Abstract
Skeletal muscle regulates central nervous system (CNS) function and health, activating the muscle-to-brain axis through the secretion of skeletal muscle-originating factors (“myokines”) with neuroprotective properties. However, the precise mechanisms underlying these benefits in the context of Alzheimer’s disease (AD) remain poorly understood. To investigate muscle-to-brain axis signaling in response to amyloid β (Aβ)-induced toxicity, we generated 5xFAD transgenic female mice with enhanced skeletal muscle function (5xFAD;cTFEB;HSACre) at prodromal (4-months old) and late (8-months old) symptomatic stages. Skeletal muscle TFEB overexpression reduced Aβ plaque accumulation in the cortex and hippocampus at both ages and rescued behavioral neurocognitive deficits in 8-month-old 5xFAD mice. These changes were associated with transcriptional and protein remodeling of neurotrophic signaling and synaptic integrity, partially due to the CNS-targeting myokine prosaposin (PSAP). Our findings implicate the muscle-to-brain axis as a novel neuroprotective pathway against amyloid pathogenesis in AD.
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Introduction
Multiple studies have demonstrated that the loss of neurotrophic signaling and synaptic connections are early events during Alzheimer’s disease (AD) pathogenesis. Indeed, deficits in neurotrophic factor abundance alongside widespread changes in synapse number, structure, and function have been reported in the CNS of persons with, and animal models of, AD [1,2,3,4]. Furthermore, these deficits correlate well with cognitive abnormalities in persons with AD, even more so than other pathological markers of the disease [1, 3]. This suggests that targeting neurotrophic signaling or synaptic function/number may be a critical step in developing new generations of AD disease-modifying therapeutics.
The muscle-to-brain axis has recently arisen as a powerful regulator of CNS health and function [5,6,7,8,9]. This novel signaling axis is mediated by circulating factors collectively known as “myokines,” which are secreted from skeletal muscle in response to multiple physiological and pathological conditions with high metabolic demand [10]. Through mechanisms that remain poorly understood, these circulating myokines can promote CNS rejuvenation and neuroprotection, reducing neuroinflammation, reactivating declining neurogenesis, and reducing the accumulation of protein aggregates [5, 11,12,13,14,15], all key features of AD pathogenesis. However, to date, the precise mechanisms that facilitate myokine-dependent neuroprotection in the context of AD remain poorly understood.
We have previously shown that activation of the muscle-to-brain axis via targeted overexpression transcription factor EB (TFEB) in skeletal muscle can protect against age-associated cognitive decline and reduce degenerative neuropathological hallmarks in the MAPT P301S mouse model of tauopathy [5]. We observed robust reductions in neuroinflammation and rescue of declining neurotrophic signaling in the hippocampus of both aged (24-months-old) and MAPT P301S transgenic mice (8-months-old) with muscle-TFEB overexpression. Furthermore, we also identified sex-dimorphic transcriptional remodeling in the CNS of muscle-TFEB overexpressing mice, with female mice displaying significant upregulation in pathways associated with synaptic physiology, neurotransmitter signaling, and voltage- and ion-gated channels, and male mice displaying upregulation of mitochondrial and ribosomal signaling [5]. We also confirmed that these neuroprotective effects were associated with increased expression and secretion of known CNS-targeting myokine cathepsin B, in addition to identifying several new potentially secreted proteins in TFEB-overexpressing muscle [5]. However, whether muscle-TFEB overexpression in skeletal muscle impacts CNS health in the presence of Aβ toxic species has yet to be explored.
Here, we report that activation of the muscle-to-brain axis using our cTFEB;HSACre (muscle-TFEB) mice also provides important neuroprotective effects in the 5xFAD model of Aβ-plaque toxicity. Muscle-TFEB overexpression reduced Aβ plaque accumulation in the cortex and hippocampus at prodromal (4-months-old) and later stages (8-months-old) of disease. Importantly, muscle-TFEB overexpression rescued neurocognitive deficits in 5xFAD mice in a battery of memory and learning behavioral tests. These neuroprotective effects appear to be independent of the modulation of neuroinflammatory states. Instead, muscle-TFEB expression promoted transcriptional remodeling of the 5xFAD CNS in pathways associated with neurotrophic and synaptic signaling, which we validate via extensive immunoblotting for neurotrophic and synaptic markers. Furthermore, we also provide evidence demonstrating our newly identified exercise-responsive myokine prosaposin (PSAP) as a potential mechanism driving these benefits.
Our results indicate that skeletal muscle TFEB-overexpression is sufficient to provide neuroprotection against amyloid pathogenesis-associated neurocognitive deficits by enhancing neurotrophic and synaptic signaling, potentially through the release of CNS-targeting myokines such as PSAP. These findings support the neuroprotective effects of the muscle-to-brain axis and provide potential pathways that can be targeted by interventions to preserve cognitive function and prevent worsening pathologies in neurodegenerative diseases.
Methods
Animals
We have previously described the generation of fxSTOP-TFEB transgenic mice [5]. For this work, cTFEB;HSACre;5xFAD transgenic mice were generated by crossing fxSTOP-TFEB females with 5xFAD (MMRRC Strain: 034840-JAX | B6SJL Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax) males. Double transgenic TFEB + /5xFAD + females were then crossed with heterozygous HSACre + males (JAX Strain No: 006139 | HSACre79) (Fig. 1A). All lines have been maintained in a C57B6/L background for over ten generations in our lab. Mice were housed in a temperature- and humidity-controlled environment on a 12-h light/dark cycle with food and water ad libitum. For all experiments, control animals were TFEB-;HSACre + and/or TFEB + ;HSACre- littermates, which we have previously demonstrated have no neurological or metabolic phenotypes at these ages [5]. To our knowledge, we did not detect any differences in plaque-associated CNS phenotypes in 5xFAD + ;TFEB + or 5xFAD + ;HSACre + double transgenic animals compared to 5xFAD single transgenic controls (Figs. 1, 2, 3, 4, and 5 and S1, S2, S3, S4, and S5) and are thus all grouped into the “AD” 5xFAD group. Mice were collected at either 4 months (5xFAD pre-symptomatic) or 8 months (5xFAD symptomatic) of age (Figs. 1, 2, 3, 4, and 5A–C and S1, S2, S3, and S4). C57B6/L males (Figs. 5D–F and S5) were 3 months old at the time of the pre-clinical intervention. All animal experimentation adhered to NIH guidelines and was approved by and performed in accordance with the University of Southern California and University of Alabama at Birmingham Institutional Animal Care and Use. The mice were not fasted prior to any of the experiments.
