Female sex mitigates motor and behavioural phenotypes in TDP-43Q331K knock-in mice

Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are overlapping neurodegenerative disorders. ALS is more commonly seen in men than women and the same may be the case for FTD. Preclinical models demonstrating sex-specific vulnerability may help to understand female resistance to ALS-FTD and thereby identify routes to therapy. We previously characterised a TDP-43Q331K knock-in mouse, which demonstrated behavioural phenotypes reminiscent of ALS-FTD in males. Here we present our behavioural observations of female TDP-43Q331K mutants. Female TDP-43Q331K knock-in mice displayed increased weight relative to wild-type and increased food intake at 20 months of age, much later than previously observed in male mutants. Spontaneous digging behaviour was initially normal and only declined in mutants in the second year of life. Gait analysis using Catwalk (https://www.noldus.com/catwalk-xt) found significant deficits in the second year of life, while nocturnal running behaviour was attenuated from ~ 250 days of life. These results indicate that while female TDP-43Q331K knock-in mice do display progressive behavioural phenotypes, these are less severe than we previously noted in male mutants. Further studies of male and female TDP-43Q331K knock-in mice may help to unravel the mechanisms underlying sex-specific vulnerability in ALS-FTD.


Scientific Reports
| (2020) 10:19220 | https://doi.org/10.1038/s41598-020-76070-w www.nature.com/scientificreports/ knock-in mouse model of ALS-FTD harbouring only a human equivalent missense mutation in the endogenous murine Tardbp gene 23 . In our analysis of breeding ratios, we found that while female TDP-43 Q331K knock-in mutants were present at Mendelian ratios, male mutants were under-represented. This suggested that males were more susceptible to deleterious effects of the TDP-43 Q331K mutation 23 . We subsequently focussed our attention on male mice, finding that male mutants displayed FTD-like deficits 23 , including executive dysfunction, weight gain due to hyperphagia 24 , and reduced digging behaviour suggestive of apathy 25 . However, whether similar phenotypes occurred in female mutants and whether these are attenuated, as they are in women compared to men, was not determined.
Here, we present results from a longitudinal study to investigate behaviour in female homozygous mutant (TDP-43 Q331K/Q331K ) knock-in mice and wild-type littermates. Given the increased incidence and severity of ALS-FTD in men [4][5][6][7] , and the increased penetrance of TARDBP mutations in males 21 , we tested the hypothesis that female sex attenuates disease caused by mutant TDP-43 Q331K .

Results
Weight gain and age-dependent increase in food intake in female mutant mice. We previously showed that male TDP-43 Q331K/Q331K mice displayed increased weight gain from 8 months of age and were also hyperphagic compared to wild-type mice 23 . We therefore weighed female wild-type and TDP-43 Q331K/ Q331K mice but found that at 8 months of age there were no significant differences in weight (23.0 ± 1.7 g and 25.7 ± 3.8 g, respectively, P = 0.9692). However, TDP-43 Q331K/Q331K mice gradually gained more weight over time and were significantly heavier than wild-type mice from 13 months of age. By 20 months, wild-type mice weighed 29.5 ± 5.0 g and TDP-43 Q331K/Q331K mice weighed 45.6 ± 7.7 g (P < 0.01; mixed-effects analysis) (Fig. 1a).
To determine if weight gain in the TDP-43 Q331K/Q331K mice could be due to hyperphagia, food intake was measured when mice were 9, 13 and 20 months old. The amount of food eaten in 72 h did not change with age and there was no significant difference between groups, although at 20 months there was a trend towards increased food intake (Fig. 1b). Wild-type and TDP-43 Q331K/Q331K mice ate 12.7 ± 2.3 g and 12.3 ± 2.2 g of food at 9 months of age (P = 0.9801), 12.2 ± 2.3 g and 11.8 ± 1.6 g of food at 13 months of age (P = 0.9633) and 11.4 g ± 1.5 g and 13.9 ± 2.8 g at 20 months (P = 0.0601 two-way ANOVA), respectively.

