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Am J Physiol Cell Physiol 292: C1156-C1166, 2007. First published October 25, 2006; doi:10.1152/ajpcell.00397.2006
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MUSCLE CELL BIOLOGY AND CELL MOTILITY

Ca2+ sparks and T tubule reorganization in dedifferentiating adult mouse skeletal muscle fibers

Lisa D. Brown,1 George G. Rodney,2 Erick Hernández-Ochoa,3 Chris W. Ward,3,4 and Martin F. Schneider3

1Biology Department, Morgan State University, Baltimore; 2Medical Biotechnology Center, University of Maryland Biotechnology Institute, Baltimore; 3Department of Biochemistry and Molecular Biology, School of Medicine and 4School of Nursing, University of Maryland Baltimore, Baltimore, Maryland

Submitted 21 July 2006 ; accepted in final form 18 October 2006


   ABSTRACT
TOP
 ABSTRACT
MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Ca+ sparks are rare in healthy adult mammalian skeletal muscle but may appear when adult fiber integrity is compromised, and occur in embryonic muscle but decline as the animal develops. Here we used cultured adult mouse flexor digitorum brevis muscle fibers to monitor occurrence of Ca2+ sparks during maintenance of adult fiber morphology and during eventual fiber morphological dedifferentiation after various times in culture. Fibers cultured for up to 3 days retain normal morphology and striated appearance. Ca2+ sparks were rare in these fibers. At 5–7 days in culture, many of the original muscle fibers exhibit sprouting and loss of striations, as well as the occurrence of spontaneous Ca2+ sparks. The average rate of occurrence of Ca2+ sparks is >10-fold higher after 5–7 days in culture than in days 1–3. With the use of fibers cultured for 7 days, application of the Ca2+ channel blockers Co2+ or nifedipine almost completely suppressed the occurrence of Ca2+ sparks, as previously shown in embryonic fibers, suggesting that Ca2+ sparks may be generated by similar mechanisms in dedifferentiating cultured adult fibers and in embryonic fibers before final differentiation. The sarcomeric disruption observed under transmitted light microscopy in dedifferentiating fibers was accompanied by morphological changes in the transverse (T) tubular system, as observed by fluorescence confocal imaging of both an extracellular marker dye and membrane staining dyes. Changes in T tubule morphology coincided with the appearance of Ca2+ sparks, suggesting that Ca2+ sparks may either be a signal for, or the result of, disruption of DHPR-ryanodine receptor 1 coupling.

calcium ion signaling; muscle remodeling; fluo 4; calcium ion imaging

CA2+ SPARKS ARE BRIEF LOCALIZED elevations of cytosolic Ca2+ generated by the opening of a small number of ryanodine receptor (RyR) Ca2+ release channels (4). In frog skeletal muscle fibers, the global Ca2+ transient during fiber depolarization appears to be made up of the near-synchronous occurrence of large numbers of Ca2+ sparks throughout the muscle fiber (15). Although spontaneous Ca2+ sparks can be easily evoked under physiological conditions in resting adult frog skeletal muscle fibers, Ca2+ sparks are not normally detected in adult mammalian skeletal muscle. In fact, in adult mammalian myofibers, spontaneous Ca2+ sparks seem to appear only when the integrity of the fiber is compromised (i.e., permeabilized or membrane disrupted; see Refs. 7, 13, and 22) or the myofiber is under acute mechanical/ionic stress (26), leading to the conclusion that Ca2+ spark activity is suppressed rather than nonexistent in adult mammalian myofibers (19).

In contrast to adult myofibers, Ca2+ sparks are normally present in embryonic mammalian skeletal muscle (7) and during early postnatal maturation of mammalian skeletal muscle (6). However, the frequency of event occurrence decreases postnatally (6) as the animal and the muscle fiber transverse (T) tubules (11) develop. Early hypotheses to explain the postnatal decline in Ca2+ sparks in mammalian skeletal muscle focused on differential expression of RyR isoforms (RyR1 and RyR3) during development; however, these hypotheses were quickly discounted as RyR1, as well as RyR3, was capable of producing Ca2+ spark-type release (7, 27). More recently, work has focused on developmental structural differences in DHPR-RyR1 coupling (1, 10, 21, 22, 31), as well as acute structural alterations at the level of the T tubules (26), showing that both are associated with Ca2+ sparks in adult mammalian muscle. We therefore hypothesized that experimentally induced alterations in T tubule morphology may be needed to allow spontaneous Ca2+ release events to occur.