Tissue collections
Animals were anesthetized with 3.8% Avertin Solution and received transcardial perfusion with 60 mL of chilled 1X PBS. Right hemibrains were post-fixed in 4% paraformaldehyde for less than 24 h before transferring to a 30% (w/v) sucrose solution for another 24 h before OCT (TissueTek, 4583) embedding and cryo-sectioning. The left hemisphere was micro-dissected into the cortex and hippocampus and flash-frozen in liquid nitrogen alongside quadricep skeletal muscle for downstream analysis. Blood was collected via cardiac puncture and transferred to an EDTA tube in a 1:100 ratio and centrifuged at 1500 × g for 15 min at 4 °C to separate the layers. The top layer containing plasma was transferred to a 1.5-mL tube. The other layers were discarded. Tissue and plasma samples were stored at − 80 °C prior to downstream analysis. When possible, flash-frozen and OCT-embedded hemibrains from the same individual were utilized across the study, and results were confirmed in additional animals of the same genotype/age.
Immunofluorescence staining and analysis
Tissue was embedded in OCT (TissueTek, 4583), slow frozen using 2-methylbutane vapors (VWR, 103,525–278) submerged in liquid nitrogen, and stored at − 80 °C until use. All hemibrains were sectioned on a standing cryostat in 20 µm slices. All sections were permeabilized with 1X PBS + 0.1% (v/v) Triton for 15 min and blocked with 4% (w/v) BSA in 1X PBS for 1 h. Sections were stained with appropriate antibodies overnight at 4 °C; see Table S1 for full details on antibodies utilized in this project. After overnight incubation, sections were washed three times with 1X PBS and incubated with appropriate secondary antibodies for 1 h. Sections were washed three times with 1X PBS and incubated with 1:5000 Hoechst (Thermo Scientific, 62,249) for 5 min. Lastly, sections were washed three times with 1X PBS and mounted with ProLong glass (Invitrogen, P36984). Slides were imaged using a 20X or 60X objective on the Nikon A15R/SIM Confocal microscope at the UAB HRIF Confocal/Light Microscopy Core, or on Stellaris 5 (Leica Microsystems, 8,119,637).
Aβ plaque load was quantified following an established protocol [16] in ImageJ. Images included 2–6 biological replicates from each group and at least eleven technical replicates from anterior (n = 3), middle (n = 5), or posterior (n = 3) coronal sections. Cortical quantification spanned all six layers of the cortex and the whole morphometric structure of the hippocampus. Relative presence of glial cells in brain cryosections of the dentate gyrus of the hippocampus was quantified by the percentage of area coverage of GFAP + (astrocyte) and IBA1 + (microglia) staining using ImageJ. The number of astrocytes and the volume of microglia as a proxy for neuroinflammation were determined using the surface function available through Imaris microscopy image analysis software.
Mouse phenotyping and behavior
All behavioral experiments listed below were performed by double-blinded investigators. Unless otherwise stated, group sizes were as follows: controls (n = 10–12), 5xFAD (n = 7–8), 5xFAD;cTFEB;HSACre (n = 9). Group size changes across phenotyping tests reflect unrelated veterinary flags that required an individual’s removal from the study, such as fighting injuries, flooded cages, and/or prolapses.
Open field
Mice (8 months old) were individually placed in an open field (50 × 50 cm), illuminated to 600 lx in the center, and were allowed to explore freely for 5 min. The following behaviors were recorded: traveled distance (cm), time spent in the center (s), and velocity (cm/s). Movements were tracked via Ethovision (Noldus).
Nest building
Nest building was assessed following similarly established protocols, with minor modifications [17]. In brief, mice were transferred to individual testing cages with woodchip bedding but no environmental enrichment items such as paper towels or other nesting material, and one (~ 3 g) piece of nestlet was placed in each cage. The nests were assessed 24 h later on a rating scale of 0 (no nestlet interaction), 1 (nestlet partially torn, 50–90% nestlet remaining intact), 2 (nestlet mostly shredded but no identifiable nest site), and 3 (fully developed nest) based on nest construction.
Barnes maze
The maze was an open circular platform (75 cm in diameter), with 20 evenly spaced holes located 5 cm apart along the border with a rectangular escape box (5.5 × 11.5 × 5.5 cm) placed under one of the holes. Distinct and constant spatial cues were located around the maze. Mice completed each trial of the maze individually. On the first day, a red light was turned on; the mice were placed in the center inside a start box for 10 s and were allowed to explore the maze for 3 min. On the second day, an initial training occurred where mice were placed inside the start box for 10 s with the buzzer and light on (80 dB + 400 lx) and were guided to the escape box, where the mice remained for an additional minute before their return to the home cage. Following this, the first training session (Trial Day 1) began by placing the mice inside the start box for 10 s with the buzzer and light on. The mice were allowed to explore for 3 min or until the mice found the escape box; once they found the escape, they remained in the box for an additional minute. Mice were returned to the home cage after testing ends. Days 3–5 (Trial Day 2–4) were the same as Day 2 but did not include the initial training guide. On Day 7 (probe day), the escape box was converted into a decoy box; the mice were placed in the center of the maze inside the start box for 10 s with the buzzer and light on and were allowed to explore for 3 min. Video recordings and data were analyzed with Ethovision (Noldus).
Fear conditioning
Conditioning was carried out in Plexiglas Freeze Monitor chambers (26 cm × 26 cm × 17 cm) with speakers and lights mounted on two opposite walls and shockable grid floors. The chambers were housed in sound-proofed boxes. Sessions were recorded with real-time digital video, and recordings were calibrated to distinguish among subtle movements, such as whisker twitches, tail flicks, and freezing behavior. On Day 1, mice were habituated to the chambers in a 5-min shock-free test. On Day 2, the mice are subjected to the context and conditioned stimulus (30 s, 2800 Hz, 75 dB sound + white light) in association with foot shock (0.5 mA, 2 s, scrambled current). During this 3-min test, the mice received 1 shock during the last 2 s of a 30-s tone/light exposure. On Day 3, contextual conditioning (as determined by freezing behavior) was measured during a 5-min test in the chamber where the mice were trained (context test). The next day, cued conditioning (CS + test) was tested. The mice were placed in a novel context for 3 min; after which, they were exposed to the conditioned stimuli (white light + tone) for 3 min. To create a novel context, the chamber was covered with new walls (white opaque plastic creating a circular compartment in contrast to a clear plastic square compartment) and a new floor (white opaque plastic in contrast to a metal grid). Animals were returned to their home cages after the testing period.
