Characterization and utilization of the flexor digitorum brevis for assessing skeletal muscle function
The ability to assess skeletal muscle function and delineate regulatory mechanisms is essential to uncovering therapeutic approaches that preserve functional independence in a disease state. Skeletal muscle provides distinct experimental challenges due to inherent differences across muscle groups, including fiber type and size that may limit experimental approaches. The flexor digitorum brevis (FDB) possesses numerous properties that offer the investigator a high degree of experimental flexibility to address specific hypotheses. To date, surprisingly few studies have taken advantage of the FDB to investigate mechanisms regulating skeletal muscle function. The purpose of this study was to characterize and experimentally demonstrate the value of the FDB muscle for scientific investigations.
First, we characterized the FDB phenotype and provide reference comparisons to skeletal muscles commonly used in the field. We developed approaches allowing for experimental assessment of force production, in vitro and in vivo microscopy, and mitochondrial respiration to demonstrate the versatility of the FDB. As proof-of principle, we performed experiments to alter force production or mitochondrial respiration to validate the flexibility the FDB affords the investigator.
The FDB is made up of small predominantly type IIa and IIx fibers that collectively produce less peak isometric force than the extensor digitorum longus (EDL) or soleus muscles, but demonstrates a greater fatigue resistance than the EDL. Unlike the other muscles, inherent properties of the FDB muscle make it amenable to multiple in vitro- and in vivo-based microscopy methods. Due to its anatomical location, the FDB can be used in cardiotoxin-induced muscle injury protocols and is amenable to electroporation of cDNA with a high degree of efficiency allowing for an effective means of genetic manipulation. Using a novel approach, we also demonstrate methods for assessing mitochondrial respiration in the FDB, which are comparable to the commonly used gastrocnemius muscle. As proof of principle, short-term overexpression of Pgc1α in the FDB increased mitochondrial respiration rates.
The results highlight the experimental flexibility afforded the investigator by using the FDB muscle to assess mechanisms that regulate skeletal muscle function.
KeywordscDNA electroporation Mitochondrial respiration Muscle stimulation Skeletal muscle function
Extensor digitorum longus
Electron transport chain
Flexor digitorum brevis
Green fluorescent protein
Krebs Ringer Buffer
Mitotracker deep red
Physiological cross-sectional area
Peroxisome proliferator-activated receptor gamma coactivator 1-alpha
Yellow fluorescent protein
Skeletal muscle is susceptible to a number of genetic, environmental, and age-related pathologies that impair the tissue’s normal mechanical and metabolic function. This often leads to the development of comorbidities and sometimes death. Defining the mechanisms that regulate the development of skeletal muscle dysfunction is critical for designing therapeutic interventions. Investigators currently employ a variety of established methods for answering such questions, but are often experimentally hampered by unique inherent heterogeneity between muscle groups and cells within the same muscle tissue. Muscles commonly used for functional and mechanistic experiments include the extensor digitorum longus (EDL), soleus, plantaris, gastrocnemius, tibialis anterior (TA), and/or the quadriceps. These muscles each offer unique advantages across a host of methodologies including measuring isometric force production, susceptibility to muscle injury, mitochondrial respiration, protein content, and histology. For example, the EDL is frequently used for measures of isometric force production or susceptibility to stretch-induced injury in order to better understand and assess the efficacy of interventions targeting Duchenne muscular dystrophy [1, 2, 3] and/or aging [4, 5, 6]. Meanwhile, studies investigating metabolic diseases such as obesity and type II diabetes commonly measure skeletal muscle mitochondrial respiration using the red portion of the gastrocnemius muscle [7, 8, 9]. However, due to inherent differences across muscles, investigators are often forced to apply specific experimental approaches for each muscle. This specificity can limit the broad interpretation of the results.
Mechanistically driven research often utilizes DNA manipulation to alter protein expression in skeletal muscle. The electroporation of cDNA or shRNA into muscles often delivers inconsistent results due to both the size of the muscle and anatomical location, which each impede uniform distribution of cDNA. These factors can lead to low transduction efficiencies, making physiological and biochemical assays unreliable. To overcome this technical limitation, investigators have tagged their gene of interest and used immunohistochemical procedures to determine changes in tagged fibers that are known to express their gene of interest. Unfortunately, this approach limits the assays that can be employed and rules out most functional assays. While transgenic models have proven a valuable resource, they remain a costly, time-consuming, and uncertain endeavor. In contrast, the flexor digitorum brevis's (FDB) unique anatomical location coupled with its size makes the muscle amenable to cDNA electroporation allowing for high transduction efficiencies.
