001     280787
005     20250907001910.0
024 7 _ |a 10.1016/j.cell.2025.05.029
|2 doi
024 7 _ |a pmid:40532699
|2 pmid
024 7 _ |a 0092-8674
|2 ISSN
024 7 _ |a 1097-4172
|2 ISSN
024 7 _ |a altmetric:178143270
|2 altmetric
037 _ _ |a DZNE-2025-00971
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Woo, Marcel S
|b 0
245 _ _ |a The immunoproteasome disturbs neuronal metabolism and drives neurodegeneration in multiple sclerosis.
260 _ _ |a [Cambridge, Mass.]
|c 2025
|b Cell Press
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1756207020_31525
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Inflammation, aberrant proteostasis, and energy depletion are hallmarks of neurodegenerative diseases such as multiple sclerosis (MS). However, the interplay between inflammation, proteasomal dysfunction in neurons, and its consequences for neuronal integrity remains unclear. Using transcriptional, proteomic, and functional analyses of proteasomal subunits in inflamed neurons, we found that interferon-γ-mediated induction of the immunoproteasome subunit, proteasome 20S beta 8 (PSMB8) impairs the proteasomal balance, resulting in reduced proteasome activity. This reduction causes the accumulation of phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3 (PFKFB3), a key metabolic regulator, leading to enhanced neuronal glycolysis, reduced pentose phosphate pathway activity, oxidative injury, and ferroptosis. Neuron-specific genetic and systemic pharmacological targeting of PSMB8 or PFKFB3 protected neurons in vitro and in a mouse model of MS. Our findings provide a unifying explanation for proteasomal dysfunction in MS and possibly other neurodegenerative diseases, linking inflammation to metabolic disruption, and presenting an opportunity for targeted neuroprotective therapies.
536 _ _ |a 353 - Clinical and Health Care Research (POF4-353)
|0 G:(DE-HGF)POF4-353
|c POF4-353
|f POF IV
|x 0
536 _ _ |a 351 - Brain Function (POF4-351)
|0 G:(DE-HGF)POF4-351
|c POF4-351
|f POF IV
|x 1
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: pub.dzne.de
650 _ 7 |a excitotoxicity
|2 Other
650 _ 7 |a ferroptosis
|2 Other
650 _ 7 |a glycolysis
|2 Other
650 _ 7 |a immunoproteasome
|2 Other
650 _ 7 |a interferon-γ
|2 Other
650 _ 7 |a metabolism
|2 Other
650 _ 7 |a multiple sclerosis
|2 Other
650 _ 7 |a neurodegeneration
|2 Other
650 _ 7 |a neuroinflammation
|2 Other
650 _ 7 |a Proteasome Endopeptidase Complex
|0 EC 3.4.25.1
|2 NLM Chemicals
650 _ 7 |a Phosphofructokinase-2
|0 EC 2.7.1.105
|2 NLM Chemicals
650 _ 7 |a Interferon-gamma
|0 82115-62-6
|2 NLM Chemicals
650 _ 7 |a PFKFB3 protein, mouse
|0 EC 2.7.1.105
|2 NLM Chemicals
650 _ 7 |a Psmb10 protein, mouse
|0 EC 3.4.25.1
|2 NLM Chemicals
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a Proteasome Endopeptidase Complex: metabolism
|2 MeSH
650 _ 2 |a Proteasome Endopeptidase Complex: genetics
|2 MeSH
650 _ 2 |a Multiple Sclerosis: metabolism
|2 MeSH
650 _ 2 |a Multiple Sclerosis: pathology
|2 MeSH
650 _ 2 |a Multiple Sclerosis: immunology
|2 MeSH
650 _ 2 |a Neurons: metabolism
|2 MeSH
650 _ 2 |a Neurons: pathology
|2 MeSH
650 _ 2 |a Mice
|2 MeSH
650 _ 2 |a Phosphofructokinase-2: metabolism
|2 MeSH
650 _ 2 |a Glycolysis
|2 MeSH
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Interferon-gamma: metabolism
|2 MeSH
650 _ 2 |a Mice, Inbred C57BL
|2 MeSH
650 _ 2 |a Inflammation: metabolism
|2 MeSH
650 _ 2 |a Disease Models, Animal
|2 MeSH
650 _ 2 |a Pentose Phosphate Pathway
|2 MeSH
650 _ 2 |a Ferroptosis
|2 MeSH
650 _ 2 |a Neurodegenerative Diseases: metabolism
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Female
|2 MeSH
650 _ 2 |a Encephalomyelitis, Autoimmune, Experimental
|2 MeSH
700 1 _ |a Brand, Johannes
|b 1
700 1 _ |a Bal, Lukas C
|b 2
700 1 _ |a Moritz, Manuela
|b 3
700 1 _ |a Walkenhorst, Mark
|b 4
700 1 _ |a Vieira, Vanessa
|b 5
700 1 _ |a Ipenberg, Inbal
|b 6
700 1 _ |a Rothammer, Nicola
|b 7
700 1 _ |a Wang, Man
|b 8
700 1 _ |a Dogan, Batuhan
