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  1. Article ; Online: Adipocyte death triggers a pro-inflammatory response and induces metabolic activation of resident macrophages.

    Lindhorst, Andreas / Raulien, Nora / Wieghofer, Peter / Eilers, Jens / Rossi, Fabio M V / Bechmann, Ingo / Gericke, Martin

    Cell death & disease

    2021  Volume 12, Issue 6, Page(s) 579

    Abstract: A chronic low-grade inflammation within adipose tissue (AT) seems to be the link between obesity and some of its associated diseases. One hallmark of this AT inflammation is the accumulation of AT macrophages (ATMs) around dead or dying adipocytes, ... ...

    Abstract A chronic low-grade inflammation within adipose tissue (AT) seems to be the link between obesity and some of its associated diseases. One hallmark of this AT inflammation is the accumulation of AT macrophages (ATMs) around dead or dying adipocytes, forming so-called crown-like structures (CLS). To investigate the dynamics of CLS and their direct impact on the activation state of ATMs, we established a laser injury model to deplete individual adipocytes in living AT from double reporter mice (GFP-labeled ATMs and tdTomato-labeled adipocytes). Hence, we were able to detect early ATM-adipocyte interactions by live imaging and to determine a precise timeline for CLS formation after adipocyte death. Further, our data indicate metabolic activation and increased lipid metabolism in ATMs upon forming CLS. Most importantly, adipocyte death, even in lean animals under homeostatic conditions, leads to a locally confined inflammation, which is in sharp contrast to other tissues. We identified cell size as cause for the described pro-inflammatory response, as the size of adipocytes is above a critical threshold size for efferocytosis, a process for anti-inflammatory removal of dead cells during tissue homeostasis. Finally, experiments on parabiotic mice verified that adipocyte death leads to a pro-inflammatory response of resident ATMs in vivo, without significant recruitment of blood monocytes. Our data indicate that adipocyte death triggers a unique degradation process and locally induces a metabolically activated ATM phenotype that is globally observed with obesity.
    MeSH term(s) Adipocytes/pathology ; Animals ; Female ; Humans ; Inflammation/physiopathology ; Lipid Metabolism/physiology ; Macrophages/pathology ; Mice ; Obesity/physiopathology
    Language English
    Publishing date 2021-06-05
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2541626-1
    ISSN 2041-4889 ; 2041-4889
    ISSN (online) 2041-4889
    ISSN 2041-4889
    DOI 10.1038/s41419-021-03872-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Macrophages in obesity are characterised by increased IL-1β response to calcium-sensing receptor signals.

    Thrum, Stephan / Sommer, Miriam / Raulien, Nora / Gericke, Martin / Massier, Lucas / Kovacs, Peter / Krasselt, Marco / Landgraf, Kathrin / Körner, Antje / Dietrich, Arne / Blüher, Matthias / Rossol, Manuela / Wagner, Ulf

    International journal of obesity (2005)

    2022  Volume 46, Issue 10, Page(s) 1883–1891

    Abstract: Objective: Obesity is complicated by inflammatory activation of the innate immune system. Stimulation of the calcium-sensing receptor (CaSR) by extra-cellular calcium ions ([Ca: Methods: [Ca: Results: Both MDM and AT readily responded with ... ...

    Abstract Objective: Obesity is complicated by inflammatory activation of the innate immune system. Stimulation of the calcium-sensing receptor (CaSR) by extra-cellular calcium ions ([Ca
    Methods: [Ca
    Results: Both MDM and AT readily responded with concentration-dependent IL-1β release already at low, near physiological concentrations to addition of [Ca
    Conclusions: Obesity renders macrophages more susceptible to [Ca
    MeSH term(s) Calcium/metabolism ; Humans ; Inflammasomes/metabolism ; Interleukin-1beta/metabolism ; Lipopolysaccharides/metabolism ; Macrophages/metabolism ; NLR Family, Pyrin Domain-Containing 3 Protein/metabolism ; Obesity/metabolism ; RNA, Messenger/metabolism ; Receptors, Calcium-Sensing/metabolism
    Chemical Substances IL1B protein, human ; Inflammasomes ; Interleukin-1beta ; Lipopolysaccharides ; NLR Family, Pyrin Domain-Containing 3 Protein ; RNA, Messenger ; Receptors, Calcium-Sensing ; Calcium (SY7Q814VUP)
    Language English
    Publishing date 2022-08-05
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 752409-2
    ISSN 1476-5497 ; 0307-0565
    ISSN (online) 1476-5497
    ISSN 0307-0565
    DOI 10.1038/s41366-022-01135-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Autoimmune arthritis induces paired immunoglobulin-like receptor B expression on CD4

