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Hanashima, C.

Publications and source records attributed to Hanashima, C..

2 recordsLinked to original sources

Most early-born subplate neurons persist as Layer 6b neurons in the adult mouse neocortex

Subplate neurons (SpNs) are among the earliest-born neurons in the mammalian neocortex and play key roles in radial migration and transient circuit formation. It has long been assumed that most SpNs undergo extensive postnatal cell death, leaving only a small remnant population that contributes to layer 6b (L6b) in adulthood. However, the extent to which SpNs actually persist as L6b neurons has remained unresolved, partly because previous studies lacked quantitative, whole-cortex analyses that account for postnatal cortical expansion. Here, we performed a comprehensive birthdating analysis using multiple EdU injections spanning the entire neurogenic window of SpNs in mice, combined with whole-neocortex 3D tissue clearing to measure subplate and L6b volumes. This approach allowed us to directly estimate the total number and distribution of SpN-derived neurons in adulthood. We found that most early-born SpNs persist as L6b neurons, and that the apparent postnatal reduction in SpN density reflects tangential cortical expansion rather than neuronal loss. Moreover, surviving SpNs comprise diverse neuronal subtypes reminiscent of those present at early postnatal stages. Together, these findings demonstrate that, in rodents, the majority of adult L6b neurons originate from SpNs, revising the long-held view that the subplate is a largely transient neuronal population.

neuroscience↗

Post-synaptic competition between calcineurin and PKA regulates mammalian sleep-wake cycles

Phosphorylation of synaptic proteins is a pivotal biochemical reaction that controls the sleep-wake cycle in mammals. Protein phosphorylation in vivo is reversibly regulated by kinases and phosphatases. In this study, we investigated a pair of kinases and phosphatases that reciprocally regulate sleep duration. Through comprehensive screening of Protein kinase A (PKA) and phosphoprotein phosphatase (PPP) family genes via the generation of 40 gene knockout mouse lines including post-natal CRISPR targeting, we identified a regulatory subunit of PKA (Prkar2b), a regulatory subunit of protein phosphatase (PP) 1 (Pppr1r9b), and catalytic and regulatory subunits of PP2B (calcineurin) (Ppp3ca and Ppp3r1) as sleep control genes. AAV-mediated stimulation of PKA and PP1/calcineurin activities confirmed PKA as a wake-promoting kinase, while PP1 and calcineurin function as sleep-promoting phosphatases. The importance of these phosphatases in sleep regulation is supported by the dramatic changes in sleep duration associated with their increased and decreased activity, ranging from approximately 17.3 hours/day (PP1 expression) to 6.7 hours/day (post-natal CRISPR targeting of calcineurin). For these phosphatases to exert their sleep-promoting effects, localization signals to the excitatory post-synapse were necessary. Furthermore, the wake-promoting effect of PKA localized to the excitatory post-synapse negated the sleep-promoting effect of calcineurin, suggesting that PKA and calcineurin construct a hierarchical phosphorylation control network for sleep regulation at excitatory post-synapses.

neuroscience↗