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Sarhadi, M.

Publications and source records attributed to Sarhadi, M..

2 recordsLinked to original sources

Deciphering auditory neuroprogenitor stemness for large-scale neuronal screening

Sensorineural hearing loss can arise from damage to sensory hair cells, auditory neurons or their synaptic connections, with auditory neuropathy and cochlear synaptopathy highlighting the importance of neural integrity for hearing. The mammalian cochlea has limited capacity to regenerate lost auditory neurons. Understanding the molecular programs that sustain cochlear progenitor expansion and neurogenic competence could support neuronal regeneration and provide renewable models for auditory drug discovery. We previously established that WNT activation combined with dual SMAD inhibition (CHIR-DS) supports scalable expansion and neuronal differentiation of mouse auditory neuroprogenitors (ANPGs). Here, we characterize the transcriptional, chromatin and metabolic changes associated with the induced state. RNA-seq and ATAC-seq identified reduced Id1 and Id2 expression and increased accessibility at proneural basic helix-loop-helix motifs, alongside transcriptional enrichment of translation, mTOR and glucose-metabolism programs. Compared with growth-factor controls, CHIR-DS-treated ANPGs showed slight increase in glycolysis at early passage. However, after long-term expansion, both glycolysis and mitochondrial respiration were markedly enhanced. Human fetal ANPGs also responded to CHIR-DS with increased sphere growth and retained neural differentiation capacity, providing proof of concept beyond the mouse system. Finally, neurons derived from stemness-induced ANPGs (siANs) supported a 384-well reporter assay and a 2,560-compound pilot screen that nominated candidate neurite-outgrowth enhancers. Together, these findings validate the pathway basis of ANPG stemness induction, characterize the resulting molecular and metabolic state, and demonstrate human feasibility and a neuronal screening application.

neuroscience↗

Developmental gene expression patterns driving species-specific cortical features

The cerebral cortex shows species-specific variations in size and organization, likely accounting for distinct behavioral abilities. These structural differences may reflect evolutionary changes in the developmental expression of shared genes. To investigate this possibility, we compared cell-type-specific gene expression across species in the developing mouse and human neocortex, and human cortical organoids, by generating a shared transcriptional reference framework. This identified genes with conserved/divergent expression patterns, providing a molecular foundation to interrogate species-specific cellular properties. Using this resource, we discovered that the transcription factor JUNB is expressed in human but not mouse progenitors. Through cell-type-specific gain- and loss-of-function experiments in mice and human organoids, we demonstrate that JUNB bidirectionally controls human cortical features, including progenitor proliferation rates, neuronal production timing, and total neuronal output. This reveals how cell-type-specific regulation of shared genes during development can drive species-specific cortical features, providing a framework for understanding the molecular basis of cortical evolution.

neuroscience↗