    Rothe, Kathrin / Raulien, Nora / Köhler, Gabriele / Pierer, Matthias / Quandt, Dagmar / Wagner, Ulf

    European journal of immunology

    2017  Volume 47, Issue 9, Page(s) 1457–1467

    Abstract: The chronic, destructive autoimmune arthritis in SKG mice, which closely resembles human rheumatoid arthritis, is the result of self-reactive T cells escaping thymic deletion. Since the inhibitory receptor LIR-1 is up-regulated on auto-reactive T cells ... ...

    Abstract The chronic, destructive autoimmune arthritis in SKG mice, which closely resembles human rheumatoid arthritis, is the result of self-reactive T cells escaping thymic deletion. Since the inhibitory receptor LIR-1 is up-regulated on auto-reactive T cells in human rheumatoid arthritis, the role of its murine ortholog PIR-B was investigated. Peripheral CD4
    MeSH term(s) Animals ; Antigens, CD/metabolism ; Arthritis, Experimental/immunology ; Arthritis, Rheumatoid/immunology ; CD4-Positive T-Lymphocytes/immunology ; Cells, Cultured ; Female ; Humans ; Interferon-gamma/metabolism ; Interleukin-17/metabolism ; Leukocyte Immunoglobulin-like Receptor B1 ; Mice ; Mice, Inbred BALB C ; Mice, Inbred Strains ; RNA, Small Interfering/genetics ; Receptors, Immunologic/genetics ; Receptors, Immunologic/metabolism
    Chemical Substances Antigens, CD ; Interleukin-17 ; LILRB1 protein, human ; Leukocyte Immunoglobulin-like Receptor B1 ; Pirb protein, mouse ; RNA, Small Interfering ; Receptors, Immunologic ; Interferon-gamma (82115-62-6)
    Language English
    Publishing date 2017-09
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 120108-6
    ISSN 1521-4141 ; 0014-2980
    ISSN (online) 1521-4141
    ISSN 0014-2980
    DOI 10.1002/eji.201646747
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Cross-talk between lipid and protein carbonylation in a dynamic cardiomyocyte model of mild nitroxidative stress.

    Griesser, Eva / Vemula, Venukumar / Raulien, Nora / Wagner, Ulf / Reeg, Sandra / Grune, Tilman / Fedorova, Maria

    Redox biology

    2016  Volume 11, Page(s) 438–455

    Abstract: Reactive oxygen and nitrogen species (ROS/RNS) play an important role in the regulation of cardiac function. Increase in ROS/RNS concentration results in lipid and protein oxidation and is often associated with onset and/or progression of many ... ...