The FDB is a skeletal muscle located in the base of the foot that has previously been used to isolate and culture single muscle fibers. For reasons that are unclear, investigators have generally limited use of the FDB to isolated fiber imaging-based approaches or satellite cell function in culture [10, 11, 12, 13]. In this study, we demonstrate the utility of the FDB as a model for assessing skeletal muscle function across a range of methodologies commonly used within the skeletal muscle research community, including isometric force production, in vitro and in vivo imaging, and mitochondrial respiration. The full utility of the FDB is best demonstrated in studies combining these physiological tests with genetic manipulation (cDNA electroporation), thus allowing the investigator to manipulate cellular protein levels efficiently in a setting that allows for accurate functional outcome analyses.
All mice were 3–11-month-old C57BL/6 males at the time of testing. Mice were purchased from Jackson laboratories, housed in a temperature (22 °C) and light-controlled facility, and given free access to food and water. Mice were euthanized via isoflurane overdose. All animal procedures and usage were approved by the Institutional Review Committee at East Carolina University. Animal care complied with the Guide for the Care and Use of Laboratory Animals, Institute of Laboratory Animal Resources, Commission on Life Sciences, National Research Council (Washington: National Academy Press, 1996).
After dissection of the FDB, the muscles were placed in fresh culture media (DMEM with glutamine, 2% sterile-filtered FBS, 0.1% gentamycin) supplemented with 4 mg/ml collagenase A (Roche – 11088793001) for 90–120 min at 37 °C in 5% CO2 as previously described . The FDB muscle was placed in 2 mL of culture media without collagenase and gently triturated against the wall of the dish to release the fibers from the bundle using the cut end of a P1000 pipette tip. Isolated myofibers were adhered to glass bottom dishes that were coated with entactin-collagen-laminin (ECL Cell attachment matrix, #08110 Millipore). Fibers were returned to 37 °C in 5% CO2 for several hours and subsequently imaged as described below.
FDB muscle fiber length
The FDB muscles of male and female C57BL/6 mice were tied at the proximal tendon and three medial toe tendons with silk suture and fastened to a metal clip to maintain resting tension. Myofibers were isolated as described above, but were not adhered to glass bottom plates. Myofibers were imaged using a ×4 objective and an EVOS XL core microscope and accompanying software (Life Technologies, Bothell, WA). The lengths of approximately 1000 myofibers were measured in ImageJ (version 1.6.0, NIH, Bethesda, MD). When isolated, the myofibers were no longer at tension and therefore did not represent optimal length. To account for this change in myofiber length, a conversion factor was utilized using sarcomere length, as previously described by Dr. Richard Lieber . When at optimal length, the assumed mouse muscle optimal sarcomere length of a myofiber is 2.5 μm across . To normalize myofiber lengths to sarcomere length, we measured sarcomere length in a subset of 30 myofibers. The distance between 10 sarcomeres of each myofiber was measured, and an average sarcomere length was calculated across all 30 myofibers. The optimal sarcomere length (2.5 μm) divided by the average measured sarcomere length produced a conversion factor of 1.14, which was used to normalize all measured myofiber lengths to optimal sarcomere length.
Individual fiber type and fiber size
Muscle fiber type analysis of the FDB was conducted on samples from C57BL/6 mice, as previously described . Sections were probed with primary antibodies against myosin heavy chain type I (BA-F8), IIa (SC-71), IIb (BF-F3) (Development Studies Hybridoma Bank, Univ of Iowa), and anti-dystrophin (Rb-9024, Thermo Fisher, Waltham, MA), then imaged using an EVOS FL auto microscope and accompanying software (Life Technologies, Bothell, WA). Fiber type and fiber cross-sectional area (CSA) were assessed using ImageJ, as previously described .
