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Single-Fiber Myosin Heavy-Chain Isoform Composition of Rodent Laryngeal Muscle
Modulation by Thyroid Hormone
Ya Zhen Wu, MD;
Michael J. Baker, MS;
Roger L. Crumley, MD;
Vincent J. Caiozzo, PhD
Arch Otolaryngol Head Neck Surg. 2000;126:874-880.
ABSTRACT
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Background Studies have shown that canine laryngeal muscle contains a large number of muscle fibers that coexpress varying combinations of myosin heavy-chain (MyHC) isoforms. Currently, it is not clear whether this phenomenon is unique to canine laryngeal muscle or occurs in all mammals.
Objectives To examine the single-fiber MyHC isoform composition of rodent laryngeal muscle and to examine the plasticity of single-fiber MyHC isoform composition via manipulation of thyroid state.
Results (1) Findings of single-fiber electrophoretic analyses clearly demonstrate that most fibers in both the posterior cricoarytenoid and thyroarytenoid muscles exhibit MyHC polymorphism. However, the proportions and patterns of polymorphism appear to be muscle specific. (2) Although the fast type IIL isoform was observed in fibers from both muscles, it was always coexpressed in combination with other MyHC isoforms (ie, no pure type IIL fibers were found), and always represented a minor proportion of the total MyHC pool. (3) Altering the thyroid state proved a useful tool for exploring the scope of MyHC isoform expression in these muscles. While the posterior cricoarytenoid muscle seemed more sensitive to the thyroid state, transitions in both muscles were primarily confined to the fast type IIX and IIB MyHC isoforms.
Conclusion The findings of this study support the concept that single-fiber MyHC polymorphism occurs commonly in mammalian laryngeal muscle.
INTRODUCTION
LITTLE IS KNOWN about the biochemical and mechanical properties of laryngeal muscle despite their central role in fundamental processes like swallowing, phonation, and breathing. Within this context, there has been a growing interest in the myosin heavy-chain (MyHC) isoform composition of laryngeal muscle. Myosin heavy chains are the molecular motors of muscle, and convert chemical energy into mechanical work and heat. By using electrophoretic and immunohistochemical techniques, 4 adult MyHC isoforms have been identified in the hind-limb muscles of a number of mammalian species. These have been classified as the slow type I, fast type IIA, fast type IIX, and fast type IIB MyHC isoforms.1-2 With respect to rate of adenosine triphosphate hydrolysis and maximum shortening velocity, MyHC isoforms can be ranked as type I slower than type IIA, type IIX slower than type IIB (slowest to fastest).3 On this basis, MyHC isoforms have been characterized as "physiological markers," providing insight into the mechanical properties of a fiber.
Recent studies have begun to characterize the MyHC isoform composition of laryngeal muscles.4-11 In addition to the slow and fast MyHC isoforms typically found in the rodent hind-limb musculature, DelGaudio et al11 reported that the rodent posterior cricoarytenoid (PCA) and thyroarytenoid (TA) muscles also expressed an "atypical" MyHC isoform, which these investigators classified as type IIL.11 A similar finding was also made in rabbit laryngeal muscle by Lucas et al.6 However, Lucas et al suggested that the additional laryngeal MyHC isoform was really identical to that found previously in the extraocular musculature (ie, the extraocular myosin [EOM]).6 More recently, Jung et al5 showed that the rodent type IIL and EOM MyHC isoforms are, in fact, the same. While the findings of these whole-muscle analyses have provided an important database, ultimately it is more important to understand how these MyHC isoforms are distributed at the single-fiber level. As a consequence, we recently examined the MyHC isoform composition of single fibers from canine laryngeal muscles.9-10 These studies demonstrate that many single fibers in canine laryngeal muscle coexpress various combinations of MyHC isoforms (ie, polymorphic or hybrid fibers). Currently, it is not clear, however, whether such a phenomenon (ie, single-fiber MyHC polymorphism) is unique to canine laryngeal muscle or occurs across a broad spectrum of mammalian laryngeal muscle.
