, INTRODUCTION
Aging is characterized by a universal, progressive time-dependent functional decline that occurs across multiple organ systems, resulting in increased vulnerability to death [1,2]. This multi-step deterioration represents the main risk factor for several debilitating pathologies, including cardiovascular diseases, cancer, neurodegeneration, and osteoporosis [3,4]. Importantly, the increased number of adults in the elderly population and improvements in healthcare and sanitary conditions have led to worldwide interest in the discovery of effective measures to slow or reverse the aging process. Although several contributors, such as cellular senescence, oxidative stress, and dysregulation of energy homeostasis, are known to be involved in age-associated physiologic changes [5,6], heterochronic parabiosis experiments have highlighted the critical role of circulating factors in the aging process [7-9]. In detail, the exposure of old mice to young blood rejuvenated aged organs and tissues [10,11], whereas an exchange with old blood rapidly inhibited the physiologic functions of young mice [12]. Based on these backgrounds, researchers in this field continue to dedicate their efforts to identifying pro-youthful or pro-aging factors in blood [9,13].
Sarcopenia corresponds to a gradual and generalized skeletal muscle disorder that involves the accelerated loss of muscle mass and function [14-16]. Among the multifactorial causes, cellular and molecular changes during aging contribute to an imbalance between the anabolic and catabolic pathways of muscle protein, and this condition commonly occurs in older people [17]. Sarcopenia is thus considered to be a key component of aging phenotypes. Although sarcopenia has long been considered as an unavoidable outcome of aging, the perception that it should be overcome has been increased due to advances in knowledge (i.e., skeletal muscle homeostasis might be reversible) [18,19]. Importantly, sarcopenia is strongly associated with increased vulnerability to falls, frailty, and death [17,20]. Consequently, the identification of factors affecting muscle metabolism has become the focus of intense research to extend health span in old age.
C C motif chemokine ligand 11 (CCL11), also denoted as eotaxin-1, exerts biologic effects via C-C chemokine receptors (CCRs) [21]. CCL11 is well known as a potent chemoattractant for eosinophils and is thus mainly implicated in allergic responses [22,23]. Accumulating evidence indicates that CCL11 may also play a pivotal role in age-related degeneration. Comparison of young isochronic and heterochronic cohorts revealed that plasma CCL11 level was markedly higher in heterochronic parabionts [8]. Consistently, a positive correlation was found between circulating CCL11 concentration and chronological age in both mice and humans, and systemic CCL11 injection decreased neurogenesis and cognitive performance in young mice [8]. Further, exogenous CCL11 disturbed bone remodeling by stimulating preosteoclast migration and resultant bone resorption [24]. In addition to the secreted feature of CCL11, these results suggest that this protein could be a potential systemic pro-aging factor and could be involved in muscle metabolism and age-associated sarcopenia. To clarify this possibility, we examined the effects of CCL11 on in vitro muscle biology and its clinical relevance for sarcopenia parameters in older adults.
METHODS
Cell culture and reagents
Mouse C2C12 myoblasts were purchased from the American Type Culture Collection (ATCC, Manassas, VA, USA) and maintained in Dulbecco’s Modified Eagle’s medium (DMEM) supplemented with 10% fetal bovine serum, 20 mM hydroxyethyl piperazine ethane sulfonic acid, 2 mM L-glutamine, 100 U/mL penicillin, and 0.1 mg/mL streptomycin (Life Technologies Corp., Carlsbad, CA, USA) at 37°C in a humidified atmosphere containing 5% CO2. To induce myogenesis, cells were grown to 90% confluency in maintenance media and switched to differentiation media (DMEM with 2% horse serum) for 3 or 4 days of culture. Recombinant CCL11 was purchased from R&D Systems (cat. no. 420-ME-100; Minneapolis, MN, USA).
