Nanopattern surface improves cultured human myotube maturation
Skeletal Muscle volume 11, Article number: 12 (2021)
In vitro maturation of human primary myoblasts using 2D culture remains a challenging process and leads to immature fibers with poor internal organization and function. This would however represent a valuable system to study muscle physiology or pathophysiology from patient myoblasts, at a single-cell level.
Human primary myoblasts were cultured on 800-nm wide striated surface between two layers of Matrigel, and in a media supplemented with an inhibitor of TGFβ receptor. Gene expression, immunofluorescence, and Ca2+ measurements upon electrical stimulations were performed at various time points during maturation to assess the organization and function of the myotubes.
We show that after 10 days in culture, myotubes display numerous functional acetylcholine receptor clusters and express the adult isoforms of myosin heavy chain and dihydropyridine receptor. In addition, the myotubes are internally well organized with striations of α-actinin and STIM1, and occasionally ryanodine receptor 1. We also demonstrate that the myotubes present robust Ca2+ responses to repetitive electrical stimulations.
The present method describes a fast and efficient system to obtain well matured and functional myotubes in 2D culture allowing thorough analysis of single-cell Ca2+ signals.
Skeletal myofibers are large multinucleated cells with an exceptional level of internal organization dedicated to produce strength upon nerve activation. Acetylcholine, released from nerve terminals, induced membrane depolarization (action potential) that is sensed by voltage-gated Ca2+ channels, Cav1.1, also called dihydropyridine receptor (DHPR). The conformational change of DHPR is transmitted to the ryanodine receptor 1 (RyR1), a Ca2+ channel localized at the terminal cisternae of sarcoplasmic reticulum (SR). The opening of RyR1 leads to a strong release of Ca2+ from the SR and eventually muscle contraction, an overall process called excitation–contraction (EC) coupling. Because of the size and organization of muscle fibers, and even if important progresses were accomplished over the years, it remains challenging to obtain well differentiated and matured myofibers in vitro. Several models of myogenesis were designed to generate muscle tissue that could be eventually engrafted in damaged/diseased muscles , to provide suitable models to study pathophysiological mechanisms of the disease [2, 3], or to understand the various steps of muscle formation [4, 5]. The sources of cells used to perform in vitro culture are diverse, such as C2C12 mouse cell line or primary myoblasts of murine or human origin. As well, cultures derived from human iPSC are used with promising outcomes [6, 7]. In the recent years, several studies have highlighted the benefits of establishing 3D compared with 2D culture. Indeed, 3D approaches promote the level of maturation and contractility of myotubes/myofibers and allow to keep cells longer in culture. The improved internal architecture, the presence of acetylcholine receptor (AChR) clusters, and the higher contractility are among the main advantages of 3D versus 2D culture . However, 2D cultures are likely more appropriate for single-cell level analysis, but myotubes differentiated on 2D frequently do not mature properly with often a lack of striations and the appearance of small/broken cells  . One cue demonstrated to promote a higher level of myotube maturation is the cell alignment. Indeed, skeletal muscles are composed of very long and aligned fibers, an organization that could be recapitulated, at least partially, in culture. To promote such alignment, self-fabricated substrates are usually created, which are nonetheless complicated to establish and require special lab equipment [9,10,11].
In the present study, we describe an in vitro maturation system that uses striated surface to culture human primary myoblasts. We report evidence of clear beneficial effects of growing and differentiating muscle cells on a striated surface, both at structural and functional levels. We show that on this surface, myocytes display rapidly a high level of internal organization and numerous AChR clustering. Finally, this culture model allows thorough analysis of single-cell robust and repetitive Ca2+ transients elicited by electrical field stimulations.
Human primary myoblasts were isolated from semitendinous muscle samples obtained after orthopedic surgery (surgical waste) on patients without known muscular diseases. All samples were collected anonymously after obtaining a written consent and approval by the University of Geneva (protocol CCER no. PB_2016-01793 (12-259) accepted by the Swiss Regulatory Health Authorities and approved by the “Commission Cantonale d'Ethique de la Recherche” from the Geneva Cantonal Authorities, Switzerland). The purification of myoblasts was performed as previously described .