Grip strength
Mice were placed in the testing room 1 h before starting and were subjected to a standardized grip strength test. In brief, mice were placed on a TSE Systems grip strength meter that allowed for a 2-paw grip. Once mice gripped the meter, they were gently pulled by the base of the tail, parallel to the table surface, until they released their grip. The force exerted as the moment of release was recorded as the grip strength. Measurements were repeated three times with a 1-min rest interval.
Gene expression analysis
Assays were performed as described previously [5]. In brief, 100 ng aliquots of hippocampal RNA were extracted using the PureLink RNA kit (Invitrogen, 12183018A) and run via the Nanostring nCounter analysis system (NanoString Technologies, Seattle, WA, USA) at the University of Alabama Nanostring Core. After codeset hybridization overnight, the samples were washed and immobilized to a cartridge using the NanoString nCounter Prep Station. Cartridges were scanned in the nCounter Digital Analyzer at 555 fields of view for the maximum level of sensitivity. Raw reads and the Nanostring Mm_AD30_v1.1 probe annotation codeset were imported into the Nanostring proprietary software, nSolver 4.0, and QC was performed following company protocol guidelines.
Counts for target genes were normalized to housekeeping genes included in the panel. Specifically, background correction was performed using the negative control at the cutoff of mean + 2 standard deviation. Housekeeping genes were used for normalization based on geometric mean. All p-values were adjusted using a false discovery rate (FDR) correction of 1% for multiple comparisons. Differential expression and pathway scoring analysis, as well as graphical QC representation, were performed in the nSolver Advanced Analysis software 2.0 using a custom analysis to utilize generated normalized counts. Differential gene expression values were presented as 5xFAD vs. 5xFAD;cTFEB:HSACre hippocampal RNA expression counts. A p-value < 0.05 was considered significant. Volcano plots were generated with the ggplot2 package in RStudio [18] using significant genes and a predetermined cutoff value. The pathway scoring module summarizes a single score from the data from a pathway’s genes.
Protein extraction
Protein lysates from skeletal muscle or cortex tissue from female 5xFAD, control, or 5xFAD;cTFEB;HSACre mice were prepared as previously described [5, 7, 8] with a few modifications. Flash-frozen perfused tissues (quadriceps and cortex) were added to a 2.0-mL plastic tube with silica beads (MP Biomedical, 116,913,100) and homogenized using a FastPrep-24 5G bead grinder and lysis system (MP Biomedical, 116,005,500) in radioimmunoprecipitation assay (RIPA) lysis and extraction buffer (Invitrogen, 89,900), 1X Halt Protease and Phosphatase Inhibitor Cocktail (Invitrogen, 78,442), and 1% (w/v) SDS. The supernatant was transferred to a new 1.5-mL plastic tube and centrifuged (Eppendorf, 5425R) at 1500 × g for 10 min at 4 °C to remove debris. The resulting supernatant was transferred onto a new 1.5-mL plastic tube. Protein concentration was quantified using a Pierce™ BCA Protein Assay (ThermoFisher Scientific, 237,227) and frozen at − 80 °C until downstream analysis.
Synaptosome extraction
Total protein lysates and synaptosomes were extracted from 3-month-old C57BL/6 male mice following previously established protocols [19, 20] with a few modifications. In brief, flash-frozen perfused cortex tissue was added to a 2.0-mL plastic tube with silica beads (MP Biomedical, 116,913,100) and homogenized using a FastPrep-24 5G bead grinder and lysis system (MP Biomedical, 116,005,500) in 1 mL of Buffer A, which consisted of 10 mM HEPES (Millipore Sigma, H3375) (pH 7.4), 2 mM EDTA (Millipore Sigma, E4884), 5 mM sodium orthovanadate (Millipore Sigma, S6508), 30 mM sodium fluoride (Millipore Sigma, 201,154), 20 mM β-glycerol phosphate (Millipore Sigma, G5422), and protease inhibitor cocktail (Millipore Sigma, P2714), all diluted in 50 mL of water to a total volume of 50 mL. Tissue homogenates were then split onto two 1.5-mL plastic tubes.
To extract total protein lysates, 3% (v/v) Triton X-100 (Millipore Sigma, X100) was added to tissue homogenates and allowed to incubate in ice for 30 min with gentle shaking followed by centrifugation at 10,000 × g for 15 min at 4 °C. The resulting supernatant was transferred onto a new 1.5-mL tube; protein concentration was quantified using a Pierce™ BCA Protein Assay (ThermoFisher Scientific, 237,227) and frozen at − 80 °C until downstream analysis.
To extract synaptosomes, total homogenates were centrifuged for 500 × g for 5 min at 4 °C, and the resulting supernatant was separated from the nuclear pellet and transferred onto a new 1.5-mL tube followed by centrifugation at 10,000 × g for 15 min at 4 °C. The cytosolic supernatant was transferred onto a new 1.5-mL tube, while the pellet containing the crude synaptosome fraction was dissolved in 200 µL Buffer B, which consisted of 10 mM HEPES (pH 7.4), 2 mM EDTA, 2 mM EGTA (Millipore Sigma, E3889), 5 mM sodium orthovanadate, 30 mM sodium fluoride, 20 mM β-glycerol phosphate and 1% (v/v) Triton X-100 protease inhibitor cocktail, all diluted in 50 mL of water to a total volume of 50 mL. Protein concentration was quantified using a Pierce™ BCA Protein Assay and frozen at − 80 °C until downstream analysis.