Isometric force production
Isometric force production and fatigue was assessed in EDL (n = 5), soleus (n = 4), and FDB (n = 6) muscles of C57BL/6 mice, as previously described  with slight modifications. The FDB was exposed and the proximal tendon was secured using silk suture. Fine-tip forceps were placed under the three medial toe tendons and pulled gently down toward the toes before the three tendons (Fig. 1) were secured with silk suture. We tied the three medial tendons because it is not possible to tie one of the toes due to anatomical location, and tying the fourth tendon does not, in our experience, result in a different absolute force (data not shown). Each tendon was then cut just above the knot, and the FDB was gently lifted away from the foot. Micro-scissors were used to remove any remaining connective tissue, releasing it from the foot. The muscle was then tied to a force transducer and suspended in oxygenated Krebs Ringer Buffer (KRB—[mM] 115 NaCl, 2.5 KCl, 1.8 CaCl2, 2.2 Na2HPO4, 0.85 NaH2PO4) at room temperature. The muscle length was then adjusted until the FDB produced a peak twitch force, at which point the optimal resting tension (Lo) was set and the muscle was allowed to equilibrate for 10 min. Soleus muscles were prepared by tying a double square knot at the distal soleus tendon. The tendon was cut above the knot and the posterior muscles were gently pulled away from the leg revealing the proximal soleus tendon, which was tied with a double square knot. The EDL was dissected and tied as previously described . EDL and soleus muscles were equilibrated in oxygenated room temperature KRB at resting tension for 10 min. Following equilibration, muscle tension was optimized by performing maximal twitch stimulations and adjusting the muscle length until peak force was achieved. Twitch stimulations were performed 30 s apart to avoid fatiguing the muscle. Muscles were then stimulated 60 s apart at 10, 20, 40, 60, 80, 100, and 120 Hz to generate a force frequency curve. Muscles were rested for an additional 1 min before completing a 10-min stimulation protocol to determine fatigue resistance. The fatigue protocol stimulated muscles at 30 Hz every 2 s for a period of 600 s for a total of 300 contractions. Optimal muscle length was recorded and muscles were blotted to remove excess KRB before being weighed. An optimum voltage of 20 V was established prior to the experiments to ensure maximal stimulation of the FDB, EDL, and soleus (data not shown). Absolute muscle force data were converted to specific force (N/cm2) using previously described equations for the mathematical estimation of muscle CSA  and physiological cross-sectional area (PCSA) . The primary difference between CSA and PCSA is the inclusion of the muscle fiber length to muscle length ratio in the PCSA equation. We used both corrected methods to provide a wider compatibility with the literature.
Passive contractile properties
Passive contractile properties were assessed in EDL and FDB muscles from C57BL/6 male mice (n = 4), as previously described , with slight modifications. The EDL and FDB muscles dissected and tied to a force transducer as described above. Muscles were equilibrated for 10 min in oxygenated KRB at room temperature. Following equilibration, muscle tension was optimized by performing maximal twitch stimulations and adjusting the muscle length until peak force was achieved. Twitch stimulations were performed 30 s apart to avoid fatiguing the muscle. The muscle reference length was measured as the Lo before undergoing a passive stretch of 105, 110, 115, 120, 125, and 130% of Lo. Muscles were blotted to remove excess KRB and then weighed. Data were corrected to CSA and PCSA.
Cardiotoxin (CTX) injury
Comparisons were made in C57BL/6 mice between a CTX-treated FDB (Naja nigricollis, #02152238, MP Biomedicals, Santa Ana, CA) and PBS-treated contralateral FDB 4 days (n = 4) and 10 days post-treatment (n = 2). Sterile 8-mm-long 31G syringes were prepared with 10 μL of 10 μM CTX or 10 μL of sterile 1× PBS, as previously described . Following isoflurane-induced anesthesia, the base of the feet of four mice was cleaned with alcohol wipes. CTX was injected at the proximal portion of the foot with the needle positioned under the skin and toward the toes. PBS was injected into the contralateral foot. Mice were sacrificed at the appropriate time, and FDBs were dissected for the measurement of force production, as described above. Data were corrected to PCSA.
Hematoxylin and eosin staining
FDB muscles subjected to 10 days CTX treatment were flash frozen in optimal cutting temperature (OCT) solution for sectioning and H&E staining, as previously described .
