|Home | About | Journals | Submit | Contact Us | Français|
The robust axonal growth and regenerative capacities of young neurons decrease substantially with age. This developmental downregulation of axonal growth may facilitate axonal pruning and neural circuit formation but limits functional recovery following nerve damage. While external factors influencing axonal growth have been extensively investigated, relatively little is known about the intrinsic molecular changes underlying the age-dependent reduction in regeneration capacity. We report that developmental downregulation of LIS1 is responsible for the decreased axonal extension capacity of mature dorsal root ganglion (DRG) neurons. In contrast, exogenous LIS1 expression or endogenous LIS1 augmentation by calpain inhibition restored axonal extension capacity in mature DRG neurons and facilitated regeneration of the damaged sciatic nerve. The insulator protein CTCF suppressed LIS1 expression in mature DRG neurons, and this reduction resulted in excessive accumulation of phosphoactivated GSK-3β at the axon tip, causing failure of the axonal extension. Conversely, sustained LIS1 expression inhibited developmental axon pruning in the mammillary body. Thus, LIS1 regulation may coordinate the balance between axonal growth and pruning during maturation of neuronal circuits.
The progressive growth of the vertebrate nervous system during embryonic and early postnatal development results in an overabundance of neural connections, requiring targeted elimination to facilitate functional circuit organization (Luo and O'Leary, 2005). An important regressive event is the ‘pruning’ or selective removal of superfluous synapses, axon branches, and dendrites. Axon elimination can occur at different levels, involving small-scale pruning of axon terminals or larger-scale removal of entire collaterals (Vanderhaeghen and Cheng, 2010). Improper pruning in humans has been implicated in various disease states such as autism and schizophrenia (Rosenthal, 2011; Saugstad, 2011). In both flies and mammals, developmental pruning of entire axon branches occurs within a relatively short period of time (Nakamura and O'Leary, 1989; Watts et al., 2003).
Developmental pruning of larger axon segments resembles the fragmentation and eventual disintegration of the distal axon segment following peripheral nerve transection, an active process known as Wallerian degeneration (Conforti et al., 2014). This degeneration allows proximal axons of the peripheral nervous system to regenerate and reinnervate targets, enabling at least partial functional recovery. In contrast to peripheral axons, the repair capacity of central axons is more limited and declines further with age. This unique characteristic of the peripheral nervous system stems at least in part from the ability of Schwann cells (SCs) to provide a proregenerative microenvironment (Son and Thompson, 1995) involving debris clearance, upregulation of membrane-bound and diffusible cues for axonal guidance and organization (Parrinello et al., 2010), and release of prosurvival factors. With advancing age, however, both the speed and the extent of functional recovery decrease following peripheral nerve injury. A number of explanations have been proposed for slower and less complete functional recovery of peripheral axons with age. Adult peripheral axons may regenerate less vigorously than embryonic axons due to intrinsic changes, such as decreased axonal transport by cytoskeletal proteins (Brunetti et al., 1987; McQuarrie and Lasek, 1989; Tashiro and Komiya, 1994). Alternatively, older axons may have fewer trophic factor receptors (Ferguson and Son, 2011; Uchida and Tomonaga, 1987). In addition, the periaxonal milieu provided by SCs in older animals has lower concentrations of growth and guidance factors (Bosse, 2012; Komiyama and Suzuki, 1992; Martini, 1994). Finally, impaired neuron-Schwann cell signaling may limit functional recovery by reducing the accuracy of target reinnervation (Kawabuchi et al., 2011). This downregulation of axon regeneration with age may be necessitated by the axon pruning process. One hypothesis is that, to ensure efficient axon pruning, the capacity for axon regeneration must be suppressed.
LIS1 was originally identified as a gene mutated in lissencephaly (Dobyns, 1989; Dobyns et al., 1993; Reiner et al., 1993), a developmental brain disorder caused by defective neuronal migration and consequent cortical dysplasia. Regulation of the motor protein dynein by LIS1 has been intensively investigated (Kardon and Vale, 2009; Vallee and Tsai, 2006; Wynshaw-Boris, 2007). Movement of dynein toward the minus end of the microtubule network is essential for retrograde transport. We previously reported that LIS1 suppresses dynein motility on microtubules in an idling state, which is essential for plus-end-directed (anterograde) transport of dynein by kinesin-1 (Yamada et al., 2008). Some isolated lissencephaly sequence cases (40%) are caused by LIS1 haploinsufficiency. We found that in utero administration of calpain inhibitors rescued phenotypes of Lis1+/− mice, including excessive neuronal apoptosis and migration deficits resulting in cortical dysplasia (Yamada et al., 2009). In addition, the blood brain barrier (BBB)-permeable calpain inhibitor SNJ1945, delivered perinatally or in utero via pregnant dams, rescued defective neuronal migration in Lis1+/− mice (Toba et al., 2013).
