Protocol describes induction and quantification of axon outgrowth in adult mouse DRG neurons, indicating a method for studying nerve regeneration.
Adult dorsal root ganglion (DRG) neurons provide a powerful model to study axon growth. Dissociated lumbar L3-L5 DRG neurons extend axons de novo in culture, enabling the measurement of baseline outgrowth. Here, we present a protocol for inducing and quantifying injury-primed axon outgrowth in adult mouse DRG neurons. We describe steps for sciatic nerve conditioning injury, isolating and culturing injured L3-L5 DRG neurons, and quantifying axon outgrowth. This protocol is compatible with cytoskeletal imaging and molecular profiling of injury-induced changes.
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Seburn et al. (2026) studied this question.
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