Size homeostasis is a fundamental process in biology and is particularly important for large cells such as neurons. We previously proposed a motor-dependent length-sensing mechanism wherein reductions in microtubule motor levels would be expected to accelerate neuronal growth, and validated this prediction in dynein heavy chain 1 Loa mutant (Dync1h1Loa) sensory neurons. Here, we describe a new mouse model with a conditional deletion allele of exons 24 and 25 in Dync1h1. Homozygous Islet1-Cre-mediated deletion of Dync1h1 (Isl1-Dync1h1−/−), which deletes protein from the motor and sensory neurons, is embryonic lethal, but heterozygous animals (Isl1-Dync1h1+/−) survive to adulthood with ∼50% dynein expression in targeted cells. Isl1-Dync1h1+/− sensory neurons reveal accelerated growth, as previously reported in Dync1h1Loa neurons. Moreover, Isl1-Dync1h1+/− mice show mild impairments in gait, proprioception and tactile sensation, similar to what is seen in Dync1h1Loa mice, confirming that specific aspects of the Loa phenotype are due to reduced dynein levels. Isl1-Dync1h1+/− mice also show delayed recovery from peripheral nerve injury, likely due to reduced injury signal delivery from axonal lesion sites. Thus, conditional deletion of Dync1h1 exons 24 and 25 enables targeted studies of the role of dynein in neuronal growth.
Neurons must extend axons over long distances during development to reach their targets and establish functional circuits, and these extended neuronal arbors constitute a vulnerability that is prone to neurological disease (Albus et al., 2013; Sleigh et al., 2019; Terenzio et al., 2017). A number of studies have described neurological disorders resulting from aberrations in signaling pathways implicated in neuronal size control (Nikolaeva et al., 2017; Sundberg and Sahin, 2020) or in intracellular transport (Sleigh et al., 2019). Dync1h1 encodes the heavy chain of the cytoplasmic dynein 1 motor protein, which plays a key role in retrograde axonal transport in neurons. Various mutations in human DYNC1H1 have been associated with neurological diseases, including spinal muscular atrophy, Charcot–Marie–Tooth disease, and infantile developmental and epileptic encephalopathy (Hoang et al., 2017; Marzo et al., 2019; Su et al., 2022). Accordingly, a number of dynein mutant mouse lines have been generated as models of neurological disease (Terenzio et al., 2018a).
Prolonged Dync1h1 depletion has been shown to disturb long microtubule transport and alignment in distal axonal segments of superior cervical ganglia neurons, leading to a significant decrease in axonal length (Ahmad et al., 2006). In contrast, we previously demonstrated that partial Dync1h1 deletion in dorsal root ganglia (DRG) neurons results in axonal growth acceleration (Rishal et al., 2012). The Dync1h1 legs at odd angles (Loa) mouse mutant was originally described with an autosomal dominant mild neurodegenerative disease phenotype (Hafezparast et al., 2003). We subsequently found that heterozygous Loa sensory neurons have accelerated axonal growth (Rishal et al., 2012). Thus, the dynein complex links intracellular transport with size control in neurons (Rishal and Fainzilber, 2019; Rishal et al., 2012). However, interpretation of those results was complicated by the fact that the Loa mutation is a single nucleotide change rather than a clear loss of function allele. Dync1h1Loa mice and other described mutants are invariably non-viable as homozygotes, and the adult heterozygous animals have mild to severe neurodegeneration phenotypes (Terenzio et al., 2018a), raising the possibility that specific aspects of the phenotype might be due to effects of the point mutation rather than reduction in dynein levels. An allele deletion model allowing focus on specific neuronal cell types would be of great utility to resolve such issues.
Here, we describe a new conditional deletion allele for Dync1h1 in the mouse. Islet1-Cre-induced homozygous deletion mice are not viable, but heterozygosity is well tolerated. The heterozygous mice have normal life span and fertility and mutant sensory neurons show the expected decrease in dynein levels, and increased axonal growth. Moreover, Islet1-Cre Dync1h1+/− adult animals present deficits in motor and proprioception coordination, and delays in recovery from peripheral nerve injury. Thus, this new conditional Dync1h1 allele enables targeted confirmation of dynein roles in neuronal growth control, and will facilitate comprehensive studies of the physiological roles of dynein.
