Microglial G.sub.i-dependent dynamics regulate brain network hyperexcitability
Microglial surveillance is a key feature of brain physiology and disease. Here, we found that G.sub.i-dependent microglial dynamics prevent neuronal network hyperexcitability. By generating Mg.sup.PTX mice to genetically inhibit G.sub.i in microglia, we show that sustained reduction of microglia bra...
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Published in | Nature neuroscience Vol. 24; no. 1; pp. 19 - 23 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Nature Publishing Group
01.01.2021
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Abstract | Microglial surveillance is a key feature of brain physiology and disease. Here, we found that G.sub.i-dependent microglial dynamics prevent neuronal network hyperexcitability. By generating Mg.sup.PTX mice to genetically inhibit G.sub.i in microglia, we show that sustained reduction of microglia brain surveillance and directed process motility induced spontaneous seizures and increased hypersynchrony after physiologically evoked neuronal activity in awake adult mice. Thus, G.sub.i-dependent microglia dynamics may prevent hyperexcitability in neurological diseases. |
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AbstractList | Microglial surveillance is a key feature of brain physiology and disease. Here, we found that G.sub.i-dependent microglial dynamics prevent neuronal network hyperexcitability. By generating Mg.sup.PTX mice to genetically inhibit G.sub.i in microglia, we show that sustained reduction of microglia brain surveillance and directed process motility induced spontaneous seizures and increased hypersynchrony after physiologically evoked neuronal activity in awake adult mice. Thus, G.sub.i-dependent microglia dynamics may prevent hyperexcitability in neurological diseases. Merlini, Rafalski et al. show that dynamic microglial brain surveillance prevents hyperexcitability and seizures by G.sub.i-dependent microglia-neuron interactions in response to evoked neuronal activity to maintain physiological network synchronization. Microglial surveillance is a key feature of brain physiology and disease. Here, we found that G.sub.i-dependent microglial dynamics prevent neuronal network hyperexcitability. By generating Mg.sup.PTX mice to genetically inhibit G.sub.i in microglia, we show that sustained reduction of microglia brain surveillance and directed process motility induced spontaneous seizures and increased hypersynchrony after physiologically evoked neuronal activity in awake adult mice. Thus, G.sub.i-dependent microglia dynamics may prevent hyperexcitability in neurological diseases. |
Audience | Academic |
Author | Palop, Jorge J Sampson, Daniel Naranjo Merlini, Mario Kim, Keun-Young Rios Coronado, Pamela E Tognatta, Reshmi Acevedo, Rosa Meza Thomas, Reuben Cabriga, Belinda Sozmen, Elif G Petersen, Mark A Coughlin, Shaun R Rafalski, Victoria A Ellisman, Mark H Bardehle, Sophia Dean, Terry, Jr Mendiola, Andrew S Ma, Keran Ryu, Jae Kyu Yan, Zhaoqi Bushong, Eric A Haberl, Matthias G Akassoglou, Katerina |
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SubjectTerms | Brain diseases Development and progression Health aspects Neural circuitry Physiological aspects Seizures (Medicine) |
Title | Microglial G.sub.i-dependent dynamics regulate brain network hyperexcitability |
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