Here, we demonstrate that physiological LIS1 downregulation via the DNA-binding zinc finger protein CCCTC-binding factor (CTCF) (Ong and Corces, 2014) is responsible for the age-dependent decrease in axonal regenerative capacity of dorsal root ganglion (DRG) neurons. Our findings uncovered a surprising mechanism for the coordination between axonal extension and pruning by the regulation of LIS1 expression.
DRG neurons are a favored model to study axonal regeneration because they possess two axonal branches, one of which projects into the peripheral and the other into the central nervous system. We isolated DRG neurons at various postnatal stages from Lis1+/+ (wild-type, WT) and Lis1+/− (Lis1−/− nulls die immediately after implantation) mice (Hirotsune et al., 1998) and examined the potential for axonal extension in cell culture. Axon length of each DRG neuron was defined as the sum of all projections including branches. At postnatal day (P)3, WT DRG neurons robustly extended axonal processes with extensive arborization, whereas axonal extension was significantly reduced at P15 (Fig. 1A). DRG neurons derived from P3 Lis1+/− mice showed reduced axonal extension compared to age-matched WT mice (Fig. 1A), suggesting that LIS1 insufficiency results in earlier downregulation of axonal extension and that LIS1 normally serves to maintain the robust axonal extension capacity of young neurons. We examined apoptotic cell death using an anti-active Caspase-3. There was no significant difference of apoptotic cell death between Lis1+/+ DRG neurons and Lis1+/− DRG neurons (Fig. S1A), suggesting that the reduced axonal extension of Lis1+/− DRG neurons will not be attributable to the impairment of viability. Further, we examined whether developmental changes in LIS1 protein expression regulate the neurite extension capacity of DRG neurons. Indeed, LIS1 was induced after plating and the degree of upregulation was age-dependent, with robust induction in P3 WT DRG neurons but much weaker induction at P15 as measured by western blotting (Fig. 1B).
To confirm that axon extension depends on LIS1 induction, we increased total expression by transfection of enhanced-green-fluorescent-protein (eGFP)-tagged LIS1 in WT DRG neurons. Expression of exogenous LIS1 significantly enhanced extension at both P3 and P15 (Fig. 1C). Under physiological conditions, half of the total LIS1 protein is degraded by calpain-dependent proteolysis at the plus ends of microtubules, and inhibition or knockdown of calpains protected LIS1 from proteolysis and rescued the phenotypes of Lis1+/− mice (Yamada et al., 2009). Similarly, peri- or postnatal treatment with the novel calpain inhibitor SNJ1945 rescued defective cortical neuron migration, motor deficits, aberrant neurite length and branch number, and defective retrograde transport of nerve growth factor in Lis1+/− mice (Toba et al., 2013). Thus, we examined whether endogenous LIS1 augmentation using SNJ1945 (Fig. S1B) also facilitates axonal extension. Consistent with exogenous LIS1 overexpression, SNJ1945 significantly enhanced axon extension at P15 (Fig. 1D; Fig. S1D), although not at P3 possibly due to limited augmentation relative to exogenous overexpression. We conclude that developmental downregulation of LIS1 expression reduces the regenerative capacity of maturing DRG neurons.
Deletion of the first coding exon of the mouse Lis1 gene results in the expression of a truncated protein, sLIS1, because of translation initiation at the second methionine (Cahana et al., 2001). Expression of sLIS1 suggests that other regulatory regions may be present outside the vicinity of the first exon, such as within the long first intron. We investigated the transcriptional regulatory region of Lis1 intron 1 using a Lis1 minigene conjugated to luciferase as an expression reporter (Fig. S2A). Luciferase reporter gene constructs carrying various deletions of intron 1 were transfected into P3 and P15 DRG neurons, followed by the dual-luciferase reporter assay. Deletion construct #59 exhibited higher luciferase activity than the full-length Lis1 minigene and all deletion constructs, suggesting that a cis-repressive element may be present in the deleted region. To narrow down the regulatory region, we created luciferase reporter gene constructs carrying various deletions within the deleted region of the construct #59. The highest luciferase activity was detected in construct #9-1 (Fig. S2B), defining the repressor region within a span of 4.5–10 kbp from the start of the first intron. Further, we applied in silico prediction of repressors that specifically bind to this region and found a potential binding site for CTCF. Therefore, we examined the function of CTCF in the age-dependent repression of LIS1. We have examined the CTCF expression by western blotting, and found that there was no significant difference between P3 DRG neurons and P15 DRG neurons (Fig. S2C). CTCF has been found in a subset of domain boundaries (Ong and Corces, 2014). Interacting CTCF boundaries showed a unique enrichment for H3K27me3 within the loops. Presumably, CTCF mediated LIS1 downregulation will not be simply attributable to the up regulation of CTCF, rather to histone modifications.