Immunoblot analysis
Western blot analyses were conducted as previously described [5]. In brief, 5–10 µg (synaptosome preps) or 20–40 µg (for total tissue) of homogenized protein lysates were mixed in appropriate volumes with NuPAGE LDS sample buffer (ThermoFisher Scientific, NP0007) and NuPAGE sample reducing reagent (ThermoFisher Scientific, NP0004) and were denatured at 70 °C for 10 min. Samples were then loaded per lane onto Any kDa, 4–15% or 10% Mini-PROTEAN TGX Stain-Free Precast Gels (BioRad, 4,568,123, 4,568,083, or 4,568,033). Gels were activated by exposure to UV light for 45 s using a Chemidoc (BioRad, 12,003,153), and protein lanes were transferred onto a 0.45 µm PVDF membrane (BioRad, 1,704,275) using the BioRad Turbo Transfer system (BioRad, 1,704,150). Post-transfer membranes were blocked in 5% (w/v) BSA in TBS + 0.1% (v/v) Tween-20 (TBST) or 5% (w/v) skimmed milk in TBST at RT for 1 h. Membranes blocked with milk were washed three times with TBST to remove excess milk prior to incubation with primary antibodies. Skeletal muscle membranes were incubated with anti-FLAG or PSAP antibodies. Cortex membranes were incubated with anti-brain derived neurotrophic factor (BDNF), neurotrophin 4 (NTF4), synaptosomal-associated protein 25 (SNAP25), synaptophysin 1 (SYP1), synaptotagmin 1 (SYT1), synapsin 1 (SYN1), post-synaptic density protein (PSD95), synaptosome associated protein 97 (SAP97), SAP102, glutamate ionotropic receptor AMPA type subunit 1 (GluA), actin β, PSAP/saposin-C, or β tubulin 3; see Table S1 for full details. Finally, all membranes were subjected to gentle shaking at 4 °C overnight, washed three times with 1X TBST, and incubated with appropriate secondary antibodies for 1–2 h with gentle shaking at RT. Membranes were washed twice with TBST and once with TBS and imaged using Chemidoc (BioRad, 12,003,153). All data were analyzed using densitometry analysis normalized to an appropriate loading control (Total StainFree, actin β, or tubulin depending on lysate origin) in ImageLab. All experiments included at least 4–6 biological replicates per group.
Prosaposin ELISA
Blood was collected from mice via cardiac puncture, and plasma was separated using standard coagulation/centrifugation protocols as described above. Collected plasma was diluted 1:2222 and processed through a mouse PSAP ELISA kit (Abcam, ab277399) following the manufacturer’s protocol. In brief, 100 µL of standard calibrator or sample was added to a plate and allowed to incubate for 2.5 h with gentle shaking at RT. Wells were washed 4X with wash buffer, and 100 µL of biotinylated anti-PSAP antibody was added to each well and allowed to incubate for 1 h with gentle shaking at RT. Wells were then washed four times with wash buffer, and 100 µL of HRP-streptavidin concentrate was added to each well and allowed to incubate for 45 min with gentle shaking at RT. After four washes, 100 µL of TMB substrate reagent was added to each well and allowed to incubate for 30 min at RT. Finally, 50 µL of stop solution was added to each well, and the plate was read immediately at 450 nm (Tecan, 30,190,085). The concentration of PSAP was determined using a standard serially diluted curve of known concentration.
PS18 administration
An 18-mer derived peptide (LSELIINNATEELLIKGL; PS18) from the amino-terminal hydrophilic sequence of the rat saposin-C domain was obtained from Phoenix Pharmaceuticals (324–431), dissolved in dimethyl sulfoxide (DMSO), which was diluted in sterile normal saline (0.9%) into a solution with 1% DMSO (v/v) the day before injections. Each mouse was subcutaneously injected with a final concentration of 2.0 mg/kg PS18 or 1% DMSO alone once a day for 7 days. Mice were sacrificed on the 8th day, and tissue was collected and processed as described above.
Statistical analysis
All statistical analyses were conducted using Prism (GraphPad Software, La Jolla, CA). All data were analyzed using either one-way ANOVA followed by post hoc multiple comparisons, 2-way ANOVA followed by post hoc multiple comparisons for genotype × testing day/time × outcome, or independent t-tests, as appropriate. The level of significance (α) was always set at 0.05. All data were prepared for analysis with standard spreadsheet software (Microsoft Excel).
Results
Conditional skeletal muscle TFEB overexpression reduces Aβ accumulation and rescues neurocognitive behavioral deficits in 5xFAD female mice
Previous work from our lab has shown that skeletal muscle-TFEB overexpression is sufficient to improve learning and memory and reduce neuroinflammation and CNS protein aggregation during healthy aging and in the MAPT P301S mouse model of tauopathy [5]. To investigate whether muscle-TFEB overexpression is also neuroprotective in the context of another primary neuropathological hallmark of AD (i.e., Aβ), we generated 5xFAD;cTFEB;HSACre triple transgenic mice to achieve muscle-TFEB overexpression in the well-characterized plaque-toxicity 5xFAD transgenic background [21] (Fig. 1A). For this work, we focused our intervention on 5xFAD transgenic female mice only, as they exhibit an earlier and more severe phenotypic presentation of AD-associated pathology than their male counterparts [22], including more severe behavioral deficits, a stronger neuroinflammatory response associated with Aβ plaque deposition, and other metabolic deficits. These observations also align with the known increased prevalence and risk for AD in human females compared to males [23].
We first confirmed robust skeletal muscle 3x-FLAG-TFEB overexpression via immunoblotting in skeletal muscle lysates of 5xFAD;TFEB;HSACre but not 5xFAD;TFEB or 5xFAD;HSACre littermates (hereafter referred to as 5xFAD, Fig. 1B). There were no significant changes in the levels of TFEB protein expression between 4 months (early symptomatic) and 8 months of age (late symptomatic) in 5xFAD;cTFEB;HSACre skeletal muscle (Fig. S1A). Importantly, we also saw no detectable exogenous expression of TFEB in the CNS of 5xFAD;TFEB;HSACre mice via immunoblotting of cortical lysates from the same individuals (Fig. 1B). This confirms inducible and specific TFEB expression at stable levels in skeletal muscle across two stages of disease progression in this model (Fig. 1B), similar to what we observed in our MAPT P301S;cTFEB;HSACre model [5].
Given the profound decreases in the accumulation of neurotoxic hyperphosphorylated tau in our MAPT P301S work [5], we first examined whether overexpression of TFEB in skeletal muscle modifies the accumulation of Aβ in the CNS of 5xFAD mice. Consistent with previous work deep-phenotyping the progressive age-associated increase in plaque burden in this model [24], the 6E10 + fraction of the 5xFAD cortex and hippocampus increased from around 1% at 4 months of age up to ~ 8–10% at 8 months of age. Interestingly, we detected significant reductions in the 6E10-positive fraction area in the 5xFAD;cTFEB;HSACre cortex (Figs. 1C, D, and S1B) and hippocampus (Figs. 1E, F and S1C) at both ages compared to their 5xFAD littermates.