Generation of a conditional deletion allele for Dync1h1
We established a floxed Dync1h1 allele targeting exons 24 and 25 of the Dync1h1 gene, using available embryonic stem cell (ESC) clones (Skarnes et al., 2011). The floxed allele was generated by transfection of the parental ESC line with an Flp recombinase plasmid, leading to removal of the LacZ-NeoR cassette, and subsequent efficient germline transmission of the Dync1h1 floxed allele. After recombination, exons 24 and 25 are deleted leading to a frameshift mutation prior to the motor domain of DYNC1H1 protein. This is the same targeting strategy recently used by Baehr and collaborators for analyses of Dync1h1 roles in the retina and photoreceptor systems (Dahl et al., 2021a,b). Details of the mouse generation strategy and genotyping are presented in Fig. S1 and Materials and Methods.
Dync1h1 conditional exons 24–25 mice were bred with Islet1 (Isl1) Cre mice. The Isl1 promoter drives expression in motor and sensory neurons (Srinivas et al., 2001), but also in heart and limb progenitors (Yang et al., 2006). Homozygous Isl1-Cre deletions of Dync1h1 were embryonic lethal, but heterozygous mice (henceforth termed Isl1-Dync1h1+/−) were viable and used for further characterization. Isl1-Dync1h1+/− survived to adulthood and no evident abnormalities were noticed in their postnatal growth rates or life span compared to their wild-type (WT) counterparts.
Reduced Dync1h1 expression in heterozygous Isl1-Dync1h1 mice
We examined dynein mRNA and protein levels in cultured DRG sensory neurons, as Dync1h1Loa neuron outgrowth investigations were previously conducted in this cell type. Quantitative (q)PCR and western blot analyses revealed a significant reduction of both Dync1h1 mRNA (Fig. 1A) and protein (Fig. 1B) in neurons cultured for 24 h in vitro. This was further confirmed by immunostaining (Fig. 1C,D; Fig. S2A,B). Proximity ligation assay (PLA) was then used to detect spatial coincidence of DYNC1H1 with importin β1, a known component of dynein complexes in axoplasm and cytoplasm (Hanz et al., 2003; Perry et al., 2012). A clear decrease of axonal PLA signals for DYNC1H1–importin β1 in heterozygous neurons confirms that reduced dynein expression is reflected in the prevalence of functional dynein complexes in the mutant (Fig. 1E,F; Fig. S2C,D).
Neuronal growth phenotype in heterozygous Isl1-Dync1h1 conditional knockout neurons
Isl1-Dync1h1+/− mice presented abnormal hind limb posture when suspended by the tail (Fig. S3), similar to the phenotype previously reported for whole-body mutant Dync1h1Loa animals (Hafezparast et al., 2003), and indicative of motor and/or proprioceptive phenotypes (Chen et al., 2007). In previous work, we had demonstrated enhanced neuronal growth of Dync1h1Loa sensory neurons due to perturbation of a postulated dynein-dependent length-sensing mechanism (Rishal et al., 2012). We tested this prediction of increased growth by cross-breeding Isl1-Dync1h1+/− mice with Thy1-YFP mice (Feng et al., 2000) to obtain animals that express YFP primarily in large proprioceptive sensory neurons. Time-lapse imaging of axon outgrowth from YFP-expressing neurons in culture reveal significantly accelerated growth of Isl1-Dync1h1+/− genotype neurons, both at low culture densities that provide superior conditions for enhanced growth (Fig. 2), and at higher densities comparable to the conditions used in previous studies on Dync1h1Loa mice (Fig. S4).
