In vivo , peripheral nerve injury enables adult dorsal root ganglion (DRG) neurons to support regeneration of their spinal cord axons (Richardson & Issa, Nature 309:79,1984. It is not known which of the genes induced by this injury are needed for regeneration. In vitro, combined expression of GAP-43 and CAP-23, two prominent growth cone proteins, can mimic peripheral nerve injury in triggering the extension of long axons by adult DRG neurons (Bomze et. al, this volume). To determine whether replacement of these two proteins is sufficient to induce regeneration in vivo, we made bilateral dorsal column lesions that sever the central axons of DRG neurons in wild-type mice and in transgenic animals expressing both GAP-43 and CAP-23. A segment of peripheral nerve (sciatic) was resected on one side and grafted into the lesion site. After 1-4 months, diI was introduced into the distal end of the graft to retrogradely label the cell bodies of those axons that had regenerated into the graft. DRG subjected to the pe...

Previous attempts to model motoneuron action potentials, spike frequency adaptation, and steady-state repetitive discharge behavior have relied on geometrically simple models that do not explicitly represent the myelinated axon of the neuron. However, there is evidence that action potential initiation (API), from current injection into the cell body or excitatory synaptic input, takes place not in the cell body or initial segment, but in a node of the myelinated axon. The goal of this study was to develop motoneuron models that represent the complete neuronal architecture, and the ion channel type and density in the different neural elements. The models consisted of a myelinated axon, initial segment, soma, and either a three-dimensional branching dendritic tree or a single equivalent tapering cylinder. The nodes of the axon had fast sodium (INa), persistant sodium (INap), slow potassium, and leakage (IL) channels. The initial segment had INa, INap, delayed rectifier potassium (IKdr), and IL channels. The ...

It is widely believed that axons in the central nervous system of adult mammals do not regrow following injury. This failure is thought, at least in part, to underlie the limited recovery of function following injury to the brain or spinal cord. Some studies of fixed tissue have suggested that, counter to dogma, norepinephrine (NE) axons regrow following brain injury. Here, we have used in vivo two-photon microscopy in layer 1 of the primary somatosensory cortex in transgenic mice harboring a fluorophore selectively expressed in NE neurons. This protocol allowed us to explore the dynamic nature of NE axons following injury with the selective NE axon toxin N -(2-chloroethyl)- N -ethyl-2-bromobenzylamine (DSP4). Following DSP4, NE axons were massively depleted and then slowly and partially recovered their density over a period of weeks. This regrowth was dominated by new axons entering the imaged volume. There was almost no contribution from local sprouting from spared NE axons. Regrown axons did not appear ...

It is widely believed that axons in the central nervous system of adult mammals do not regrow following injury. This failure is thought, at least in part, to underlie the limited recovery of function following injury to the brain or spinal cord. Some studies of fixed tissue have suggested that, counter to dogma, norepinephrine (NE) axons regrow following brain injury. Here, we have used in vivo two-photon microscopy in layer 1 of the primary somatosensory cortex in transgenic mice harboring a fluorophore selectively expressed in NE neurons. This protocol allowed us to explore the dynamic nature of NE axons following injury with the selective NE axon toxin N-(2-chloroethyl)-N-ethyl-2-bromobenzylamine (DSP4). Following DSP4, NE axons were massively depleted and then slowly and partially recovered their density over a period of weeks. This regrowth was dominated by new axons entering the imaged volume. There was almost no contribution from local sprouting from spared NE axons. Regrown axons did not appear to ...

Mitogen-activated protein kinase kinase kinases (MAP3Ks) dual leucine kinase (DLK) and leucine zipper kinase (LZK) are essential mediators of axon damage responses, but their responses are varied, complex, and incompletely understood. To characterize their functions in axon injury, we generated zebrafish mutants of each gene, labeled motor neurons (MNs) and touch-sensing neurons in live zebrafish, precisely cut their axons with a laser, and assessed the ability of mutant axons to regenerate in larvae, before sex is apparent in zebrafish. DLK and LZK were required redundantly and cell autonomously for axon regeneration in MNs but not in larval Rohon–Beard (RB) or adult dorsal root ganglion (DRG) sensory neurons. Surprisingly, in dlk lzk double mutants, the spared branches of wounded RB axons grew excessively, suggesting that these kinases inhibit regenerative sprouting in damaged axons. Uninjured trigeminal sensory axons also grew excessively in mutants when neighboring neurons were ablated, indicating that...