Previous studies have reported increased levels of amyloid precursor protein (APP) and pro-amyloidogenic APP-protease BACE1 [25,26,27,28] and decreased levels of non-amyloidogenic APP-protease ADAM10 [29, 30] concentrations in the brains of 5xFAD mice, likely acting as major drivers of Aβ-plaque accumulation in this model. Interestingly, we detected a significant reduction in total soluble APP levels, accompanied by a slight increase in ADAM10 and a decrease in BACE1 protein levels in 4 months of age 5xFAD;cTFEB;HSACre cortex (Fig. S1D). This suggested that muscle-TFEB overexpression reduced Aβ accumulation through modulation of APP processing. However, these changes were not detectable at 8 months of age (Fig. S1E), despite significant overall reductions in Aβ-plaque burden at this age (Fig. 1C, D), indicating a transient, age-dependent modulation of Aβ accumulation.
We have previously reported that muscle-TFEB overexpression improves cognitive performance in aged mice compared to age-matched controls [5]. Given the significant reductions in plaque burden observed in the CNS of 5xFAD;cTFEB;HSACre mice at 8 months of age (Fig. 1C–F), we next interrogated behavioral phenotypes in our cohorts at this symptomatic stage. As previously reported [24, 31, 32], 5xFAD transgenic mice weighed less than their control littermates at 8 months of age, a phenotype believed to reflect on-going metabolic imbalance (Fig. 1G). Interestingly, the body weight of age-matched 5xFAD;cTFEB;HSACre mice was not significantly different than their control littermates (Fig. 1G), consistent with our previous findings that muscle-TFEB overexpression improves overall skeletal muscle and metabolic health [5, 33]. We found no differences among any of the groups on grip strength tests (Fig. 1H), consistent with mild to no muscle weakness in this model at this age [24].
We next evaluated neurocognitive performance in our cohorts using a battery of tests with well-characterized deficits for the 5xFAD model, beginning with nest building to assess general behavior, well-being, and sensorimotor gating [34]. While control animals scored high on a 24-h nest-building test (average score of 2.1, maximum score of 3), 5xFAD transgenic mice scored quite poorly (average score of 0.4), rarely exhibiting interest in the provided nestlet (Fig. 1I). Conversely, 5xFAD;cTFEB;HSACre mice had significantly higher nesting scores (average score of 1.4), displaying increased interactions with the nestlets and building more complex nests (Fig. 1I). This score was not significantly different than the one observed in control mice.
Female 5xFAD transgenic mice have well-characterized deficits in spatial learning and memory in the Barnes maze [24, 35], spending less time in the target quadrant (Fig. 1J) and a longer latency to the target hole (Fig. 1K) than their control littermates even during training days (Fig. S2D, E). Interestingly, 5xFAD;cTFEB;HSACre mice performed at the same level as control animals in both metrics during probe day testing (Fig. 1J, K), spending more time in the target zone and escaping the maze faster than their 5xFAD counterparts, without any significant differences in motor activity among any of our cohorts (Fig. S2A–C). Finally, 5xFAD;cTFEB;HSACre mice performed equally as well as their control littermates and significantly better than their 5xFAD littermates when we assessed associative learning memory via fear conditioning testing (Fig. 1L). Collectively, this battery of neurocognitive tests suggests that muscle-TFEB overexpression rescues neurocognitive deficits in decision-making, spatial memory, and associative learning in 8-month-old 5xFAD mice.
Skeletal muscle TFEB overexpression does not alter neuroinflammation markers in the CNS of 5xFAD female mice
Neuroinflammation, the chronic activation of glial cell toward pro-inflammatory phenotypes, is a well-characterized pathological hallmark of AD [36] that is recapitulated in the brains of 5xFAD mice [37]. Given the robust reductions in morphological and transcriptional markers of neuroinflammation we observed in response to skeletal muscle TFEB overexpression in the context of tau toxicity [5], we wondered whether neuroinflammation was once again a target of skeletal muscle-TFEB-dependent neurotrophic signaling in 5xFAD;cTFEB;HSACre mice. To assess glial activation in situ, we first examined astroglial morphology in the dentate gyrus of the hippocampus (Figs. 2A and S3A), a well-documented metric of glial inflammatory states [38]. As expected, and reflecting the high degree of neuroinflammation of this model at symptomatic stages of the disease [24], we detected a large age-dependent increase in the GFAP-positive (astrocytes) and IBA1-positive (microglial) fractions of the hippocampus in 5xFAD transgenic mice compared to their control littermates (Figs. 2B and S3B). We also confirmed significant increases in morphological markers of pro-inflammatory states, including the volume of hippocampal IBA1 + microglia (Fig. 2C) (suggesting pro-phagocytic/reactive state) and the number of GFAP + astrocytes (Fig. 2D) (suggesting pro-inflammatory/reactive states) in the 5xFAD hippocampus relative to their control littermates. However, and in opposition to what we observed in our MAPT P301S;cTFEB;HSACre model [5], the fraction area coverage, microglial volume, or astrocyte number in the hippocampus of 5xFAD;cTFEB;HSACre mice was comparable to that observed in 5xFAD mice at either age examined (Figs. 2A–D and S3A–D).
As a second measure of neuroinflammatory states, we performed a targeted transcriptional analysis in hippocampal RNA lysates using the Nanostring mouse Neuroinflammation panel containing 757 genes covering the core pathways and processes that define neuroimmune interactions. This revealed only 11 downregulated and 7 upregulated neuroimmune genes in the 5xFAD;cTFEB;HSACre hippocampus relative to their 5xFAD counterparts (Fig. 2E). None of the 24 Nanostring functional neuroinflammation pathway scores in this panel were significantly different among groups (not shown). GO biological process analysis of the differentially expressed genes identified mostly unrelated signaling pathways, including response to inorganic substance, positive regulation of molecular function, and cellular response to stress (Fig. S3E). Top Reactome terms included some immune-associated pathways like toll-like receptor cascades, death receptor signaling, and the innate immune system (Fig. 2F). We also confirmed no differences in expression levels of classical neuroinflammatory markers Ccl2, Il6, or Nfkβ in hippocampal RNA lysates (not shown).