Myoblasts were seeded either on a conventional dish with a flat surface (FluoroDishTM, Cat n°FD34-100; WPI), or on a nanopattern surface (Anisotropic Nano-Fabricated Surface, ANFS, Nanosurface Biomedical), that has ridges and grooves of 800-nm and 600-nm deep. Both surfaces were coated with Matrigel (Corning Matrigel Basement Membrane Matrix Growth Factor Reduced, Phenol Red Free, #356321) diluted at 1:100 in Ham's F-10 (ThermoFisher) as previously described . Cells were expanded in a growth medium (GM; see Table 1), and when they reached around 90% of confluency, the differentiation was triggered by replacing GM with a differentiation medium (DM; see Table 1). At the time, cells were placed in DM, and during the first 3–4 days in differentiation, the medium was supplemented with 10 μM of TGFβ receptor I inhibitor (SB431542, #S4317, Sigma). After 4 days in differentiation, the TGFβ inhibitor was removed, and a thick layer of Matrigel diluted at 1:3 in DM was added to limit cell detachment , and then half of the medium was changed every 2 days.
Human myotubes were fixed in PBS with 4% paraformaldehyde, permeabilized and blocked in PBS containing 0.3% of Triton X-100 and 5% goat serum. Proteins of interest were revealed by incubation of specific primary antibodies overnight at 4 °C, followed by incubation of fluorophore-conjugated secondary antibodies for 75 min at room temperature. Primary and secondary antibodies and their dilution are listed in Table 2. Nuclei were stained using ProLong® Gold Antifade Reagent with DAPI (ref. P36931, Life Technologies). To detect acetylcholine receptors, α-bungarotoxin (α-BTX, B13422, Invitrogen) was added together with the secondary antibodies. Images were acquired either with a widefield AxioImager M2 microscope (widefield microscopy, Zeiss, Germany) through a 20× objective (EC Plan-Apochromat 20×/ 0.8), or with a confocal Nikon A1r spectral microscope (Nikon; Japan) through a 60× objective (1.4 CFI Plan Apo Lambda). Three random fields were acquired for each dish, with a minimum of two dishes per experimental condition. Clusters of AChR bigger than 5 μm2 were considered for analysis. Analysis of the images were performed using ImageJ software. For display purposes, some pictures were rotated and rescaled to have the same resolution.
Nuclei segmentation analysis
Nuclei were detected based on their DAPI fluorescent channel using Cellpose 0.1.0.1 pretrained model , with automated detection of the diameter. Then the segmentation masks and the acquired images were processed with Matlab 2020b. Briefly, myocyte enhancer factor 2C (MEF2C) or Myogenic differentiation 1 (MyoD)-positive nuclei were analyzed if their individual area was between 40 and 200 μm2. Nuclei were considered as part of a cluster if their nearest neighbor distance was below 3 μm border-to-border. For each isolated nucleus (i.e., not part of a cluster), orientation in the field of view and eccentricity (that informed about the shape of the nuclei) were computed. Nuclei detection and segmentation was performed by Nicolas Liaudet from the Bioimaging core facility of the University of Geneva (https://www.unige.ch/medecine/bioimaging).
Myotubes were loaded with Cal520-AM (5 μM, AAT Bioquest®) and 0.1% Pluronic F-127 (Invitrogen, cat. No P3000MP), in the dark at 37 °C in Ca2+-containing solution. Following an incubation of 90 min, cells were washed and kept for 30 min to allow de-esterification of the dye. Fluorescence was recorded using a Zeiss Axio Observer A1 microscope equipped with a Lambda XL illumination system (Sutter Instrument, Novato, CA, USA). The excitation wavelength was 480 nm (ET480/20×; Chroma), and emission was collected through a T505lpxr dichroic mirror (Chroma) and a 510WB40 filter (Omega Optical) by a cooled 16-bit CMOS camera (pco.Edge sCMOS, Visitron Systems, Puchheim, Germany). An attenuation filter was added at the excitation side to limit phototoxicity (694/SP BrightLine HC shortpass filter, AHF analysentechnik AG, Germany). Acetylcholine (10 μM, A2661, Sigma-Aldrich) or electrical stimulations (see below) were applied to elicit Ca2+ responses. Image acquisition was performed at 3.3 Hz with the VisiWiew software, version 126.96.36.199 (Visitron Systems, Puchheim, Germany). The fluorescence intensity was expressed as F/Fo to normalize the data.