Immunofluorescence
Differentiated C2C12 cells were fixed in 4% paraformaldehyde for 15 minutes, washed twice with phosphate buffered saline (PBS), permeabilized in 0.01 M sodium citrate buffer containing 0.1% Triton X-100 for 10 minutes, and washed twice with PBS. The cells were blocked with 2% bovine serum albumin (BSA) in PBS for 1 hour and subsequently incubated with anti-myosin heavy chain (MyHC) antibody (MF20; Developmental Studies Hybridoma Bank, Iowa City, IA, USA) at 4°C overnight. Cells were incubated with Alexa Flour 555-conjugated secondary antibodies (Cell Signaling, Danvers, MA, USA; 1:1,000 dilution) for 1 hour and washed with PBST (0.2% Tween-20 in PBS). Thereafter, they were incubated with 4,6-diamidino-2-phenyindole (DAPI; Sigma-Aldrich, St. Louis, MO, USA; 1:10,000 dilution) for 2 minutes and washed with PBS. The samples were mounted using Fluoromount G (Southern Biotech, Birmingham, AL, USA) and images were captured using a fluorescence microscope (Carl Zeiss, Jena, Germany). The area of the MyHC-stained myotubes was calculated using the ZEN 2 (blue edition) software (Carl Zeiss). Fusion index (%) was calculated using the following equation: 100×number of nuclei in MyHC+ myotubes per total number of nuclei in MyHC+ myocytes and myotubes.
Western blot analysis
Cells were lysed in radioimmunoprecipitation assay (RIPA) buffer (50 mM Tris-HCl [pH 7.4], 150 mM NaCl, 1% Triton X-100, 1 mM ethylenediaminetetraacetic acid, 1 mM ethylene glycol tetraacetic acid, 0.1% sodium dodecyl sulfate [SDS], 1% sodium deoxycholate, 1 mM Na3VO4, 1 mM sodium fluoride, 1 mM phenylmethylsulfonyl fluoride, and protease inhibitor cocktail). After a 30-minute incubation on ice, the lysates were centrifuged at 14,000 rpm for 20 minutes at 4°C. The protein concentration was measured with a bicinchoninic Acid (BCA) protein assay kit (Pierce Chemical Co., Rockford, IL, USA). Protein samples were separated by SDS-polyacrylamide gel electrophoresis (PAGE), transferred to a polyvinylidene fluoride membrane, and immunoblotted with antibodies [25]. The primary antibodies were: MyHC (MF20); myogenin (sc-12732) and CCR5 (sc-178933) (Santa Cruz Biotechnology, Dallas, TX, USA); and β-tubulin (T2200; Sigma-Aldrich).
Quantitative reverse-transcription polymerase chain reaction
Total RNA was extracted using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s protocol. After first-strand cDNA synthesis with the Superscript III First-Strand Synthesis System (Invitrogen) using oligo dT primers, quantitative reverse-transcription polymerase chain reaction was performed in triplicate on a Light Cycler 480 SYBR Green I Master (Roche, Mannheim, Germany) [26]. The primers for myogenin (NM_031189.2) and MyHC (NM_001013397.2) were obtained from Applied Biosystems (Foster City, CA, USA). The threshold cycle (Ct) value for each gene was normalized to the Ct value of the 18S rRNA (NR_003278.3).
Ligand and receptor binding assay
Recombinant CCL11 was coated onto the wells of maxisorp 96-well microtiter plates and incubated for 18 hours at 4°C. Each well was washed three times with PBST (0.2% Tween-20 in PBS). Thereafter, the plates were blocked with 2% BSA in PBST for 2 hours. Cell lysates were added to the plates and incubated for 2 hours. The wells were then washed three times [27]. Preparations of the CCR5 antibody (Santa Cruz Biotechnology) in blocking solution were added to the plates and allowed to react for 2 hours. After washing, horseradish peroxidase (HRP)-linked antibody (Cell signaling Technology) was added and the lysates were incubated for 2 hours; this was followed by five rounds of washes. The reaction was developed with 100 μL tetramethylbenzidine (TMB) substrate solution and stopped with 100 μL of 1 N H2SO4. The absorbance in the microtiter plates was measured at 450 nm using a microplate reader (Infinite 200 PRO; Tecan Life Sciences, Zürich, Switzerland).
Study participants
We consecutively recruited Koreans who visited the Division of Geriatrics, Department of Internal Medicine, Asan Medical Center (AMC, Seoul, Korea) to undergo a comprehensive geriatric assessment between July 2019 and April 2020 [28]. Participants whose life expectancy was expected to be less than 1 year owing to end-stage renal failure, symptomatic heart failure, or malignancy were excluded. After the exclusion of ineligible participants, blood samples were collected from 79 eligible participants with their consent. This study was approved by the AMC Institutional Review Board (no. 2020-0259). Written informed consent was obtained from all enrolled participants.