Altogether, our morphological and transcriptional analyses indicate minimal changes in neuroinflammatory states in the hippocampus of 5xFAD;cTFEB;HSACre mice relative to their 5xFAD littermates, despite robust reductions in Aβ accumulation (Fig. 1C–F). Furthermore, it indicates that the observed behavioral neurocognitive improvements in 5xFAD;cTFEB;HSACre mice (Fig. 1I–L) likely occur through a mechanism independent of neuroinflammatory-associated pathways.
Skeletal muscle TFEB overexpression promotes transcriptional remodeling associated with synaptic function in the CNS of 5xFAD female mice
Given the mild transcriptional effects observed with the Nanostring Neuroinflammation panel in 5xFAD;cTFEB;HSACre hippocampi (Fig. 2E), we next proceeded to directly interrogate AD-associated signaling using the Nanostring Alzheimer’s Disease panel. Importantly, this panel was built utilizing the 5xFAD model in addition to human samples, creating a much more targeted disease profile [39,40,41]. We identified 15 differentially expressed genes in 5xFAD;cTFEB;HSACre hippocampal RNA lysates when compared to their 5xFAD littermate controls (Fig. 3A). Of these, 12 were downregulated and only 3 were upregulated, reflecting the high degree of disease-association built into the panel footprint [39,40,41]. Two of these genes were associated with protein aggregation (Kctd1, potassium channel tetramerization domain containing 1) [42] and Aβ amyloidosis formation (Phyhip, phytanoyl-CoA 2-hydroxylase interacting protein) [43], consistent with our findings of reduced plaque abundance (Fig. 1C–F) and potential reductions in APP pro-amyloidogenic processing (Fig. S1D) in the CNS of 5xFAD;HSACre mice. Strikingly, many of the other downregulated genes coded for multiple hits on the synaptic regulatory network, including Stxbp5l (a syntaxin-binding protein), protein kinase C-related genes Prkca and Prkcb, Arhgef9, and Mef2c. Additional significantly downregulated genes that were associated with different aspects of synaptic signaling were Kcng5 (potassium voltage-gated channel subfamily J member 5), Chrm1 (acetylcholine receptor), Pde1a (phosphodiesterase-1), and Cnler2/Cnksr2 (connector enhancer of kinase suppressor of Ras 2). Consistent with transcriptional targeting of the synaptic signaling network in the CNS of 5xFAD;HSACre mice, we also detected significant upregulation of neurotrophic-associated Gss (glutathione synthetase), as well as Cbln1 (precerebellin), another promoter of synaptic plasticity [44] (Fig. 3A). Analysis of Nanostring functional pathway scores confirmed a profound rescue of gene signature scores for vesicle trafficking (Fig. 3B), neuronal connectivity (Fig. 3C), and chromatin modification (Fig. 3D), all of which are pathways known to be dysregulated in symptomatic 5xFAD female mice [22, 45]. Interestingly, we also observed non-significant trends for the rescue of the lipid metabolism signature gene cluster (Fig. 3E), another classical pathological hallmark of AD [46].
We next performed gene set enrichment analysis on the differentially expressed genes in the 5xFAD;cTFEB;HSACre hippocampi, which confirmed significant changes in gene pathways associated with pre- and post-synaptic membrane potential and transmission pathways (GO Biological Processes, Fig. 3F), and trafficking of GLUR2 containing AMPA receptors and VEGFR2 mediated signaling (GO Reactome, Fig. 3G). Altogether, this transcriptional analysis strongly suggests that muscle-TFEB overexpression transcriptionally promotes remodeling of the synaptic networks in 5xFAD female transgenic mice.
Skeletal muscle TFEB overexpression increases levels of synaptic proteins in the CNS of 5xFAD female mice
To validate whether these transcriptional changes associated with increased synaptic function (Fig. 3) could underlie the behavioral improvements we observed in 5xFAD;cTFEB;HSACre transgenic mice (Fig. 1I–L), we assayed levels of synaptic proteins in cortical lysates of all our groups (Fig. 4). We first confirmed previously reported deficits in levels of neurotrophic factors such as brain-derived neurotrophic factor (BDNF, particularly of the cleaved, secreted form) and neurotrophin 4 (NTF4) (Fig. 4A) in the cortex of an 8-month-old 5xFAD transgenic mice [47,48,49,50]. Interestingly, while the pre-synaptic protein markers SNAP25, SYP1, and SYT1 were unchanged in 5xFAD cortical lysates at this age, post-synaptic markers PSD95, SAP102, and SAP97 showed significant reductions in 5xFAD transgenic mice (Fig. 4B). These markers were not altered in 5xFAD 4-month-old mice (Fig. S4A–C), confirming their reflection of neuropathological processes occurring in symptomatic stages in this model. Strikingly, protein levels of most of these pre- and post-synaptic markers were significantly increased in the 5xFAD;cTFEB;HSACre cortex at 8 months of age, even to levels above their littermate controls (Fig. 4A, B). Overall, this data strongly implicates improvements in synaptic function, likely driven by increases in neurotrophic signaling, as a potential mechanism underlying the neuroprotective benefits observed in 5xFAD;TFEB;HSACre transgenic mice.
Skeletal muscle-targeted TFEB overexpression increases the release of CNS-targeting myokine Prosaposin in 5xFAD;cTFEB;HSACre transgenic mice
We have previously demonstrated that muscle-TFEB overexpression is a powerful activator of the muscle-to-brain axis [5]. We further identified several potentially secreted proteins in TFEB-overexpressing skeletal muscle as potential new myokines with CNS targeting effects, including the precursor to lysosomal sphingolipid hydrolase activator proteins known as prosaposin (PSAP) [5]. Various studies have recently highlighted a potential neuroprotective effect for PSAP, whether as the full-length protein, saposin C (one of its biologically active cleavage products), or a saposin C-derived 18-mer derived peptide (PS18). Indeed, PSAP and its derivatives prevent neuronal degeneration and axonal loss [51, 52] and stimulate nerve regeneration [53], neuronal growth [54], and neuroprotection in neurodegenerative model systems [11, 55,56,57]. Furthermore, PSAP has recently been shown to be secreted from skeletal muscle in response to muscle metabolic stressors, including exercise and PGC1α-overexpression [58, 59]. Building on this body of evidence, we posited that PSAP may act as pivotal myokine facilitating muscle-to-brain crosstalk in our 5xFAD;cTFEB;HSACre mice.