    Abstract Reactive oxygen and nitrogen species (ROS/RNS) play an important role in the regulation of cardiac function. Increase in ROS/RNS concentration results in lipid and protein oxidation and is often associated with onset and/or progression of many cardiovascular disorders. However, interplay between lipid and protein modifications has not been simultaneously studied in detail so far. Biomolecule carbonylation is one of the most common biomarkers of oxidative stress. Using a dynamic model of nitroxidative stress we demonstrated rapid changes in biomolecule carbonylation in rat cardiomyocytes. Levels of carbonylated species increased as early as 15min upon treatment with the peroxynitrite donor, 3-morpholinosydnonimine (SIN-1), and decreased to values close to control after 16h. Total (lipids+proteins) vs. protein-specific carbonylation showed different dynamics, with a significant increase in protein-bound carbonyls at later time points. Treatment with SIN-1 in combination with inhibitors of proteasomal and autophagy/lysosomal degradation pathways allowed confirmation of a significant role of the proteasome in the degradation of carbonylated proteins, whereas lipid carbonylation increased in the presence of autophagy/lysosomal inhibitors. Electrophilic aldehydes and ketones formed by lipid peroxidation were identified and relatively quantified using LC-MS/MS. Molecular identity of reactive species was used for data-driven analysis of their protein targets. Combination of different enrichment strategies with LC-MS/MS analysis allowed identification of more than 167 unique proteins with 332 sites modified by electrophilic lipid peroxidation products. Gene ontology analysis of modified proteins demonstrated enrichment of several functional categories including proteins involved in cytoskeleton, extracellular matrix, ion channels and their regulation. Using calcium mobilization assays, the effect of nitroxidative stress on the activity of several ion channels was further confirmed.
    MeSH term(s) Aldehydes/metabolism ; Animals ; Autophagy/genetics ; Ketones/metabolism ; Lipid Peroxidation/genetics ; Molsidomine/administration & dosage ; Molsidomine/analogs & derivatives ; Myocytes, Cardiac/drug effects ; Myocytes, Cardiac/metabolism ; Nitrogen/metabolism ; Oxidative Stress/genetics ; Proteasome Endopeptidase Complex/drug effects ; Proteasome Endopeptidase Complex/metabolism ; Protein Carbonylation/genetics ; Proteolysis/drug effects ; Rats ; Reactive Nitrogen Species/metabolism ; Reactive Oxygen Species/metabolism
    Chemical Substances Aldehydes ; Ketones ; Reactive Nitrogen Species ; Reactive Oxygen Species ; linsidomine (5O5U71P6VQ) ; Molsidomine (D46583G77X) ; Proteasome Endopeptidase Complex (EC 3.4.25.1) ; Nitrogen (N762921K75)
    Language English
    Publishing date 2016-12-28
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2701011-9
    ISSN 2213-2317 ; 2213-2317
    ISSN (online) 2213-2317
    ISSN 2213-2317
    DOI 10.1016/j.redox.2016.12.028
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Cross-talk between lipid and protein carbonylation in a dynamic cardiomyocyte model of mild nitroxidative stress

    Eva Griesser / Venukumar Vemula / Nora Raulien / Ulf Wagner / Sandra Reeg / Tilman Grune / Maria Fedorova

    Redox Biology, Vol 11, Iss , Pp 438-

    2017  Volume 455

    Abstract: Reactive oxygen and nitrogen species (ROS/RNS) play an important role in the regulation of cardiac function. Increase in ROS/RNS concentration results in lipid and protein oxidation and is often associated with onset and/or progression of many ... ...

    Abstract Reactive oxygen and nitrogen species (ROS/RNS) play an important role in the regulation of cardiac function. Increase in ROS/RNS concentration results in lipid and protein oxidation and is often associated with onset and/or progression of many cardiovascular disorders. However, interplay between lipid and protein modifications has not been simultaneously studied in detail so far. Biomolecule carbonylation is one of the most common biomarkers of oxidative stress. Using a dynamic model of nitroxidative stress we demonstrated rapid changes in biomolecule carbonylation in rat cardiomyocytes. Levels of carbonylated species increased as early as 15 min upon treatment with the peroxynitrite donor, 3-morpholinosydnonimine (SIN-1), and decreased to values close to control after 16 h. Total (lipids+proteins) vs. protein-specific carbonylation showed different dynamics, with a significant increase in protein-bound carbonyls at later time points. Treatment with SIN-1 in combination with inhibitors of proteasomal and autophagy/lysosomal degradation pathways allowed confirmation of a significant role of the proteasome in the degradation of carbonylated proteins, whereas lipid carbonylation increased in the presence of autophagy/lysosomal inhibitors. Electrophilic aldehydes and ketones formed by lipid peroxidation were identified and relatively quantified using LC-MS/MS. Molecular identity of reactive species was used for data-driven analysis of their protein targets. Combination of different enrichment strategies with LC-MS/MS analysis allowed identification of more than 167 unique proteins with 332 sites modified by electrophilic lipid peroxidation products. Gene ontology analysis of modified proteins demonstrated enrichment of several functional categories including proteins involved in cytoskeleton, extracellular matrix, ion channels and their regulation. Using calcium mobilization assays, the effect of nitroxidative stress on the activity of several ion channels was further confirmed. Keywords: Nitroxidative stress, Cardiomyocytes, Lipid oxidation, Protein oxidation, Lipid-protein adducts, Carbonylation
    Keywords Medicine (General) ; R5-920 ; Biology (General) ; QH301-705.5
    Subject code 572
    Language English
    Publishing date 2017-04-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article ; Online: Cross-talk between lipid and protein carbonylation in a dynamic cardiomyocyte model of mild nitroxidative stress

    Griesser, Eva / Vemula, Venukumar / Raulien, Nora / Wagner, Ulf / Reeg, Sandra / Grune, Tilman / Fedorova, Maria

    Redox Biology. 2016,

    2016  

    Abstract: Reactive oxygen and nitrogen species (ROS/RNS) play an important role in the regulation of cardiac function. Increase in ROS/RNS concentration results in lipid and protein oxidation and is often associated with onset and/or progression of many ... ...

