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 inNature neuroscience Vol. 24; no. 1; pp. 19 - 23
Main Authors Merlini, Mario, Rafalski, Victoria A, Ma, Keran, Kim, Keun-Young, Bushong, Eric A, Rios Coronado, Pamela E, Yan, Zhaoqi, Mendiola, Andrew S, Sozmen, Elif G, Ryu, Jae Kyu, Haberl, Matthias G, Sampson, Daniel Naranjo, Petersen, Mark A, Bardehle, Sophia, Tognatta, Reshmi, Dean, Terry, Jr, Acevedo, Rosa Meza, Cabriga, Belinda, Thomas, Reuben, Coughlin, Shaun R, Ellisman, Mark H, Palop, Jorge J, Akassoglou, Katerina
Format Journal Article
LanguageEnglish
Published 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.
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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