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024 7 _ |a 10.1002/glia.23507
|2 doi
024 7 _ |a pmid:30277599
|2 pmid
024 7 _ |a 0894-1491
|2 ISSN
024 7 _ |a 1098-1136
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024 7 _ |a altmetric:48195495
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037 _ _ |a DZNE-2020-06662
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Fülle, Lorenz
|b 0
245 _ _ |a CCL17 exerts a neuroimmune modulatory function and is expressed in hippocampal neurons.
260 _ _ |a Bognor Regis [u.a.]
|c 2018
|b Wiley-Liss
264 _ 1 |3 online
|2 Crossref
|b Wiley
|c 2018-09-12
264 _ 1 |3 print
|2 Crossref
|b Wiley
|c 2018-10-01
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 1744892447_19520
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336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Chemokines are important signaling molecules in the immune and nervous system. Using a fluorescence reporter mouse model, we demonstrate that the chemokine CCL17, a ligand of the chemokine receptor CCR4, is produced in the murine brain, particularly in a subset of hippocampal CA1 neurons. We found that basal expression of Ccl17 in hippocampal neurons was strongly enhanced by peripheral challenge with lipopolysaccharide (LPS). LPS-mediated induction of Ccl17 in the hippocampus was dependent on local tumor necrosis factor (TNF) signaling, whereas upregulation of Ccl22 required granulocyte-macrophage colony-stimulating factor (GM-CSF). CCL17 deficiency resulted in a diminished microglia density under homeostatic and inflammatory conditions. Further, microglia from naïve Ccl17-deficient mice possessed a reduced cellular volume and a more polarized process tree as assessed by computer-assisted imaging analysis. Regarding the overall branching, cell surface area, and total tree length, the morphology of microglia from naïve Ccl17-deficient mice resembled that of microglia from wild-type mice after LPS stimulation. In line, electrophysiological recordings indicated that CCL17 downmodulates basal synaptic transmission at CA3-CA1 Schaffer collaterals in acute slices from naïve but not LPS-treated animals. Taken together, our data identify CCL17 as a homeostatic and inducible neuromodulatory chemokine affecting the presence and morphology of microglia and synaptic transmission in the hippocampus.
536 _ _ |a 342 - Disease Mechanisms and Model Systems (POF3-342)
|0 G:(DE-HGF)POF3-342
|c POF3-342
|f POF III
|x 0
542 _ _ |i 2018-09-12
|2 Crossref
|u http://doi.wiley.com/10.1002/tdm_license_1.1
542 _ _ |i 2018-09-12
|2 Crossref
|u http://onlinelibrary.wiley.com/termsAndConditions#vor
588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 7 |a Ccl17 protein, mouse
|2 NLM Chemicals
650 _ 7 |a Ccl22 protein, mouse
|2 NLM Chemicals
650 _ 7 |a Ccr4 protein, mouse
|2 NLM Chemicals
650 _ 7 |a Chemokine CCL17
|2 NLM Chemicals
650 _ 7 |a Chemokine CCL22
|2 NLM Chemicals
650 _ 7 |a Lipopolysaccharides
|2 NLM Chemicals
650 _ 7 |a Receptors, CCR4
|2 NLM Chemicals
650 _ 7 |a Tumor Necrosis Factor-alpha
|2 NLM Chemicals
650 _ 7 |a enhanced green fluorescent protein
|2 NLM Chemicals
650 _ 7 |a Green Fluorescent Proteins
|0 147336-22-9
|2 NLM Chemicals
650 _ 7 |a Granulocyte-Macrophage Colony-Stimulating Factor
|0 83869-56-1
|2 NLM Chemicals
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a Chemokine CCL17: genetics
|2 MeSH
650 _ 2 |a Chemokine CCL17: metabolism
|2 MeSH
650 _ 2 |a Chemokine CCL22: metabolism
|2 MeSH
650 _ 2 |a Female
|2 MeSH
650 _ 2 |a Gene Expression
|2 MeSH
650 _ 2 |a Granulocyte-Macrophage Colony-Stimulating Factor: metabolism
|2 MeSH
650 _ 2 |a Green Fluorescent Proteins: genetics
|2 MeSH
650 _ 2 |a Green Fluorescent Proteins: metabolism
|2 MeSH
650 _ 2 |a Hippocampus: immunology
|2 MeSH
650 _ 2 |a Hippocampus: pathology
|2 MeSH
650 _ 2 |a Homeostasis: physiology
|2 MeSH
650 _ 2 |a Inflammation: metabolism
|2 MeSH
650 _ 2 |a Inflammation: pathology
|2 MeSH
650 _ 2 |a Lipopolysaccharides
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Mice, Inbred C57BL
|2 MeSH
650 _ 2 |a Mice, Transgenic
|2 MeSH
650 _ 2 |a Microglia: immunology
|2 MeSH
650 _ 2 |a Microglia: pathology
|2 MeSH
650 _ 2 |a Monocytes: immunology
|2 MeSH
650 _ 2 |a Monocytes: pathology
|2 MeSH
650 _ 2 |a Neuroimmunomodulation: physiology
|2 MeSH
650 _ 2 |a Neurons: immunology
|2 MeSH
650 _ 2 |a Neurons: pathology
|2 MeSH
650 _ 2 |a Receptors, CCR4: metabolism
|2 MeSH
650 _ 2 |a Synaptic Transmission: physiology
|2 MeSH
650 _ 2 |a Tumor Necrosis Factor-alpha: metabolism
|2 MeSH
700 1 _ |a Offermann, Nina
|0 P:(DE-HGF)0
|b 1
700 1 _ |a Hansen, Jan Niklas
|0 P:(DE-HGF)0
|b 2
700 1 _ |a Breithausen, Björn
|b 3
700 1 _ |a Erazo, Anna Belen
|b 4
700 1 _ |a Schanz, Oliver
|b 5
700 1 _ |a Radau, Luca
|b 6
700 1 _ |a Gondorf, Fabian
|b 7
700 1 _ |a Knöpper, Konrad
|b 8
700 1 _ |a Alferink, Judith
|b 9
700 1 _ |a Abdullah, Zeinab
|b 10
700 1 _ |a Neumann, Harald
|b 11
700 1 _ |a Weighardt, Heike
|b 12
700 1 _ |a Henneberger, Christian
|0 P:(DE-2719)2811625
|b 13
|u dzne
700 1 _ |a Halle, Annett
|0 P:(DE-2719)2812038
|b 14
|u dzne
700 1 _ |a Förster, Irmgard
|0 P:(DE-HGF)0
|b 15
|e Corresponding author
773 1 8 |a 10.1002/glia.23507
|b : Wiley, 2018-09-12
|n 10
|p 2246-2261
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|t Glia
|v 66
|y 2018
|x 0894-1491
773 _ _ |a 10.1002/glia.23507
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856 4 _ |u https://pub.dzne.de/record/140340/files/DZNE-2020-06662_Restricted.pdf
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914 1 _ |y 2018
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Marc 21