Electric field stimulations
A chamber containing platinum electrodes (RC-37FS, Cat.64-0366, Warner Instruments) was inserted into the culture dish. For the experiments performed with cells grown on the nanopattern surface, the electrodes were oriented in a transversal direction compared with the long axis of the cells. The chamber was connected to an electric field stimulator (A310 Accupulser, World Precision Instruments), where the parameters of the stimulation were set up, and to an electric field isolator (A385 Stimulus isolator, World Precision Instruments) to supply a constant current.
Myotubes were stimulated with repetitive bursts of 1 s at 10 Hz every 10 s (each stimulation lasts 2 ms), at 70 V for 3 min. Three to four rounds of stimulations were performed on each cell culture. Stimulations were performed on a medium containing (mM) 135 NaCl, 5 KCl, 1 MgCl2, 10 Hepes, 10 glucose, 0.050 EGTA, and 2 CaCl2, pH 7.4 (NaOH). The analysis of Ca2+ transient parameters was performed with MatLab (R2020b).
Quantitative and conventional real-time quantitative polymerase chain reaction (RT-PCR)
RNA was isolated using TRI Reagent Solution (AM9738, Invitrogen™) from myoblasts, myotubes differentiated for 4 and 10 days, and from adult muscles, according to the manufacturer’s instructions. Quantification of the samples, quality control, reverse transcription, and real-time quantitative polymerase chain reaction (RT-qPCR) were all performed at the iGE3 Genomic Platform of the University of Geneva (https://ige3.genomics.unige.ch/). Following the measurement of sample concentration, quality of the RNA was determined using the Agilent RNA 6000 Nano Kit and analyzed with the Agilent 2100 Bioanalyzer instrument (Agilent Technologies, Germany). From the total RNA, 0.5 μg was reverse transcribed with the PrimeScript™ RT reagent kit (TaKaRa, Bio Company, Japan) according to the manufacturer’s instruction. The expression of genes listed in Table 3 was evaluated during the differentiation and maturation of the myotubes and compared with the expression in the adult tissue. RT-qPCR was performed on 7900HT instrument (Applied Biosystems™). Raw threshold-cycle (Ct) values obtained with SDS 2.2 (Applied Biosystems™) were imported into Excel. Normalization factor and fold changes were calculated using the GeNorm method . The level of gene expression was normalized for two housekeeping genes (B2M coding for β2 microglobulin and EEF1A1). Fold changes obtained for each condition were normalized to the adult tissues.
For conventional PCR, cDNA from myotubes differentiated for 4 and 10 days and from adult muscle were used. DNA fragments of Cav1.1 splice variant, Cav1.1a (adult; 350 bp) and Cav1.1e (embryonic; 250 bp), were separated in 2.2% agarose gel electrophoresis. Each DNA fragment was further sequenced by Fasteris DNA Sequencing Service (Fasteris SA, Switzerland).
For the analysis of nuclei clusters and shape, statistical analysis based on Wilcoxon rank sum tests were conducted on the median number of nuclei in clusters and on the median eccentricity of each acquisition. The null hypothesis between nuclei cultured on nanopattern and flat surfaces was considered as rejected if the p values were below the significant level of 0.05. For all other experiments, data are mean ± SEM, and the statistically significant differences were determined using a Student t test, where * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.00001.
Myotube differentiation on flat versus striated surfaces
We first evaluated the benefit of growing and differentiating human primary myoblasts on a nanopattern surface (ANSF, see Methods section) compared with those on a flat surface. We analyzed the level of myotube differentiation after 4 days in DM, by immunolabeling the cells with α-actinin and the transcription factor MEF2C (Fig. 1a). The fusion index (number of nuclei within myotubes/total number of nuclei) and the percentage of MEF2C positive nuclei were similar between the two surfaces (Fig. 1b, c). However, organization of myotubes was notably different. On the flat surface, myotubes were mainly randomly oriented, while on the nanopattern surface, they were tightly aligned parallel to the striations (Fig. 1a). The position and the shape of the nuclei were also different (Fig. 1d, e): nuclei were frequently found as aggregates of up to 20 nuclei on flat surface (median value between 2 and 7), while the aggregates contained less nuclei (up to 8) on the nanopattern surface (median from 2 to 4; Fig. 1f), and the nuclei displayed predominantly a linear arrangement along the axis of the cells (Fig. 1e). As well, nuclei of cells grown on the nanopattern were more elongated (eccentricity close to 1), as compared with nuclei of cells grown on a flat surface (Fig. 1g). As dispersion and alignment of myonuclei are reminiscent of the sequence of events taking place during myotube maturation , these results suggested that the maturation of myotubes is more advanced when grown on a striated surface than on a flat surface.