Isl1-Dync1h1+/− mice reveal deficits in motor coordination, gait and tactile sensitivity
Dync1h1Loa mice and other dynein heavy chain heterozygous point mutant animals have clear behavioral deficits, including abnormal hind limb positioning and decreased grip strength (Terenzio et al., 2018a). The phenotype was associated with motor and sensory abnormalities, a loss of 50% motor neurons in embryonic day (E)18.5 embryos, and an 86% reduction in muscle spindles in hind limbs by 13 weeks postnatally (Hafezparast et al., 2003). The loss of proprioceptive sensory neurons at the L4 level has been shown to precede the loss of motor neurons, leading to early-onset sensory neuropathy (Chen et al., 2007). We evaluated locomotion deficits, impaired balance and muscular weakness in Isl1-Dync1h1+/− animals, using catwalk and rotarod tests (Dumont, 2011). Isl1-Dync1h1+/− mice revealed mild but significant impairments in both assays (Fig. 3A,B). Alterations in tactile sensitivity were also observed (Fig. 3C), whereas, in contrast there were no deficits in heat sensitivity (Fig. 3D). The similar phenotypes of Isl1-Dync1h1+/− and Dync1h1Loa animals might be caused by the same motor and sensory abnormalities that have been found in Dync1h1Loa mice and other dynein heavy chain heterozygous point mutant animals, indicating that these are likely a consequence of partial loss of Dync1h1 function.
Impairment in regeneration response to peripheral nerve injury in Isl1-Dync1h1+/− mice
Previous studies have shown a critical role for dynein in retrograde signaling after peripheral nerve injury (Rishal and Fainzilber, 2014; Terenzio et al., 2017). We therefore examined the injury responses of sensory neurons in Isl1-Dync1h1+/− mice. Sciatic nerve conditioning lesion (Smith and Skene, 1997) enhances the elongating growth of WT sensory neurons cultured from L3, L4 and L5 DRG, but there was no such effect on Isl1-Dync1h1+/− neurons (Fig. 4; Fig. S4). The dynein-deficient neurons exhibited enhanced growth in culture under basal conditions, comparable with elongated growth of WT neurons after injury (Fig. 4; Fig. S5). This enhanced growth might mask any potential effect of the conditioning lesion.
To test whether increased axonal outgrowth of Isl1-Dync1h1+/− sensory neurons might be due to ‘pre-conditioning’ caused by reduced levels of Dync1h1, we assessed expression levels of activating transcription factor 3 (ATF3), a well-established indicator of the regenerative state (Seijffers et al., 2007). Analyses were conducted on DRG from WT or Isl1-Dync1h1+/− mice, under naive conditions or 3 days after sciatic nerve injury. ATF3 immunoreactivity was low in naive neurons from both WT and Isl1-Dync1h1+/− mice (Fig. 5A). This finding does not support the possibility of a preconditioning effect due to a decrease in Dync1h1. However, Isl1-Dync1h1+/− neurons show reduced upregulation of ATF3 after injury (Fig. 5), indicative of a deficit in retrograde injury signaling.
We then proceeded to examine functional recovery from sciatic nerve lesion in Isl1-Dync1h1+/− mice in vivo. Mouse gait parameters were evaluated on a catwalk apparatus before crush injury of the sciatic nerve, and over a time course up to 28 days post-lesion (Fig. 6). As expected, both WT and Isl1-Dync1h1+/− mice reduced usage of the injured limb immediately after injury, with gradual recovery of different gait parameters over time after lesion (Fig. 6). Differences between WT and Isl1-Dync1h1+/− mice were apparent through the recovery time course, with Isl1-Dync1h1+/− mice showing somewhat reduced recovery of the injured limb at the time points assayed during the recovery phase (Fig. 6B–D).
To test nerve regeneration after injury, we harvested sciatic nerves from WT and Isl1-Dync1h1+/− mice 3 days after injury along with naive counterparts, prepared longitudinal cryosections, and immunostained them for Scg10 (also known as Stmn2), a marker for regenerating axons (Shin et al., 2014). There was little or no expression of Scg10 in uninjured axons, and marked upregulation after injury in both genotypes (Fig. 7). However, Dync1h1+/− axons show significantly lower upregulation of Scg10 than WT axons at 1 mm distal to the injury site (Fig. 7), consistent with the delayed regeneration observed above (Fig. 6).