CTCF binds to multiple DNA sequences through various combinations of 11 zinc fingers and mediates transcriptional activation/repression and chromatin insulation depending on the biological context (Ong and Corces, 2014). To address whether CTCF suppresses LIS1 expression, we transfected P3 and P15 WT DRG neurons with eGFP-CTCF or siRNA against CTCF. Expression of eGFP-CTCF significantly suppressed endogenous LIS1 expression (Fig. 2A), whereas CTCF depletion by siRNA enhanced endogenous LIS1 expression (Fig. 2B). Therefore, we conclude that CTCF negatively regulates LIS1 expression. Further, exogenous expression of eGFP-CTCF significantly reduced axonal extension at P3 and more mildly suppressed axonal extension at P15 (Fig. 2C), again consistent with the notion that LIS1 confers greater axonal extension capacity. Moreover, co-transfection of td-Tomato-Lis1 with eGFP-CTCF rescued the decreased axonal extension at P3 (Fig. 2C). On the other hand, CTCF depletion by siRNA transfection in P3 DRG neurons had no effect on axonal extension, whereas depletion at P15 significantly enhanced extension (Fig. 3). Thus, we conclude that CTCF controls the age-dependent downregulation of LIS1 and concomitant loss of axonal extension capacity.
GSK3 is a key regulator of neurogenesis, polarization, neurite outgrowth, and plasticity (Hur and Zhou, 2010). GSK3 regulates microtubule growth and stability by phosphorylating microtubule-associated proteins (MAPs) such as Tau, MAP1b, CRMP-2, and APC. Mutation or absence of these proteins alters the formation and growth of axons. GSK3-mediated phosphorylation of MAPs such as MAP1B and Tau appears to reduce microtubule binding, thereby creating a population of dynamically unstable microtubules (Trivedi et al., 2005). We previously demonstrated that LIS1 arrests dynein motility and that kinesin-1 transports a LIS1-dynein-tubulin complex to the plus ends of microtubules via mNUDC (Yamada et al., 2010, 2008). Therefore, we explored whether LIS1 expression modulates GSK3 function via regulation of its dynein-dependent transport. Indeed, GSK-3β was elevated in the growth cones of DRG neurons from Lis1+/− mice compared to Lis1+/+ mice (Fig. 4A), and this aberrant accumulation of GSK-3β was reversed by administration of SNJ1945 (Fig. 4A). These results suggest that elevated LIS1 expression in young neurons serves to prevent GSK-3β accumulation in growth cones, concomitant MAP phosphorylation, and ensuing destabilization of microtubule dynamics, thereby allowing for axonal extension. We examined actin organization within the growth cone of Lis1+/+ DRG neurons and Lis1+/− DRG neurons. Curiously, growth cones of the Lis1+/− DRG neurons were characterized by thicker and longer filopodia, which are formed by robust actin bundles (Fig. 4B). GSK-3β can influence actin filament dynamics through activating Rac/Arf6 and Rho GTPases and thus contributing to the formation of lamellipodia at the cell front (Hur and Zhou, 2010). Excessive pool of GSK-3β may stabilize actin bundles, which leads to thicker and longer filopodia at the growth cone.
To determine whether this GSK-3β accumulation occurs via LIS1 effects on axonal transport, we conducted live cell imaging of P3 DRG neurons expressing td-Tomato-tagged GSK-3β. The fusion protein exhibited robust bidirectional movement, suggesting that the subcellular distribution of GSK-3β relies on the activity of motor proteins, including kinesin and dynein. While there was no significant difference in the speed of retrograde GSK-3β movement between Lis1+/− and Lis1+/+ axons (Fig. 4C,D,F; Movie 1), the ratio of retrograde to anterograde movement was significantly lower in DRG neurons from Lis1+/− mice (Fig. 4C-E; Movie 1). This decreased frequency of retrograde movement in Lis1+/− DRG neurons was rescued by the addition of SNJ1945 (Fig. 4C-E; Movie 1). We conclude that LIS1 expression is essential for the retrograde transport of GSK-3β and prevention of distal accumulation in growth cones.
