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Mubuchi, A.

Publications and source records attributed to Mubuchi, A..

2 recordsLinked to original sources

Neuronal activity induces aggrecan expression to drive perineuronal net formation in cortical neurons

Synaptic plasticity, driven by activity-dependent changes in neuronal connectivity, underlies learning and memory. However, the mechanisms that sustain long-term synaptic stabilization are not well understood. Perineuronal nets (PNNs), which are lattice-like extracellular matrix structures that enwrap neurons, are thought to stabilize synapses. However, the mechanisms regulating their formation remain unclear. Here, we found that neuronal activity induces transcription of aggrecan, a core PNN component, which in turn promotes PNN assembly. In primary cultured mouse cortical neurons, pharmacological stimulation of neuronal activity robustly increased aggrecan expression, whereas activity blockade suppressed it. Among the PNN-related genes examined, aggrecan alone exhibited strong activity-dependent transcriptional regulation. Analysis of published in vivo datasets revealed selective upregulation of aggrecan in parvalbumin-positive interneurons following sensory stimulation. This regulation required calcium influx through voltage-gated calcium channels and was dependent on cAMP response element binding protein (CREB) signaling and chromatin remodeling. These findings reveal a novel molecular link between neuronal activity and PNN formation, providing insights into the mechanisms underlying the long-term stabilization of neural circuits.

neuroscience↗

Assembly of neuron- and radial glial cell-derived extracellular matrix molecules promotes radial migration of developing cortical neurons

Radial neuronal migration is a key neurodevelopmental event for proper cortical laminar organization. The multipolar-to-bipolar transition, a critical step in establishing neuronal polarity during radial migration, occurs in the subplate/intermediate zone (SP/IZ), a distinct region of the embryonic cerebral cortex. It has been known that the extracellular matrix (ECM) molecules are enriched in the SP/IZ. However, the molecular constitution and functions of the ECM formed in this region remain poorly understood. Here, we identified neurocan (NCAN) as a major chondroitin sulfate proteoglycan in the SP/IZ. NCAN binds to both radial glial cell-derived tenascin-C (TNC) and hyaluronan (HA), a large linear polysaccharide, forming a ternary complex of NCAN, TNC, and HA in the SP/IZ. Developing cortical neurons make contact with the ternary complex during migration. The enzymatic or genetic disruption of the ternary complex impairs radial migration by suppressing the multipolar-to-bipolar transition. Furthermore, both TNC and NCAN promoted the morphological maturation of cortical neurons in vitro. The present results provide evidence for the cooperative role of neuron- and radial glial cell-derived ECM molecules in cortical development.

neuroscience↗