KIFC1 (also called HSET or kinesin-14a) is best known as a multifunctional motor protein essential for mitosis. The present studies are the first to explore KIFC1 in terminally postmitotic neurons. Using RNA interference to partially deplete KIFC1 from rat neurons (from animals of either gender) in culture, pharmacologic agents that inhibit KIFC1, and expression of mutant KIFC1 constructs, we demonstrate critical roles for KIFC1 in regulating axonal growth and retraction as well as growth cone morphology. Experimental manipulations of KIFC1 elicit morphological changes in the axon as well as changes in the organization, distribution, and polarity orientation of its microtubules. Together, the results indicate a mechanism by which KIFC1 binds to microtubules in the axon and slides them into alignment in an ATP-dependent fashion and then cross-links them in an ATP-independent fashion to oppose their subsequent sliding by other motors. SIGNIFICANCE STATEMENT Here, we establish that KIFC1, a molecular motor w...

Recording the spiking activity from subcellular compartments of neurons such as axons and dendrites during mouse behavior with 2-photon calcium imaging is increasingly common yet remains challenging due to low signal-to-noise, inaccurate region-of-interest (ROI) identification, movement artifacts, and difficulty in grouping ROIs from the same neuron. To address these issues, we present a computationally efficient preprocessing pipeline for subcellular signal detection, movement artifact identification, and ROI grouping. For subcellular signal detection, we capture the frequency profile of calcium transient dynamics by applying fast Fourier transform (FFT) on smoothed time-series calcium traces collected from axon ROIs. We then apply bandpass filtering methods (e.g., 0.05–0.12 Hz) to select ROIs that contain frequencies that match the power band of transients. To remove motion artifacts from z -plane movement, we apply principal component analysis on all calcium traces and use a bottom-up segmentation chang...

Recording the spiking activity from subcellular compartments of neurons such as axons and dendrites during mouse behavior with 2-photon calcium imaging is increasingly common yet remains challenging due to low signal-to-noise, inaccurate region-of-interest (ROI) identification, movement artifacts, and difficulty in grouping ROIs from the same neuron. To address these issues, we present a computationally efficient pre-processing pipeline for subcellular signal detection, movement artifact identification, and ROI grouping. For subcellular signal detection, we capture the frequency profile of calcium transient dynamics by applying Fast Fourier Transform (FFT) on smoothed time-series calcium traces collected from axon ROIs. We then apply band-pass filtering methods (e.g. 0.05 to 0.12 Hz) to select ROIs that contain frequencies that match the power band of transients. To remove motion artifacts from z-plane movement, we apply Principal Component Analysis on all calcium traces and use a Bottom-Up Segmentation ch...

The initial outgrowth of peripheral axons in developing embryos is thought to occur independently of neurotrophins. However, the degree to which peripheral neurons can extend axons and elaborate axonal arborizations in the absence of these molecules has not been studied directly because of exquisite survival requirements for neurotrophins at early developmental stages. We show here that embryonic sensory neurons from BAX-deficient mice survived indefinitely in the absence of neurotrophins, even in highly dissociated cultures, allowing assessment of cell autonomous axon outgrowth. At embryonic day 11 (E11)–E13, stages of rapid axon growth toward targets in vivo , Bax −/− sensory neurons cultured without neurotrophins were almost invariably unipolar and extended only a rudimentary axon. Addition of neurotrophins caused outgrowth of a second axon and a marked, dose-dependent elongation of both processes. Surprisingly, morphological responses to individual neurotrophins differed substantially. Neurotrophin-3 (...

Understanding the bioenergetics of axon extension and maintenance has wide ranging implications for neurodevelopment and disease states. Glycolysis is a pathway consisting of ten enzymes and separated into preparatory and payoff phases, the latter producing ATP. Using embryonic chicken sensory neurons, we report that glycolytic enzymes are found through the axon and the growth cone. Pharmacological inhibition of glycolysis in the presence of NGF impairs axon extension and growth cone dynamics within minutes without affecting axon maintenance. Experiments using microfluidic chambers show the effect of inhibiting glycolysis on axon extension is local along distal axons and can be reversed by promoting mitochondrial respiration. Knock down of GAPDH simplifies growth cone morphology and is rescued by shRNA resistant GAPDH expression. Rescue of GAPDH using killer red (KR) fused to GAPDH followed by localized chromophore assisted light inactivation of KR-GAPDH in distal axons halts growth cone dynamics. Consider...