The dynein heavy chain Dync1h1 is an essential gene in multicellular organisms, and accordingly all constitutive Dync1h1 mouse mutants described to date are embryonic lethal when homozygous (Terenzio et al., 2018a). Heterozygous mutants are mostly viable, although they typically have progressively worsening neurodegeneration phenotypes, and given that the mutation is organism-wide, the origin of a specific deficit might be unclear. For example, a number of studies in both Dync1h1Loa and Dync1h1Cra mice have suggested that their originally described motor phenotypes might be a secondary consequence of earlier effects in sensory neurons (Chen et al., 2007; Dupuis et al., 2009; Ilieva et al., 2008). Alleles allowing cell type and/or temporal specificity in targeting dynein will be of value in resolving such issues. Moreover, potential confounding or masking effects are less likely in a deletion allele as compared to an expressed mutant with altered amino acid sequence. Indeed, a recent study reported photoreceptor maintenance phenotypes upon conditional deletion of Dync1h1 exons 24 and 25 in retinal cells (Dahl et al., 2021a) that were not reported previously in Dync1h1 point mutant mice.
The Dync1h1 allele described herein enables Cre-driven deletion of dynein with expected effects on dynein expression and function in targeted cell types and tissues. Our previous work had postulated roles for dynein in retrograde injury signaling (Rishal and Fainzilber, 2014), and in intrinsic length-sensing and regulation of axonal growth rates (Rishal et al., 2012). The length-sensing model predicts axon length increase upon partial reduction of dynein levels (Rishal and Fainzilber, 2019; Rishal et al., 2012), and initial experiments in sensory neurons of Dync1h1Loa mice supported this prediction (Rishal et al., 2012). The results reported above in Isl1-Dync1h1+/− sensory neurons further support the model, with clearly enhanced outgrowth of heterozygous dynein-knockout neurons. Thus, the Isl1-Dync1h1+/− model phenocopies the effects of Dync1h1Loa on sensory neuron growth in vitro and on limb proprioception in vivo. These functional phenotypes likely reflect similar motor and sensory abnormalities, as previously described in Dync1h1Loa mice and other dynein heavy chain heterozygous point mutant animals. Taken together, these findings suggest that the sensory and motor phenotypes observed in the Dync1h1Loa mutant are caused by loss of dynein function, rather than a dominant-negative effect of mutant Loa Dync1h1 (Garrett et al., 2014; Ori-McKenney et al., 2010).
In vivo characterization of Isl1-Dync1h1+/− mice reveal further parallels with Dync1h1Loa in limb coordination (Hafezparast et al., 2003), and altered proprioception and gait (Ilieva et al., 2008). The Isl1-Dync1h1+/− mice also show changed tactile, but not thermal, sensitivity, indicating differential physiological impacts of dynein reduction in distinct sensory neuron subtypes. As regards injury response, Isl1-Dync1h1+/− neurons do not exhibit enhanced growth after conditioning lesion, and injury-induced upregulation of ATF3 is attenuated in heterozygous neurons. Impaired regeneration was also observed in the in vivo analyses, including delayed recovery from sciatic nerve injury, based on gait analysis and immunostaining for the regeneration marker Scg10. Taken together, these data indicate that the enhanced basal neuronal growth of dynein heterozygote neurons is not sufficient to overcome other deficiencies caused by the deletion. Similar findings were described previously for importin β1 (KPNB1) 3′UTR mutant mice, which have deficiencies in retrograde injury signaling and sciatic nerve regeneration (Perry et al., 2012), and also accelerated growth of sensory neurons in culture (Doron-Mandel et al., 2021; Perry et al., 2016). Additional studies utilizing neuron-subtype-specific Cre drivers will be required to dissect the underlying mechanisms.
A number of rare neurological diseases have been genetically associated with mutations in the DYNC1H1 gene. These diseases include motor neuron diseases such as spinal muscular atrophy with lower extremity predominance (SMA-LED) or Charcot–Marie–Tooth disease (Becker et al., 2020; Harms et al., 2012; Scoto et al., 2015; Weedon et al., 2011), and also neurodevelopmental defects (Poirier et al., 2013) and/or epilepsy (Lin et al., 2017; Matsumoto et al., 2021). A retrospective analysis of all published mutations revealed domain-specific genotype-phenotype correlations [i.e. mutations in the dimerization domain with reductions in lower limb strength in DYNC1H1-NMD (neuromuscular disorders) and motor domain with cerebral malformations in DYNC1H1-NDD (neurodevelopmental disorders) (Becker et al., 2020)]. Elucidating the origin of these diverse clinical presentations will benefit from the availability of the dynein deletion allele model, potentially allowing determination of specific cell types linked to each disease.