We have previously utilized enzymatically dissociated adult mouse flexor digitorum brevis (FDB) muscle fibers to characterize the process of dedifferentiation of adult skeletal muscle fibers in culture. Fibers cultured for up to 3 days in serum-containing medium retain normal morphology and striated appearance. At 5–7 days in culture, many fibers begin to exhibit a change in the adult morphology, characterized by sprouting, fusion with mononuclear cells (presumably myoblasts), and loss of striations, generally beginning at their ends (2). Whether or not the morphological loss of striations and drastic changes in fiber shape observed in cultured fibers represent only fiber remodeling to the developmentally preceding terminal myotube stage, or whether this is true dedifferentiation to a precursor cell type (8, 18), remains to be determined. Similar morphological regression and/or reversion to a precursor cell type occurs in vivo in muscle diseases (3) and presumably also accompanies in vivo muscle regeneration after muscle damage. Possible reversion of muscle fibers to precursor cell types (17, 25) has important implications for remodeling of muscle and for "engineered" muscle or other tissues. In addition to the pronounced morphological changes observed during fiber dedifferentiation in culture, functional changes were also evident. Multiple or delayed Ca2+ transients in response to brief field stimulation were often observed in dedifferentiated fibers (2), indicating alterations in action potential initiation and possibly in excitation contraction (EC) coupling.

Here we use dissociated adult mouse FDB muscle fibers to monitor the occurrence of Ca2+ sparks during periods of maintained adult fiber morphology, and during eventual fiber morphological dedifferentiation after various times in culture. We find that Ca2+ sparks are extremely rare in acutely dissociated adult mouse FDB fibers or in fibers maintained for up to 3 days in culture in serum-containing medium. At 5–7 days in culture, the frequency of Ca2+ sparks increases, coincident with the changes in morphology indicative of dedifferentiation. As in embryonic fibers (6), Ca2+ channel blockers almost completely suppress the occurrence of Ca2+ sparks in adult fibers cultured for longer than 7 days. These observations suggest that Ca2+ sparks may be generated by similar mechanisms in dedifferentiating cultured adult fibers and in embryonic fibers before final differentiation. Also, changes in T tubule morphology in dedifferentiated fibers coincided with the appearance of Ca2+ sparks, suggesting that Ca2+ sparks may either be a signal for, or the result of, disruption of DHPR-RyR1 coupling.


   MATERIALS AND METHODS
TOP
 ABSTRACT
 MATERIALS AND METHODS
RESULTS
 DISCUSSION
 REFERENCES
 
Preparation of isolated adult mouse skeletal muscle fibers. Single muscle fibers from the FDB muscle were enzymatically dissociated and cultured using a modified protocol previously described (16). Briefly, FDB muscles were incubated in minimal essential media containing 10% FBS and 0.2% Type I collagenase at 37°C for 2.5 h. To release single fibers, the FDB muscles were then triturated gently in media without collagenase. The fibers were then plated on laminin-coated cover slip floors of culture dishes in serum-containing media and incubated in 5% CO2 at 37°C until use. For cultures maintained in serum-free media, the serum-containing media was replaced after 1 h of plating with minimal essential media containing 5 µg/ml apotransferrin, 5 ng/ml sodium selenite, and 5 µg/ml insulin. All images and data presented here were obtained from living cultured fibers bathed in Ringer solution (in mM: 145 NaCl, 4 KCl, 1.8 CaCl2, 1 MgSO4, 10 glucose, and 10 HEPES-Na2, pH 7.4) with or without additions, as indicated, and studied at room temperature.

Imaging local Ca2+ sparks. Cultures of FDB fibers were loaded by exposure to 20 µM fluo 4-AM (Ca2+ indicator dye; Invitrogen, Carlsbad, CA) prepared in Ringer solution for ~45–60 min followed by a rest period of 15 min to allow for dye deesterification. Both fibers that appeared normal and dedifferentiating fibers were imaged for spontaneous Ca2+ sparks on an inverted microscope [Olympus IX-71 with a x60, 1.3 numerical aperture (NA) water-immersion objective] coupled to a Bio-Rad CellMap IC laser scanning confocal imaging system (LSCM). Fibers that appeared normal were characterized by a striated appearance, rounded ends, and no sprouts and exhibited no visible signs of damage. Dedifferentiating fibers were characterized by loss of striations and sprouting either at the ends or from the middle of the fiber. In the basal condition, a sequence of 50 x-y images (512 x 512 pixels; 0.18 µm pixel; 2 ms/line) were collected at 3-s intervals shortly after deesterification of the fluo 4-AM. In each myofiber, an image sequence was taken at each end and near the midpoint of the myofiber. In a subset of the myofibers, imaging was repeated following application of Ringer solution containing Ca2+ channel blockers (5 µM nifedipine or 5 mM CoCl2). Image sequences were processed, and the frequency of sparks was determined as described in Chun et al. (6). In brief, Ca2+ sparks were identified using a modified automatic detection method as previously described (5, 6). In this method, the mean fiber fluorescence image was determined by a pixel-by-pixel average of a 25-image sequence. In each sequence, potential local Ca2+ release events were identified as contiguous pixels exhibiting fluorescence ≥1.5 SDs above the mean fiber fluorescence. Regions selected as local Ca2+ events were identified in {Delta}F/F (where F is fluorescence) images as contiguous regions of pixels having fluorescence values greater than or equal to two SD above the mean fluorescence for the same pixel, and were selected by the criterion that at least one pixel within the two SD area must exceed three SD above the mean.