|b 9
700 1 _ |a Loreth, Desirée
|b 10
700 1 _ |a Mayer, Christina
|b 11
700 1 _ |a Nagel, Darwin
|b 12
700 1 _ |a Wagner, Ingrid
|b 13
700 1 _ |a Pfeffer, Lena Kristina
|b 14
700 1 _ |a Landgraf, Peter
|b 15
700 1 _ |a van Ham, Marco
|b 16
700 1 _ |a Mattern, Kuno M-J
|b 17
700 1 _ |a Winschel, Ingo
|b 18
700 1 _ |a Frantz, Noah
|b 19
700 1 _ |a Sonner, Jana K
|b 20
700 1 _ |a Grosshans, Henrike K
|b 21
700 1 _ |a Miguela, Albert
|b 22
700 1 _ |a Bauer, Simone
|b 23
700 1 _ |a Meurs, Nina
|b 24
700 1 _ |a Müller, Anke
|b 25
700 1 _ |a Binkle-Ladisch, Lars
|b 26
700 1 _ |a Salinas, Gabriela
|b 27
700 1 _ |a Jänsch, Lothar
|b 28
700 1 _ |a Dieterich, Daniela C
|b 29
700 1 _ |a Riedner, Maria
|b 30
700 1 _ |a Krüger, Elke
|b 31
700 1 _ |a Heppner, Frank L
|0 P:(DE-2719)2812386
|b 32
|u dzne
700 1 _ |a Glatzel, Markus
|b 33
700 1 _ |a Puelles, Victor G
|b 34
700 1 _ |a Engler, Jan Broder
|b 35
700 1 _ |a Nyengaard, Jens Randel
|b 36
700 1 _ |a Misgeld, Thomas
|0 P:(DE-2719)2810727
|b 37
|u dzne
700 1 _ |a Kerschensteiner, Martin
|b 38
700 1 _ |a Merkler, Doron
|b 39
700 1 _ |a Meyer-Schwesinger, Catherine
|b 40
700 1 _ |a Friese, Manuel A
|b 41
773 _ _ |a 10.1016/j.cell.2025.05.029
|g Vol. 188, no. 17, p. 4567 - 4585.e32
|0 PERI:(DE-600)2001951-8
|n 17
|p 4567 - 4585.e32
|t Cell
|v 188
|y 2025
|x 0092-8674
856 4 _ |y OpenAccess
|u https://pub.dzne.de/record/280787/files/DZNE-2025-00971.pdf
856 4 _ |u https://pub.dzne.de/record/280787/files/DZNE-2025-00971%20SUP.zip
856 4 _ |u https://pub.dzne.de/record/280787/files/DZNE-2025-00971.pdf?subformat=pdfa
|x pdfa
|y OpenAccess
909 C O |o oai:pub.dzne.de:280787
|p openaire
|p open_access
|p VDB
|p driver
|p dnbdelivery
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 32
|6 P:(DE-2719)2812386
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 37
|6 P:(DE-2719)2810727
913 1 _ |a DE-HGF
|b Gesundheit
|l Neurodegenerative Diseases
|1 G:(DE-HGF)POF4-350
|0 G:(DE-HGF)POF4-353
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
|4 G:(DE-HGF)POF
|v Clinical and Health Care Research
|x 0
913 1 _ |a DE-HGF
|b Gesundheit
|l Neurodegenerative Diseases
|1 G:(DE-HGF)POF4-350
|0 G:(DE-HGF)POF4-351
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
|4 G:(DE-HGF)POF
|v Brain Function
|x 1
914 1 _ |y 2025
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2025-01-01
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2025-01-01
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
|d 2025-01-01
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1190
|2 StatID
|b Biological Abstracts
|d 2025-01-01
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0600
|2 StatID
|b Ebsco Academic Search
|d 2025-01-01
915 _ _ |a OpenAccess
|0 StatID:(DE-HGF)0510
|2 StatID
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b CELL : 2022
|d 2025-01-01
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1030
|2 StatID
|b Current Contents - Life Sciences
|d 2025-01-01
915 _ _ |a WoS
|0 StatID:(DE-HGF)0113
|2 StatID
|b Science Citation Index Expanded
|d 2025-01-01
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2025-01-01
915 _ _ |a IF >= 60
|0 StatID:(DE-HGF)9960
|2 StatID
|b CELL : 2022
|d 2025-01-01
915 _ _ |a Peer Review
|0 StatID:(DE-HGF)0030
|2 StatID
|b ASC
|d 2025-01-01
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0160
|2 StatID
|b Essential Science Indicators
|d 2025-01-01
915 _ _ |a Creative Commons Attribution CC BY 4.0
|0 LIC:(DE-HGF)CCBY4
|2 HGFVOC
915 _ _ |a Nationallizenz
|0 StatID:(DE-HGF)0420
|2 StatID
|d 2025-01-01
|w ger
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2025-01-01
920 1 _ |0 I:(DE-2719)1810007
|k AG Heppner
|l Neuroimmunology
|x 0
920 1 _ |0 I:(DE-2719)1110000-4
|k AG Misgeld
|l Neuronal Cell Biology
|x 1
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a UNRESTRICTED
980 _ _ |a I:(DE-2719)1810007
980 _ _ |a I:(DE-2719)1110000-4
980 1 _ |a FullTexts


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21