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Demyelinating injuries in the central nervous system trigger a regenerative process that relies on coordinated responses from multiple cell types, including the innate immune system. Here, we propose that a maladaptive chronic immune response may be initiated when microglia’s capacity to clear myelin debris is overwhelmed, leading to a self-propagating immune response that impairs remyelination and causes further tissue damage. We aim to identify the molecular checkpoints in microglia/macrophages that drive this process, with a focus on interferon signaling.
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Creators and SubmitterViews: 30
Created: 3rd Aug 2026 at 08:27
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Projects: TRR 274: Checkpoints of Central Nervous System Recovery
Institutions: Universitätsmedizin Göttingen
Projects: CRC1002: Modulatory Units in Heart Failure, TRR 274: Checkpoints of Central Nervous System Recovery, SFB 1190: Compartmental Gates and Contact Sites in Cells
Web page: Not specified
https://rdp.sfb274.de/ (Research Data Platform) https://gepris.dfg.de/gepris/projekt/408885537 (DFG Gepris entry) The central nervous system (CNS) is a terminally differentiated tissue, where any insult carries a heightened risk - yet the tissue response to these insults is variable and can range from irreversible destruction to almost complete recovery. The rules that instruct these divergent outcomes are still unknown. The aim of this CRC is therefore to understand the biology of the multicellular ...
Programme: Sonderforschungsbereiche/Collaborative Research Centers
Public web page: https://www.sfb274.de/
After demyelinating injury of the central nervous system, resolution of the mounting acute inflammation is crucial for the initiation of a regenerative response. Here, we aim to identify fatty acids and lipid mediators that govern the balance of inflammatory reactions within demyelinating lesions. Using lipidomics, we identify bioactive lipids in the resolution phase of inflammation with markedly elevated levels of n-3 polyunsaturated fatty acids. Using fat-1 transgenic mice, which convert n-6 ...
Submitter: Camilla Giudici
Investigation: A06 - Linking lipid metabolism to inflammation ...
Assays: Shotgun proteomics (mouse)
Snapshots: No snapshots
Understanding the complexity of cellular function within a tissue necessitates the combination of multiple phenotypic readouts. Here, we developed a method that links spatially-resolved gene expression of single cells with their ultrastructural morphology by integrating multiplexed error-robust fluorescence in situ hybridization (MERFISH) and large area volume electron microscopy (EM) on adjacent tissue sections. Using this method, we characterized in situ ultrastructural and transcriptional ...
Submitter: Camilla Giudici
Investigation: A06 - Linking lipid metabolism to inflammation ...
Assays: Expression profiling: Spatial Transcriptomics correlated Electron Micros...
Snapshots: No snapshots
Oligodendrocytes extend numerous cellular processes that wrap multiple times around axons to generate lipid-rich myelin sheaths. Myelin biogenesis requires an enormously productive biosynthetic machinery for generating and delivering these large amounts of newly synthesized lipids. Yet, a complete understanding of this process remains elusive. Utilizing volume electron microscopy, we demonstrate that the oligodendroglial endoplasmic reticulum (ER) is enriched in developing myelin, extending into ...
Submitter: Camilla Giudici
Investigation: A06 - Linking lipid metabolism to inflammation ...
Assays: Bottom-up proteomics (mouse)
Snapshots: No snapshots
Submitter: Camilla Giudici
Assay type: Proteomics
Technology type: Mass Spectrometry
Investigation: A06 - Linking lipid metabolism to inflammation ...
Organisms: Mouse
SOPs: No SOPs
Data files: Proteomics analysis of myelin from GLTP KO mous...
Snapshots: No snapshots
Submitter: Camilla Giudici
Assay type: Experimental Assay Type
Technology type: Technology Type
Investigation: A06 - Linking lipid metabolism to inflammation ...
Organisms: Mouse
SOPs: No SOPs
Data files: Spatial Transcriptomics correlated Electron Mic...