In agreement with this, we confirmed that, as predicted by our previous proteomics studies in young and aged cTFEB;HSACre transgenic mice [5], total PSAP protein levels were twice as high in 8-month-old 5xFAD;cTFEB;HSACre skeletal muscle relative to 5xFAD transgenic muscle (Fig. 5A). Interestingly, we also detected a milder but still significant increase in PSAP and its cleaved isoform saposin C in the cortex of the same mice (Fig. 5B), suggesting systemic elevations of PSAP levels in 5xFAD;cTFEB;HSACre transgenic mice. Consistent with this hypothesis, ELISA testing confirmed large increases in circulating PSAP protein in 5xFAD;cTFEB;HSACre plasma (~ 200,000 pg/ml) compared to either control or 5xFAD plasma (~ 100,000 pg/ml) (Fig. 5C), strongly suggesting that skeletal muscle PSAP overproduction via TFEB overexpression results in increased PSAP secretion into circulation.
Multiple studies have demonstrated that supplementation of individual myokines in the periphery results in potent neurotrophic effects in the CNS [60,61,62,63]. To test the potential role of PSAP-signaling as a novel myokine mediating the synaptic remodeling observed in the CNS of 5xFAD;cTFEB;HSACre mice, we subcutaneously injected 3-month-old C57B6/L male mice once a day for 7 days with PS18 (Fig. 5D), an 18-mer derived peptide from the amino-terminal hydrophilic sequence of the rat saposin C-domain. This PS18 injection paradigm has previously been shown to effectively target the CNS, reducing Aβ1–42 neurotoxicity and memory deficits [64]. Consistent with our hypothesis that peripheral PSAP-signaling mediates the synaptic remodeling observed in the 5xFAD;cTFEB;HSACre CNS, immunoblot analysis of cortical lysates revealed a robust increase in both pro- and active BDNF isoforms in PS18-injected animals relative to their DMSO-injected controls (Fig. 5E). To obtain direct insights into changes localized to the synaptic compartment, we next isolated cortical synaptosome fractions enriched in pre- and post-synaptic machinery from the cortex of PS18 and DMSO-injected mice. Immunoblot analyses of cortical synaptosomes showed that peripheral PS18 injection increased the abundance of pre-synaptic protein SNAP25 and post-synaptic protein PSD95 (Fig. 5F) as well as trends toward increases for SYP1, SYT1, and SAP97 in cortical synaptosome-enriched fractions from PS18-injected animals (Fig. S5B), similar to what we observed in 5xFAD;cTFEB;HSACre cortices (Fig. 4). Altogether, these provocative data suggest that peripheral supplementation of PS18 is sufficient to activate neurotrophic signaling and promote synapse remodeling in the CNS. Furthermore, it implies that the neurocognitive benefits seen in 5xFAD;cTFEB;HSACre mice can be attributed, at least in part, to increased secretion of muscle-originating PSAP and/or PSAP derivates into circulation.
Discussion
Over the last decade, growing evidence has suggested that the periphery contributes to the etiology of neurodegenerative diseases, including AD [5, 12, 13, 63, 65,66,67]. In particular, activation of the muscle-to-brain axis and its associated myokines collectively target central markers of CNS dysfunction, decreasing neuroinflammation and reducing proteotoxicity in the CNS, all key factors in AD pathogenesis [23]. Indeed, peripheral delivery of CNS-targeting circulating factors such as Fncd5/irisin [63], platelet factor-4 (Pf4) [68], and glycosylphosphatidylinositol-specific phospholipase D1 (Gpld1) [69] all individually promote significant neurotrophic remodeling of the mouse brain, although the precise mechanisms driving these benefits remain unknown. Here, we provide direct evidence demonstrating benefits in the CNS after enhancing skeletal muscle TFEB signaling in the context of Aβ-induced toxicity and validate PSAP-associated signaling as a new myokine system with CNS-targeting effects.
Similar to what we previously reported in a model of tau-associated toxicity [5], we discovered that overexpression of TFEB in skeletal muscle (Fig. 1B) significantly improves multiple disease-associated hallmarks in 5xFAD female transgenic mice. Indeed, we confirmed robust reductions in plaque accumulation (Fig. 1C–F) and profound synaptic remodeling (Figs. 3 and 4) in the hippocampus and cortex of 5xFAD;cTFEB;HSACre transgenic mice. This is consistent with our previous work showing that expression of many genes related to synaptic transmission and plasticity is transcriptionally remodeled in the hippocampus of young and aged female cTFEB;HSACre transgenic mice, even in the absence of AD-associated pathologies [5]. Importantly, we confirm that these biochemical findings translate into a significant rescue of behavioral performance across a battery of neurocognitive tests (Fig. 1G–L) in symptomatic 5xFAD mice with skeletal muscle-TFEB overexpression. These results thus imply, for the first time, that activation of the muscle-to-brain axis via skeletal muscle-TFEB overexpression is a powerful augmenter of neurotrophic signaling and synaptic network remodeler of the CNS.
One of the most interesting findings from this study was the mild effect of muscle-TFEB overexpression on markers of neuroinflammation (Figs. 2 and S3). Whereas we observed major reductions in both morphometric and transcriptional markers of neuroinflammation in the dentate gyrus of the hippocampus of our MAPT P301S;cTFEB;HSACre mice [5], we failed to detect similar changes in the same brain region of 5xFAD;cTFEB;HSACre mice. We did detect some modest transcriptional expression differences in the 5xFAD;cTFEB;HSACre hippocampus using the targeted Nanostring neuroinflammation panel (Fig. 2E, F), raising the possibility that these non-canonical inflammatory signaling pathways may not translate into detectable morphological changes in astrocytes and microglia at the ages examined. Indeed, our previous results in MAPT P301S mice displayed a sex-dimorphic neuroinflammatory rescue associated with muscle-TFEB overexpression. This suggests that in our current study, the protective effects on neuroinflammation in 5xFAD;cTFEB;HSACre female mice may be concealed due to a differential inflammatory baseline derived from sex. Interestingly, we have previously reported a similar uncoupling between mild modifications of neuroinflammation markers and robust neurocognitive improvements in our aged cTFEB;HSACre mice without any AD-associated transgenes [5]. This suggests that skeletal muscle TFEB overexpression may promote differential muscle-to-brain axis signaling in a CNS-pathology and/or sex-specific manner, although this hypothesis remains untested.