To summarize, our results on heterozygous Dync1h1 deletion in sensory neurons confirm model predictions and previous findings from Dync1h1Loa mice on a dynein-dependent mechanism that regulates neuronal growth. The Dync1h1 conditional allele provides a new model for targeted studies on dynein functions in specific cell types.
MATERIALS AND METHODS
All animal experiments were approved by the IACUC (Animal Care and Use Committee) at the Weizmann Institute of Science. Mice were bred and maintained at the Veterinary Resources Department. Experiments were carried out on animals between 2 and 6 months old. In this work, all mice used for experimentation have a BALB/cN/C57BL/6/129×1/SvJ/ICR mixed genetic background strain. The C57BL/6YFP16 mice (Feng et al., 2000) and Isl1-Cre (129X1/SvJ/ICR) (Srinivas et al., 2001) mice were maintained at the Veterinary Resources of the Weizmann Institute. According to the IACUC guidelines, animals were kept at 24.0±0.5°C in a humidity-controlled room under a 12 h light–12 h dark cycle with all the time access to food and water. Mice used for behavioral tests were kept at the same conditions in a reverse dark–light cycle room.
Mutant mouse line establishment
The Dync1h1 conditional mutant mouse line was established at the Institut Clinique de la Souris - PHENOMIN (http://www.phenomin.fr). Three clones EPD0284-5-C04, EPD0284-5-D04 and EPD0284-5-H02 were ordered from the Mutant Mouse Resource Research center (https://www.mmrrc.org/). All three clones contained the standard knockout first with the potential conditional International Mouse Phenotyping Consortium (IMPC) allele. The critical exons 24 (ENSMUSE00000116212) and 25 (ENSMUSE00000116247) are floxed. The deletion of these exon leads to a frame shift. Proper homologous recombination was confirmed by Southern blotting using an internal probe (Neo probe) (Codner et al., 2021). Four restriction enzymes were used, all showed a single band at the expected size, confirming the correct recombination at the Dync1h1 locus for all three clones. Two additional digests were used to confirm the presence of the 3′ LoxP. This latter site was also confirmed by PCR. The three clones were karyotyped by chromosome spreading and Giemsa staining and microinjected in BALB/cN blastocysts. Even if good chimeras were obtained (until 85% of percentage of chimerism), none gave germline transmission.
Hypothesizing that the absence of germline transmission might indicate lethality upon implementation of the knockout first strategy, we decided to remove the flipped LacZ-NeoR cassette directly in an ESC clone in vitro in order to obtain the conditional knockout allele (tm1c) (Fig. S1). Electroporation with a plasmid expressing the FlpO recombinase (cloned under a pCAG promoter) was performed on clone EPD0284-5-D04. Different subclones were obtained and analyzed by PCR. Two PCR sets were used and confirmed the excision of the flipped cassette. One positive subclone was microinjected in BALB/cN blastocysts, male chimeras were obtained and germline transmission was achieved (tm1c allele; conditional knock-out).
Genotyping of Isl1-Dync1h1+/− mice was performed on genomic DNA isolated from ears as shown in Fig. S1B,C using following primers: LoxP F, 5′-CCATTGTCCCCCTGGTTTCATCC-3′; LoxP R, 5′-CTGTGTCAGTTGCAGACAGTTTCTACG-3′; Intron23 F, 5′-GCTGCCTGAACTCCCAGTTTTCCG-3′.
The presence of Cre gene was correlated with excision of the floxed exons, that is knockout, as shown in Fig. S1B.
Cultures and antibodies
Culture of sensory neurons from DRG were performed as previously described (Terenzio et al., 2018b). Adult DRG were dissociated by enzymatic treatment (papain and a mix of collagenase/dispase), triturated in Hanks’ balanced salt solution (HBSS)-supplemented with 10 mM glucose and 5 mM HEPES pH 7.35, and recovered by centrifugation (1000 g for 8 min) through 20% Percoll. Sensory neurons obtained from this procedure were then subjected to immunostaining. Primary antibodies used in this study are the following: chicken anti-NFH (Abcam, ab72996, 1:2000), rabbit anti-Dync1h1 (Proteintech, 12345-1-AP, 1:500), mouse anti-importin β1 (monoclonal, generated in-house), rabbit anti β-III tubulin (Abcam, ab18207, 1:2000), recombinant rabbit monoclonal anti-ATF3 (Abcam, ab207434, 1:1000, for IF) and rabbit polyclonal anti-Stathmin2/Scg10 (Novus, NBP1-49461, 1:1000, for immunofluorescence). Secondary antibodies used for immunostaining are anti-chicken-IgY, -mouse-IgG or -rabbit-IgG conjugated to Alexa Fluor 488, 594 or 647 (Jackson ImmunoResearch, 1:1000). Secondaries for immunoblotting were HRP-conjugated anti-rabbit-IgG antibodies (Bio-Rad Laboratories, 1:10,000).