Age-dependent deficits in marble burying behaviour in mutant females.
A subset of male TDP-43 Q331K/Q331K mice were previously found to display reduced spontaneous digging as determined by the marble burying assay from as early as 5 months of age 23 . This may reflect apathy or reduced motivation, both of which are features of FTD 25 . We therefore examined marble burying behaviour in female wild-type and TDP-43 Q331K/Q331K mice from 8 to 20 months of age but found no significant differences between genotypes at any given age although there was a trend towards reduced digging from 14 months onwards (Fig. 1c). At 9 months of age, wild-type mice buried 8.5 ± 1.4 marbles and TDP-43 Q331K/Q331K mice buried 8.9 ± 0.7 marbles (P = 0.9966), whereas at 14 months wild-type mice buried 8.4 ± 1.2 marbles and TDP-43 Q331K/Q331K mice buried 6.2 ± 2.9 marbles (P = 0.0495). When mice reached 20 months of age wild-type mice buried 7.75 ± 1.6 marbles and TDP-43 Q331K/Q331K mice buried 6.4 ± 2.7 marbles (P = 0.5513, mixed-effects analysis). These results indicate that innate exploratory digging behaviours are largely intact in female mutant mice, although they may be affected in older age.
Gait deficits in aged mutant females. Our previous study showed that male TDP-43 Q331K/Q331K mice have reduced Rotarod performance from ~ 6 months of age, which was likely due to increased body weight rather than impaired motor coordination 23 . To test for motor coordination in female mice, we carried out detailed gait analysis using the Catwalk gait analysis system (Noldus, https ://www.noldu s.com/catwa lk-xt). TDP-43 Q331K/Q331K mice had normal hindlimb base of support (BOS, the distance between the hind paws during the step cycle) from 8 to 14 months of age, but significantly wider hindlimb BOS at 20 months of age, when compared to wildtype mice (26.9 ± 5.3 mm and 23.5 ± 2.6 mm, respectively; overall P < 0.05, two-way ANOVA) (Fig. 2a). While this could be due to impaired motor coordination it could also be explained by the increased body weight.
TDP-43 Q331K/Q331K mice also showed decreased hindlimb swing time (time between successive paw placements) and increased swing speed (average speed of paw travelling during the swing phase). The hindlimb swing time and swing speed of wild-type mice at 20 months were 0.09 ± 0.01 s and 0.65 ± 0.12 m/s, respectively, and were 0.07 ± 0.01 s and 0.83 ± 0.16 m/s for TDP-43 Q331K/Q331K mice. This suggests that TDP-43 Q331K/Q331K mice walk faster than wild-type mice (Fig. 2b, c). However, the overall duration of the runs and hindlimb stride length showed no significant difference between the two groups at 20 months of age (data not shown). Together with swing speed and time, these results suggest that TDP-43 Q331K/Q331K mice take faster steps than wild-type mice.
Under normal conditions mice walk in a diagonal stepping pattern with only two diagonally opposed paws on the surface at any one time 26 . An increase in the percentage of time spent on 3 or 4 paws indicates instability whilst walking. Female wild-type mice spent the majority of their time on diagonal paws, and relatively little time on 3 and 4 paws from 10 to 20 months of age ( Fig. 2d-f). In contrast, TDP-43 Q331K/Q331K mice spent significantly more time on 3 and 4 paws (Fig. 2 d-f). This difference was most pronounced at 20 months of age, by which time wild-type mice were spending 71.4 ± 8.8% of time on diagonal paws and 5.04 ± 4.1% of time on 4 paws, whereas mutants spent 58.1 ± 8.1% of time on diagonal paws and 14.1 ± 5.6% of time on 4 paws. These changes indicate that TDP-43 Q331K/Q331K mice stand for longer durations of the step cycle and may develop a less steady gait with age.
Reduced running in mutant mice. To gain further insight into the motor performance of female TDP-43 Q331K/Q331K mice we measured voluntary wheel running, an assay that can be performed without disruption to Scientific Reports | (2020) 10:19220 | https://doi.org/10.1038/s41598-020-76070-w www.nature.com/scientificreports/ the normal murine diurnal rhythm in a minimally stressful environment 27 . Behaviour was monitored daily in mice that had unlimited access to a running wheel, which was linked to a sensor to measure time spent running, total distance run, and speed. As they aged, both wild-type and TDP-43 Q331K/Q331K mice showed a progressive decline in total time and distance run per night, but this deterioration was more marked in mutants ( Fig. 3a, b). Wild-type mice had a decrease from 286 ± 102 to 109 ± 56 min of running per night and mutants had a decrease from 252 ± 107 to 33 ± 30 min of running per night between 8 and 20 months of age (overall P < 0.0001, two-way ANOVA). Wild-type mice retained their average speed from 250 to 600 days of age, but mutants declined over time and became significantly slower. By 20 months of age wild-type mice were running 2.2 ± 1.81 km per night at 1.12 ± 0.35 km/h, whereas TDP-43 Q331K/Q331K mice were running 0.50 ± 0.61 km per night at 0.68 ± 0.38 km/h (Fig. 3c). This suggests that female TDP-43 Q331K/Q331K mice have reduced physical performance compared to wild-types.