To further characterize the differentiation process on both surfaces, we used immunostaining against the transcription factors paired box 7 (Pax7) and MyoD to evaluate the proportion of reserve cells in our two cultures (Supplemental Fig. 1A). During the early step of differentiation in vitro, reserve cells escape the terminal differentiation and commit to a quiescent state . These cells express Pax7, but not MyoD (Pax7+/MyoD-), while myotubes express MyoD and downregulate Pax7 (Pax7-/MyoD+). We did not observe a difference between surfaces in the percentage of Pax7-positive cells (Supplemental Fig. 1B), indicating that the striated surface did not interfere with the establishment of reserve cells. MyoD-positive nuclei were, however, slightly more frequent on the striated surface (Supplemental Fig. 1C). Hence, the nanopatterned striated surface seems to favor specifically myotube maturation but not the entire process of myogenesis.
Ca2+ response to electrical field stimulation on flat versus striated surfaces
We then investigated whether aligned myotubes obtained from the striated surface were functionally more advanced compared with those grown on a flat surface. To this end, we recorded Ca2+ responses after electrical field stimulation to assess the level of EC coupling. Four-day-old myotubes were electrically stimulated by repetitive bursts (1 s at 10 Hz, every 10 s) for 3 min. Myotubes grown on either surface responded by transient cytosolic Ca2+ elevations after stimulation. To note, while less than 45% myotubes cultured on a flat substrate displayed Ca2+ elevation upon stimulation, this percentage increased to more than 95% when the myotubes were grown on nanopattern (Fig. 2a, b). We cannot exclude that a small percentage of myotubes grown on a flat surface did not display a Ca2+ response to electrical field stimulation because of a suboptimal orientation of the cell compared with the electrodes. However, as the myotubes on the flat surface grow in all directions, they are less sensitive to an optimal orientation, and this could not explain the low percentage of responding cells that we observed on the flat surface. Hence, this increased response to electrical field stimulations strongly suggests that myotubes grown on a striated pattern are not only better organized but are also functionally more mature.
Gene expression during maturation on striated surface
The poor myotube organization and their progressive detachment on a flat substrate prevent keeping our cultures for more than 4 to 5 days. On the contrary, myotubes adhere better when cultured on nanopattern, and after addition of a second thick layer of Matrigel, we could keep them for up to 10–12 days in culture and study accurately their maturation. Under these conditions, the width of the myotubes remained stable over time (19.7 ± 1.1 μm to 19.8 ± 0.7 μm at 4 and 10 days, respectively; data not shown).
To obtain a broad overview of the myotube maturation achieved on nanopattern surface, we analyzed several parameters, the first one being the gene expression of Ca2+-handling proteins (Cav1.1α1s, RyR1, and sarco-endoplasmic Ca2+ ATPase (SERCA)1/2) and myosin heavy-chain isoforms, by RT-qPCR in cultured myotubes (at 4 and 10 days) and, for comparison, in adult muscle sample. As expected, the expression of all these genes increased between myoblasts and differentiated myotubes, while their expression remained stable between 4 and 10 days in culture (Fig. 3a). Transcript levels of CACNA1S, RYR1, MYH7 (encoding the isoform expressed in slow fibers), and ATP2A2 (encoding SERCA2) were less than 10-fold lower in myotubes compared with those in adult fibers. On the contrary, genes encoding proteins abundant in fast fibers (MYH1, MYH2, and ATP2A1) were between 10- and more than 100-fold less expressed in myotubes than in adult tissue. Transcript levels of MYH3 (coding the embryonic myosin heavy chain) slightly decreased between 4- and 10-day old myotubes, and they were higher in myotubes than in the adult tissue (Fig. 3a). In parallel, we assessed the expression of the embryonic and adult isoforms of the Cav1.1α1s subunit, namely the Cav1.1e and the Cav1.1a, respectively. Immature myotubes express predominantly the Cav1.1e isoform (that lacks exon 29), while it represents less than 10% of the transcripts in differentiated muscle . Using conventional PCR analysis, we detected two bands corresponding to the embryonic and adult isoforms of Cav1.1 both at 4 and 10 days, while on the adult tissue, only the Cav1.1a was expressed (Fig. 3b). Sequencing the PCR product confirmed that the lower band found in myotubes lacks exon 29 (Fig. 3c). Furthermore, the ratio of Cav1.1e and Cav1.1a expression decreased between 4- and 10-day old myotubes (Fig. 3d), highlighting a shift towards the expression of the adult Cav1.1 channel with time in culture.
