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Microglia enable cross-modal plasticity by removing inhibitory synapses.
Hashimoto, Akari; Kawamura, Nanami; Tarusawa, Etsuko; Takeda, Ikuko; Aoyama, Yuki; Ohno, Nobuhiko; Inoue, Mio; Kagamiuchi, Mai; Kato, Daisuke; Matsumoto, Mami; Hasegawa, Yoshihiro; Nabekura, Junichi; Schaefer, Anne; Moorhouse, Andrew J; Yagi, Takeshi; Wake, Hiroaki.
Affiliation
  • Hashimoto A; Department of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.
  • Kawamura N; KOKORO-Biology Group, Laboratories for Integrated Biology, Graduate School of Frontier Biosciences, Osaka University, Suita 565-0871, Japan.
  • Tarusawa E; KOKORO-Biology Group, Laboratories for Integrated Biology, Graduate School of Frontier Biosciences, Osaka University, Suita 565-0871, Japan.
  • Takeda I; Department of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.
  • Aoyama Y; Department of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.
  • Ohno N; Department of Anatomy, Division of Histology and Cell Biology, Jichi Medical University, Shimotsuke 329-0498, Japan; Division of Ultrastructural Research, National Institute for Physiological Sciences, Okazaki 444-8585, Japan.
  • Inoue M; Department of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.
  • Kagamiuchi M; Department of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.
  • Kato D; Department of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.
  • Matsumoto M; Section of Electron Microscopy, Supportive Center for Brain Research, National Institute for Physiological Sciences, Okazaki 444-8585, Japan; Department of Developmental and Regenerative Neurobiology, Institute of Brain Science, Nagoya City University Graduate School of Medical Sciences, Nagoya 467-
  • Hasegawa Y; Department of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.
  • Nabekura J; Division of Homeostatic Development, National Institute for Physiological Sciences, Okazaki 444-8585, Japan; Department of Physiological Sciences, Graduate University for Advanced Studies, SOKENDAI, Hayama 240-0193, Japan.
  • Schaefer A; Center for Glial Biology, Department of Neuroscience and Psychiatry, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029-6574, USA; Max Planck Institute for Biology of Ageing, 50931 Cologne, Germany.
  • Moorhouse AJ; School of Biomedical Sciences, The University of New South Wales, Sydney, NSW 2052, Australia.
  • Yagi T; KOKORO-Biology Group, Laboratories for Integrated Biology, Graduate School of Frontier Biosciences, Osaka University, Suita 565-0871, Japan.
  • Wake H; Department of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan; Division of Multicellular Circuit Dynamics, National Institute for Physiological Sciences, Okazaki 444-8585, Japan; Center for Optical Scattering Image Science, Kobe University, K
Cell Rep ; 42(5): 112383, 2023 05 30.
Article in En | MEDLINE | ID: mdl-37086724
Cross-modal plasticity is the repurposing of brain regions associated with deprived sensory inputs to improve the capacity of other sensory modalities. The functional mechanisms of cross-modal plasticity can indicate how the brain recovers from various forms of injury and how different sensory modalities are integrated. Here, we demonstrate that rewiring of the microglia-mediated local circuit synapse is crucial for cross-modal plasticity induced by visual deprivation (monocular deprivation [MD]). MD relieves the usual inhibition of functional connectivity between the somatosensory cortex and secondary lateral visual cortex (V2L). This results in enhanced excitatory responses in V2L neurons during whisker stimulation and a greater capacity for vibrissae sensory discrimination. The enhanced cross-modal response is mediated by selective removal of inhibitory synapse terminals on pyramidal neurons by the microglia in the V2L via matrix metalloproteinase 9 signaling. Our results provide insights into how cortical circuits integrate different inputs to functionally compensate for neuronal damage.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Visual Cortex / Microglia Limits: Animals Language: En Journal: Cell Rep Year: 2023 Document type: Article Affiliation country: Japan Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Visual Cortex / Microglia Limits: Animals Language: En Journal: Cell Rep Year: 2023 Document type: Article Affiliation country: Japan Country of publication: United States