Phosphorylation of GSK-3β at Ser9 renders it inactive (Dudek et al., 1997), whereas phosphorylation at Tyr216, which lies within the activation loop between subdomains VII and VIII of the catalytic domain, is necessary for functional activity (Hughes et al., 1993). A constitutively active GSK-3β mutant inhibited axon formation, whereas multiple axons formed from a single neuron when GSK-3β activity was reduced by small molecule inhibitors, a peptide inhibitor, or siRNAs (Jiang et al., 2005). To estimate the level of GSK-3β activity at the tip of the DRG neurons, we double-labeled DRG neurons from Lis1+/− and Lis1+/+ mice with an antibody against total GSK-3β and another against either (inactive) GSK-3β phosphorylated at Ser9 (pS9-GSK-3β) (Fig. 5) or active GSK-3β phosphorylated at Tyr 216 (pY216-GSK-3β) (Fig. 6) and determined the inactive/total and active/total GSK-3β ratios. The pS9-GSK-3β/GSK-3β ratio in the growth cones of P3 DRG neurons from Lis1+/− mice was significantly lower than in growth cones of P3 Lis1+/+ mice (Fig. 5A,B,D). Conversely, the pY216-GSK-3β/GSK-3β ratio in the growth cones of P3 DRG neurons from Lis1+/− mice was significantly higher than in growth cones of P3 Lis1+/+ mice (Fig. 6A,B,D). Further, this aberrant accumulation of GSK-3β in Lis1+/− mice was rescued by SNJ1945 (Fig. 5C,D and Fig. 6C,D). Collectively, we conclude that GSK-3β is overactivated in the growth cones of P3 DRG neurons from Lis1+/− mice, which will suppress axonal extension.
We previously reported that a calpain inhibitor upregulates LIS1 (Yamada et al., 2009) and facilitates neuronal circuit formation (Toba et al., 2013). To investigate whether endogenous LIS1 augmentation using SNJ1945 facilitates axonal regeneration after injury, we subjected mice to sciatic nerve (SN) axotomy, a common model of peripheral nerve injury in rodents (Magill et al., 2007), and compared regrowth and functional recovery between SNJ1945-treated and untreated groups. The left SN was transected at the obturator tendon level in 4-week-old WT mice, and the extent of injury and subsequent regeneration were evaluated by light and electron microscopy. Following nerve injury, Toluidine Blue staining of nerve cross sections revealed changes in the distal nerve stump characteristic of Wallerian degeneration, such as massive axonal swelling. Treatment with SNJ1945 had no obvious effect on SN regeneration at one week (Fig. 7A; Fig. S3A), but treated mice exhibited significantly more numerous myelinated SN fibers at one month (Fig. 7B) and numerically greater numbers at three months (Fig. 7C) and six months (Fig. 7D) after transection (results summarized in Fig. 7E). Transected SNs from control mice exhibited only partial regeneration with hypomyelination compared to SNJ1945-treated mice at the same times after injury. This suggests that SNJ1945-induced enhancement of axonal L1S1 accelerates regeneration of the injured sciatic nerve (Fig. 7B-E).
In principle, this accelerated regeneration after injury could be mediated by facilitation of proximal axon growth, protection against proximal regression, accelerated distal Wallerian degeneration, or a combination. Previous studies examining the sequence of events following injury revealed at least three morphologically discernible phases (Wang et al., 2012). 72 h after transection, rapid fragmentation and cytoskeletal breakdown occurred along the full length of the distal axon, followed by increased microglial influx to clear axonal remnants. So, to distinguish among these possible mechanisms, we initiated SNJ1945 treatment one week after transection, beyond the early phase of degeneration. Although this latency attenuated initial recovery and remyelination of transected SN at one week, remyelination was still significantly augmented at one month (Fig. 7E,F). We conclude that SNJ1945 treatment facilitates axon regeneration rather than removal of distal debris.
To examine the efficacy of SNJ1945 treatment on functional motor recovery, walking-track analysis was performed using the sciatic function index (SFI) (de Medinaceli et al., 1984). Control transection model mice displayed prolonged functional deficits (Fig. 7G; Figs S3B and S3C, Movies 2 and 3) and significantly lower SFI values throughout the 12-week assessment period compared to SNJ1945-treated mice (Fig. 7G; Figs S3B and S3C, Movies 2 and 3). These results suggest that SNJ1945 promotes SN reinnervation of appropriate muscle targets for motor function recovery but upregulates LIS1 expression.