PSAP is a complex multifunctional protein, playing roles both intracellularly (as a regulator of lysosomal function) and extracellularly as a secreted factor [52, 70]. The extracellular presence of full-length prosaposin suggests a discrete function for full-length prosaposin beyond its role as the saposin precursor protein. Indeed, full-length PSAP was recently found to be enriched in skeletal muscle exudates [58]. Furthermore, expression levels of PSAP are significantly increased in both skeletal muscle and plasma of exercised (running) rats [59], suggesting PSAP secretion is responsive to skeletal muscle-targeting interventions. In agreement with this, and using unbiased proteomics analysis, we had previously also predicted PSAP as one of the most highly upregulated secreted proteins in cTFEB;HSACre skeletal muscle [5]. Here, we validate our previous findings and extend them to our new disease model, showing significant increases in the PSAP protein locally in skeletal muscle (Fig. 5A) and systemically in circulation (plasma; Fig. 5C) of 5xFAD;cTFEB;HSACre transgenic mice. To further support this notion, we also demonstrate significant enhancement of neurotrophic and pre- and post-synaptic markers in the CNS after peripheral injections of a prosaposin-derived 18-mer active peptide (PS18). We thus propose that PSAP and its derivatives may represent a novel myokine with CNS-targeting effects. Indeed, PSAP levels in skeletal muscle and plasma appear to be positively regulated by exercise [59] and exercise-like states [5, 58] (Fig. 5). Second, peripheral delivery of prosaptides has been reported to have strong neuroprotective effects in the context of multiple neurotoxic insults [70] (Fig. 5). Third, at least some prosaptides have been shown to cross the blood–brain barrier (BBB) [71, 72], consistent with previous work on other CNS-targeting myokines [10]. Additional research into the specific mechanisms underlying the CNS benefits of PSAP/PS18 should yield fascinating insights into novel regulators of brain health and function.
Of note, whereas we report increases in BDNF protein levels in 5xFAD;cTFEB;HSACre (Fig. 4A) and PS18-injected whole cortical lysates (Fig. 5E), we only detected changes in synaptic protein markers in synaptosome-enriched fractions from PS18-injected mouse cortices (Figs. 5F and S5B). We believe this reflects the effects of chronic increased circulating PSAP (and its derivates) in our 5xFAD;cTFEB;HSACre mice vs. the acute activation of PSAP-signaling associated with peripheral PS18 delivery. Thus, although endogenous PSAP is enriched in the brain and has a well-known history of exhibiting neuroprotective actions (reviewed here [52, 70]), our work shows for the first time a role for muscle-originating peripheral PSAP in mediating CNS-targeting neuroprotective effects.
For this work, we focused our studies on 5xFAD;cTFEB;HSACre transgenic female mice only, due to their earlier and more severe phenotypic presentation of AD-associated pathology than their male counterparts [22]. To our knowledge, this is the first time that female mice have been utilized as a screening platform to identify new regulators of the muscle-to-brain axis. Importantly, however, we demonstrate similar synaptic remodeling and activation of neurotrophic signaling in the cortex of healthy male mice after PS18 delivery, suggesting that activation of the muscle-to-brain axis via peripheral PSAP-signaling achieves similar benefits in both sexes. This is particularly relevant in light of the male focus of myokine research to date [69, 73,74,75] and the accumulating evidence indicating the influence of biological sex on the brain benefits of both exercise [76] and myokine signaling [5]. Additional studies investigating any sex-dimorphic responses in the CNS in response to myokine supplementation should enhance our understanding of the mechanisms by which the muscle-to-brain axis benefits brain health.
Two central gaps in knowledge in our current understanding of CNS-targeting myokines currently remain. First, the mechanism of transport of these myokines through circulation is a highly debated topic in the field. Many studies have identified myokines as part of the cargo contained within extracellular vesicles (EVs), including those originating from skeletal muscle [77]. However, delivery of recombinant free proteins and/or AAV-packaged versions of myokines into peripheral circulation has also successfully targeted the CNS, suggesting that vesicle-bound entities may not be necessary for activation of the muscle-to-brain axis. Importantly, the content and abundance of myokines in circulation are highly responsive to exercise [63, 74, 77, 78], suggesting they may act as direct modulators of muscle-targeting interventions with known neurotrophic effects [5, 79]. Second gap in knowledge is the ability (and necessity) of myokines to cross the BBB. While some work supports the potential transmembrane transport, diffusion, or signal-transduction of these myokines across the BBB [63, 74], to date, the mechanisms that transmit the peripheral signal into the CNS remain unknown. Full-length PSAP is unlikely to cross the BBB, so it may be instead carried within EVs as they are known to traverse across BBB [80,81,82,83] or it could be enzymatically digested to more soluble forms such as saposin C or PS18-like fragments. Either way, these cleavage products of PSAP have come to be collectively known as “prosaptides” due to their reported neurotrophic effects. Additional research is needed to clarify these on-going questions.
Overall, this work connects, for the first time, skeletal muscle TFEB overexpression to increased secretion of PSAP into circulation and validates PSAP as a novel myokine with CNS-targeting effects in an Aβ-induced toxicity AD model (i.e., 5xFAD). Ultimately, this work reveals a potentially new mechanism of muscle-to-brain communication during neurodegenerative disease through neuroprotective muscle-originating secreted protein signatures, “reuniting the body from the neck down” [84].
Data availability
All data generated or analyzed during this study is included in the published article and/or is available upon request.
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Acknowledgements
We thank all members of the Cortes lab past and present that contributed their support to this work. We also thank C. Finch for providing us with the necessary reagents and intellectual discussion throughout.
Funding
Open access funding provided by SCELC, Statewide California Electronic Library Consortium. This work was supported by the National Institutes of Health NIH R01 AG077536 (to C.J.C.), NIA T32 AG052374 (training grant to I.M. and A.B.) and AARF-21–851362 (to A.B).
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Taha, H.B., Birnbaum, A., Matthews, I. et al. Activation of the muscle-to-brain axis ameliorates neurocognitive deficits in an Alzheimer’s disease mouse model via enhancing neurotrophic and synaptic signaling. GeroScience (2024). https://doi.org/10.1007/s11357-024-01345-3
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DOI: https://doi.org/10.1007/s11357-024-01345-3