Organization of muscle-specific proteins and Ca2+ responses
Skeletal muscles have a highly organized internal architecture with striated pattern of most of the muscle-specific proteins. To evaluate how mature are myotubes grown on the nanopattern surface, we performed immunostaining of α-actinin, RyR1, and the SR Ca2+ sensor stromal interaction molecule 1 (STIM1) after 10–12 days of differentiation. As shown on Fig. 4a, the staining of all these proteins appeared striated, and the distance between two z lines was of around 2.7 μm, close to what is found in the adult human muscle (2.5 μm; Fig. 4b and Supplemental figure 2). Over time, the typical perpendicular alignment of α-actinin appeared first (at around 4 days) followed by STIM1 (at 8–10 days) and eventually RyR1 (Fig. 4c–e). The striations of α-actinin and STIM1 were observed in a consistent way, while the RyR1 doublets were seldom obtained (in about 20% of the cultures) after 10 days of myotube maturation. We further noticed that on myotubes at that stage, the nuclei were mostly localized at the cell periphery (Fig. 4f). Importantly, already after 6 days in DM, the myotubes displayed frequently spontaneous contractions, in around 30–40% of the cultures (Movie 1).
Next, we analyzed the presence of AChR clusters at different times of maturation. Both number and size of clusters significantly increased within 2, 4, and 10 days of culture (Fig. 5a–d). The shape of the clusters is known to change during maturation, with the emergence of branched structures with time . We detected only very few clusters with such rearrangement of the AChR after 10 days of maturation, most of the clusters being oval-shaped. However, AChR were functional, as shown by the rapid cytosolic Ca2+ elevation elicited by application of 10 μM acetylcholine (Fig. 5e–g). By comparison, on the flat surface at day 4 of differentiation, the AChR were more dispersed on the myotubes and did not form proper clusters (Supplemental Figure 3). In addition, only 64% of the myotubes displayed a Ca2+ response when stimulated with 10 μM ACh, compare with the 97% of responding myotubes grown on the nanopattern surface (Supplemental Figure 3).
Lastly, we assessed Ca2+ responses to electrical stimulations. Four- and 10-day-old myotubes were stimulated for 3 min with repetitive bursts every 10 s (Fig. 6a). The amplitude and the decay time of the first cytosolic Ca2+ elevation were very similar at early and later stages of maturation (Fig. 6b, c). As well, the amplitude of the last transient compared with the first one (percentage of remaining Ca2+), that depicts the sustained nature of the response was also not significantly different between the two time points (Fig. 6d). Hence, myotubes already displayed robust EC coupling after 4 days when cultured on nanopattern striated surface.
We reported here a simple in vitro culture model of human primary myoblasts that presents greater level of myotube maturation compared with commonly used 2D cultures.
Our culture model combined various procedures that foster myotube maturation. First, cells were grown between two layers of Matrigel that provided an extracellular matrix limiting cell detachment, as previously reported . Second, cells were grown on a striated pattern surface that favors alignment and maturation of myotubes [11, 20, 21]. This surface is a fabricated pattern with grooves and ridges of 800-nm width and 600-nm depth, dimensions that were previously described to favor myotube maturation , even if larger striations (up to 1600 nm) also led to an enhanced maturation . In addition, we added during the initial 4 days of differentiation an inhibitor of TGFβ receptor, a procedure that was shown to improve cell fusion , MYH expression, and sarcomere organization [23, 24].
As expected, the myotubes grown on a striated surface were very well aligned, with nuclei being also more elongated, initially aligned in the middle of the myotubes while moving at the cell periphery with time in culture, hence recapitulating the progression of nuclei movement occurring in vivo . Yet, we did not notice differences, neither in fusion index nor in percentage of MEF2C-positive nuclei, between flat and grooved surfaces after 4 days of differentiation. This is somehow in contradiction with what was previously reported, where differentiation performed on striated surfaces enhanced the fusion index [20, 21]. It should be pointed out, however, that human primary cells cultured in our laboratory has a high fusion index (around 60%), higher than what was reported in the abovementioned studies. In line with the fusion index, the percentage of Pax7-positive cells was also similar between the two surfaces. Hence, our culture system did not favor the initial steps of differentiation but presents the advantage to promote cell alignment and to maintain cells for longer time in culture allowing their maturation.