Immature neuronal networks formed by axonal and dendritic sprouting subsequently undergo extensive pruning to form functional circuits. This pruning includes distinct processes for removal of axons, axon branches, and dendrites (Luo and O'Leary, 2005). It is speculated that, to ensure efficient axonal pruning, the capacity for axonal regeneration must be suppressed. We hypothesized that developmental LIS1 downregulation may be associated with axon and dendrite pruning because pruning and growth/regeneration require reciprocal effects on growth-associated processes such as cytoskeletal dynamics.
We first examined the association of axonal extension during cortical development with LIS1 expression. Like DRG neurons, cortical neurons isolated from P3 mice exhibited robust axonal outgrowth, whereas cortical neurons isolated from P15 or P60 mice showed markedly reduced outgrowth potential (Fig. S4A). Thus, as in peripheral neurons, LIS1 downregulation was coupled to the maturation of cortical neurons (Fig. S4B). We conclude that the parallel age-dependent reduction of axonal growth potential and LIS1 expression observed in the DRG is recapitulated in the central nervous system.
We next examined neuronal circuit maturation in vivo under modulation of LIS1 or CTCF expression to assess effects on pruning. We focused on the post-mammillary component of the mouse fornix, a tract of axons that extends beyond the mammillary bodies and into the midbrain in the first postnatal week as the fornix-mammillary projection is established but progressively regresses until it is no longer detectable by the third postnatal week (Stanfield et al., 1987). To visualize the developing fornix, Fezf2-Gfp bacterial artificial chromosome (BAC) transgenic mice (Fezf2-Gfp), in which GFP expression is regulated by the promoter for the transcription factor Fezf2 (Gong et al., 2003; Kwan et al., 2008), were transfected with control, LISI, CTCF, or CTCF-targeted shRNA expression vectors by in utero gene transfer (Tabata and Nakajima, 2001). Transfection of a red fluorescent td-Tomato control plasmid at embryonic day (E)12.5 (Fig. 8A,B) revealed numerous labeled fornix fibers extending into and beyond the mammillary body at P15, and this post-mammillary population was markedly diminished by P18 (Fig. 8B) and completely absent at P21 (Fig. 8B,F). However, a substantial fraction of the post-mammillary component survived at P21 in mice transfected with td-Tomato-Lis1, with the labeled axons confined to a sharply defined fiber bundle at the dorsolateral aspect of the mammillary nuclei (Fig. 8C,F). Similarly, when CTCF was depleted by a targeted shRNA, survival of the post-mammillary component was significantly increased at P21 compared to controls, with labeled fascicles continuing into the mammillary body (Fig. 8D,F) (Alant et al., 2013). In contrast, the post-mammillary component underwent premature regression in mice overexpressing td-Tomato-CTCF, as surviving fascicles extending into the mammillary body were clearly diminished at P15 (Fig. 8E,F). Thus, CTCF-dependent LIS1 suppression is critical for axonal regression during development.
We provided evidence that endogenous LIS1 is a key regulator of the balance between neural circuit formation and regenerative capacity in both the developing peripheral and the central nervous systems. DRG neurons exhibited an age-dependent reduction in axonal extension potential that was paralleled by downregulation of LIS1 expression. Further, extension potential was also reduced in young DRG neurons from Lis1+/− mice. In both P15 WT and P3 Lis1+/− neurons, low extension potential was rescued by exogenous LIS1 overexpression and by endogenous LIS1 augmentation using the calpain inhibitor SNJ1945. In addition, we show that LIS1 is physiologically regulated by the insulator protein CTCR. LIS1 augmentation by SNJ1945 (Toba et al., 2013) promoted axonal extension, which suggests a novel approach for improving peripheral nerve regeneration after injury. A recent report provided evidence that the endogenous calpain inhibitor calpastatin functions as a determinant of axonal survival both during development and after injury (Yang et al., 2013). Therefore, calpastatin induction is a promising approach for blocking LIS1 suppression by calpains, thereby reinducing robust axonal growth. Oral SNJ1945 treatment in particular is a promising approach because SNJ1945 has low toxicity and high BBB permeability (Toba et al., 2013). Indeed, oral SNJ1945 markedly accelerated recovery of motor function following sciatic nerve transection in mice.