Functional status and sarcopenia assessment
Experienced nurses were charged with collecting participants’ information, such as demographic characteristics and surgical or medical histories, through detailed interviews and reviews of medical records. Handgrip strength of the dominant side was measured using Jamar hydraulic hand dynamometer (Patterson Medical, Warrenville, IL, USA) [29]. Participants were instructed to sit comfortably, bend their elbow at 90 degrees, and hold the dynamometer as tightly as possible. The maximum value was adapted after all tests were conducted twice at intervals of 1 minute or more. Time to complete 5 chair stands (s) and usual gait speed (m/sec) from a 4-m walk were assessed [30]. The short physical performance battery (SPPB) consists of gait speed, standing balance, and repeated chair stands [31]. In the standing balance test, including tandem stance, semi-tandem stance, and side-by-side stance, the participants were instructed to stand for up to 10 seconds. Ranging from 0 to 12 points, a higher SPPB score indicates better lower extremity function.
A bioelectrical impedance analyzer (InBody S10; InBody, Seoul, Korea) with measuring frequencies of 1, 5, 50, 250, 500, and 1,000 kHz was used to evaluate the body compositions, including muscle mass (whole body lean body mass minus bone mineral content) [32]. Appendicular skeletal muscle mass (ASM) was defined as the sum of the muscle mass of both arms and legs. Skeletal muscle mass index (SMI) was calculated by adjusting the ASM to the height squared to achieve an objective comparison of muscle mass between participants [33]. Lastly, sarcopenia was classified according to the 2019 Consensus Guidelines from the Asian Working Group for Sarcopenia [34]. Briefly, older patients with low muscle mass (SMI <7.0 kg/m2 in men, <5.7 kg/m2 in women), weak muscle strength (handgrip strength <28 kg in men, <18 kg in women), and/or poor physical performance (5-time chair stand test ≥12 seconds, gait speed <1.0 m/sec, or SPPB score ≤9 points) were diagnosed with sarcopenia.
Measurement of CCL11 in human serum
Blood samples were collected from the antecubital vein of each participant. After sample centrifugation at 3,000 rpm for 5 minutes at 4°C, the supernatants were carefully collected to exclude cell components. All samples that displayed clotting or hemolysis were discarded. Prior to determining the serum concentrations, the serum samples were stored at −80°C. Serum CCL11 level was measured using a quantikine enzyme-linked immunosorbent assay (ELISA) kit (Cat. No. DTX00; R&D Systems) in accordance with the manufacturer’s instructions. The lower limit of detection of the kit was 5 pg/mL, and the intra- and inter-assay coefficients of variation were less than 5.3% and 11.5%, respectively.
Statistical analysis
The in vitro data are expressed as mean±standard error of mean of at least three independent experiments conducted with triplicate measurements, unless otherwise specified. The Mann-Whitney U test and the analysis of variance (ANOVA) with post hoc analysis via Tukey’s honest significance test were used to evaluate the significance of the differences between two groups and between ≥3 groups, respectively.
The clinical data are presented as mean±standard deviation or numbers and percentages, unless otherwise specified. The Student’s t tests for continuous variables and chi-square tests for categorical variables were used to compare the baseline characteristics of the study participants according to sarcopenia status. Kolmogorov-Smirnov testing revealed that serum CCL11 concentrations were normally distributed (P=0.302). The relationship between age and serum CCL11 level was investigated using Pearson correlation analysis. Before and after adjustments for sex, age, and body mass index (BMI), analysis of covariance (ANCOVA) was used to generate and compare the estimated means with 95% confidence intervals (CIs) in serum CCL11 level according to the status of sarcopenia and the related parameters. The association between serum CCL11 level and sarcopenia parameters was examined using a linear regression analysis. ANCOVA was also used to generate and compare the estimated means with 95% CIs in sarcopenia parameters according to the serum CCL11 quartiles. All statistical analyses were performed using the SPSS version 18.0 (SPSS Inc., Chicago, IL, USA). P<0.05 was considered statistically significant.