We analyzed then several parameters during 10–12 days in culture: the expression level of muscle-specific genes, the internal organization of the myotubes, and their Ca2+ responses to ACh and electrical stimulations, in order to provide a broad overview of the processes taking place over time, both morphologically and functionally.
Although the myotube diameter remained stable during time in culture, the number and size of AChR clusters increased between 2 and 10 days of maturation. At 10 days of differentiation, almost all myotubes displayed clusters of AChR, which reflects a greater maturation of myotubes compared with conventional 2D cultures where only a minority of myotubes have AChR clusters after 2 weeks in culture . The clusters remained however essentially homogenous, without a sign of lacunarity or pretzel structures, like it was reported in 3D culture  or on surfaces coated with various laminin , morphological changes that reflect the maturation of AChR clusters [19, 26]. AChRs were however functional as shown by the Ca2+ elevations elicited by ACh stimulation. The amplitude of the response was akin to the one elicited by electrical stimulation, in line with what was reported on human 3D myobundles . On the contrary, 4-day-old myotubes grown on a flat surface have a diffuse pattern of AChR and not all myotubes responded to ACh stimulation by a Ca2+ elevation.
Interestingly, the genes expressed predominantly in slow fibers (MYH7 and ATP2A2) were expressed in 10-day-old myotubes at levels closer to adult tissue, than the ones expressed in fast fibers (MYH1&2 and ATP2A1). Hence, even if there was a mixed expression of genes from slow and fast fibers, like it is frequently observed in cultured myotubes [28, 29] , myotubes appear to mature preferentially towards a slow phenotype. This slow phenotype resembles the one observed during the establishment of a human muscle cell line HMCL-7304 , with a higher abundance of slow MYH. This slow phenotype is however different to what is observed in vivo when regeneration happens in the absence of innervation, where fibers follow what is called the “default pathway” toward a fast phenotype . The reasons of this maturation towards a slow phenotype are unclear, but this may, at least partially, explain the kinetics of the Ca2+ responses triggered by ACh or electrical stimulation that we measured. Indeed, even if myotubes in culture are known to have slower Ca2+ recovery phase than adult fibers , we were anticipating a faster decay time associated with enhanced maturation, which was not the case. Certainly, the slow Ca2+ kinetics of the response also reflects the fact that the system did not sufficiently mature to have an obvious impact on the Ca2+ repumping efficiency. During muscle development, a splice variant of Cav1.1 lacking exon 29, namely Cav1.1Δ29 or Cav1.1e is expressed, characterized by distinct biophysical properties compared with the adult Cav1.1 isoform: a higher Ca2+ current amplitude together with a 30-mV left shift of the activation potential [18, 33]. The expression of Cav1.1e was also reported in human myotubes in culture, leading us to evaluate its expression. Our results show that the embryonic Cav1.1e is expressed both at 4 and 10 days, and interestingly, the ratio between the two, embryonic and adult isoforms, decreased with time in culture, confirming an enhanced fiber maturation at 10 days.
We also assessed the organization level of several proteins over time in culture. As already reported , the transverse alignment of α-actinin occurred rapidly after the induction of differentiation. Indeed, after 4 days in culture, a substantial number of cells displayed this typical arrangement, and the striations get sharper with longer time in culture. The distance between two Z lines in 10-day-old myotubes was around 2.7 μm, close to the size of adult human sarcomeres (2.5 μm). Furthermore, after 7–8 days in culture, the SR resident Ca2+ sensor STIM1 also appeared striated, with an important level of colocalization on the Z lines. This localization of STIM1 is consistent with findings obtained in muscle adult tissue, where STIM1 was reported to be present both at a region corresponding to the I band (around the Z lines), as well as on the longitudinal SR  [36, 37]. A proper RyR1 localization in doublet was however infrequently obtained, even after 12 days of maturation. On the few cases where such matured arrangement of RyR1 was observed, it always took place after STIM1 was perpendicularly organized. Even if RyR1 doublets were seldom observed, the high level of internal organization achieved within 10 days was to our knowledge not obtained with human cells cultured in 2D. Advanced maturation were obtained with human iPSC but after a significantly longer time (50 days to obtain titin striations , or after 2 weeks to obtain α-actinin striations of myotubes derived from induced myogenic progenitor cells . Hence, the advantage of growing the myotubes on a striated surface, beside the improvement of cell adhesion, is that myotubes remain thin and elongated which likely promotes their internal organization and thus maturation.
