Proneurogenic Ligands Defined by Modeling Developing Cortex Growth Factor Communication Networks

The neural stem cell decision to self-renew or differentiate is tightly regulated by its microenvironment. Here, we have asked about this microenvironment, focusing on growth factors in the embryonic cortex at a time when it is largely comprised of neural precursor cells (NPCs) and newborn neurons. We show that cortical NPCs secrete factors that promote their maintenance, while cortical neurons secrete factors that promote differentiation. To define factors important for these activities, we used transcriptome profiling to identify ligands produced by NPCs and neurons, cell-surface mass spectrometry to identify receptors on these cells, and computational modeling to integrate these data. The resultant model predicts a complex growth factor environment with multiple autocrine and paracrine interactions. We tested this communication model, focusing on neurogenesis, and identified IFNγ, Neurturin (Nrtn), and glial-derived neurotrophic factor (GDNF) as ligands with unexpected roles in promoting neurogenic differentiation of NPCs in vivo. •Model of cortical neuron-cortical precursor communication from transcriptome data•Integration of cell-surface proteome of neurons/precursors into communication model•Cortical neuron-precursor communication model predicts proneurogenic ligands•IFNγ, Nrtn, and GDNF predicted by the model stimulate embryonic neurogenesis Yuzwa et al. use transcriptome and cell-surface proteome profiling of developing cortical neural precursors and neurons to model cell-cell communication between these two cell types. Testing the resulting integrated model identifies growth factors that promote genesis of neurons.