Preservation of functional motor units in mutant mice.
To determine if the motor deficits in female mutants were due to neuromuscular dysfunction, we looked for evidence of denervation by measuring compound muscle action potentials (CMAP) in the hindlimbs of 12-month-old mice. However, we found no significant differences in CMAP amplitudes between wild-type and mutant females (36.5 ± 5.4 mV and 39.2 ± 8.9 mV, respectively; n = 3 per genotype; P = 0.6689, unpaired t-test) (Fig. 4). This suggests that functional motor units are preserved in mutant mice and that the motor deficits they display are not due to neuromuscular denervation. Nonetheless, a more detailed analysis with a larger sample size and at more timepoints may be of value in determining if female mutants are vulnerable to denervation. Food intake at 9, 13 and 20 months of age (n = 10 per genotype (9 months); 9 wild-type, 8 mutants (13 months); 8 wild-type, 9 mutants (20 months)) (overall P = 0.3260; two-way ANOVA). (c) Marble burying from 8 to 20 months of age (n = 10 per genotype (8, 9, 10 and 12 months); 9 per genotype (14 months); 8 per genotype (20 months)) shows no significant difference between groups (P = 0.6689; unpaired t-test). Error bars represent mean ± s.e.m, except in (c) where they are median ± interquartile range. ***P < 0.001.

Discussion
Epidemiological studies show that women are significantly less likely to develop ALS-FTD than men. Preclinical models of ALS-FTD that recapitulate this sex difference could help to understand the reasons for the protection conferred by female sex, which may in turn help towards developing therapies. In this study we found that female TDP-43 Q331K knock-in mice develop motor and behavioural deficits similar to those previously observed in male mutants, but that these phenotypes were less severe in females ( Table 1). The clearest indicator of this was the striking weight gain seen in mutants, which occurred later in life and to a lesser extent in females than in males. Similarly, while food intake and marble burying behaviour were significantly increased and decreased respectively in male mutants, female mutants showed only trends towards such changes. The gradual increase in weight gain in both male and female TDP-43 Q331K/Q331K mice may be attributable to the role of TDP-43 in fat metabolism regulated by Tbc1d1 28,29 , which is most likely independent of oestrogen 30 . However, the hyperphagia observed in female mice at 20 months when oestrogen levels have dropped 31 may directly result from release of the appetite stimulating gut hormone ghrelin, normally under tonic inhibition by oestradiol 32 . Thus, further studies of TDP-43 Q331K mice promise to help unravel how female sex protects against ALS-FTD. Determining differences due to biological sex in other animal models of ALS/FTD is more challenging due to confounding factors such as genetic background and transgene expression levels. Nonetheless, some studies have reported sex-specific behavioural differences in mouse models of ALS and FTD. A transgenic TDP-43 A315T mutant mouse shows earlier disease onset and more rapid disease progression in males than females, accompanied by reduced lifespan 33 , although females perform worse in spatial learning tasks 34 . Female TDP-43 M323K knock-in mice harbouring a missense mutation in the endogenous Tardbp gene display an age-dependent decrease in grip strength, while males are normal 35 . Mouse models of other ALS and FTD-linked genes present a more complex picture. Males overexpressing human mutant superoxide dismutase 1 (SOD1 G93A ) show earlier disease onset than females 36 , although this is dependent on genetic background 37,38 . However, the opposite is observed in females harbouring an inducible D83G point mutation in murine Sod1, which demonstrate earlier impairment in Rotarod performance, though males reach end-stage sooner 39 . Female SOD1 G37R mice also have increased maladaptive axonal arborisation compared to males, which corresponds to neuronal loss and muscular denervation 40 . In contrast, transgenic female mice expressing the G118V mutation in profilin1 (PFN1) reach end-stage earlier than males, although age of disease onset is unaffected by sex 41 . Similarly, female transgenic mice expressing a mutant form of chromosome 9 open reading frame 72 (C9ORF72), the most common known genetic cause of ALS-FTD 3 , have reduced body weight while male mutants are unaffected 42 . This suggests an intricate regulation of sex-specific behaviours in diverse animal models.
Scientific Reports | (2020) 10:19220 | https://doi.org/10.1038/s41598-020-76070-w www.nature.com/scientificreports/ mutations in C9ORF72 have been shown to be more commonly seen in women than men with ALS 43 , although this difference is not observed in C9ORF72-related FTD 43 . Mutations in progranulin (GRN) are also more common in women 43 , and mutations in T-cell restricted intracellular antigen 1 (TIA1) have, to date, been found exclusively in women 44 . Mutations in microtubule-associated protein tau (MAPT) by contrast are not specific to either sex 43 . A likely explanation for sex differences in neurodegenerative disease is the role of reproductive hormones. Oestrogens, specifically 17β-oestradiol, can exert neuroprotective effects in both males and females by signalling . c Mean speed run per 24 h (P < 0.0001; two-way ANOVA). All data are from 230 to 618 days of age (n = 8-10 wild-type, 7-10 mutants). Error bars represent mean ± s.e.m. ****P < 0.0001.
Scientific Reports | (2020) 10:19220 | https://doi.org/10.1038/s41598-020-76070-w www.nature.com/scientificreports/ through oestrogen receptors, which are widely distributed in the brain 45 . These effects range from maintenance of cognition and response to injury, to dendritic spine maturation and adult neurogenesis 46 . This is in keeping with findings from patients with ALS in whom the sex differences in incidence and prevalence diminish with age 4 . This may well be due to the reduction in levels of oestrogen in post-menopausal women 5 . The protective effects of sex hormones are not only restricted to neurons, which constitutively produce oestradiol, but also glia 45 . Astrocytes show sex differences in their development, number and morphology, in addition to functional characteristics like glutamate uptake and their response to cannabinoids, gonadotrophic hormones, and harmful stimuli such as environmental toxins 47 . Microglia, the innate immune cells of the central nervous system, develop sex-specific transcriptional differences in adulthood, although it is debated which sex develops a more pro-inflammatory phenotype 48 . This may contribute to sex-specific differences in ALS-FTD, given that microglia play key roles during development and ageing, express high levels of the FTD-linked gene GRN 49 , and have been implicated in disease pathogenesis by several mouse models of ALS [50][51][52] .
The effects of sex hormones on brain mitochondrial metabolism have also been well documented 53 . For example, 17β-oestradiol can transcriptionally regulate and increase the function of components of the respiratory chain while reducing oxidative stress in brain mitochondria. Cerebral expression of the oestrogen receptors ERα and ERβ is also sexually dimorphic 53 . Incidentally, female transgenic mutant SOD1 mice have delayed onset of mitochondrial dysfunction in the spinal cord compared to males 54 , possibly resulting from ERα-dependent activation of the mitochondrial unfolded protein response 55 . This transcriptional programme for restoration of proteostasis can also be activated by TDP-43 56 . Hormonal regulation may also affect disease course in ALS through regulation of the expression of a group of muscle-specific microRNAs 57 Table 1. Summary of differences between male and female TDP-43 Q331K mice in age of onset of behavioural phenotypes, compared to wild-type. a Earliest age at which food intake was measured. b Statistical trend. c As male mice on the C57BL/6 background have low baseline levels for this task 69 .
Phenotype (compared to wild-type)