Finally, we assessed the ability of myofibers to elicit cytosolic Ca2+ transients upon electrical field stimulation. Already at 4 days of culture, electrical stimulations resulted in large Ca2+ transients of almost all myotubes, highlighting a functional EC coupling. This time frame is rapid if we compared it to the 8 days needed to obtain 50% of myotubes responding to electrical stimulation with classical 2D culture of human cells . We analyzed at 4 and 10 days of culture three parameters out of these Ca2+ recordings, the amplitude of the first transient, the kinetic of the Ca2+ recovery phase, and the sustained nature of the signals during the 3-min stimulation. None of these parameters significantly changed between 4 and 10 days, showing that even if the cells displayed a better internal organization at 10 days, this did not correlate with an improved Ca2+ signals. This is however in agreement with the expression levels of RYR1, CACNA1S, and ATP2A1/2 that remain stable during the maturation period we analyzed.
Overall, we proposed a 2D culture system of human myotubes that reach after 10 days a high level of maturation, with the presence of numerous functional AChR clusters, the expression of adult MYH, increased adult CACNA1S isoform expression, and a high level of internal fiber organization. Further improvements are however required to obtain myofibers that resemble more the adult organization and function. Nevertheless, this rapid and easy-to-perform 2D culture, which does not require sophisticated technology, presents certainly great advantages for further single-cell studies designed to investigate the processes of skeletal muscle maturation.
Availability of data and materials
The datasets used during the current study are available from the corresponding author upon request.
Myocyte enhancer factor 2C
Myogenic differentiation 1
Paired box 7
Ryanodine receptor 1
Stromal interaction molecule 1
Sarco-endoplasmic Ca2+ ATPase
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We thank Prof. Laurent Bernheim for his fruitful discussions and critical reading of the manuscript and Olivier Dupont for his excellent technical assistance. We thank also Prof. Perrine Castets for providing us with α-BTX and for critical reading of the manuscript.
The study is supported by the Swiss National Foundation, grant 310030_166313 (M.F.) and the Foundation Marcel Levaillant (M.F.).
Ethics approval and consent to participate
This study was approved by the University of Geneva under the protocol CCER No PB_2016-01793 (12-259).
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The authors declare that they have no competing interests.
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Spontaneous myotube contraction on 6-day old culture on nanopattern surface.
The reserve cell population is not affected by the surface pattern. (A) Immunofluorescence of nuclei of 4-day old myotubes on Flat (upper panel) or nanopattern surface (ANFS, lower panel). Cell nuclei were stained using an antibody against Pax7 (in green), MyoD (in red) and all nuclei were counterstained with DAPI (in blue). Scale bar: 50 μm. Images shown are representative of six independent experiments. (B, C) Percentage of Pax7 positive nuclei (B) and MyoD positive nuclei (C). Error bars are Mean ± SEM. Supplementary Figure 2. Length of the sarcomere on culture myotubes and on adult tissue. (A-B) Representative images of 10-day old myotubes cultured on nanopattern surface (A) and adult human muscle tissue (B) Scale bar: 10 μm. (C-D) Corresponding line profiles (white dotted line) of α-actinin normalized fluorescence intensity. Supplemental Figure 3. Organization of AChR clusters and Ca2+ response to acetylcholine on flat and striated surface. (A) Representative images of 4-day old myotubes cultured on flat (left panel) and nanopattern surface (right panel) and immunolabeled for α-actinin (red) and α-bungarotoxin (α-BTX, green) together with a DAPI staining (blue). Scale bar: 50 μm. (B) Myotubes were loaded with 5 μM Cal520-AM to measure changes in cytosolic Ca2+ and stimulated with 10 μM of acetylcholine (ACh). Traces represent the mean ± SEM of Ca2+ responses of myotubes differentiated for 4 day on flat surface (left panel) and striated surface (right panel). (C) Statistical evaluation of the amplitude of the peak following ACh stimulation. Error bars are Mean ± SEM. (D) Bar chart representing the percentage of responding cells on both surfaces. Data were obtained from three independent experiments.
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Brunetti, J., Koenig, S., Monnier, A. et al. Nanopattern surface improves cultured human myotube maturation. Skeletal Muscle 11, 12 (2021). https://doi.org/10.1186/s13395-021-00268-3