Line scan images. The temporal profiles of the Ca2+ spark were assessed with linescan (x-t; distance-time) images (5-s acquisition time, 2 ms/line, 512 pixels/line, 0.18 µm/pixel) of fluorescence of fluo 4-loaded fibers. Regions of interest (ROI) in which potential Ca2+ sparks occurred were detected by an automatic computer detection algorithm (20) as modified from Cheng et al. (5). Images were corrected for PMT offset and then converted to {Delta}F by subtraction of the spatial (x) pattern of resting fluorescence (F) along the fiber averaged in time over the entire duration, excluding the contribution of potential Ca2+ spark ROIs. {Delta}F images were then normalized pixel-by-pixel by F and smoothed 3 x 3 to create {Delta}F/F normalized images.

Fiber resting Ca2+ concentration measurements. Intracellular free Ca2+ measurements were carried out with a ratiometric fluorescence method using the Ca2+ fluorescent probe indo 1. Fibers were rinsed with Ringer solution and loaded with indo 1-AM (4 µM; Invitrogen) for 45 min at room temperature. After being loaded, fibers were washed with dye-free Ringer solution followed by a rest time interval of 20 min to allow deesterification of the probe. Intracellular free Ca2+ measurements were performed at room temperature. A photometry system, data acquisition board PCI-6221, and custom-made software written in LabView (National Instruments, Austin, TX) were used to acquire and analyze fluorescence data. Fibers were illuminated with a xenon-arc lamp (300 W, Lambda LS; Sutter Instruments, Novato, CA) only during recording of light signals to minimize photobleaching. The ratiometric method and the calibration procedure have been published elsewhere (12). The ratio (R) of the dual emission fluorescence of the free and Ca2+-bound forms of indo 1 (at 485 and 405 nm, respectively) were separated, filtered, and collected by two photomultipliers. The light signals were collected from a spot of ~15 µm diameter. This procedure allowed the recording at various locations in the same fibers and reduced ultraviolet light exposition. Intracellular calibration experiments were performed to convert ratios to Ca2+ concentration ([Ca2+]). Rmin was determined by exposing the muscle fibers to a zero Ca2+ Ringer solution with 20 µM 4-bromo A-23187, a nonfluorescent Ca2+ ionophore (Invitrogen), pH 7.4. When the fluorescence reached a steady minimum value (Rmin), fibers were exposed to a high-Ca2+ (20 mM) Ringer solution and 20 µM 4-bromo A-23187 to estimate Rmax. The following equation published by Grynkiewicz et al. (12) and modified to correct for dye compartmentalization by Zhou et al. (31) was used to convert ratios to [Ca2+]

Formula
where b is the ratio of the 485-nm signals at zero and saturating [Ca2+]. Keff and R0 are effective values of the dissociation constant and Rmin, respectively. We assumed a constant and similar contribution of volume of sarcoplasmic reticulum (SR) and mitochondria in adult and dedifferentiated muscle fibers (<10% of total) as that reported by Zhou et al. (31) in myotubes. Keff was calculated to be 400 nM. When translating ratios into [Ca2+], the Keff acts as a constant scaling factor; hence, any possible underestimation in Keff will not markedly affect the differences observed in the results.

Block of plasma membrane and T tubule Ca2+ channels. Ca2+ channel blockers were applied either by draining the chamber and adding blockers at the final desired concentration in Ringer solution or by removing 1 ml of the 2-ml solution in the chamber and adding 1 ml of 2x concentration of inhibitor in Ringer solution.

Visualization of T tubular system in living fibers. T tubules of FDB fibers were visualized by using three alternative procedures, as follows: 1) sulforhodamine B staining: Cultured myofibers were exposed to the fluorescent dye sulforhodamine B (100 µM; Polysciences, Rydal, PA) in Ringer solution. After a brief incubation, this extracellular marker dye diffuses into the T tubular system (9) and allows visualization of the T tubule morphology by confocal fluorescence microscopy (excitation: 550 nm; emission: >585 nm). Because sulforhodamine B dye remained in the external solution during T tubular imaging, the high fluorescence outside the fiber was eliminated after using the background subtraction rolling ball algorithm process in ImageJ (ImageJ, NIH, Bethesda, MD; http://rsb.info.nih.gov/ij/); 2) membrane marker FM4–64: FDB fibers were loaded with the lypophilic styryl membrane marker FM4–64 (4 µM; Invitrogen) in Ringer solution for 5 min. High-resolution images (excitation: 488 nm; emission: >650 nm) were obtained on a Zeiss LSM 510 with a x63 NA 1.4 oil objective. Pixel dimensions were 0.12 x 0.12 µm in x and y and 0.2 µm in the z-axis. Deconvolution and three-dimensional reconstruction was performed using the commercially available software package Volocity (Improvision); 3) di-8-ANEPPS staining: FDB fibers were stained with the voltage-sensitive dye pyridinium, 4-[2-(6-(dioctylamino)-2-naphthalenyl) ethenyl]-1-(3-sulfopropyl)-, inner salt (di-8-ANEPPS) (5 µM; in Ringer solution for 1 h; excitation: 488 nm; emission: >600 nm; Invitrogen). Fibers stained with di-8-ANEPPS were imaged on a Bio-Rad CellMap IC LSMC system (x60, 1.3 NA water-immersion objective; pixel dimensions 0.15 x 0.15 µm in x and y). Alternatively, di-8-ANEPPS-stained fibers were imaged on a Fluoview 500 LSCM system (x60, 1.3 NA water-immersion objective; pixel dimensions 0.2 x 0.2 µm in x and y). Images of the T tubular network were obtained with 512 x 512 pixel x-y images (average of 16 images). Some di-8-ANEPPS-stained fibers were also loaded with fluo 4 (20 µM; 1 h) to monitor Ca2+ sparks. For sequential imaging of Ca2+ sparks and T tubule networks, fluo 4 and di-8-ANEPPS were excited at 488 nm, and emission intensity was measured using BP 520/40-nm and a LP 600-nm filters, respectively.


