).”
BackgroundInfluentialMaranville, J., Baxter, S. S., Witonsky, D., Chase, M., & Rienzo, A. D. (2013) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2013.08.005 · Cited by 28
Maranville, J., Baxter, S. S., Torres, J., & Rienzo, A. D. (2011) · The Pharmacogenomics Journal · doi:10.1038/tpj.2011.55 · Cited by 29
“direct disruption of cell membranes or interaction or modulation of T cell receptor activity (27)), they act primarily through the regulation of gene expression (28).”
Genomic effects of glucocorticoids
Grbeša, I., & Hakim, O. (2016) · PROTOPLASMA · doi:10.1007/s00709-016-1063-y · Cited by 30
“Other, non-genomic activities of GCs have been discussed elsewhere (Stahn and Buttgereit 2008; Alangari 2010; Zen et al. 2011).”
BackgroundDexamethasone premedication suppresses vaccine-induced immune responses against cancer
Vormehr, M., Lehar, S. M., Kranz, L. M., Tähtinen, S., Oei, Y. A., Javinal, V., Delamarre, L., Walzer, K. C., Diken, M., Kreiter, S., et al. (2020) · OncoImmunology · doi:10.1080/2162402x.2020.1758004 · Cited by 28
“Moreover, direct interactions with a variety of pathways have been described.(2-5) As a result, GCS have a plethora of downstream effects and can modulate the immune system in various ways, which are still not fully understood.”
BackgroundEpigenetics, pregnancy and autoimmune rheumatic diseases
Pacini, G., Paolino, S., Andréoli, L., Tincani, A., Gerosa, M., Caporali, R. F., Iagnocco, A., Ospelt, C., Smith, V. M., & Cutolo, M. (2020) · Autoimmunity Reviews · doi:10.1016/j.autrev.2020.102685 · Cited by 32
“It directly modulates virtually all immune cells, essentially exerting an antiinflammatory and immunomodulatory effect [87,88].”
BackgroundPanin, L. E., Mokrushnikov, P. V., Kunitsyn, V. G., & Зайцев, Б. Н. (2010) · The Journal of Physical Chemistry B · doi:10.1021/jp911917a · Cited by 29
Restoring immune suppression in the multiple sclerosis brain
Koning, N., Uitdehaag, B. M. J., Huitinga, I., & Hoek, R. M. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.09.005 · Cited by 28
“Glucocorticoids (GCs) are known for their broad anti-inflammatory properties (Stahn and Buttgereit, 2008).”
BackgroundHapgood, J. P., & Tomasicchio, M. (2010) · Archives of Virology · doi:10.1007/s00705-010-0678-0 · Cited by 28
“This can occur through direct DNA binding by the GR to glucocorticoid response elements (GREs) or via tethering to other transcription factors, thereby activating or repressing gene transcription [22, 23, 31, 32].”
BackgroundPsychological and endocrine factors and pain after mastectomy
Nishimura, D., Kosugi, S., Onishi, Y., Ihara, N., Wakaizumi, K., Nagata, H., Yamada, T., Suzuki, T., Hashiguchi, S., & Morisaki, H. (2017) · European Journal of Pain · doi:10.1002/ejp.1014 · Cited by 28
“Glucocorticoids are known to exert strong anti-inflammatory effects (Stahn and Buttgereit, 2008) and to inhibit the release of prostaglandins via the arachidonic acid pathway, and hence, play a role in the regulation of pain perception (Flower and Blackwell, 1979).”
Background
Metadata
- Authors
- Stahn, C., & Buttgereit, F.
- Affiliations
- Charité – Universitätsmedizin Berlin (DE)
- Berlin Institute of Health at Charité - Universitätsmedizin Berlin (DE)
- Corresponding author
- Buttgereit, Frank
- ORCID
- Buttgereit, Frank
- Venue
- Nature Clinical Practice Rheumatology
- Published
- 2008-09-02
- Volume
- 4
- Issue
- 10
- Pages
- 525-533
- ISSN
- 1745-8382 (ISSN-L)
- 1745-8390
- OpenAlex
- W1968436319
- Cited by
- 594
- References
- 65
- Citations by year
- 2026: 19 · 2025: 26 · 2024: 29 · 2023: 40 · 2022: 49 · 2021: 33 · 2020: 46 · 2019: 40 · 2018: 26 · 2017: 35 · 2016: 27 · 2015: 37 · 2014: 41 · 2013: 31 · 2012: 29
- FWCI
- 2.66
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Clinical Practice Rheumatology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Estrogen and related hormone effects
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Keywords
- glucocorticoids, glucocorticoid receptor, genomic mechanisms, transcriptional activation, transrepression, steroid hormone receptors, selective glucocorticoid receptor agonists, adverse effects, anti-inflammatory activity, immunosuppression, rheumatic diseases
- MeSH terms
- Anti-Inflammatory Agents, Cell Membrane, Dose-Response Relationship, Drug, Glucocorticoids, Humans, Immunosuppressive Agents, Ligands, Receptors, Glucocorticoid, Rheumatology, Transcriptional Activation, Genomics
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