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GABA-receptive microglia selectively sculpt developing inhibitory circuits.

Cell (2021-07-08)
Emilia Favuzzi, Shuhan Huang, Giuseppe A Saldi, Loïc Binan, Leena A Ibrahim, Marian Fernández-Otero, Yuqing Cao, Ayman Zeine, Adwoa Sefah, Karen Zheng, Qing Xu, Elizaveta Khlestova, Samouil L Farhi, Richard Bonneau, Sandeep Robert Datta, Beth Stevens, Gord Fishell
RESUMEN

Microglia, the resident immune cells of the brain, have emerged as crucial regulators of synaptic refinement and brain wiring. However, whether the remodeling of distinct synapse types during development is mediated by specialized microglia is unknown. Here, we show that GABA-receptive microglia selectively interact with inhibitory cortical synapses during a critical window of mouse postnatal development. GABA initiates a transcriptional synapse remodeling program within these specialized microglia, which in turn sculpt inhibitory connectivity without impacting excitatory synapses. Ablation of GABAB receptors within microglia impairs this process and leads to behavioral abnormalities. These findings demonstrate that brain wiring relies on the selective communication between matched neuronal and glial cell types.

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Nucleasas Benzonase®, ≥250 units/μL, ≥90% (SDS-PAGE), recombinant, expressed in E. coli, buffered aqueous glycerol solution
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DAPI, for nucleic acid staining
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Anticuerpo anti-NeuN (conejo), from rabbit, purified by affinity chromatography
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Anticuerpo anti-transportador de glutamato vesicular 1, serum, Chemicon®
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Anticuerpo anti-NeuN purificado, from guinea pig, purified by affinity chromatography
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Anti-GABA B Receptor R2 Antibody, serum, from guinea pig
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Anti-Glutamate Decarboxylase Antibody, 65 kDa isoform, clone GAD-6, clone GAD-6, Chemicon®, from mouse