   RESULTS
TOP
 ABSTRACT
 MATERIALS AND METHODS
 RESULTS
DISCUSSION
 REFERENCES
 
Effects of serum treatment on muscle fiber morphology. As previously observed (2), adult FDB myofibers cultured in serum-containing media retained their morphology until approximately day 5, at which time the myofibers begin to dedifferentiate (Fig. 1). Dedifferentiation was characterized by sprouting at the myofiber ends and in some cases in the middle of the myofiber. In addition to sprouting, the normal striated appearance characteristic of freshly dissociated fibers became intermittent and irregular in myofibers cultured for ≥5 days. Furthermore, free cells, presumably fibroblasts from the connective tissue and freed satellite cells, proliferated and reached confluency by day 5. In many cases, it was apparent that these proliferating cells fused with each other and possibly with the muscle fibers. However, dedifferentiating myofibers could readily be distinguished from newly formed myotubes (Fig. 1) until approximately day 10 in culture. At this time, both fibers and myotubes appeared as flattened, fused structures (not shown).


Figure 1
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  		Fig. 1. A single representative isolated adult flexor digitorum brevis (FDB) muscle fiber cultured on a laminin-coated cover slip in serum-containing media. Transmitted light images of the same fiber were taken 1 day (A), 3 days (B), 5 days (C), and 7 days (D) after plating. The images show the gradual transition from the adult fiber appearance to a myotube-like morphology, including branches and fine projections. The culture was returned to the tissue culture incubator for 2-day intervals between acquisitions of successive images. Scale bar = 0.1 mm.

 
Time course of appearance of Ca2+ release events in cultured muscle fibers. In our previous study, multiple or delayed Ca2+ transients in response to a single field stimulus were observed in dedifferentiated fibers cultured in serum-containing media but were not observed in any fibers cultured in serum-free media. Based on these findings, as well as the gross morphology under the light microscope, we hypothesized that alterations in T tubular structure and a concomitant disorganization of EC coupling proteins may account for these observations. Our first aim in the present study was to monitor the occurrence of Ca2+ sparks using fluo 4 fluorescence images from fibers cultured in serum-containing media. We reasoned that if the normal EC coupling architecture was altered (locally disrupted DHPR-RyR interactions) spontaneous localized Ca2+ release events may be revealed. Ca2+ release events, indicated by local elevations of fluo 4 fluorescence, were exceedingly rare in adult mouse skeletal muscle fibers during the first days in culture (Fig. 2A). In contrast, Ca2+ events became increasingly evident in adult mouse skeletal muscle fibers between 5 and 7 days in culture in serum-containing medium (Fig. 2B). As described above, this time of myofiber culture often resulted in significant myofiber sprouting, a condition that was evident in Fig. 2B, left.


Figure 2
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  		Fig. 2. Local Ca2+ sparks events in single muscle fibers after 1 day (A) and after 7 days (B) in culture. Six representative images of 2 different fibers are shown for each condition (a–f). Note the appearance of Ca2+ events in the fibers cultured for 7 days.

 
Figure 3A presents 50 successive raw x-y fluo 4 fluorescence images recorded at the myofiber end in a fiber from a 7-day culture. In Fig. 3B, the same image sequence is displayed as a {Delta}F series in which the ROIs of identified sparks (>2 SD above mean fiber F) are displayed. In the images collected, we observed the events to be of variable spatial extent, and there were numerous instances of Ca2+ events recurring at the same location in successive image frames (Fig. 3B). For example, frames 20–22 each had a detected event at the same location near the center, toward the end of the fiber, whereas frames 24–29 each showed an event at the same location at another spot in the fiber (Fig. 3B). Because each x-y image is a "snap shot" acquired over a particular brief interval of time, we cannot tell from x-y images whether the events were continuous between frames or were turning off and back on between x-y image frames.


