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Toro-Tapia, G.

Publications and source records attributed to Toro-Tapia, G..

2 recordsLinked to original sources

Gαi2 coordinates neuronal microtubule and neurofilament networks to regulate axon initiation in vivo

Neurons possess a highly polarised morphology, established through axon formation. However, the mechanisms regulating stable axon initiation during embryonic development remain poorly understood. Here, using fixed-tissue super-resolution and high-resolution live-tissue imaging in developing chick spinal cord, we demonstrate that the multifunctional G-protein Gi2 coordinates the interconnected neurofilament and microtubule networks to achieve stable axon outgrowth. Before axon initiation, microtubule network orientation shifts towards the site of the future axon where coiled Gi2-associated neurofilaments accumulate asymmetrically before unfurling into the initiating axon behind microtubules. Crucially, Gi2 is associated with neurofilaments and microtubules at points of contact. Gi2 depletion reduces engagement between these cytoskeletal networks, and leads to impaired passage of neurofilaments into initiating axons and disrupted axon outgrowth, supporting a role for Gi2 in regulating microtubule-driven incorporation of neurofilaments in nascent axons. These findings advance mechanistic understanding of polarity establishment and offer an enriched view of cytoskeletal regulation during axon formation.

developmental biology↗

Ciliary cAMP regulates Shh signal interpretation to drive polarisation of differentiating neurons

Cellular differentiation is characterised by transitions in cell-state through reinterpretation of extracellular signals. However, the mechanisms facilitating context-dependent signal interpretation remain poorly understood. Differentiating neurons remodel a molecularly distinct primary cilium as they switch from canonical to non-canonical Shh signalling. Here, using long-term live-tissue imaging, we demonstrate that the opposing Shh signalling modulators Smo and GPR161 simultaneously accumulate in the remodelled primary cilium. The correct balance of Smo and GPR161 leads to elevated ciliary cAMP levels, which suppresses Gli transcription factor activation and regulates actin dynamics to drive neuron polarisation. Notably, disrupting this balance through Smo hyperactivation or GPR161 depletion results in reduced ciliary cAMP, inappropriate activation of canonical Shh signalling, dysregulated actin dynamics and initiation of multiple unstable axon-like projections. Thus, this study identifies shifts in ciliary cAMP levels as a key regulator of cellular signal interpretation, and links primary cilium-mediated signal transduction to precise control of cytoskeletal organisation.

developmental biology↗