Dync1h1 gene expression analysis by qPCR
The mRNA level of Dync1h1 was quantified by qPCR analysis. RNA was extracted from DRG neurons grown 24 h in culture using the Oligotex mRNA Mini kit (Quiagen). Superscript III (Invitrogen) was used to synthesize cDNA and qPCR reactions were prepared in a total volume of 20ul using PerfeCTa SYBR Green (Quanta Biosciences, Gaithersburg, USA) and performed on a ViiA7 System (Applied Biosystem). 18S was used as housekeeping gene for normalization, and data were analyzed using the comparative ΔΔCt method (Livak and Schmittgen, 2001). The sequences of the primers are as follows: 18S forward, 5′-AAACGGCTACCACATCCAAG-3′; 18S reverse, 5′-CCTCCAATGGATCCTCGTTA-3′; Dync1h1 forward, 5′-CCAACAGCTTGGCGTTCAT-3′; and Dync1h1 reverse, 5′-GGGACGACACTGGCTTGTCT-3′.
DYNC1H1 protein expression analysis by western blotting
Western blot analysis was conducted on DRG neurons cultured for 24 h. Cells were harvested and lysed in RIPA buffer. Proteins were then boiled in 5× Laemmli sample buffer, fractionated by SDS-PAGE, and transferred to 4–15% gradient gels using a Bio-Rad transfer apparatus according to the manufacturer's protocol. Membranes were incubated for 1 h at room temperature in a blocking solution of 5% milk in 10 mM Tris-HCl pH 8.0, 150 mM NaCl and 0.5% Tween 20 (TBST), washed and incubated with the rabbit anti-Dync1h1 antibody and rabbit anti-β-III tubulin antibody overnight at 4°C. The following day, they were washed and incubated with HRP-conjugated anti-rabbit-IgG antibodies for 1 h. Images were captured with the ECL system (Amersham Biosciences) and the signal quantified using Fiji software.
Proximity ligation assay (PLA) (Gullberg et al., 2004) was used to detect spatial coincidence of DYNC1H1 and importin β1 proteins. PLA was performed according to manufacturer's instructions using Duolink (Sigma; PLA probe anti-mouse minus DUO92004, anti-rabbit plus DUO92002, and detection kit red DUO92008). After the PLA protocol, cells were immunostained with chicken anti-NFH antibody. The images were taken using Fluoview (FV10i), a fully automated confocal laser–scanning microscope at a 60× magnification with a water immersion objective (Olympus UPLANSAPO, NA 1.2). The PLA signal was quantified with the ‘analyze particles’ function of Fiji software, using a mask based on intensity of NFH staining and dividing the number of PLA-positive puncta by the NFH stained area excluding cell body.
Axon outgrowth analysis
For outgrowth analysis, Isl1-Dync1h1+/− and WT mice were crossed with Thy1–YFP mice (Feng et al., 2000). DRG neurons from adult mice were plated on a 96-well glass-bottom plate (Cellvis) coated with 0.01% poly-L-lysine (Sigma P4832; 50 ml) and laminin (7 μg/ml final concentration; Thermo Fisher Scientific; 23017015). After seeding, neurons were imaged at 6, 12, 24, 36, 48 and 72 h after plating using an ImageXpress Micro (Molecular Devices), a fully automated spinning disc confocal microscope with a built-in CO2 incubator, at a 10× magnification. The cells were analyzed using the MetaXpress software (Molecular Devices). The total outgrowth parameter was defined as the sum of all process lengths. The maximum process length parameter was defined as the sum of the length of the longest process plus the lengths of all branches associated with it. Only growing cells were included in analysis.