    Abstract Reactive oxygen and nitrogen species (ROS/RNS) play an important role in the regulation of cardiac function. Increase in ROS/RNS concentration results in lipid and protein oxidation and is often associated with onset and/or progression of many cardiovascular disorders. However, interplay between lipid and protein modifications has not been simultaneously studied in detail so far. Biomolecule carbonylation is one of the most common biomarkers of oxidative stress. Using a dynamic model of nitroxidative stress we demonstrated rapid changes in biomolecule carbonylation in rat cardiomyocytes. Levels of carbonylated species increased as early as 15 min upon treatment with the peroxynitrite donor, 3-morpholinosydnonimine (SIN-1), and decreased to values close to control after 16 h. Total (lipids + proteins) vs. protein-specific carbonylation showed different dynamics, with a significant increase in protein-bound carbonyls at later time points. Treatment with SIN-1 in combination with inhibitors of proteasomal and autophagy/lysosomal degradation pathways allowed confirmation of a significant role of the proteasome in the degradation of carbonylated proteins, whereas lipid carbonylation increased in the presence of autophagy/lysosomal inhibitors. Electrophilic aldehydes and ketones formed by lipid peroxidation were identified and relatively quantified using LC-MS/MS. Molecular identity of reactive species was used for data-driven analysis of their protein targets. Combination of different enrichment strategies with LC-MS/MS analysis allowed identification of more than 167 unique proteins with 332 sites modified by electrophilic lipid peroxidation products. Gene ontology analysis of modified proteins demonstrated enrichment of several functional categories including proteins involved in cytoskeleton, extracellular matrix, ion channels and their regulation. Using calcium mobilization assays, the effect of nitroxidative stress on the activity of several ion channels was further confirmed.
    Keywords ROS ; RNS ; OS ; CVDs ; HF ; IR ; CM ; SIN-1 ; oxoLPPs ; DMEM/F12 ; 7-AAD ; DCFDA ; CHH ; PFA ; TCE ; DNPH ; MTBE ; AMC ; DTT ; pepA ; IAA ; HRP ; ARP ; BSO ; 8OHQ ; POPA ; DMF ; LC3 ; LDH ; TPBS ; DDA ; Cu(8OHQ) ; oxPC ; LDs ; HNE ; MDA ; PTMs ; HHE ; LOX ; MCO ; ECM ; MyBP-C ; VDCC ; RyR ; IP3R ; Nitroxidative stress ; Cardiomyocytes ; Lipid oxidation ; Protein oxidation ; Lipid-protein adducts ; Carbonylation
    Language English
    Publishing place Elsevier B.V.
    Document type Article ; Online
    Note Pre-press version
    ZDB-ID 2701011-9
    ISSN 2213-2317
    ISSN 2213-2317
    DOI 10.1016/j.redox.2016.12.028
    Database NAL-Catalogue (AGRICOLA)

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  7. Article ; Online: Calcium-sensing receptor-mediated NLRP3 inflammasome response to calciprotein particles drives inflammation in rheumatoid arthritis.

    Jäger, Elisabeth / Murthy, Supriya / Schmidt, Caroline / Hahn, Magdalena / Strobel, Sarah / Peters, Anna / Stäubert, Claudia / Sungur, Pelin / Venus, Tom / Geisler, Mandy / Radusheva, Veselina / Raps, Stefanie / Rothe, Kathrin / Scholz, Roger / Jung, Sebastian / Wagner, Sylke / Pierer, Matthias / Seifert, Olga / Chang, Wenhan /
    Estrela-Lopis, Irina / Raulien, Nora / Krohn, Knut / Sträter, Norbert / Hoeppener, Stephanie / Schöneberg, Torsten / Rossol, Manuela / Wagner, Ulf

    Nature communications

    2020  Volume 11, Issue 1, Page(s) 4243

    Abstract: Increased extracellular ... ...