We also demonstrated that CTFC is involved in the physiological downregulation of LIS1. CTCF contains a highly conserved DNA-binding domain with 11 zinc fingers, enabling it to function as a major insulator for numerous target genes. In fact, CTCF is present at 55,000–65,000 sites in the mammalian genome (Ong and Corces, 2014). Depletion of CTCF at P15 facilitated axonal extension through LIS1 overexpression, whereas CTCF overexpression at P3 suppressed axonal extension by LIS1 downregulation. In contrast, however, individual projection neurons in CTCF-cKO mice exhibited significantly reduced average dendritic lengths (Hirayama et al., 2012) rather than overextension. This contradictory result may indicate distinct regulatory mechanisms for axons and dendrites or arise because of different KO procedures. In the NEX-Cre mice used by Hirayama et al. (2012) for disruption of CTCF in post-mitotic neurons, the most prominent Cre activity was observed in the neocortex and hippocampus beginning at around E11.5 (Goebbels et al., 2006). Within the dorsal telencephalon, Cre-mediated recombination was substantial in hippocampal pyramidal neurons, dentate gyrus hilar mossy cells, and granule cells, but absent from proliferating neural precursors (Goebbels et al., 2006). In the current study, an shRNA against CTCF was transfected into E12.5 embryos to examine the effect of depletion of CTCF on post-mammillary fornix pruning. Thus, the discrepancy may be attributable to the earlier developmental stage of CTCF disruption, which in turn could influence numerous subsequent developmental processes. Alternatively, CTCF functions in neural development may be region-specific.
We found that LIS1 regulates axonal extension via transport of GSK-3β. GSK-3β is a multifunctional serine/threonine kinase known to regulate axon growth (Hur and Zhou, 2010) by phosphorylating MAPs such anaphase-promoting complex (APC) that control microtubule dynamics. When GSK3 activity is inhibited, APC binds to a microtubule plus end, by which it anchors spindle microtubules to the kinetochore and astral microtubules to the cell cortex (Hur and Zhou, 2010). By regulating microtubule assembly, GSK3 signaling is a key determinant of neuronal polarity and axonal extension. Indeed, inhibition of GSK-3β by small molecule inhibitors, peptide inhibitors, or shRNA, induced multiple functional axons (Jiang et al., 2005). We found that GSK-3β accumulated in the axons of P3 DRG neurons from Lis1+/− mice, with a significantly lower ratio of inactive to total GSK-3β (pS9-GSK-3β/GSK-3β) and a significantly higher ratio of active to total GSK-3β (pY216-GSK-3β/GSK-3β) compared to WT mice, indicative of greater GSK-3β activity (Dudek et al., 1997; Hughes et al., 1993). Retrograde transport of GSK-3β was significantly lower in Lis1+/− DRG neurons than in Lis1+/+ DRG neurons, whereas anterograde transport was similar, which could account for the abnormal GSK-3β accumulation at the axon tip. We speculate that accumulation of GSK-3β at the axon tip impairs cytoskeletal dynamics, limiting axonal extension.
Selective elimination of axons, axon collaterals, dendrites, dendritic branches, and synapses without loss of the parent neuron occurs during normal development and in response to injury or degenerative diseases in the adult brain. Widespread overproduction or overextension of axonal projections, dendritic branches, and synaptic connections requires both small-scale and large-scale pruning to establish precise connectivity, and these same or similar growth and pruning mechanisms may be reactivated for neural plasticity in the adult nervous system (Luo and O'Leary, 2005). For example, the axons of retinal ganglion cells initially overshoot their future termination zone in the superior colliculus. Later, axon segments distal to the termination zone are pruned through local degeneration (Feldheim and O'Leary, 2010). In developing rats, great numbers of fibers extending through the fornix initially grow well beyond the mammillary bodies and into the mesencephalic and pontine tegmentum. This post-mammillary component of the fornix is almost completely eliminated during the first few postnatal weeks (Stanfield et al., 1987). Remaining improper connections or excessive pruning may result in neuropsychiatric diseases, such as schizophrenia, depression, attention deficit/hyperactivity disorder, and autism (Liston et al., 2011; Rosenthal, 2011; Saugstad, 2011). It will be of great interest to explore whether regulators of motor proteins and microtubule organization are involved in neuropsychiatric diseases via effects on neural circuit pruning.
While the intrinsic regenerative potential of axons may be partially suppressed for efficient pruning in the maturing nervous system, this decreased potential limits regeneration following traumatic injury and in pathological conditions such as Alzheimer's disease, Parkinson's disease, multiple sclerosis, and amyotrophic lateral sclerosis. A previous report indicated that calpastatin induction facilitated regeneration of damaged neurons. Consistent with this finding, the calpain inhibitor SNJ1945 enhanced sciatic nerve regeneration after injury via augmentation of LIS1. Therefore, our study identifies a novel therapeutic approach to peripheral nerve injury.
