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Leaman, S.

Publications and source records attributed to Leaman, S..

2 recordsLinked to original sources

Functional recruitment of astrocyte-derived neurons into the mouse visual cortex

Inducing neurogenesis from glia could permit circuit remodeling and neuron replacement in the brain. Indirect evidence suggests that glia-to-neuron reprogramming is feasible, but the dynamics of conversion have not been directly observed, and it remains unclear whether glia-derived cortical neurons can functionally integrate into brain circuits. Here, we use two-photon imaging to visualize the reprogramming of astroglia into induced neurons in the mouse cortex in vivo. We track the emergence of spontaneous neuron-like calcium transients in astrocyte-derived induced neurons, demonstrating their functional activity in vivo. Importantly, these induced neurons exhibit orientation tuned, visually evoked calcium responses, demonstrating their functional integration into cortical circuitry - a prerequisite for their utility in circuit repair. Thus, astrocytes can be recruited to generate functional neurons in the postnatal cortex, enabling circuit remodeling in perinatal injury or neurodevelopmental disorders without relying on external cellular sources.

neuroscience↗

Dlx2 reprograms the transcriptome and laminar position of glia-derivedAscl1-induced interneurons

Direct lineage reprogramming of glial cells into neurons offers a promising strategy to repair diseased brain circuits, but engineering defined neuronal subtypes remains challenging. We found that a phospho-site-deficient Ascl1 variant, Ascl1SA6, but not wildtype Ascl1, induces hallmarks of parvalbumin fast-spiking interneurons, raising the question of how closely these induced neurons resemble canonical cortical interneurons and what transcriptional events underlie this process. Single-cell transcriptomic analysis revealed that Ascl1SA6-induced neurons only partially recapitulated canonical interneuron programs and failed to induce the transcription factor Dlx2 and its downstream targets. Co-expression of Dlx2 with Ascl1SA6 restored a more canonical interneuron-like transcriptome, including genes involved in migration, and resulted in neurons occupying laminar positions more typical of endogenous interneurons. These findings provide molecular insights into how Ascl1 posttranslational modifications regulate its transcriptional activity and demonstrate a strategy to engineer induced cortical interneurons that more closely resemble their native counterparts, offering a framework for layer-specific restoration of inhibitory circuits in neurological diseases.

neuroscience↗