    Abstract Increased extracellular Ca
    MeSH term(s) Animals ; Arthritis, Rheumatoid/immunology ; Calcinosis ; Calcium/metabolism ; Cells, Cultured ; Humans ; Inflammasomes/metabolism ; Inflammation ; Interleukin-1beta/metabolism ; Mice ; Monocytes/metabolism ; NLR Family, Pyrin Domain-Containing 3 Protein/deficiency ; NLR Family, Pyrin Domain-Containing 3 Protein/metabolism ; Phosphates/metabolism ; Pinocytosis ; Receptors, Calcium-Sensing/deficiency ; Receptors, Calcium-Sensing/metabolism ; Signal Transduction ; THP-1 Cells ; alpha-2-HS-Glycoprotein/metabolism
    Chemical Substances Inflammasomes ; Interleukin-1beta ; NLR Family, Pyrin Domain-Containing 3 Protein ; Phosphates ; Receptors, Calcium-Sensing ; alpha-2-HS-Glycoprotein ; Calcium (SY7Q814VUP)
    Keywords covid19
    Language English
    Publishing date 2020-08-25
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-020-17749-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Inhibition of nicotinamide phosphoribosyltransferase modifies LPS-induced inflammatory responses of human monocytes.

    Schilling, Erik / Wehrhahn, Janine / Klein, Carina / Raulien, Nora / Ceglarek, Uta / Hauschildt, Sunna

    Innate immunity

    2012  Volume 18, Issue 3, Page(s) 518–530

    Abstract: Recent studies have identified enzymes that use NAD as a substrate, thus contributing to its net consumption. To maintain the intracellular pool, NAD is re-synthesized by a salvage pathway using nicotinamide, the by-product generated by the enzymatic ... ...

    Abstract Recent studies have identified enzymes that use NAD as a substrate, thus contributing to its net consumption. To maintain the intracellular pool, NAD is re-synthesized by a salvage pathway using nicotinamide, the by-product generated by the enzymatic cleavage of NAD. Enzymes involved in NAD re-synthesis include nicotinamide phosphoribosyltransferase (NAMPT) and nicotinamide mononucleotide adenylyltransferase. Our studies show, that NAMPT was substantially up-regulated by LPS in primary human monocytes, suggesting that it may be especially required during the process of monocyte activation. To evaluate the contribution of the NAD rescue pathway to LPS-induced biological responses in human monocytes, we used APO866, a well-characterized inhibitor of NAMPT. Concomitant with the inhibition of NAMPT, LPS-induced TNF-α protein synthesis declined, while TNF-α mRNA levels were minimally affected. Moreover, APO866 strongly decreased the production of reactive oxygen species (ROS), increased surface expression of the NAD-consuming enzyme CD38, and modified the production of selective eicosanoids. We further demonstrate that protein ADP-ribosylation was strongly reduced, indicating a possible link between this post-translational protein modification and human monocyte inflammatory responses. Despite a substantial reduction in intracellular NAD levels, activated monocytes were resistant to apoptosis, while resting monocytes were not. Taken together, our data suggest that activated monocytes strongly depend on the NAD salvage pathway to mount an appropriate inflammatory response. Their survival is not affected by NAD-depletion, probably as a result of LPS-mediated anti-apoptotic signals.
    MeSH term(s) ADP-ribosyl Cyclase 1/genetics ; ADP-ribosyl Cyclase 1/metabolism ; Acrylamides/pharmacology ; Apoptosis/drug effects ; Apoptosis/immunology ; Cells, Cultured ; Eicosanoids/metabolism ; Humans ; Inflammation/immunology ; Inflammation Mediators/metabolism ; Lipopolysaccharides/immunology ; Lipopolysaccharides/metabolism ; Monocytes/drug effects ; Monocytes/immunology ; NAD/immunology ; Nicotinamide Phosphoribosyltransferase/antagonists & inhibitors ; Nicotinamide Phosphoribosyltransferase/genetics ; Nicotinamide Phosphoribosyltransferase/metabolism ; Piperidines/pharmacology ; Protein Processing, Post-Translational/drug effects ; Protein Processing, Post-Translational/immunology ; Reactive Oxygen Species/metabolism ; Tumor Necrosis Factor-alpha/genetics ; Tumor Necrosis Factor-alpha/metabolism ; Up-Regulation
    Chemical Substances Acrylamides ; Eicosanoids ; Inflammation Mediators ; Lipopolysaccharides ; N-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(pyridin-3-yl)acrylamide ; Piperidines ; Reactive Oxygen Species ; Tumor Necrosis Factor-alpha ; NAD (0U46U6E8UK) ; Nicotinamide Phosphoribosyltransferase (EC 2.4.2.12) ; ADP-ribosyl Cyclase 1 (EC 3.2.2.6)
    Language English
    Publishing date 2012-06
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1753-4267
    ISSN (online) 1753-4267
    DOI 10.1177/1753425911423853
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Fatty Acid Oxidation Compensates for Lipopolysaccharide-Induced Warburg Effect in Glucose-Deprived Monocytes.

