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USP18 lack in microglia causes destructive interferonopathy of the mouse brain
Open accessAbstract
Microglia are tissue macrophages of the central nervous system (CNS) that control tissue homeostasis. Microglia dysregulation is thought to be causal for a group of neuropsychiatric, neurodegenerative and neuroinflammatory diseases, called "microgliopathies". However, how the intracellular stimulation machinery in microglia is controlled is poorly understood. Here, we identified the ubiquitin-specific protease (Usp) 18 in white matter microglia that essentially contributes to microglial quiescence. We further found that microglial Usp18 negatively regulates the activation of Stat1 and concomitant induction of interferon-induced genes, thereby terminating IFN signaling. The Usp18-mediated control was independent from its catalytic activity but instead required the interaction with Ifnar2. Additionally, the absence of Ifnar1 restored microglial activation, indicating a tonic IFN signal which needs to be negatively controlled by Usp18 under non-diseased conditions. These results identify Usp18 as a critical negative regulator of microglia activation and demonstrate a protective role of Usp18 for microglia function by regulating the Ifnar pathway. The findings establish Usp18 as a new molecule preventing destructive microgliopathy.
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“Inappropriate upregulation of type I IFN signaling and ISG expression in the CNS have been linked to several interferonopathies including Aicardi-Goutieres syndrome and ubiquitin specific peptidase 18 (USP18)-deficiency in humans.”
From Interferon signaling modulates Down syndrome-associated Alzheimer’s disease pathology in a mouse model (2025) · cites this paper as [81]
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“which inhibits microglial activation by specifically blocking IFN-induced transcription”
From Microglial depletion prevents extracellular matrix changes and striatal volume reduction in a model of Huntington's disease (2020) · cites this paper as Goldmann et al., 2015
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Cites
Amyloid oligomers exacerbate tau pathology in a mouse model of tauopathy
Selenica, M.-L. B., Brownlow, M., Jimenez, J. P., Lee, D. C., Pena, G., Dickey, C. A., Gordon, M. N., & Morgan, D. (2013) · Neurodegenerative Diseases · doi:10.1159/000337230 · Cited by 10,359
Polazzi, E., Mengoni, I., Caprini, M., Peña‐Altamira, E., Kurtys, E., & Monti, B. (2012) · Neurosignals · doi:10.1159/000337115 · Cited by 9,023
Hershko, A., & Ciechanover, A. (1998) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.67.1.425 · Cited by 8,840
Defective LPS Signaling in C3H/HeJ and C57BL/10ScCr Mice: Mutations in Tlr4 Gene
Poltorak, A., He, X., Smirnova, I., Liu, M.-Y., Huffel, C. V., Du, X., Birdwell, D., Alejos, E., Silva, M., Galanos, C., et al. (1998) · Science · doi:10.1126/science.282.5396.2085 · Cited by 7,631
Microglia: Active sensor and versatile effector cells in the normal and pathologic brain
Hanisch, U.-K., & Kettenmann, H. (2007) · Nature Neuroscience · doi:10.1038/nn1997 · Cited by 3,676
Fate Mapping Reveals Origins and Dynamics of Monocytes and Tissue Macrophages under Homeostasis
Yona, S., Kim, K.-W., Wolf, Y., Mildner, A., Varol, D., Breker, M., Strauss-Ayali, D., Viukov, S., Guilliams, M., Misharin, A., et al. (2013) · Immunity · doi:10.1016/j.immuni.2012.12.001 · Cited by 3,245
Initiative, T. A. D. N., Hollingworth, P., CHARGE consortium, EADI1 consortium, Harold, D., Sims, R., Gerrish, A., Lambert, J.-C., Carrasquillo, M. M., Abraham, R., et al. (2011) · Nature Genetics · doi:10.1038/ng.803 · Cited by 1,997