Snapshots: No snapshots
Corpus callosum dissections were lysed in 300 µL STET lysis buffer (1% (v/v) Triton X-100, 150 mM NaCl, 2 mM EDTA, 50 mM TrisHCl pH 7.5) with a Precellys Evolution homogenizer (Bertin, Germany) using 0.5 mL soft tissue homogenization kit CK14 applying two cycles of 30 s with a speed of 6500rpm. After 15 min incubation on ice, samples were centrifuged at 16,000×g for 15 min to remove undissolved material and cell debris. The supernatant was transferred to a fresh protein lobind tube (Eppendorf, ...
Submitter: Camilla Giudici
Assay type: Proteomics
Technology type: Technology Type
Investigation: A06 - Linking lipid metabolism to inflammation ...
Organisms: Mouse
SOPs: No SOPs
Data files: Proteomic and lipidomic profiling of demyelinat...
Snapshots: No snapshots
After demyelinating injury of the central nervous system, resolution of the mounting acute innate inflammation is crucial for the initiation of a regenerative response. To identify factors in lesion recovery after demyelination injury, we used a toxin-induced model, in which a single dose of lysolecithin is injected into the corpus callosum to induce a focal demyelinating lesion. Afterwards, we investigated the proteome of demyelinating lesions at different time points post injection (dpi) in a ...
Creators: None
Submitter: Camilla Giudici
Investigations: A06 - Linking lipid metabolism to inflammation ...
Studies: Proteomic and lipidomic profiling of demyelinat...
Assays: Shotgun proteomics (mouse)
Current spatial transcriptomics methods provide molecular and spatial information but no morphological readout. Here, we present STEM - a method that correlates multiplexed error-robust FISH with electron microscopy from neighboring tissue sections of the same sample. STEM links transcriptional and spatial organization of single cells with ultrastructural morphology of the tissue in vivo. Using STEM to characterize demyelinated white-matter lesions allowed us to link morphology of myelin-laden ...
Creators: None
Submitter: Camilla Giudici
Tryptic in solution digestion of the purified myelin fraction was performed according to the filter-aided sample preparation (FASP) protocol (Erwig et al., 2019) originally described by Manza et al., 2005; followed by LC-MS-analysis. In brief, purified myelin fractions corresponding to 10 µg myelin protein were dissolved and lysed in lysis buffer (1% ASB-14, 7 M urea, 2 M thiourea. 10 mM DTT 0.1 M Tris pH 8.5). Homogenised samples were diluted with lysis buffer containing 2% CHAPS to reduce ASB-14 ...
Creators: None
Submitter: Camilla Giudici
Investigations: A06 - Linking lipid metabolism to inflammation ...
Studies: Nonvesicular lipid transfer drives myelin growt...
Assays: Bottom-up proteomics (mouse)
Abstract (Expand)
Authors: Jianping Wu, Georg Kislinger, Jerome Duschek, Ayşe Damla Durmaz, Benedikt Wefers, Ruoqing Feng, Karsten Nalbach, Wolfgang Wurst, Christian Behrends, Martina Schifferer, Mikael Simons
Date Published: 11th Nov 2024
Publication Type: Journal Article
DOI: 10.1038/s41467-024-53511-y
Citation: Nat Commun 15(1):9756.
Abstract (Expand)
Authors: Peter Androvic, Martina Schifferer, Katrin Perez Anderson, Ludovico Cantuti-Castelvetri, Hanyi Jiang, Hao Ji, Lu Liu, Garyfallia Gouna, Stefan A. Berghoff, Simon Besson-Girard, Johanna Knoferle, Mikael Simons, Ozgun Gokce
Date Published: 11th Jul 2023
Publication Type: Journal Article
DOI: 10.1038/s41467-023-39447-9
Citation: Nat Commun 14(1):4115.
Abstract
Authors: Horst Penkert, Alix Bertrand, Vini Tiwari, Stephan Breimann, Stephan A. Müller, Paul M. Jordan, Mathias J. Gerl, Christian Klose, Ludovico Cantuti-Castelvetri, Mar Bosch-Queralt, Ilya Levental, Stefan F. Lichtenthaler, Oliver Werz, Mikael Simons
Date Published: 1st Oct 2021
Publication Type: Journal Article
DOI: 10.1016/j.celrep.2021.109898
Citation: Cell Reports 37(4):109898.
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https://orcid.org/0000-0002-3794-7295