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Microglial displacement of inhibitory synapses provides neuroprotection in the adult brain

Author

Listed:
  • Zhihong Chen

    (Lerner Research Institute, Cleveland Clinic)

  • Walid Jalabi

    (Lerner Research Institute, Cleveland Clinic)

  • Weiwei Hu

    (Lerner Research Institute, Cleveland Clinic
    School of Basic Medical Sciences, Zhejiang University)

  • Hyun-Joo Park

    (Lerner Research Institute, Cleveland Clinic)

  • John T. Gale

    (Lerner Research Institute, Cleveland Clinic
    Center for Neurological Restoration, Neurological Institute, Cleveland Clinic)

  • Grahame J. Kidd

    (Lerner Research Institute, Cleveland Clinic)

  • Rodica Bernatowicz

    (Lerner Research Institute, Cleveland Clinic)

  • Zachary C. Gossman

    (Lerner Research Institute, Cleveland Clinic)

  • Jacqueline T. Chen

    (Lerner Research Institute, Cleveland Clinic)

  • Ranjan Dutta

    (Lerner Research Institute, Cleveland Clinic)

  • Bruce D. Trapp

    (Lerner Research Institute, Cleveland Clinic)

Abstract

Microglia actively survey the brain microenvironment and play essential roles in sculpting synaptic connections during brain development. While microglial functions in the adult brain are less clear, activated microglia can closely appose neuronal cell bodies and displace axosomatic presynaptic terminals. Microglia-mediated stripping of presynaptic terminals is considered neuroprotective, but the cellular and molecular mechanisms are poorly defined. Using 3D electron microscopy, we demonstrate that activated microglia displace inhibitory presynaptic terminals from cortical neurons in adult mice. Electrophysiological recordings further establish that the reduction in inhibitory GABAergic synapses increased synchronized firing of cortical neurons in γ-frequency band. Increased neuronal activity results in the calcium-mediated activation of CaM kinase IV, phosphorylation of CREB, increased expression of antiapoptotic and neurotrophic molecules and reduced apoptosis of cortical neurons following injury. These results indicate that activated microglia can protect the adult brain by migrating to inhibitory synapses and displacing them from cortical neurons.

Suggested Citation

  • Zhihong Chen & Walid Jalabi & Weiwei Hu & Hyun-Joo Park & John T. Gale & Grahame J. Kidd & Rodica Bernatowicz & Zachary C. Gossman & Jacqueline T. Chen & Ranjan Dutta & Bruce D. Trapp, 2014. "Microglial displacement of inhibitory synapses provides neuroprotection in the adult brain," Nature Communications, Nature, vol. 5(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms5486
    DOI: 10.1038/ncomms5486
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    Cited by:

    1. Ru-Siou Hsu & Ssu-Ju Li & Jen-Hung Fang & I-Chi Lee & Li-An Chu & Yu-Chun Lo & Yu-Jen Lu & You-Yin Chen & Shang-Hsiu Hu, 2022. "Wireless charging-mediated angiogenesis and nerve repair by adaptable microporous hydrogels from conductive building blocks," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    2. Faith H. Brennan & Yang Li & Cankun Wang & Anjun Ma & Qi Guo & Yi Li & Nicole Pukos & Warren A. Campbell & Kristina G. Witcher & Zhen Guan & Kristina A. Kigerl & Jodie C. E. Hall & Jonathan P. Godbout, 2022. "Microglia coordinate cellular interactions during spinal cord repair in mice," Nature Communications, Nature, vol. 13(1), pages 1-20, December.

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