Naj, A. C., Jun, G., Beecham, G. W., Wang, L.-S., Vardarajan, B. N., Buros, J., Gallins, P. J., Buxbaum, J. D., Jarvik, G. P., Crane, P. K., et al. (2011) · Nature Genetics · doi:10.1038/ng.801 · Cited by 1,901
Microglial physiology: unique stimuli, specialized responses
Ransohoff, R. M., & Perry, V. H. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132528 · Cited by 1,858
von Büdingen, H. ‐., Palanichamy, A., Lehmann‐Horn, K., Michel, B., & Zamvil, S. S. (2015) · European Neurology · doi:10.1159/000377675 · Cited by 1,475
Microglia emerge from erythromyeloid precursors via Pu.1- and Irf8-dependent pathways
Kierdorf, K., Erny, D., Goldmann, T., Sander, V., Schulz, C., Perdiguero, E. G., Wieghofer, P., Heinrich, A., Riemke, P., Hölscher, C., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3318 · Cited by 1,457
Self-citationType I Inteferon Gene Induction by the Interferon Regulatory Factor Family of Transcription Factors
Honda, K., Takaoka, A., & Taniguchi, T. (2006) · Immunity · doi:10.1016/j.immuni.2006.08.009 · Cited by 1,386
Microglia and brain macrophages in the molecular age: from origin to neuropsychiatric disease
Prinz, M., & Priller, J. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3722 · Cited by 1,329
Self-citationImmunomodulatory functions of type I interferons
González-Navajas, J. M., Lee, J., David, M., & Raz, E. (2012) · Nature reviews. Immunology · doi:10.1038/nri3133 · Cited by 1,030
The tumour suppressor CYLD negatively regulates NF-κB signalling by deubiquitination
Kovalenko, A., Chable-Bessia, C., Cantarella, G., Israël, A., Wallach, D., & Courtois, G. (2003) · Nature · doi:10.1038/nature01802 · Cited by 1,018
CYLD is a deubiquitinating enzyme that negatively regulates NF-κB activation by TNFR family members
Trompouki, E., Hatzivassiliou, E., Tsichritzis, T., Farmer, H., Ashworth, A., & Mosialos, G. (2003) · Nature · doi:10.1038/nature01803 · Cited by 964
Loss of the cylindromatosis tumour suppressor inhibits apoptosis by activating NF-κB
Brummelkamp, T. R., Nijman, S. M. B., Dirac, A. M. G., & Bernards, R. (2003) · Nature · doi:10.1038/nature01811 · Cited by 947
Selective transfer of exosomes from oligodendrocytes to microglia by macropinocytosis
Fitzner, D., Schnaars, M., van Rossum, D., Krishnamoorthy, G., Dibaj, P., Bakhti, M., Regen, T., Hanisch, U.-K., & Simons, M. (2011) · Journal of Cell Science · doi:10.1242/jcs.074088 · Cited by 866
International MS Genetics Consortium, De Jager, P. L., Jia, X., Wang, J., de Bakker, P. I. W., Ottoboni, L., Aggarwal, N. T., Piccio, L., Raychaudhuri, S., Tran, D., et al. (2009) · Nature Genetics · doi:10.1038/ng.401 · Cited by 800
Lgr6 Marks Stem Cells in the Hair Follicle That Generate All Cell Lineages of the Skin
Snippert, H. J., Haegebarth, A., Kasper, M., Jaks, V., van Es, J. H., Barker, N., van de Wetering, M., van den Born, M., Begthel, H., Vries, R. G., et al. (2010) · Science · doi:10.1126/science.1184733 · Cited by 751
A new type of microglia gene targeting shows TAK1 to be pivotal in CNS autoimmune inflammation
Goldmann, T., Wieghofer, P., Müller, P. F., Wolf, Y., Varol, D., Yona, S., Brendecke, S. M., Kierdorf, K., Staszewski, O., Datta, M., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3531 · Cited by 688
Self-citationInteractions Between Gut Microbiota and Host Metabolism Predisposing to Obesity and Diabetes
Musso, G., Gambino, R., & Cassader, M. (2011) · Annual Review of Medicine · doi:10.1146/annurev-med-012510-175505 · Cited by 598
Luther, K., Torosantucci, A., Brakhage, A. A., Heesemann, J., & Ebel, F. (2006) · Cellular Microbiology · doi:10.1111/j.1462-5822.2006.00796.x · Cited by 582
Rademakers, R., Baker, M., Nicholson, A. M., Rutherford, N. J., Finch, N., Soto-Ortolaza, A., Lash, J., Wider, C., Wojtas, A., DeJesus-Hernandez, M., et al. (2012) · Nature Genetics · doi:10.1038/ng.1027 · Cited by 571
Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation
Zhang, X., Bogunovic, D., Payelle-Brogard, B., Francois-Newton, V., Speer, S. D., Yuan, C., Volpi, S., Li, Z., Sanal, O., Mansouri, D., et al. (2015) · Nature · doi:10.1038/nature13801 · Cited by 558
UBP43 (USP18) Specifically Removes ISG15 from Conjugated Proteins
Malakhov, M. P., Malakhova, O. A., Kim, K. I., Ritchie, K. J., & Zhang, D. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m109078200 · Cited by 531
Gall, A., Treuting, P., Elkon, K. B., Loo, Y.-M., Gale, M., Barber, G. N., & Stetson, D. B. (2012) · Immunity · doi:10.1016/j.immuni.2011.11.018 · Cited by 510
Constitutive Type I Interferon Modulates Homeostatic Balance through Tonic Signaling
Gough, D. J., Messina, N. L., Clarke, C. J. P., Johnstone, R. W., & Levy, D. E. (2012) · Immunity · doi:10.1016/j.immuni.2012.01.011 · Cited by 492
Mildner, A., Mack, M., Schmidt, H., Brück, W., Djukic, M., Zabel, M. D., Hille, A., Priller, J., & Prinz, M. (2009) · Brain · doi:10.1093/brain/awp144 · Cited by 445
Self-citationUBP43 is a novel regulator of interferon signaling independent of its ISG15 isopeptidase activity
Malakhova, O. A., Kim, K. I. I., Luo, J.-K., Zou, W., Kumar, K. G., Fuchs, S. Y., Shuai, K., & Zhang, D. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601149 · Cited by 443
Prinz, M., Schmidt, H., Mildner, A., Knobeloch, K., Hanisch, U., Raasch, J., Merkler, D., Detje, C. N., Gutcher, I., Mages, J., et al. (2008) · Immunity · doi:10.1016/j.immuni.2008.03.011 · Cited by 387
Self-citationHwang, S. Y., Hertzog, P. J., Holland, K. A., Sumarsono, S. H., Tymms, M. J., Hamilton, J. A., Whitty, G. A., Bertoncello, I., & Kola, I. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.24.11284 · Cited by 378
Guerreiro, R. J., Lohmann, E., Brás, J. M., Gibbs, J. R., Rohrer, J. D., Gurunlian, N., Dursun, B., Bilgic, B., Hanagasi, H., Gurvit, H., et al. (2013) · JAMA Neurology · doi:10.1001/jamaneurol.2013.579 · Cited by 374 · cited 1×
“…as Csf1r in hereditary diffuse leukoencephalopathy with spheroids (Rademakers et al , 2012), CD33 in Alzheimer’s disease (Hollingworth et al , 2011; Naj et al , 2011), Trem2 in frontotemporal dementia (Guerreiro et al , 2013), and Tnfrsf1a and Irf8 in multiple sclerosis (De Jager et al , 2009).”
Identification of a microglia phenotype supportive of remyelination
Olah, M., Amor, S., Brouwer, N., Vinet, J., Eggen, B., Biber, K., & Boddeke, H. W. G. M. (2012) · Glia · doi:10.1002/glia.21266 · Cited by 358
Self-citationDeubiquitylation and regulation of the immune response
Sun, S. (2008) · Nature reviews. Immunology · doi:10.1038/nri2337 · Cited by 356
Type I IFN Contributes to NK Cell Homeostasis, Activation, and Antitumor Function
Swann, J. B., Hayakawa, Y., Zerafa, N., Sheehan, K. C. F., Scott, B., Schreiber, R. D., Hertzog, P. J., & Smyth, M. J. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.12.7540 · Cited by 340
Protein ISGylation modulates the JAK-STAT signaling pathwayPreprint
Malakhova, O. A., Yan, M., Malakhov, M. P., Yuan, Y., Ritchie, K. J., Kim, K. I., Peterson, L. F., Shuai, K., & Zhang, D. (2003) · Genes & Development · doi:10.1101/gad.1056303 · Cited by 317
Immunity by ubiquitylation: a reversible process of modification
Liu, Y., Penninger, J. M., & Karin, M. (2005) · Nature reviews. Immunology · doi:10.1038/nri1731 · Cited by 260
Reiley, W. W., Jin, W., Lee, A. J., Wright, A., Wu, X., Tewalt, E. F., Leonard, T. O., Norbury, C. C., Fitzpatrick, L. R., Zhang, M., et al. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20062694 · Cited by 255
Regulation of T cell development by the deubiquitinating enzyme CYLD
Reiley, W. W., Zhang, M., Jin, W., Losiewicz, M., Donohue, K. B., Norbury, C. C., & Sun, S.-C. (2006) · Nature Immunology · doi:10.1038/ni1315 · Cited by 198
Functional diversity of microglia – how heterogeneous are they to begin with?