Dorsal root ganglia from P3 and P15 mice were dissociated using a previous method (Lindsay, 1988) with modifications. The cells were plated onto Matrigel-coated dishes (Corning, NY, USA) and cultured in DMEM (Wako Chemicals, Osaka, Japan) supplemented with 10% heat-inactivated fetal bovine serum (Nichirei Biosciences, Tokyo, Japan), 10 ng/ml 2.5S mNGF (Sigma Aldrich, St. Louis, MO, USA), and 5 mM uridine/deoxyfluorouridine (Sigma Aldrich) for 48 h. Neurons were then transfected with the eGFP-LIS1 expression vector using the Neon Transfection System (Invitrogen). Mouse cortical neurons were isolated from P3, P15, and P60 mice. Briefly, cortical tissue was dissected and dissociated by trypsin digestion and trituration in serum-free medium (Hilgenberg and Smith, 2007) and maintained in Neurobasal medium supplemented with B27 (Invitrogen), GlutaMAX (Invitrogen), and penicillin/streptomycin. Fusion constructs of GSK-3β with td-Tomato or eGFP were transfected into DRG neurons to image GSK-3β migration. Particles in axons were tracked using an IX70 inverted microscope (Olympus) equipped with a stage cell incubator held at 37°C (MATS-LH, Tokai Hit, Fujinomiya, Japan). The images were captured with a digital CCD camera (EM-CCD C9100-13, Hamamatsu Photonics, Hamamatsu, Japan) and analyzed using MetaMorph software (MDS Analytical Technologies, Orleans Drive Sunnyvale, CA, USA).
Cells or tissues were lysed in phosphate-buffered saline containing 0.2% NP-40. For immunoblotting, proteins were separated by SDS-PAGE under reducing conditions, followed by electrophoretic transfer to PVDF membranes. Membranes were probed using antibodies against βIII-tubulin (Abcam), CTCF (Abcam), GAPDH (Abcam), and LIS1, followed by visualization using a secondary antibody conjugated to alkaline phosphatase or horseradish peroxidase. Blots were developed using the BCIP/NBT phosphatase substrate system (Roche, Basel, Switzerland) or enhanced chemiluminescence technique (Amersham ECL Prime Western Blotting Detection Reagent RPN2232, GE Healthcare Biosciences, UK) on a LAS-3000 lumino-image analyzer system (GE Healthcare Biosciences). Deprotected and double-stranded 21-nucleotide RNAs targeting mouse CTCF were synthesized by Sigma Aldrich.
Cells were fixed with 4% (w/v) paraformaldehyde for 15 min at room temperature and permeabilized using 0.2% Triton X-100 for 5 min at room temperature. The cells were then blocked using 5% (w/v) BSA in PBS and incubated with an anti-βIII-tubulin antibody (Abcam), an anti-LIS1 antibody, an anti-GSK-3β antibody (BD Biosciences), an anti-pS9-GSK-3β antibody (Cell Signaling Technology, CST, Danvers, USA), anti-pY216-GSK-3β antibody (BD Biosciences), and anti-active Caspase-3 antibody (Abcam) followed by incubation with Alexa 488-conjugated anti-mouse IgG, Alexa 555-conjugated anti-rabbit IgG, and/or Alexa 647-conjugated anti-rabbit IgG (Molecular Probes, Eugene, OR, USA) as appropriate. Actin filament was stained by Rhodamine Phalloidin Conjugate (Thermo Fisher Sceintific). Nuclei were counterstained using 100 nM 4′,6-diamidino-2-phenylindole (DAPI). Each incubation was performed for 1 h at room temperature. Slides were mounted in FluorSave Reagent (345789, Calbiochem, La Jolla, CA, USA). Immunofluorescence was measured under a laser scanning confocal microscope (TCS-SP5, Leica, or LSM 700, Carl Zeiss) under the control of accessory software (LAS AF, Leica, or ZEN 2012, Carl Zeiss). Nuclei were labeled with DAPI (Thermo Fisher Scientific).
A BAC clone carrying murine Lis1 was obtained from Advanced Geno Techs (Tsukuba, Japan). The Lis1 minigene was cloned into the luciferase reporter vector pGL4.23 (Promega, Madison, WI, USA). Luciferase was conjugated in-frame to the end of Lis1 exon II. For luciferase reporter assays, approximately 5×104 DRG neurons per well were seeded in 6-well plates and cotransfected with luciferase constructs and Renilla control reporter vector (phRL-TK, Promega) at a ratio of 10:1 by electroporation using the Neon Transfection System (Invitrogen). 24 h after transfection, cells were lysed with Passive Lysis Buffer (Promega), and luciferase activity was measured using the Dual-Luciferase Assay System (Promega).