Figure 3
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  		Fig. 3. Ca2+ sparks appear in both the periphery and the center of dedifferentiating muscle fibers. A: 50 sequential full-frame fluorescence images of a muscle fiber loaded with fluo 4 after being maintained in a serum-containing culture for 7 days. B: events selected from A as being within the selection criteria of contiguous pixels >2 SD above the mean of the same pixel, with at least one pixel >3 SD above the mean. Each selected event is shown within an enclosing box in the image. Successive images were recorded at 3-s intervals.

 
With the use of line scan imaging, both rapidly rising and decaying fluorescence signals (Fig. 4, A, B, and F), similar to Ca2+ sparks in frog and mammalian myofibers, and much slower rising and decaying events (Fig. 4, C, D, and E), as seen in developing mammalian myofibers, were observed. Taken together, either long-duration events or repetitively occurring events (both seen in Fig. 4) could account for the appearance of events that occur in the same spatial location in successive x-y frames (Fig. 3B).


Figure 4
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  		Fig. 4. {Delta}F/F (where F is fluorescence) line scan images from intact dedifferentiating adult mouse muscle fibers. Above each {Delta}F/F image is the mean temporal profile centered at the peak {Delta}F/F. These records represent a sampling of the various different time courses of local Ca2+ release events recorded from dedifferentiating fibers using line scan imaging. A, B, and F: line scan images and time courses of both rapidly rising and decaying fluorescence signals. Note that these signals are quite similar to Ca2+ sparks observed in frog and mammalian myofibers. C, D, and E: line scan images and time courses of slower rising and decaying events. Note that these records are similar to Ca2+ signals as seen in developing mammalian myofibers.

 
Appearance of Ca2+ events between 5 and 7 days in culture coincides with changes in morphology indicative of dedifferentiation. Fibers dedifferentiating in serum-containing medium did not begin to exhibit Ca2+ events until after 3 days in culture (Fig. 5A). Fibers from the same culture that maintained their normal morphology did not begin to show Ca2+ events until after 5 days in culture. After 5 days in culture, the average rate of occurrence of Ca2+ sparks was more than 20-fold higher in the dedifferentiating fibers than in the fibers that appeared normal after 5 days in culture. Unlike the serum-containing cultures, fibers maintained in serum-free media exhibited very few Ca2+ events during a culture period of up to 7 days (Fig. 5A), even though dedifferentiation was seen in some fibers. Thus some serum factor may be needed in addition to dedifferentiation for the occurrence of Ca2+ release events. We have previously shown that, similar to FDB muscle fibers cultured in serum-free media, resting [Ca2+] values were not statistically different in FDB muscle fibers cultured in serum-containing media during the time of culture from day 1 to day 4 (2). Here we also used the ratiometric methods with indo 1-loaded FDB fibers for evaluating resting [Ca2+] during the time of culture at days 1 and 3 (differentiated stage) and days 5 and 7 (dedifferentiated stage) in FDB fibers cultured in serum-containing media. Figure 5B shows that resting [Ca2+] in FDB fibers cultured in serum-containing media is maintained around 60 nM during the time of culture from day 1 to day 7. Average resting [Ca2+] values from days 3, 5, and 7 were not statistically different from day 1 at P < 0.05. Thus the increase in event frequency during fiber dedifferentiation over time in serum-containing media cannot be attributed to a rise in resting [Ca2+] since indo 1 fluorescence ratio measurements indicted no significant change in [Ca2+] from 1 to 7 days in culture (Fig. 5B).


Figure 5
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  		Fig. 5. Frequency of Ca2+ events in both normal and dedifferentiated adult FDB fibers and resting Ca2+ concentration ([Ca2+]) after various times in culture. A: fibers were cultured in either serum-containing media or serum-free media. Frequency of Ca2+ event fibers increases as fiber dedifferentiation increases. In serum-containing media, the no. of fibers included with normal appearance was 15, 20, 9, and 3 and 0, 0, 11, and 5 with dedifferentiated appearance at the successive time points, and in serum-free media was 25, 16, 19, and 10 with normal appearance and 0, 2, 5, and 7 with dedifferentiated appearance at the successive time points. Statistical significance was determined using a 2-way ANOVA test. Significance (P < 0.05) was found between the dedifferentiating fibers in serum-containing media and all the other groups at both days 5 and 7. B: intracellular resting [Ca2+] during fiber dedifferentiation. Bar graph summarizing mean resting [Ca2+] evaluated by ratiometric photometry in indo 1-loaded FDB fibers cultured in serum-containing media at four different stages (days 1, 3, 5, and 7) after fiber plating. Transmitted light images at top of each column shows the typical appearance of FDB fibers for each stage. Scale bar = 10 µm; nos. in parentheses represent sample size.