Hanisch, U.-K. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00065 · Cited by 195
Type I interferonopathies: Mendelian type I interferon up-regulation
Crow, Y. J. (2014) · Current Opinion in Immunology · doi:10.1016/j.coi.2014.10.005 · Cited by 194
Schulz, S., Chachami, G., Kozaczkiewicz, L., Winter, U., Stankovic‐Valentin, N., Haas, P., Hofmann, K., Urlaub, H., Ovaa, H., Wittbrodt, J., et al. (2012) · EMBO Reports · doi:10.1038/embor.2012.125 · Cited by 184
Altorok, N., Coit, P., Hughes, T. K., Koelsch, K. A., Stone, D. U., Rasmussen, A., Radfar, L., Scofield, R. H., Sivils, K. L. M., Farris, A. D., et al. (2013) · Arthritis & Rheumatology · doi:10.1002/art.38264 · Cited by 171
Dysregulation of protein modification by ISG15 results in brain cell injuryPreprint
Ritchie, K. J., Malakhov, M. P., Hetherington, C. J., Zhou, L., Little, M.-T., Malakhova, O. A., Sipe, J. C., Orkin, S. H., & Zhang, D. (2002) · Genes & Development · doi:10.1101/gad.1010202 · Cited by 159
Candidate genes for type 1 diabetes modulate pancreatic islet inflammation and β ‐cell apoptosis
Santín, I., & Eizirik, D. L. (2013) · Diabetes Obesity and Metabolism · doi:10.1111/dom.12162 · Cited by 143
Liu, X., Li, H., Zhong, B., Blonska, M., Gorjestani, S., Yan, M., Tian, Q., Zhang, D., Lin, X., & Dong, C. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20122327 · Cited by 130
Ketscher, L., Hannß, R., Morales, D. J., Basters, A., Guerra, S., Goldmann, T., Hausmann, A., Prinz, M., Naumann, R., Pekosz, A. S., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1412881112 · Cited by 128
Self-citationThe deubiquitinase activity of A20 is dispensable for NF‐κB signaling
De, A., Dainichi, T., Rathinam, C. V., & Ghosh, S. (2014) · EMBO Reports · doi:10.15252/embr.201338305 · Cited by 125
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Wieghofer, P., Knobeloch, K., & Prinz, M. (2014) · Glia · doi:10.1002/glia.22727 · Cited by 118
Self-citationRaasch, J., Zeller, N., van Loo, G., Merkler, D., Mildner, A., Erny, D., Knobeloch, K.-P., Bethea, J. R., Waisman, A., Knust, M., et al. (2011) · Brain · doi:10.1093/brain/awq359 · Cited by 106
Self-citationHristova, M., Cuthill, D., Zbarsky, V., Acosta‐Saltos, A., Wallace, A. S., Blight, K., Buckley, S. M. K., Peebles, D., Heuer, H., Waddington, S. N., et al. (2009) · Glia · doi:10.1002/glia.20896 · Cited by 105
Honke, N., Shaabani, N., Zhang, D., Iliakis, G. E., Xu, H. C., Häussinger, D., Recher, M., Löhning, M., Lang, P. A., & Lang, K. S. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003650 · Cited by 63
Basters, A., Geurink, P. P., Oualid, F. E., Ketscher, L., Casutt, M. S., Krause, E., Ovaa, H., Knobeloch, K., & Fritz, G. (2014) · FEBS Journal · doi:10.1111/febs.12754 · Cited by 62
Self-citationVogel, S. N., & Fertsch, D. (1984) · Infection and Immunity · doi:10.1128/iai.45.2.417-423.1984 · Cited by 53
Search for Specific Biomarkers of IFNβ Bioactivity in Patients with Multiple Sclerosis
Malhotra, S., Bustamante, M. F., Miralles, F. C. P., Río, J., de Villa, M. C. R., Vegas, E., Nonell, L., Deisenhammer, F., Fissolo, N., Nurtdinov, R., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023634 · Cited by 52
Richer, É., Prendergast, C., Zhang, D., Qureshi, S. T., Vidal, S. M., & Malo, D. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000890 · Cited by 41
Self-citationMalhotra, S., Morcillo-Suárez, C., Nurtdinov, R., Río, J., Sarró, E., Moreno, M., Castilló, J., Navarro, A., Montalbán, X., & Comabella, M. (2013) · European Journal of Neurology · doi:10.1111/ene.12193 · Cited by 39
Type I Interferons as Ambiguous Modulators of Chronic Inflammation in the Central Nervous System
Prinz, M., & Knobeloch, K. (2012) · Frontiers in Immunology · doi:10.3389/fimmu.2012.00067 · Cited by 36
Self-citationDiagnostic criteria for primary progressive mutiple sclerosis: a position paper.