Male 23 Female
Weight gain 8 13 Increased food intake 9 a 20 b Reduced marble burying 5 14 b Gait defects 6 20 Reduced running n/a c 8

Muscle denervation None None
Scientific Reports | (2020) 10:19220 | https://doi.org/10.1038/s41598-020-76070-w www.nature.com/scientificreports/ testosterone on the brain are, however, more elusive, with multiple mechanisms both conferring neuroprotection and enhancing neurodegeneration [58][59][60][61][62][63] . Abundant evidence indicates sexual dimorphism in varied neurodegenerative diseases. Males have a twofold increased risk of Parkinson's disease, and also present with more marked non-motor symptoms compared to females 64 . In contrast, females are more likely to develop Alzheimer's disease 65 , particularly those with the APOEε4 allele 66 , and women with Huntington's disease show a faster rate of progression than men 67 . Our findings add to a growing body of evidence suggesting that the influence of biological sex in neurodegenerative diseases is complex, resulting not only from genetic architecture, age, epigenomic and transcriptomic factors, but also from the effects of reproductive hormones on glial and neuronal cells, and organelle function. We conclude that the TDP-43 Q331K/Q331K knock-in mouse, which displays sex-specific behavioural differences, can be utilised as a tool to investigate female resistance to ALS-FTD and thereby help towards developing therapies for this disease spectrum.