Skeletal muscle high-resolution mitochondrial respirometry
Preparation of permeabilized gastrocnemius and FDB muscle fiber bundles
Respirometry was conducted on isolated permeabilized gastrocnemius and FDB muscle bundles excised from the same limb of C57BL/6 mice (n = 4). A portion of the red gastrocnemius was dissected and used for the preparation of permeabilized fiber bundles, as previously described . Red gastrocnemius muscle was used as the comparative tissue as it is commonly used to assess murine skeletal muscle mitochondrial respiration [8, 21]. The protocol for preparing permeabilized FDB muscle fiber bundles was adapted from previously described methods on the permeabilization of red gastrocnemius muscle bundles  and is outlined below. The FDBs were dissected and immediately added to ice-cold buffer X ([mM]—7.23 K2EGTA, 2.77 CaK2EGTA, 20 imidazole, 20 taurine, 5.7 ATP, 14.3 phosphocreatine, 6.56 MgCl2·6H2O, 50 MES, pH 7.1, 295 mosmol/kgH2O). Using a dissecting microscope, connective tissue, fat, and blood vessels were removed carefully to avoid muscle loss. FDBs were cut into bundles and divided into groups of three to four bundles weighing 1.5–2.0 mg wet weight. Bundle groups were then permeabilized in buffer X containing 22.5 μg/ml saponin with continuous rotation at 4 °C for 5 min. Muscle bundles were promptly transferred to ice-cold buffer Z ([mM]—110 K-MES, 35 KCl, 1 EGTA, 5 K2HPO4, 3 MgCl2·6H2O, 5 mg/ml BSA, pH 7.4, 295 mosmol/kgH2O) and washed with continuous rotation at 4 °C for 15 min.
Measurements of high-resolution O2 consumption were made using the OROBOROS Oxygraph-2K (Oroboros Instruments, Innsbruck, Austria) at 37 °C with a starting oxygen concentration of ~ 300–350 μM as previously described . Experiments were conducted in buffer Z containing 20 mM creatine monohydrate and 25 μM blebbistatin. Mitochondrial respiration was assessed by the sequential addition of substrates at a final concentration of pyruvate 4 mM, malate 0.5 mM, glutamate 5 mM, ADP 2.5 mM, succinate 5 mM, cytochrome c 5 μM, rotenone 10 μM, antimycin A 5 μM, ascorbic acid 2 mM, and TMPD 0.5 mM (N,N,N′,N′-tetramethyl-p-phenylenediamine dihydrochloride). Integrity of the mitochondrial membrane was confirmed by excluding gastrocnemius muscle bundles and FDB muscle bundles that produced a > 10 or > 20% increase in respiration, respectively, following exogenous cytochrome c addition. A different exclusion criteria was used for the gastrocnemius and FDB muscle bundles as preliminary testing indicated a greater percent increase in respiration was common in FDB fiber bundles compared to gastrocnemius fiber bundles, following the addition of cytochrome c. Upon completion of the protocol, muscle bundles were rinsed in distilled H2O, freeze-dried (Labconco, Kansas City, MO), and weighed (Orion Cahn C-35, Thermo Electron, Beverly, MA). Respiration rates for intact gastrocnemius muscle bundles are commonly corrected to dry weight; however, due to differences in connective tissue content of the two muscle groups, JO2 values were also corrected to total protein and citrate synthase (CS) activity. CS activity was measured using kit CS0720. Chemicals and reagents were purchased from Sigma Aldrich.
FDB muscle fibers were isolated from C57BL/6 mice and attached to 35-mm glass bottom dishes coated with ECL, as previously discussed. Isolated myofibers were stained with mitotracker deep red (M2246, Thermo Fisher) and NucBlue (R37605, Thermo Fisher) in DMEM for 30 min. Fibers were washed three times with 2 mL KRB. Fibers were imaged using a single photon confocal laser scanning microscope with a ×60 oil immersion objective (Olympus, Plan Apochromat, NA 1.35) and excitation was achieved using the 405- and 488-nm lines of a multiline argon laser.
Second harmonic generation describes the optical effect produced from the passage of laser pulses through highly polarized, non-centro-symmetrical materials such as myosin. When polarized at the appropriate wavelength, these materials emit light at half the wavelength of that entering, producing high-resolution images without the need for fluorescent probes that are subject to photobleaching and phototoxicity. Furthermore, the near infrared wavelengths used allow for deep tissue penetration without the need for invasive procedures . C57BL/6 mice were anesthetized before having the skin covering the FDB removed, exposing the FDB muscle. Once exposed, the FDB was hydrated with sterile KRB and the mouse was laid prone on a glass cover slip (#1.5, Leica), as previously described  (Fig. 1C). Myosin and nicotinamide-containing molecules were excited at 900 and 720 nm using a mode locked Ti:Sapphire pulsed laser (Mai Tai Deep See HP series, Spectra-Physics, Santa Clasa, CA), and emission was recorded using non-descanned detection with a FV10 MRV/G filter set at 450 and 420 nm, respectively. All images were taken using a ×60 oil immersion objective (Plan Apochromat, NA 1.35) and an Olympus FV1000 LSM operating FV10-ASW 4.2 acquisition software.
