Primary neuronal cultures derived from mouse tissue serve as an essential model for investigating neuronal development and function. Despite this, comprehensive developmental and sex-specific transcriptomic profiles in primary neurons have not been defined. Here, we perform multiplexed RNA sequencing of neurons derived from male and female cortices across time. We validate this approach by assessing established neuronal maturation genes and identify highly stable genes to serve as controls across development. Next, using linear modeling and temporal regression, we define developmentally regulated transcripts, longitudinal expression dynamics, and gene signatures associated with transition states throughout development. Unexpectedly, this also reveals sex-specific effects on autosomal genes that emerge only after neuronal maturation even in the absence of in vivo cues. Most notably, neuropeptide genes Cortistatin and Neurokinin A are more highly expressed in female neurons. Furthermore, exposure to these neuropeptides elicits distinct transcriptional responses in male- versus female-derived cultures. These findings provide a valuable resource and reveal sex-specific autosomal transcriptional signatures that emerge in neurons maintained ex vivo.
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Paranjapye et al. (2026) studied this question.
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