Methods
Mouse model and genotyping. Mice were generated using CRISPR/Cas9 mutagenesis as described previously 23 and maintained on a C57BL/6J background by crossing with wild-type animals. Animals were bred in a specific pathogen free environment and transferred to a conventional facility under a 12-h light/dark cycle. Cages (36 × 21 × 18.5 cm) were lined with fine sawdust (eco-pure flakes 6, Datesand, UK), a plastic house was placed in each cage and paper wool (Datesand, UK) was used as bedding material. All mice were singly housed due to the use of running wheels in the home cage, with food (Harlan, UK) and water available at libitum. Animals were genotyped as described previously 23 . All experiments were conducted in accordance with the United Kingdom Animals (Scientific Procedures) Act (1986) and the United Kingdom Animals (Scientific Procedures) Act (1986) Amendment Regulations 2012, and also reviewed and approved by the University of Sheffield Animal Welfare and Ethical Review Body (AWERB). Power calculations were determined as described previously 23 . All of the behavioural testing was carried out on the same cohort of female mice. One wild-type and one mutant mouse developed skin conditions at 1 year of age and were humanely culled on compassionate grounds. One wild-type and one mutant mouse lost 20% of their bodyweight nearing the 20-month time point and were culled on compassionate grounds. One additional mutant mouse was found to be unwell at 20 months of age and was culled.
Body weight and food intake. Animals were weighed weekly in the morning as previously described 23 .
Food intake was monitored at various timepoints by weighing the food in the hopper, then re-weighing approximately 72 h later. During the 72-h period, sawdust in the cage was replaced with paper towelling to ensure any small pieces of food dropped from the top of the hopper could be included for weighing.
Marble burying. The marble burying assay was conducted as described previously 23 , except that different cages were used. Briefly, all testing was conducted in the morning and blind to genotype in cages of size 33 × 21 × 19 cm (Tecniplast) with fresh sawdust (Datesand, grade 6) placed to a height of ~ 8 cm. Ten glass marbles (1 cm) were placed evenly across the bedding. A single mouse was placed in each of the cages, the lids replaced, and left undisturbed for 30 min under white light. Mice were then removed, and the number of marbles buried by at least two thirds was scored.
Catwalk gait analysis. The Catwalk gait analysis system 7.1 (Noldus Information Technology B.V., Netherlands, https ://www.noldu s.com/catwa lk-xt) was used to capture gait parameters at 8, 10, 12, 14, and 20 months of age as previously described 38 . Mice were placed on the glass floor of the catwalk system in complete darkness and left to walk/run freely. Whenever possible, six continuous runs were recorded, with the three best runs being selected for analysis. Catwalk software 7.1 was used to label each paw print during each run and analyse the gait parameters of the mice.
Running wheel analysis. The running wheel set-up was based on an in-house protocol described previously 68 . Each cage contained a 37.8 cm circumference Fast Trac running wheel (LBS Biotech, UK) mounted at 25˚ below horizontal, on a 4 cm fixed post. The wheel was placed in the corner of each cage where the circumference was 5-10 mm from the edge of two perpendicular sides of the cage. A 5 × 10 mm neodymium magnet was glued to the underside of each Fast Trac wheel and a bicycle computer (Cateye Velo, Japan) with reed switch was fixed to the side of the cage. Time spent running, distance run, and average running speed were recorded daily.
Compound muscle action potential (CMAP) amplitude testing. Mice were placed under gaseous anaesthesia (1-2% isoflurane), with body temperature maintained using an electric heat pad (CWE, USA), and fur from the left hindlimb and lower back was removed. All recordings were made using a Dantec Keypoint Focus EMG System (Optima, UK) as previously described 38 . A grounding electrode was placed in the base of the tail (Ambu Neuroline, UK), and ring recording electrodes were placed circumferentially around the distal hindlimb muscles (Alpine Biomed, Denmark), layered with Ten20 nerve conductive paste (Pulse Medical Ltd, UK). CMAPs were acquired by applying a single, square wave electrical impulse of 0.1 ms duration to the sciatic notch using twisted pair subdermal electrodes (Ambu Neuroline, UK). The position of the subcutaneous stimulating electrodes was trialled to ensure that a response was obtained using a stimulating current of 1-2 mA. The Scientific Reports | (2020) 10:19220 | https://doi.org/10.1038/s41598-020-76070-w www.nature.com/scientificreports/ stimulation intensity was then increased until no further increase in amplitude was seen and a supramaximal response elicited.
Statistical analyses. All data was analysed using GraphPad Prism version 8 (https ://www.graph pad.com/ scien tific -softw are/prism /). Statistical significance was determined by two-way analysis of variance (ANOVA) with or without repeated measures with Sidak correction for multiple testing, mixed effects analysis, or Student's t-test. Results having P < 0.05 were considered significant in every analysis. Please note that this methods section was adapted from the PhD thesis of the first author, which can be found at https ://ethes es.white rose.ac.uk/id/eprin t/16694 re-used here under a creative commons CC BY-NC-ND 2.0 UK license (https ://creat iveco mmons .org/licen ses/by-nc-nd/2.0/uk/).