cDNA electroporation and high-resolution respirometry of skeletal muscle overexpressing Pgc1α
Electroporation of cDNA into FDBs was performed as previously described . Briefly, the feet of seven C57BL/6 male and female anesthetized mice were cleaned with an alcohol wipe and the footpads were injected with 10 μl of 2 mg/mL hyaluronidase suspended in sterile-filtered KRB using an 8-mm-long 31 gauge sterile needle. Approximately 1 h, later mice underwent anesthesia for a second time. Feet were again cleaned with an alcohol wipe and one foot received 30 μg of green fluorescent protein (GFP)-tagged PGC1α plasmid and the contralateral foot was injected with YFP cDNA. Following a full recovery from anesthesia, mice were anesthetized for a third time ~ 10 min later. Platinum electrodes were inserted under the skin and positioned perpendicular to the FDB and parallel to one another at the heel and footpad beneath the toes. The FDB was stimulated with 20 pulses of 20 ms duration at 1 Hz and 100 V . Mice were sacrificed 14 days later, and FDBs were dissected and imaged under a fluorescent microscope to confirm plasmid expression. Intact FDB muscle samples were then prepared and measured for mitochondrial respiration as outline above.
Data distributions were assessed and data that did not conform to a normal distribution were log base 10 transformed. Force frequency contractile data were analyzed via two-way ANOVA with Tukey multiple comparisons. Muscle mass, fiber type, time to max and half-relaxation, and fatigue data were analyzed via one-way ANOVA with Tukey multiple comparisons. In cases where data could not be transformed to a normal distribution, a Kruskal-Wallis test with Dunn multiple comparisons was performed. ANOVAs were completed using GraphPad Prism 7.03. Respiratory data and CS activity were analyzed via paired two-tailed t-tests with an alpha level of 0.05 using Microsoft Excel. All data are presented as mean ± SEM.
FDB fiber type and comparative characteristics
Characteristics of the FDB compared to the EDL and soleus muscles
Muscle mass (mg)
6.7 ± 0.4*
11.2 ± 0.7
10.0 ± 0.4
Optimal muscle length (mm)
9.5 ± 0.2*
14.2 ± 0.3
13.4 ± 0.3
Fiber length (mm)
0.744 ± 0.01
5.44 ± 0.12 
7.84 ± 0.22 
Fiber to muscle length ratio
0.079 ± 0.002
0.45 ± 0.004 
0.69 ± 0.006 
Fiber type %
- Type I
4.4 ± 2.9
- Type IIa
43.9 ± 1.9
- Type IIx
51.6 ± 4.8
- Type IIb
CSA (μm2 ± SD)
- Type I
488 ± 67
943 ± 198
- Type IIa
927 ± 314
634 ± 142‡
790 ± 149‡
- Type IIx
1267 ± 462
- Type IIb
772 ± 120
Isometric contractions and force production
Passive contractile properties
Using a previously described protocol  with slight modifications, we assessed the passive mechanical properties of the FDB and EDL muscles. In response to a graded increase in muscle length (strain), both the FDB and EDL recorded increasing force (mN/mm2) at each length up to 125% of Lo. At 130% Lo, both the FDB and EDL did not demonstrate any further increases in force output compared to 125% Lo. The relationship between the FDB and EDL in response to muscle lengthening was substantially altered by the method of force normalization. When normalized to CSA, the FDB consistently exhibited significantly more force than the EDL (Fig. 4G). However, when normalized to PCSA (accounting for the respective fiber length to muscle length ratios), the EDL exhibited significantly more force than the FDB (Fig. 4H).
CTX-induced muscle injury prevents force production
Comparison of mitochondrial respiration between red gastrocnemius and FDB muscle
In vitro and in vivo microscopy
cDNA electroporation-induced elevation of Pgc1α increases mitochondrial respiration in intact FDB muscle
In these experiments, we demonstrate the broad versatility of the FDB muscle as a potential tool for the assessment and investigation of skeletal muscle biology. Our findings validate the FDB muscle across a range of methodologies and highlight its inherent experimental advantages. The location of the FDB, beneath the skin, and relatively small size provide a means to accurately target and efficiently transfect cDNA for the manipulation of protein expression. Importantly, the FDB can then be used across a variety of physiological and/or biochemical-based assays. As proof of principle, in the experiments described here, we specifically demonstrate that electroporation of cDNA encoding PGC1α significantly increased mitochondrial respiration.