(2000) · Pure Amsterdam UMC · doi:10.1002/1531-8249(200006)47:6 · Cited by 2
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Metadata
- Authors
- Goldmann, T., Zeller, N., Raasch, J., Kierdorf, K., Frenzel, K., Ketscher, L., Basters, A., Staszewski, O., Brendecke, S. M., Spiess, A., Tay, T. L., Kreutz, C., Timmer, J., Mancini, G. M., Blank, T., Fritz, G., Biber, K., Lang, R., Malo, D., Merkler, D., Heikenwälder, M., Knobeloch, K., & Prinz, M.
- Affiliations
- University of Freiburg (DE)
- Erasmus MC (NL)
- University Medical Center Groningen (NL)
- Universitätsklinikum Erlangen (DE)
- McGill University (CA)
- University of Geneva (CH)
- Helmholtz Munich (DE)
- Corresponding author
- Prinz, Marco
- ORCID
- Venue
- The EMBO Journal
- Published
- 2015-04-20
- Volume
- 34
- Issue
- 12
- Pages
- 1612-1629
- ISSN
- 0261-4189 (ISSN-L)
- 1460-2075
- PMC
- PMC4475397
- OpenAlex
- W2097365950
- Cited by
- 223
- References
- 60
- Citations by year
- 2026: 14 · 2025: 19 · 2024: 15 · 2023: 23 · 2022: 11 · 2021: 35 · 2020: 22 · 2019: 25 · 2018: 15 · 2017: 22 · 2016: 14 · 2015: 7
- FWCI
- 10.33
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The EMBO Journal (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
- Archive ouverte UNIGE (University of Geneva) (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- RePub (Erasmus University Rotterdam) (submittedVersion, other-oa)
- FreiDok plus (Universitätsbibliothek Freiburg) (submittedVersion)
- mediaTUM – the media and publications repository of the Technical University Munich (Technical University Munich) (submittedVersion)
- Site cant be reached (submittedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion)
- PuSH - Publication Server of Helmholtz Zentrum München (submittedVersion)
- RePub (Erasmus University Rotterdam) (submittedVersion)
- Archive ouverte UNIGE (University of Geneva) (submittedVersion, cc-by)
- Funders
- BMBF‐funded competence network of multiple sclerosis
- DFG (SFB 992, FOR1336, ZE 894/1‐1, PR 577/8‐1, KN590/3‐2 (SPP1365), KN590/1‐3)
- Fritz‐Thyssen Foundation
- Sobek Foundation
- Gemeinnützige Hertie Foundation
- ERA‐Net NEURON initiative “NEURO‐IFN”
- Canadian Institutes of Health Research (CTP‐87520)
- Swiss National Science Foundation (PP00P3_152928)
- Klaus‐Tschira Foundation
- Gebert‐Rüf Foundation
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Keywords
- USP18, microglia, interferon signaling, STAT1, IFNAR2, IFNAR1, deubiquitination, microglial activation, neuroinflammation, interferonopathies, anti-inflammatory regulation
- MeSH terms
- Animals, Brain, Cloning, Molecular, Histological Techniques, Interferons, Microscopy, Fluorescence, Models, Neurological, Endopeptidases, Blotting, Western, Signal Transduction, Microglia, DNA Primers, Mice, Knockout, Statistics, Nonparametric, Ubiquitin Thiolesterase, Microarray Analysis, Microscopy, Electron, Transmission, Mice, Real-Time Polymerase Chain Reaction
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