For conditioning lesion experiments, mice were subjected to unilateral sciatic nerve injury and, after 3 days, DRG L3, L4 and L5 were dissociated and cultured for 24 h. The plating was done on a DMEM/F12 medium supplemented with 1× N1 medium supplement (Sigma; N6530) and 10% fetal bovine serum, as was done previously (Hanz et al., 2003). Neurons were then fixed in 4% paraformaldehyde, stained with NFH, and subjected to morphological analysis. Images were captured at 10× magnification on ImageXpress Micro (Molecular Devices), and outgrowth was analyzed using the MetaXpress software (Molecular Devices). Only ‘sprouted’ cells were included in analysis. A cell was considered sprouted when the maximum length of the process was equal to twice the cell diameter.
Immunohistochemistry on cultured neurons
Sensory neurons from WT and Isl1-Dync1h1+/− mice were grown on glass coverslips coated with poly-L-lysine and laminin for 24 or 48 h and then fixed using 4% paraformaldehyde (PFA) in 1× PBS. Blocking and permeabilization was done with 10% donkey serum and 0.2% Triton X-100 in PBS for 1 h. Coverslips with neurons were incubated overnight at 4°C with chicken anti-NFH (Abcam, ab72996, 1:2000) and rabbit anti-Dync1h1 (Proteintech, 12345-1-AP, 1:500). The next day, they were washed three times in 1× PBS and incubated for 1 h with donkey anti-chicken-IgY conjugated to Alexa Fluor 488, donkey anti-rabbit-IgG conjugated to Alexa Fluor 647 (1:1000; Jackson ImmunoResearch) and DAPI (Abcam, ab228549, 1:5000). After three washes in 1× PBS, coverslips were rinsed in ddH2O and mounted with Fluoromount-GTM.
Immunohistochemistry on cryosections
L4 DRG and sciatic nerves of adult WT and Isl1-Dync1h1+/− mice were harvested 3 days after crush injury together with non-injured controls. Then, the tissue were fixed in 4% PFA for 12 h at 4°C, washed three times in 1× PBST (10 min each), incubated overnight in 30% sucrose and subsequently embedded in OCT freezing medium (Tissue-Tek O.C.T. Compound, Sakura Cat.#4583). The 15 µm thick sections were cut with a cryostat in set of three and mounted on to glass slides. For the immunostaining, one set of each biological repeat was used. The sections were re-hydrated in 1× PBS, blocked and permeabilized with 10% donkey serum and 0.2% Triton X-100 in 1× PBS for 1 h at room temperature, and then incubated overnight with primary antibodies at 4°C. DRG sections were incubated in chicken anti-NFH (Abcam, ab72996, 1:2000) and rabbit anti-ATF3 (abcam, ab207434, 1:1000), whereas longitudinal sections of nerves were incubated in chicken anti-NFH and rabbit anti-Scg10 (Novus, NBP1-49461, 1:4000). Primary antibody solutions were carefully removed, and slides were washed three times (10 min each) at room temperature with 1× PBS and then incubated with the secondary antibodies donkey anti-chicken-IgY conjugated to Alexa Fluor 594 and donkey anti-rabbit-IgG conjugated to Alexa Fluor 488 (1:1000 each; Jackson ImmunoResearch) and DAPI (Abcam, ab228549, 1:5000) for 1 h at room temperature. After three 5-min washes in 1× PBS, slides were mounted with Fluoromount-GTM.
All fluorescence images were captured using an Olympus FV1000 Confocal laser-scanning microscope at 60× magnification with oil-immersion objective (Olympus UPLSAPO, NA 1.35) or using Fluoview (FV10i), a fully automated confocal laser–scanning microscope, with water immersion objective (Olympus UPLANSAPO 60X, NA 1.2). Image analysis was performed using Fiji software (Schindelin et al., 2012) creating a mask based on NFH channel and quantifying the mean intensity of our protein of interest. To test axonal regeneration after SN crush, the Scg10 intensity level at a distance of 1 mm distal to the injury site was divided by the Scg10 intensity level in the naive nerve. For the ATF3 experiment, we quantified both the protein intensity and the percentage of ATF3-positive nuclei of NFH neurons.