    Raulien, Nora / Friedrich, Kathleen / Strobel, Sarah / Rubner, Stefan / Baumann, Sven / von Bergen, Martin / Körner, Antje / Krueger, Martin / Rossol, Manuela / Wagner, Ulf

    Frontiers in immunology

    2017  Volume 8, Page(s) 609

    Abstract: Monocytes enter sites of microbial or sterile inflammation as the first line of defense of the immune system and initiate pro-inflammatory effector mechanisms. We show that activation with bacterial lipopolysaccharide (LPS) induces them to undergo a ... ...

    Abstract Monocytes enter sites of microbial or sterile inflammation as the first line of defense of the immune system and initiate pro-inflammatory effector mechanisms. We show that activation with bacterial lipopolysaccharide (LPS) induces them to undergo a metabolic shift toward aerobic glycolysis, similar to the Warburg effect observed in cancer cells. At sites of inflammation, however, glucose concentrations are often drastically decreased, which prompted us to study monocyte function under conditions of glucose deprivation and abrogated Warburg effect. Experiments using the Seahorse Extracellular Flux Analyzer revealed that limited glucose supply shifts monocyte metabolism toward oxidative phosphorylation, fueled largely by fatty acid oxidation at the expense of lipid droplets. While this metabolic state appears to provide sufficient energy to sustain functional properties like cytokine secretion, migration, and phagocytosis, it cannot prevent a rise in the AMP/ATP ratio and a decreased respiratory burst. The molecular trigger mediating the metabolic shift and the functional consequences is activation of AMP-activated protein kinase (AMPK). Taken together, our results indicate that monocytes are sufficiently metabolically flexible to perform pro-inflammatory functions at sites of inflammation despite glucose deprivation and inhibition of the LPS-induced Warburg effect. AMPK seems to play a pivotal role in orchestrating these processes during glucose deprivation in monocytes.
    Language English
    Publishing date 2017
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2606827-8
    ISSN 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2017.00609
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Calcium-sensing receptor-mediated NLRP3 inflammasome response to calciprotein particles drives inflammation in rheumatoid arthritis

    Elisabeth Jäger / Supriya Murthy / Caroline Schmidt / Magdalena Hahn / Sarah Strobel / Anna Peters / Claudia Stäubert / Pelin Sungur / Tom Venus / Mandy Geisler / Veselina Radusheva / Stefanie Raps / Kathrin Rothe / Roger Scholz / Sebastian Jung / Sylke Wagner / Matthias Pierer / Olga Seifert / Wenhan Chang /
    Irina Estrela-Lopis / Nora Raulien / Knut Krohn / Norbert Sträter / Stephanie Hoeppener / Torsten Schöneberg / Manuela Rossol / Ulf Wagner

    Nature Communications, Vol 11, Iss 1, Pp 1-

    2020  Volume 17

    Abstract: How extracellular calcium can trigger Nlrp3 inflammasome activation has been somewhat controversial and unclear. Here the authors show calciprotein particles are taken up by myeloid cells via calcium-sensing receptor-dependent macropinocytosis in ... ...

    Abstract How extracellular calcium can trigger Nlrp3 inflammasome activation has been somewhat controversial and unclear. Here the authors show calciprotein particles are taken up by myeloid cells via calcium-sensing receptor-dependent macropinocytosis in response to high levels of extracellular Ca2+ and this pathway might be critical to inflammatory conditions.
    Keywords Science ; Q
    Language English
    Publishing date 2020-08-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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