 
Ca2+ release events are suppressed in the presence of specific and nonspecific blockers of DHPR Ca2+ entry. Ca2+ sparks are easily detected in embryonic skeletal muscle but disappear with development and are suppressed by DHPR Ca2+ channel blockers (6). We hypothesized that the time points at which Ca2+ sparks were seen in the dedifferentiation process (i.e., increasing with T tubule disorganization) were a mirror image to the embryonic development process in which Ca2+ sparks disappear with T tubule maturation (6, 23). Because Ca2+ spark activation during development was modulated by extracellular Ca2+ influx, we next evaluated the effect of blockers of Ca2+ entry on the occurrence of Ca2+ release events in cultured FDB fibers. We first examined the effect of CoCl2, a nonspecific Ca2+ channel blocker. Dedifferentiated fibers cultured for 6–7 days were bathed in a Ringer solution and then imaged both before and after the addition of 5 mM CoCl2. Spark frequency was almost completely suppressed 15 min after application of CoCl2 (Fig. 6A), indicating extracellular Ca2+ influx may play a role in spark occurrence. Because the primary Ca2+ current in adult mammalian skeletal muscle is contributed by L-type Ca2+ channels, we then monitored the Ca2+ event rate after blocking L-type channels with nifedipine. Spark frequency significantly decreased in the first images taken a few minutes after solution change and was completely suppressed after 5 min exposure to nifedepine (5 µM; Fig. 6C). Our results with CoCl2 and nifedipine indicate that Ca2+ influx through the L-type Ca2+ channels modulates the rate of Ca2+ release events in dedifferentiating fibers.


Figure 6
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  		Fig. 6. Frequency of Ca2+ events in dedifferentiated adult FDB fibers decreases with addition of Ca2+ channel blockers. All fibers were cultured for 6–7 days in CoCl2-free, nifedipine-free, serum-containing medium before each experiment. A: fibers cultured in serum-containing media were bathed in Ringer solution and imaged both before and after the addition of 5 mM CoCl2 as indicated. B: time course of resting fiber fluorescence in the same fibers both before and after the addition of CoCl2. C: fibers cultured in serum-containing media were bathed in Ringer solution and imaged both before and after the addition of 5 µM nifedipine as indicated. D: time course of resting fiber fluorescence in the same fibers both before and after the addition of nifedipine. E: fibers cultured in serum-containing media were bathed in Ringer solution and imaged for spark activity without Ca2+ channel blocker treatment. F: time course of resting fiber fluorescence in the same fibers without Ca2+ channel blocker treatment; n = 21 in A and B, n = 10 in C and D, and n = 10 in E and F. Statistical significance was determined using a 1-way ANOVA test (P < 0.05). Groups with the same letter exhibit significant difference from each other.

 
In the presence of either CoCl2 or nifedipine, resting fiber fluorescence increased during the time course of Ca2+ event measurements (Fig. 6, B and D). This finding could potentially indicate a loss in SR Ca2+ to the cytosol, which might have resulted in partial SR depletion and thus a decrease in spark frequency. This is unlikely, however, since control experiments without the Ca2+ channel antagonists (Fig. 6, E and F) demonstrate that basal fiber fluorescence rose with a similar magnitude either with or without nifedipine or CoCl2. A tractable hypothesis to explain the rise in fluorescence level is nonevent Ca2+ release (21, 22) occurring in the fibers, an effect independent of use of the Ca2+ channel blockers.

Azumolene, a Ca2+ release modulator that suppresses the activity of the SR RyR Ca2+ release channel (28), was used to address its effect on the activity of Ca2+ sparks on day 7 dedifferentiated fibers. In fluo 4-loaded day 7 dedifferentiated fibers azumolene treatment (10 µM for 10 min) completely suppressed Ca2+ release events, indicating that RyR channel activity underlies increased Ca2+ sparks (data not shown). However, according to Zhao et al. (29) the effects of azumolene at the level of Ca2+ influx cannot be excluded. Thus further work is required 1) to determine if store-operated Ca2+ entry is present in dedifferentiated fibers cultured for seven or more days and 2) to evaluate the effect of azumolene on Ca2+ influx and Ca2+ sparks.

Appearance of Ca2+ release events coincides with changes in T tubule morphology. Based on the increased rate of Ca2+ spark occurrence coinciding with gross morphological changes seen at the light microscopic level, we next sought to evaluate T tubule morphology during the time points at which Ca2+ sparks were evident. We first used the extracellular marker dye sulforhodamine B. Muscle fibers cultured for only 1 day exhibited a normal striated pattern in scattered light (nonconfocal images; Fig. 7A) and, during exposure to sulforhodamine B (Fig. 7A'), showed a regular striated pattern running transversely across the fiber, suggesting a normal intact T tubule system. By day 7, cultured muscle fibers showed varying degrees of T tubule disorganization as indicated by the intermittent disruption of the transverse pattern of sulforhodamine B staining and the appearance of a longitudinal network of the T tubule system (Fig. 7, B' and C'). Even those fibers that appeared to have a normal striated appearance in scattered light images (Fig. 7B) showed some degree of T tubule disruption, as indicated by the breakdown of the transverse network and the appearance of the longitudinal network of the T tubule system (Fig. 7B'). These fibers may be in the early stages of dedifferentiation. Those fibers that were fully dedifferentiated did not have the transverse sarcomeric pattern in scattered light images (Fig. 7C') and exhibited more pronounced changes in the T tubule morphology, as indicated by the presence of a larger number of longitudinal bands within the T tubule system.


