| First Author | Cheng YT | Year | 2023 |
| Journal | Nature | Volume | 617 |
| Issue | 7960 | Pages | 369-376 |
| PubMed ID | 37100909 | Mgi Jnum | J:350834 |
| Mgi Id | MGI:7525568 | Doi | 10.1038/s41586-023-06010-x |
| Citation | Cheng YT, et al. (2023) Inhibitory input directs astrocyte morphogenesis through glial GABA(B)R. Nature 617(7960):369-376 |
| abstractText | Communication between neurons and glia has an important role in establishing and maintaining higher-order brain function(1). Astrocytes are endowed with complex morphologies, placing their peripheral processes in close proximity to neuronal synapses and directly contributing to their regulation of brain circuits(2-4). Recent studies have shown that excitatory neuronal activity promotes oligodendrocyte differentiation(5-7); whether inhibitory neurotransmission regulates astrocyte morphogenesis during development is unclear. Here we show that inhibitory neuron activity is necessary and sufficient for astrocyte morphogenesis. We found that input from inhibitory neurons functions through astrocytic GABA(B) receptor (GABA(B)R) and that its deletion in astrocytes results in a loss of morphological complexity across a host of brain regions and disruption of circuit function. Expression of GABA(B)R in developing astrocytes is regulated in a region-specific manner by SOX9 or NFIA and deletion of these transcription factors results in region-specific defects in astrocyte morphogenesis, which is conferred by interactions with transcription factors exhibiting region-restricted patterns of expression. Together, our studies identify input from inhibitory neurons and astrocytic GABA(B)R as universal regulators of morphogenesis, while further revealing a combinatorial code of region-specific transcriptional dependencies for astrocyte development that is intertwined with activity-dependent processes. |