All assays were performed under dim illumination (∼10 lx) during the ‘dark’ active phase of the diurnal cycle. Mice were tested with the ROTOR-ROD, catwalk, von Frey and hot plate tests as follows.
For ROTOR-ROD, mice underwent 3 days of training on the rotarod, accelerating from 0 to 40 rpm in 4 min (inclination of 10 rpm/min) during day 1 and 2. On the third day, the rotarod was accelerated from 0 to 40 in 2 min (20 rpm/min). Each day, mice were subjected to four trials with a 2 min break in between as shown previously (Ezra-Nevo et al., 2018). Latency to fall (s) was recorded and the average of the four trials per day was considered.
The catwalk test was carried on as previously described (Terenzio et al., 2020). Motivation was achieved by placing the home cage at the runway end and each mouse was tested three to five times. The collected data were analyzed using the Catwalk Ethovision XT10.6 software (Noldus Information Technology, The Netherlands). Mice showed differences in the base of support parameter (BOS), defined as the average width (cm) between the paws during each step cycle.
For the Von Frey test, mechanical sensitivity was tested by pressing filaments of different diameters on the plantar surface of the paw of the mouse. Before starting the test, mice were habituated in chambers suspended above the test apparatus wire mesh grid for an hour. Once the mice were calm, the test with the Von Frey filaments started and the response was considered positive if the paw was sharply withdrawn upon filament application, starting with 13.7 millinewton filaments and then progressing in an up-down method, as previously described (Marvaldi et al., 2020).
For the hot plate test, mice were tested for heat sensitivity at temperatures of 52°C and 55°C. Each mouse was placed in a 20 cm high Plexiglas box on the heated metal surface and the latency to initiate a nociceptive response (licking, paws shaking, jumping) was recorded.
For the catwalk assay to test regeneration in vivo, we made use of the catwalk test described above. Before sciatic nerve injury, mice were trained on the Catwalk apparatus and a baseline of both genotypes was assessed 1 day before the crush. The locomotion recovery of the mice was observed during the day 1, 5, 10, 15, 22 and 28 post-injury showing reduced recovery of the Isl1-Dync1h1+/− mice.
Quantification and statistical analysis
Data shown represent mean±s.e.m., unless otherwise noted. N represents number of independent biological repeats, n represents number of cells or sections. Statistical analyses and graphs were generated using GraphPad Prism 9 software. Pairwise analyses were conducted with an unpaired two-tailed t-test (Figs 1 and 3B,C,D; Fig. S2). Groupwise analyses were conducted by one-way ANOVA for one-factor analyses assuming equal variances (Figs 4 and 5; Fig. S5) or two-way ANOVA where >1 factor was analyzed (Figs 2, 3A and 7; Fig. S4). Statistically significant P-values are shown as *P<0.05, **P<0.01, ***P<0.001 and ****P<0.0001.
We thank the Institute Clinique de la Souris – PHENOMIN for establishment of the Dync1h1 mouse mutant line. We thank Prof. Eran Perlson, Dr. Marco Terenzio, Dr. Dalia Gordon, Dr. Michael Tsoory, Vladimir Kiss, Jérôme Sinniger, and Pierluigi Di Matteo for helpful advice and support.
Conceptualization: M.F., I.R.; Methodology: M.-C.B.; Validation: A.D.P., L.D.; Formal analysis: A.D.P., N.O.; Investigation: A.D.P.; Data curation: I.R.; Writing - original draft: A.D.P.; Writing - review & editing: L.D., M.F., I.R.; Visualization: L.M., N.O.; Supervision: M.F., I.R.; Project administration: I.R.; Funding acquisition: L.D., M.F., I.R.
This work was funded by Agence Nationale de la Recherche, France (ANR-10-JCJC-1101 to L.D.), the Motor Neuron Disease Association (Dupuis/Apr16/852-791 to L.D.), and the Israel Science Foundation (ISF 1337/18 to M.F. and I.R.). M.F. is the incumbent of the Chaya Professorial Chair in Molecular Neuroscience at the Weizmann Institute of Science. Open access funding provided by the Weizmann Institute of Science. Deposited in PMC for immediate release.
Peer review history
The peer review history is available online at https://journals.biologists.com/jcs/lookup/doi/10.1242/jcs.260220.reviewer-comments.pdf.
The authors declare no competing or financial interests.