All mouse experiments were performed with the approval of the Animal Care and Ethics Committee of Osaka City University (authorization number: OCU-08033). First, animals were anesthetized by inhalation of sevoflurane (Wako Chemicals) and intraperitoneal injection of somnopentyl (Kyoritsu, Tokyo, Japan). The left SN was exposed from where it emerges over the external obturator muscle from the sciatic notch to the trifurcation above the popliteal fossa. The nerve was sharply transected 5 mm proximal to the sciatic trifurcation, the ends were left to retract in situ, and the wound was closed (Alant et al., 2013). One week (6 mice), one month (6 mice), and six months (5 mice) after transection, the incision site was opened and three approximately 1 mm long segments of the nerve were obtained for preparation of transverse sections. The nerve segment was first fixed for a few seconds in a small drop of solution containing 2.5% glutaraldehyde and 0.5% sucrose in 0.1 M Sorensen phosphate buffer (pH 7.4) to stiffen the tissue for correct orientation and then placed in the same fixative solution for 6–8 h. SN segments were then dehydrated through a graded ethanol series (50%, 70%, 80%, 90%, and 100%) and embedded in Epon 812 resin, followed by thin sectioning at 70 nm thickness using an Ultramicrotome EM UC-6 (Leica Microsystems, Vienna, Austria). The specimens were finally stained with 0.4% lead citrate and observed under a transmission electron microscope (Hitachi).
Before SN injury and once weekly for 5 weeks thereafter, all animals were subjected to walking-track analysis based on the protocol described by Inserra et al. (1998). Paw prints were recorded by painting the hind paws with India ink and animals were tracked as they walked along a 45×6.5 cm sheet of white paper (Canson A4, 140 g/m2). The paw prints of untreated and SNJ1945-treated mice were analyzed for two parameters: (1) toe spread (TS) as measured by the distance between the first and fifth toes; and (2) print length (PL), the distance between the third toe and the hind pad. SFI was calculated according to the formula of Inserra et al. (1998):
where TS is the toe spread in mm, PL is the print length in mm, and E and N indicate the experimental and normal hind foot, respectively. Differences between the groups were assessed using the Mann–Whitney U test. A P value <0.05 was considered statistically significant.
In utero electroporation was performed using pregnant Fezf2-Gfp BAC transgenic mice as described previously (Gong et al., 2003; Kwan et al., 2008) with minor modifications. Approximately 1 μl of the plasmid solution [0.3 μg pCAG-td-Tomato, 0.3 μg pCAG-Lis1, 0.3 μg pCMV-CTCF, or 0.3 μg shRNA against CTCF (Sigma Aldrich) with 0.03% fast green] was injected into the lateral ventricle of intrauterine embryos at E12.5. The head of the embryo was placed between the disks of a forceps-type electrode (3 mm disk electrodes, CUY650P3; NEPA GENE, Chiba, Japan) and electronic pulses (30−50 V, 50 ms, five times) were applied for gene transfection into the cerebral wall.
After in utero transfection, P15, P18, and P21 mice were perfused by periodate-lysine-paraformaldehyde fixative, pH 7.4. The mouse brains were removed and immersed in the same fixative overnight at 4°C. After fixation, the brains were placed in a 20% sucrose solution, embedded in OCT compound (Sakura, Tokyo, Japan), and frozen in liquid nitrogen. The frozen blocks were cut with a cryostat into 16 μm thick sections. Immunofluorescence analyzes were conducted under a laser scanning confocal microscope (TCS-SP5, Leica, or LSM 700, Carl Zeiss) using the accessory software (LAS AF, Leica, or ZEN 2012, Carl Zeiss).
We would like to thank Dr K. Igarashi and Dr H. Kiyama for the discussion and suggestions. We also thank Senju Pharmaceutical Co., Ltd., for providing SNJ1945. We are grateful to Yukimi Kira and Yoriko Yabunaka for the technical support and Hiromichi Nishimura and Keiko Fujimoto for mouse breeding.
The authors declare no competing or financial interests.
Conceptualization: S.H., M.S.; Formal analysis: K.K., R.I.; Investigation: K.K., T.I., R.I., T.U.; Resources: T.I., T.U.; Data curation: M.S.; Writing - original draft: S.H.; Supervision: S.H., M.S.; Project administration: S.H.
This work was supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan (grant no. 2411541) to S.H. This work was also supported by the Uehara Memorial Foundation (grant no. 2015-20-252), the Naito Foundation (grant no. 2014-169), and the Takeda Science Foundation to S.H.
Supplementary information available online at http://bio.biologists.org/lookup/doi/10.1242/bio.025999.supplemental