To provide investigators a better understanding of the FDB, we performed a comprehensive phenotypic description compared to the EDL and/or soleus muscle. A novel aspect of the current study is that to the knowledge of the authors’ this is the first study to measure the muscle fiber length to muscle length ratio in the FDB of mice. This provides an important advancement in the ability to accurately compare the force-producing capacity of the FDB with other muscles, such as the EDL and soleus, for which fiber length to muscle length ratios were previously known . In the past, and in the absence of a fiber length ratio for murine FDB muscle, force has been normalized without accounting for muscle fiber lengths . This method of normalization has been employed in other investigations across other muscles such as the soleus and EDL. We have therefore normalized our data using both approaches. However, it may be important to account for the fiber length to muscle length ratio as any intervention that could affect either variable would alter force output. Examination of the force frequency curves between FDB, EDL, and soleus muscles, or the FDB and EDL muscles following passive stress exemplifies the substantial effect of accounting for the muscle fiber to muscle length ratio. Researchers should be mindful of the normalization method used when analyzing and interpreting data, and when comparing to data in the literature.
We observed an intermediate contractile phenotype in the FDB that quantitatively places it between the EDL and soleus muscles with respect to contractile kinetics. Not surprisingly, the contractile kinetics of the FDB mirror the fiber type composition, which consists predominantly of types IIx and IIa with a small percentage of type I fibers. When compared to the soleus muscle (type I = 35%, IIa = 53% and IIx = 11%, IIb = 1%) or the EDL (type I = 0%, type IIa = 3%, IIx = 25% and IIb = 72%) , the FDB presents as a more mixed phenotype. It is worth noting that the greater fatigue resistance of the FDB muscle may not be the direct result of biochemical differences, but an indirect result of a reduced oxygen diffusion distance, resulting from the smaller size of the FDB relative to the soleus and EDL. In conjunction with the EDL and soleus, the FDB provides an additional muscle in which functional outcomes can be assessed in response to experimental manipulations. Due to the unique anatomical location, the FDB is amenable to direct injections of various small molecules and/or toxins. As proof of principle, we show that the loss and recovery of isometric force production within the FDB following CTX-induced muscle injury is similar to that previously reported in the EDL . Together, these data suggest the FDB may be a valuable addition to, or substitution for, the EDL and soleus muscles when assessing skeletal muscle force production and contractile kinetics.
The FDB has a smaller fiber: muscle length ratio relative to the EDL. This ratio makes the FDB amenable to efficient single myofiber isolation, which is more challenging in the EDL and/or soleus muscles. These single myofibers can be cultured and imaged on multiple different microscopy platforms. Skeletal muscle microscopy is a valuable tool for identifying protein localization , muscle morphology , and the dynamic changes in molecules such as H2O2 [10, 30] and calcium [29, 31]. In vitro imaging of isolated FDB myofibers is well-established; however, our findings demonstrate that electroporated cDNA tagged with fluorescent proteins is retained in myofibers following isolation. This provides numerous possibilities for the manipulation of protein expression and examination of subsequent alterations to morphology and function. In addition, the combination of fluorescently labeled cDNA and specific dyes or fluorophores, such as MTDR and DAPI, may be used to image protein localization. These techniques may be further enhanced through in vivo imaging. We specifically demonstrate how two-photon confocal microscopy and principles of second harmonic generation allow for the high-resolution imaging of non-centro-symmetrical materials such as muscle myosin, nicotinamide-containing molecules, and collagen . The FDB muscle provides several advantages for using second harmonic generation microscopy. The natural prone posture of the animal may aid in reducing motion artifact due to breathing. Imaging the FDB in the fashion described is less invasive than alternative methods, such as excision of the cremaster . The amenable nature of the FDB to electroporation with fluorescently tagged cDNA may also allow for a combination of single- and two-photon microscopy, generating high-definition protein localization images.
