A P2RY12 deficiency results in sex-specific cellular perturbations and sexually dimorphic behavioral anomalies

Microglia are sexually dimorphic, yet, this critical aspect is often overlooked in neuroscientific studies. Decades of research have revealed the dynamic nature of microglial-neuronal interactions, but seldom consider how this dynamism varies with microglial sex differences, leaving a significant gap in our knowledge. This study focuses on P2RY12, a highly expressed microglial signature gene that mediates microglial-neuronal interactions, we show that adult females have a significantly higher expression of the receptor than adult male microglia. We further demonstrate that a genetic deletion of P2RY12 induces sex-specific cellular perturbations with microglia and neurons in females more significantly affected. Correspondingly, female mice lacking P2RY12 exhibit unique behavioral anomalies not observed in male counterparts. These findings underscore the critical, sex-specific roles of P2RY12 in microglial-neuronal interactions, offering new insights into basal interactions and potential implications for CNS disease mechanisms. Microglial P2RY12 shows a greater protein expression in adult females than adult malesMicroglial P2RY12 deficiency triggers morphological perturbations, especially in femalesMicroglial P2RY12 deficiency triggers sex-specific dendritic spine alterationsMicroglial P2RY12 deficiency triggers sexually dimorphic behavioral anomalies