Home > Publications Database > Neuron-glia interaction through Serotonin-BDNF-NGFR axis enables regenerative neurogenesis in Alzheimer's model of adult zebrafish brain. > print

001     145133
005     20240321221030.0
024 7 _ |a 10.1371/journal.pbio.3000585
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024 7 _ |a 1544-9173
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024 7 _ |a 1545-7885
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037 _ _ |a DZNE-2020-00492
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Bhattarai, Prabesh
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245 _ _ |a Neuron-glia interaction through Serotonin-BDNF-NGFR axis enables regenerative neurogenesis in Alzheimer's model of adult zebrafish brain.
260 _ _ |a Lawrence, KS
|c 2020
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264 _ 1 |3 online
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|c 2020-01-06
336 7 _ |a article
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336 7 _ |a ARTICLE
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520 _ _ |a It was recently suggested that supplying the brain with new neurons could counteract Alzheimer's disease (AD). This provocative idea requires further testing in experimental models in which the molecular basis of disease-induced neuronal regeneration could be investigated. We previously found that zebrafish stimulates neural stem cell (NSC) plasticity and neurogenesis in AD and could help to understand the mechanisms to be harnessed for developing new neurons in diseased mammalian brains. Here, by performing single-cell transcriptomics, we found that amyloid toxicity-induced interleukin-4 (IL4) promotes NSC proliferation and neurogenesis by suppressing the tryptophan metabolism and reducing the production of serotonin. NSC proliferation was suppressed by serotonin via down-regulation of brain-derived neurotrophic factor (BDNF)-expression in serotonin-responsive periventricular neurons. BDNF enhances NSC plasticity and neurogenesis via nerve growth factor receptor A (NGFRA)/ nuclear factor 'kappa-light-chain-enhancer' of activated B-cells (NFkB) signaling in zebrafish but not in rodents. Collectively, our results suggest a complex neuron-glia interaction that regulates regenerative neurogenesis after AD conditions in zebrafish.
536 _ _ |a 341 - Molecular Signaling (POF3-341)
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542 _ _ |i 2020-01-06
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650 _ 7 |a Brain-Derived Neurotrophic Factor
|2 NLM Chemicals
650 _ 7 |a Receptors, Nerve Growth Factor
|2 NLM Chemicals
650 _ 7 |a Zebrafish Proteins
|2 NLM Chemicals
650 _ 7 |a Serotonin
|0 333DO1RDJY
|2 NLM Chemicals
650 _ 2 |a Age Factors
|2 MeSH
650 _ 2 |a Alzheimer Disease: genetics
|2 MeSH
650 _ 2 |a Alzheimer Disease: pathology
|2 MeSH
650 _ 2 |a Alzheimer Disease: physiopathology
|2 MeSH
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a Animals, Genetically Modified
|2 MeSH
650 _ 2 |a Brain: metabolism
|2 MeSH
650 _ 2 |a Brain: physiology
|2 MeSH
650 _ 2 |a Brain-Derived Neurotrophic Factor: genetics
|2 MeSH
650 _ 2 |a Brain-Derived Neurotrophic Factor: metabolism
|2 MeSH
650 _ 2 |a Cell Communication: physiology
|2 MeSH
650 _ 2 |a Disease Models, Animal
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Mice
|2 MeSH
650 _ 2 |a Mice, Transgenic
|2 MeSH
650 _ 2 |a Nerve Regeneration: genetics
|2 MeSH
650 _ 2 |a Nerve Regeneration: physiology
|2 MeSH
650 _ 2 |a Neural Stem Cells: pathology
|2 MeSH
650 _ 2 |a Neural Stem Cells: physiology
|2 MeSH
650 _ 2 |a Neurogenesis: physiology
|2 MeSH
650 _ 2 |a Neuroglia: physiology
|2 MeSH
650 _ 2 |a Neuroimmunomodulation: physiology
|2 MeSH
650 _ 2 |a Neuronal Plasticity: physiology
|2 MeSH
650 _ 2 |a Neurons: physiology
|2 MeSH
650 _ 2 |a Receptors, Nerve Growth Factor: genetics
|2 MeSH
650 _ 2 |a Receptors, Nerve Growth Factor: metabolism
|2 MeSH
650 _ 2 |a Serotonin: genetics
|2 MeSH
650 _ 2 |a Serotonin: metabolism
|2 MeSH
650 _ 2 |a Signal Transduction: genetics
|2 MeSH
650 _ 2 |a Zebrafish
|2 MeSH
650 _ 2 |a Zebrafish Proteins: genetics
|2 MeSH
650 _ 2 |a Zebrafish Proteins: metabolism
|2 MeSH
700 1 _ |a Cosacak, Mehmet Ilyas
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700 1 _ |a Mashkaryan, Violeta
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700 1 _ |a Demir, Sevgican
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700 1 _ |a Popova, Stanislava Dimitrova
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700 1 _ |a Govindarajan, Nambirajan
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700 1 _ |a Brandt, Kerstin
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700 1 _ |a Zhang, Yixin
|b 7
700 1 _ |a Chang, Weipang
|b 8
700 1 _ |a Ampatzis, Konstantinos
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700 1 _ |a Kizil, Caghan
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773 1 8 |a 10.1371/journal.pbio.3000585
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773 _ _ |a 10.1371/journal.pbio.3000585
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LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21