In recent years, there has been a substantial increase in the utilization of methods assessing mitochondrial respiratory function, particularly so within the field of skeletal muscle-related metabolic disease. We demonstrate a novel approach, utilizing high-resolution respirometry to measure mitochondrial respiration in the FDB muscle. To validate the use of the FDB, we compared mitochondrial respiration rates between red gastrocnemius muscle and the FDB. As anticipated, respiration rates were higher in red gastrocnemius muscle. This is in part due to differences in mitochondrial content as demonstrated by greater CS activity, but also a result of the respective tissue preparation protocols. The magnitude of the difference in respiration rates was dependent on whether O2 consumption was normalized to muscle dry weight, total protein, or CS activity. Normalizing to dry weight or total protein altered respiration values as the FDB contains a relatively higher content of connective tissue compared to the gastrocnemius, thus leading to potential underestimation of FDB O2 consumption rates. While adjusting the method of normalization cannot fully account for differences in connective tissue content, when rates were normalized to CS activity, this possible underestimation was eliminated. This suggests that strong consideration to normalization must be given prior to starting any study with the FDB. CS activity was selected as an alternative normalization factor for O2 consumption rates due to its strong association with mitochondrial content . Further normalization methods, such as mitochondrial protein complex content, may be used, but interactions between the normalization factor and treatment should be considered. Investigators should also consider the size of the FDB in their study designs as this represents a limiting factor to the number of protocols and replicates that may be tested. Additionally, the FDB is too sensitive to standard mechanical separation of muscle fibers, so this should be avoided to protect mitochondrial membrane integrity.
Finally, as an overall proof of concept that the FDB affords the investigator a unique flexibility, we overexpressed GFP-tagged Pgc1α or YFP protein in the FDB for a period of 14 days using cDNA electroporation. A fluorescence imaging-based approach in combination with a CS activity assay confirmed the successful overexpressing of Pgc1α. The significantly greater complex ILEAK, complex IADP, and complex I + IIADP respiration rates in GFP-tagged Pgc1α-injected FDBs demonstrates that the electroporation of cDNA into FDBs is an effective means of manipulating the phenotype or function of the muscle. Normalizing oxygen consumption rates to CS activity resulted in no group differences compared to dry muscle weight normalization. These data suggest that Pgc1α may have a larger influence on CS activity relative to the protein complexes of the electron transport chain (ETC). More specifically, each complex of the ETC is made up of numerous proteins that are likely not all regulated by Pgc1α suggesting the necessity of additional regulators of mitochondrial function .
While there are practical advantages to using the EDL, soleus, or gastrocnemius muscles for assessing skeletal muscle isometric force production or mitochondrial respiration, these muscles are not effective targets for cDNA electroporation due primarily to their size and/or anatomical location (which impedes cDNA distribution within the muscles). Conducting mechanistic studies into the relationships between protein expression and function using such muscles therefore requires the production of muscle-specific transgenic mice. The FDB provides a time sensitive, non-invasive, and cost-effective method for assessing multiple functional indices within skeletal muscle after deliberately altering protein expression through cDNA or shRNA delivery. This combined utility provides advantages to investigators pursuing mechanistic studies in the field of skeletal muscle biology.
The use of the FDB represents an expanded tool set to the mechanism-focused investigator. We demonstrate that the FDB may act as a substitute for a number of commonly assessed skeletal muscles across a range of methodologies. In addition, the versatility of the FDB supports a number of complementary methodologies that may advance the assessment of skeletal muscle function and aid in elucidating the underlying mechanisms central to understanding skeletal muscle-related genetic disorders and disease.
We thank Dr. Jeffery Brault for providing us the cDNA for PGC-1alpha, and Drs. R. M. Lovering and P.D. Neufer for technical discussions.
This study was funded by NIH RO1AR06660 (EES), ADA 1-15-BS-170 (EES), NIH RO1HL125695 (JMM), and F32HL129632 (TER).
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
MDT wrote the manuscript, completed the experimental procedures, and contributed to the experimental design. AJA and NPB completed the experimental procedures and read drafts of the manuscript. TER contributed to designing and troubleshooting the described experimental procedures. CAS contributed to designing and troubleshooting the described experimental procedures. JMM provided intellectual insight and contributed to the project design and critical reading of the manuscript. EES contributed to the experimental analysis and design and provided critical reading revision of manuscript. All authors have read and approved the manuscript.
Ethics approval and consent to participate
Animal care and experimental procedures were approved by the Institutional Review Committee at East Carolina University and complied with the Guide for the Care and Use of Laboratory Animals, Institute of Laboratory Animal Resources, Commission on Life Sciences, National Research Council (Washington: National Academy Press, 1996).
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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