RESULTS
In vitro effects of recombinant CCL11 on muscle differentiation
To determine the potential role of CCL11 in muscle biology, we treated C2C12 myoblasts with recombinant CCL11 in vitro. While recombinant CCL11 did not affect proliferation or viability of myoblasts (data not shown), it significantly increased myotube area, myotube area per myotube, nuclei number per myotube, and fusion index in a dose-dependent manner, thereby revealing the CCL11-stimulated myogenesis (Fig. 1A). Consistently, the protein and mRNA expression levels of the myogenic differentiation markers, such as myogenin and MyHC, were markedly increased by recombinant CCL11 (Fig. 1B, C, respectively).
Among the potential receptors mediating the action of CCL11 on different types of cells [35,36], only CCR5 (i.e., not CCR2 or CCR3) was strongly expressed in both myoblasts and myotubes (Fig. 2A). A binding affinity experiment using ELISA also showed that the amount of CCL11-associated CCR5 increased as the amount of C2C12 myoblast lysate increased (Fig. 2B), indicating that CCL11 directly interacts with CCR5 in muscle cells. Aligning with these results, treating C2C12 myoblasts with CCR5 inhibitor completely attenuated recombinant CCL11-induced myogenesis (Fig. 3C). Such findings suggest that CCR5 mediates the effects of CCL11 on myogenic differentiation.
Association between circulating CCL11 level and sarcopenia parameters in humans
To investigate the clinical implication of in vitro results in aging-associated sarcopenia, we measured CCL11 level in the blood of 79 older adults. The baseline characteristics of the adults are presented in Table 1. Of the 12 cases with sarcopenia and 67 controls without sarcopenia, nine (75.0%) and 34 (50.7%) were women, respectively. The mean ages of cases and controls were 72.1±4.3 and 68.8±6.4, respectively. Participants with sarcopenia had lower weight, height, BMI, ASM, SMI, grip strength, and gait speed than those without sarcopenia. However, there were no significant differences in terms of SPPB score and time to complete 5 chair stands between the two groups.
Pearson correlation analyses with scatter plots revealed that age was positively correlated with serum CCL11 level (Supplemental Fig. S1).
Differences in serum CCL11 level according to the status of sarcopenia and related parameters were assessed using ANCOVA (Fig. 3). Before and after controlling for potential confounders, such as sex, age, and BMI, serum CCL11 concentrations were not significantly different between participants with and without sarcopenia, low muscle mass, weak muscle strength, and poor physical performance.
Linear regression analyses were adopted to investigate the association between serum CCL11 level and sarcopenia parameters (Table 2). However, serum CLL11 levels did not correlate with SMI, grip strength, SPPB score, gait speed, and time to complete 5 chair stands, regardless of the adjustment models.
To determine whether the correlation between serum CCL11 levels and sarcopenia parameters might exhibit a threshold effect rather than a gradual effect, the participants were divided into quartile groups according to serum CCL11 levels (Fig. 4). However, there was no significant difference in SMI, grip strength, SPPB score, gait speed, and time to complete 5 chair stands among the quartile groups, before and after adjusting for the confounders.
DISCUSSION
Based on backgrounds that implicated CCL11 in diverse age-related diseases, we performed experiments to observe CCL11-induced myogenesis. However, subsequent investigation to understand its clinical implications revealed no correlation between circulating CCL1 levels and muscle phenotypes in older adults. These findings indicate that the effects of CCL11 on in vitro muscle biology might not translate to humans, and that blood CCL11 level might not be a useful biomarker for sarcopenia risk assessment.
As one of efforts to find out the possible contributors explaining the development of sarcopenia, we have been particularly interested in the role of CCL11 on muscle metabolism. Previous studies reported that exogenous CCL11 treatment impaired neurogenesis, learning, memory, and bone remodeling [8,24]. Interestingly, clinical observations revealed that changes in one organ system, such as the brain, may occur alongside degenerative changes in other tissues, such as bone or muscle. Specifically, patients with cognitive dysfunction and Alzheimer’s disease were more likely to experience loss of bone mass and muscle strength [37-39]. These observations suggest that CCL11 could function as a systemic factor related to a simultaneous physiological decline with aging and be also implicated in the pathogenesis of sarcopenia. However, contrary to expectations, recombinant CCL11 promoted the differentiation of mouse C2C12 myoblasts into mature myotubes in our experiments. In other words, unlike in the brain or bone, CCL11 exhibited beneficial effects on muscle metabolism at least in vitro. Accordingly, we surmised that CCL11 may not be the direct cause of sarcopenia, but rather its level could be increased with aging to overcome poor muscle health as a compensatory mechanism.