Figure 7
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  		Fig. 7. Transmitted light (A–C) and sulforhodamine B (A'–C') images of fibers after 1 and 7 days in culture. After 1 day in culture, both transmitted light (A) and sulforhodamine-stained (A') images showed an orderly pattern of both striations and transverse (T) tubule structure. By day 7, dedifferentiating fibers exhibit various stages of disruption of T tubule structure after staining with sulforhodamine B (B' and C'). Longitudinally oriented T tubules are apparent in C'.

 
T tubule morphology was further examined using the dyes di-8-ANEPPS or FM4–64, both of which stain membranes exposed to extracellular solution. In adult mammalian skeletal muscle, the T tubule system displays a highly organized transverse pattern. In Fig. 8, T tubules were visualized by staining the fibers with 5 µM di-8-ANEPPS. In day 1 differentiated fibers (Fig. 8, B and C), T tubules were organized in a regular striated pattern, characterized by a ~2-µm sarcomere length and ~1 µm spacing between T tubule doublets. In day 7 dedifferentiated fibers (Fig. 8, E and F), the T tubular structure was reorganized and characterized by an apparent reduction in the T tubule doublet spacing, whereas more pronounced reorganization was observed near to and at the center of the sprouting site, where an almost complete disruption of the T tubules was observed (Figs. 9C and 10C). Figure 9 shows images of the T tubule system stained with FM4–64 in adult FDB fibers cultured for either 1 (Fig. 9A) or 7 (Fig. 9, B and C) days. After 1 day of culture, FDB myofibers retain the transverse spatial pattern indicative of adult skeletal muscle. After 7 days in culture, T tubule alterations were observed, with appearance of longitudinal T tubules (Fig. 9B) and as a chaotic reorganization of the T tubules (Fig. 9C).


Figure 8
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  		Fig. 8. T tubule structure reorganization during fiber dedifferentiation. Transmitted light images (average of 8 frames) of FDB fibers cultured in serum-containing media after 1 (A) and 7 (B) days in culture. B and E: laser confocal images (average of 16 frames) of the same fibers stained with pyridinium, 4-[2-(6-(dioctylamino)-2-naphthalenyl) ethenyl]-1-(3-sulfopropyl)-, inner salt (di-8-ANEPPS) from a single z-axis plane. C and F: enlarged views of the outlined regions of the fibers shown in B and E, respectively. Red traces, average intensity profile, plotted as a function of the longitudinal position, of area enclosed within white rectangles in B and E. After 7 days in culture, T tubular structure was disorganized and characterized by an apparent reduction in the T tubule spacing.

 

Figure 9
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  		Fig. 9. T tubule structure in fibers after culture for 1 and 7 days: FM4–64 staining. A: FM4–64 staining of T tubules shows a normal transverse striated pattern after 1 day in culture. B and C: after 7 days in culture, T tubules show an alteration in the transverse striated pattern, with either an occasional longitudinal T tubule (arrowhead; B) or (C) a complete loss of the transverse striated pattern with areas of the fiber void of T tubules (C).

 

Figure 10
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  		Fig. 10. T tubule reorganization and Ca2+ sparks in a di-8-ANEPPS-stained and fluo 4-loaded day 7 dedifferentiated fiber. A series of images of fluorescence of fluo-4 (50 frames) and fluorescence of di-8-ANEPPS (average of 8 images) was obtained in a sequential mode scanning in the same fiber. A: transmitted light image. B: representative single full x-y frame image showing Ca2+ sparks appearing in both the periphery and the center of day 7 dedifferentiating muscle fiber. Each selected event is shown within an enclosing box in the image. B’: 20 sequential x-y mode images of fiber shown in B. Events were selected as in Fig. 3. C: image of fluorescence of di-8-ANEPPS, showing reorganized T tubules. For comparison, enclosing boxes showing events in B, were redrawn here. Note that Ca2+ sparks usually occur in central areas, where T tubule disruption is more dramatic. Scale bars = 10 µm.

 
Recent data by Zhou et al. (31) suggest that the DHPR, which resides in the T tubule membrane, suppresses Ca2+ sparks. Thus the appearance of Ca2+ sparks in our experiments might be because of this profound reorganization of the T tubules. We directly examined the relationship between changes in T tubule organization and Ca2+ spark activity by staining fluo-4-loaded day 7 dedifferentiated fibers with di-8-ANEPPS and imaged two sequential emission bands. Despite the emission cross talk between the fluo 4 and di-8-ANEPPS signal, the dynamic range of the fluo 4 and the constant di-8-ANEPPS intensity allowed for monitoring of the occurrence of sparks. Figure 10B shows a representative image of a series of images of fluo 4 fluorescence (50 frames), illustrating the locations where sparks were more frequent. Figure 10C shows the fluorescence (average of 8 frames) of di-8-ANEPPS in the same region. Note that, in regions where sparks were frequent, T tubule structures were not present or appeared disorganized.


