Juvenile depletion of microglia reduces orientation but not high spatial frequency selectivity in mouse V1

• DOI: 10.1038/s41598-022-15503-0
• Publication Date: 2022-07-30T08:48:43Z
• Authors: Dario X. Figueroa...; Miguel Arreola; Carey Y. L. Huh; Kim Green; Sunil P. Gandhi
• Keywords: Pediatric; Neurons; 0303 health sciences; Science; Macrophage Colony-Stimulating Factor; Colony-Stimulating Factor; Q; Neurosciences; R; Article; Mice; 03 medical and health sciences; Neurological; Receptors; Receptors, Colony-Stimulating Factor; Synapses; Medicine; Animals; Microglia; Eye Disease and Disorders of Vision; Photic Stimulation; Visual Cortex

AbstractMicroglia contain multiple mechanisms that shape the synaptic landscape during postnatal development. Whether the synaptic changes mediated by microglia reflect the developmental refinement of neuronal responses in sensory cortices, however, remains poorly understood. In postnatal life, the development of increased orientation and spatial frequency selectivity of neuronal responses in primary visual cortex (V1) supports the emergence of high visual acuity. Here, we used the colony-stimulating factor 1 receptor (CSF1R) inhibitor PLX5622 to rapidly and durably deplete microglia in mice during the juvenile period in which increased orientation and spatial frequency selectivity emerge. Excitatory and inhibitory tuning properties were measured simultaneously using multi-photon calcium imaging in layer II/III of mouse V1. We found that microglia depletion generally increased evoked activity which, in turn, reduced orientation selectivity. Surprisingly, microglia were not required for the emergence of high spatial frequency tuned responses. In addition, microglia depletion did not perturb cortical binocularity, suggesting normal depth processing. Together, our finding that orientation and high spatial frequency selectivity in V1 are differentially supported by microglia reveal that microglia are required normal sensory processing, albeit selectively.