bioRxiv Science⌕ Search

Biology subjects

Masumura, R.

Publications and source records attributed to Masumura, R..

2 recordsLinked to original sources

Viral vectors with cluster of differentiation gene promoters to target specific cell types in the brain

Understanding brain function and developing targeted therapies for neurological disorders require precise access to specific cell types, but current methods are limited. Here, we report the development of cell-type specific adeno-associated virus (AAV) vectors utilizing promoters of cluster of differentiation genes (CD promoters) for targeted gene delivery in the brain. We newly identified CD promoters that induce gene expression selectively in specific cell types in the mouse brain. These AAVs enable in vivo calcium imaging and chemogenetic applications in specific cerebellar cells, revealing distinct and shared roles of two types of cerebellar interneurons. Notably, chemogenetic modulation of cerebellar molecular layer interneurons using a CD promoter rescued social behavior and motor deficits in a mouse model of autism spectrum disorder. Our findings demonstrate the utility of these AAVs in elucidating the functions of individual cell types in brain function and in developing novel, cell-type specific therapies for brain diseases.

neuroscience↗

Oligodendrocyte dependent synchronized activity orchestrates circuit maturation and brain functionalization

Synchronized spontaneous neural activity is a fundamental feature of developing central nervous systems and is thought to be essential for proper brain development. However, the mechanisms that regulate this synchronization and its long-term impact on brain function remain unclear. Here, we identify a previously unrecognized role of oligodendrocytes in orchestrating synchronized spontaneous activity during a critical developmental window, with lasting consequences for adult behavior. Using oligodendrocyte-specific genetic manipulation in the mouse cerebellum, we demonstrate that oligodendrocyte deficiency during early postnatal development, but not after weaning, disrupts the synchronization of Purkinje cell activity both during development and in adulthood. The early disruption produced persistent deficits in cerebellar-dependent behaviors, including anxiety, sociality, and motor function. Optogenetic re-synchronization in adulthood restored motor and social functions but not anxiety-like behavior, demonstrating that reduced Purkinje cell synchrony specifically drives the motor and social impairments. Our findings establish a causal link between developmental oligodendrocyte-regulated neural synchrony and the emergence of complex brain functions, which depend on the proper developmental trajectory necessary for driving brain function.

neuroscience↗