   DISCUSSION
TOP
 ABSTRACT
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
REFERENCES
 
Ca2+ sparks are discrete, localized, microscopic elevations of Ca2+ that are the result of the synchronized opening and closing of a small number of RyR Ca2+ release channels (4, 24, 13). Under normal conditions, Ca2+ sparks are thought to underlie the macroscopic efflux of Ca2+ from the RyR Ca2+ channels in the SR that occurs following depolarization of a frog skeletal muscle fiber (14, 15, 30). Thus Ca2+ sparks represent fundamental events in frog skeletal muscle EC coupling. In contrast, previous studies have shown that Ca2+ sparks are rarely seen in intact adult mammalian skeletal muscle (19, 22). Our new studies presented here identify and quantitate the reappearance and increasing frequency of Ca2+ sparks during various stages of dedifferentiation in adult mouse skeletal muscle fibers maintained in culture.

Dedifferentiation of adult FDB fibers in culture is characterized by pronounced changes in muscle fiber morphology. These changes, including loss of striations and the appearance of cytoplasmic sprouts coming out of the ends or sides of dedifferentiating fibers, can occur along the length of the fiber. The exact mechanisms underlying the observed dedifferentiation to a myotube-like structure are not known, but the morphological changes are more pronounced and enhanced by the presence of serum in the culture media (2). During this period of pronounced changes, at approximately five to seven days in serum-containing media, Ca2+ spark activity increased 25-fold when compared with fibers only cultured for one day in serum-containing media. However, results from fibers cultured in serum-free media indicate that, although dedifferentiation may be necessary for the appearance of Ca2+ release events, it may not be sufficient, and some serum factor may also be needed.

The morphological changes observed using transmitted light microscopy were also accompanied by morphological changes in the T tubular system, as observed using sulforhodamine B as an extracellular marker for the T tubule lumen or using di-8-ANEPPS or FM4–64 membrane staining and confocal fluorescence imaging. There appeared to be a transition from a transverse to a longitudinal pattern of T tubule staining as the fibers progressed toward the morphologically dedifferentiated state. A similar longitudinal orientation has previously been described and is characteristic of the early phase of T tubule development (11, 23). The orderly, transverse orientation of the T tubule occurs late in development. Thus, when dedifferentiation occurs, the transition in the T tubule orientation may indicate a transition from the mature, fully developed muscle fiber back toward an earlier developmental stage of the muscle fiber. This further supports our hypothesis that dedifferentiation may be the reverse of the development of myotubes to mature muscle fibers. There is currently considerable interest in the mechanisms underlying cellular dedifferentiation (17, 25) and the possibility of using dedifferentiated cells for tissue repairs and/or in the production of various forms of engineered tissues. It will be interesting to determine whether the local Ca2+ release events detected here in morphologically dedifferentiating skeletal muscle fibers may play a signaling or functional role in the muscle fiber dedifferentiation process.

A direct correlation between spatial distribution of the Ca2+ sparks and the areas of T tubule disruption was made, and it is clear that, as the disruption of the T tubule system progressed over time in culture, there was also an increase in the number of Ca2+ events. Thus the appearance of the Ca2+ sparks when the fibers begin to dedifferentiate may point to Ca2+ sparks being a signal for, or the result of, disruption of DHPR-RyR1 coupling. Recently, Zhou et al. (31) showed similar results when examining Ca2+ sparks in primary cultures of mammalian myotubes. In their studies, Ca2+ sparks were not detected along the periphery of the myotube, which is the primary region in which the T tubule system was developed. In contrast, Ca2+ events were detected in the central regions of the myotubes, i.e., in T tubule-free regions. In our studies, Ca2+ sparks were detected along the periphery and in the center of the dedifferentiating fibers. Likewise, T tubule disorganization was observed in the periphery and in the central regions of the fibers. We also observed that the sparks that appear in the dedifferentiating muscle fibers were suppressed in the presence of either the specific DHPR channel blocker nifedipine or the nonspecific Ca2+ channel blocker Co2+. These observations suggest that Ca2+ sparks may be generated by similar mechanisms in dedifferentiating cultured adult fibers as in embryonic fibers in which Ca2+ sparks are also blocked by the same specific and nonspecific DHPR channel blockers (6).

In conclusion, Ca2+ sparks appear in dedifferentiating adult skeletal muscle fibers. Our observations with T tubule staining, with Ca2+ channel blockers, and of the spatial distribution of Ca2+ sparks suggest that dedifferentiation may be a transition toward the embryonic state of muscle development and that Ca2+ spark occurrence is coincident with disruption of the normal T tubule and SR structure seen in normal, healthy adult skeletal muscle fibers. In this regard, the appearance of Ca2+ sparks in adult muscle may provide an indication of localized T tubule disruption.


   FOOTNOTES
 

Address for reprint requests and other correspondence: M. F. Schneider, Dept. of Biochemistry and Molecular Biology, Univ. of Maryland Baltimore School of Medicine, 108 N. Greene St., Baltimore, MD 21201 (e-mail: mschneid{at}umaryland.edu)

The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.


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