Notably, we found that the action of CCL11 on myogenesis was mediated via CCR5, not CCR3. CCL11 is a ligand for the following CCRs: CCR2, CCR3, and CCR5 [28,29]. Among these, CCL11 is known to bind to CCR3 with the highest affinity in several cell types, including eosinophils, basophils, and airway epithelial cells [35,40]. Accordingly, we opted to initially focus on the interaction between CCL11 and CCR3 in the muscle. However, CCR3 was not detected in muscle cells while the CCR3 inhibitor did not change the recombinant CCL11-induced myogenic differentiation (data not shown). On the other hand, CCR5 was strongly expressed in both myoblasts and myotubes, and CCR5 inhibitor completely reversed the myogenic differentiation stimulated by recombinant CCL11. Such results support the finding that CCR5 is the major receptor for CCL11 in skeletal muscle.
To expand on the experimental results revealing the beneficial effects of recombinant CCL11 on myotubes in vitro, we would like to elucidate its role in human muscle health. Because interventional trials cannot be conducted in humans without preclinical data confirming the safety verification, the roles of candidate factors in human muscle metabolism should be extrapolated from observational studies, which was the motivation for the present clinical study. However, an association between circulating CCL11 concentration and muscle mass, muscle strength, and physical performance was not recognized in older adults. Although the exact cause of this discrepancy could not be confirmed herein, we speculate that the physiologic CCL11 concentration in humans may not be high enough to exert the phenotypic changes expected. Specifically, CCL11 effectively promoted in vitro myogenic differentiation when administered at a dose of 10 nM (84,000 pg/mL), whereas the mean serum CCL11 level in all participants and the difference in mean serum CCL11 level between the lowest (Q1) and highest (Q4) quartiles were 159 and 165 pg/mL, respectively. Because of the relatively low concentration of circulating CCL11 in humans, the clinical relevance of CCL11 for sarcopenia may not be observed. Furthermore, there is a chance that ligands for CCR5 other than CCL11 could bias the human results which were somewhat inconsistent with those of the in vitro experiments.
Since proteomics analyses by Villeda et al. [8] found that CCL11 concentrations were increased in the blood of humans and mice during normal aging, this molecule has been receiving increased attention as a potential pro-aging factor. In the present study, we recapitulated this positive association between chronological age and circulating CCL11 levels. However, although CCL11 is known to be produced in various types of cells including chondrocytes, keratinocytes, fibroblasts, eosinophils, epithelial cells, and endothelial cells [22,24,41], the specific mechanisms underlying age-related systemic increase of CCL11 remain unclear. To fully understand the biologic role of CCL11 in age-related diseases, this question needs to be addressed by additional research.
The major strength of this study is our assessment of all required parameters for clinical research on sarcopenia, including muscle mass, handgrip strength, SPPB, 5-time chair-stand test, and gait speed, which enhance the reliability of the results [17,34]. Moreover, we diagnosed sarcopenia by adopting Asian-specific cut-off points, because muscle phenotypes can vary according to cultural backgrounds, lifestyle, ethnicities, and body size [34]. Despite the above strengths, several limitations should be considered when interpreting the data. First, we could not examine the role of blood CCL11 in the prediction of sarcopenia due to the study’s cross-sectional design. Second, our study population was exclusively Koreans. Thus, our results may not be applicable to other populations. Third, our bioelectrical impedance analysis methodology might not provide valid estimates of total body water when hydration states are altered (e.g., ascites, edema, and fluid loss), potentially leading to errors in the muscle mass assessments. Finally, uncontrolled factors that influence muscle metabolism and/or serum CCL11 level, such as 25-hydroxyvitamin D, may bias the observed findings.
In conclusion, although recombinant CCL11 stimulated in vitro myogenic differentiation, serum CCL11 concentration was not significantly different based on sarcopenia and the related parameters in older adults. Further animal interventional and clinical prospective studies are necessary to confirm the exact role of CCL11 in muscle metabolism.
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