While a database is beginning to evolve regarding the MyHC isoform composition of laryngeal muscle, very little is known about the malleability of MyHC isoform expression in laryngeal muscle. To our knowledge, the denervation studies of DelGaudio and Sciote4 and Shiotani and Flint8 are the only works that have examined laryngeal MyHC isoform plasticity. Shiotani and Flint reported that denervation primarily decreased the expression of the type IIB MyHC isoform and increased the expression of a band labeled as type IIA/IIX (ie, these investigators were unable to electrophoretically separate the IIA and IIX MyHC isoforms) in rodent laryngeal muscle.8 The expressions of the type I and type IIL MyHC isoforms were unaffected by denervation.
The thyroid state of an animal (ie, hypothyroidism, euthyroidism, or hyperthyroidism) can have a powerful effect on the expression of MyHC isoforms in hind-limb muscles.12-19 Specifically, the thyroid hormone is thought to exhibit positive regulation on the fast MyHC isoform genes, and negative regulation on the slow MyHC isoform gene. If laryngeal muscle responds to thyroid state in a manner similar to that seen in hind-limb muscle, we would hypothesize that the faster MyHC isoforms would be up-regulated by hyperthyroidism (+T3), while hypothyroidism (-T3) would produce an opposite effect.
Given this background, there were 2 primary objectives of our study. The first was to determine the MyHC isoform composition of individual muscle fibers found in the rodent PCA and TA muscles. Currently, it is not clear whether the single-fiber MyHC polymorphism in canine laryngeal muscle occurs among all mammalian species or represents a phenomenon unique to canines. The second objective was to use -T3 and +T3 as tools to gain insight into the malleability of MyHC isoform expression within rodent laryngeal muscles.
To our knowledge, the current study is the first to directly examine the single-fiber MyHC isoform composition of rodent laryngeal muscle. This approach yielded 3 unique findings. First, results of the single-fiber analyses clearly demonstrate that most fibers in both the PCA and TA muscles exhibit MyHC polymorphism. However, the proportions and patterns of polymorphism seem to be muscle specific. Second, although the type IIL isoform occurred in fibers from both muscles, it was always coexpressed in combination with other MyHC isoforms (ie, no pure type IIL fibers were found), and always represented a minor proportion of the total MyHC pool in a given fiber. Third, altering the thyroid state proved to be a useful tool for exploring the scope of MyHC isoform expression in these muscles. While the PCA muscle seemed to be more sensitive to thyroid state, transitions in both muscles were primarily confined to the fast type IIX and IIB MyHC isoforms.
MATERIALS AND METHODS
ANIMAL MODEL AND CARE
Female Sprague-Dawley rats (Taconic Farms, Germantown, NY) weighing 250 to 275 g were randomly assigned to 1 of 3 experimental groups: (1) normal control, n=5; (2) -T3, n=7; or (3) +T3, n=5. All rats were individually housed in temperature- and light-controlled quarters, and received food and water ad libitum. All experimental procedures used in this study were approved by the Institutional Animal Care and Use Committee at the University of California, Irvine.
Animals assigned to the -T3 group were thyroidectomized and given daily intraperitoneal injections of propothiouracil (12 mg/kg) for 6 weeks. This dose substantially reduces plasma T3 levels.16 Hyperthyroidism was induced through daily intraperitoneal injections of aqueous T3 (175 µg/kg) for 6 weeks. This dose induces significant hyperthyroidism, while not initiating any signs of thyrotoxicosis.15 Given that the thyroid state influences the mass of the heart (-T3 decreases; +T3 increases), heart weight was used as an index of thyroid state.
At the end of the experimental period, animals were weighed and then killed with an overdose of pentobarbital sodium (50 mg/kg). The hearts were then surgically removed and weighed. Next, a surgical laryngectomy was performed on each animal, and the larynx placed in a small glass dish filled with glycerol. Under a surgical microscope (Technival II; Jena, Germany), the PCA and TA muscles of each larynx were removed and weighed. These samples were then placed in vials containing a cooled glycerol-relaxing solution (2-mmol/L EDTA, 1-mmol/L magnesium chloride, 4-mmol/L adenosine triphosphate, 10-mmol/L imidazole, 100-mmol/L potassium chloride, pH 7.00), and stored in a -20°C freezer for 24 hours for subsequent single-fiber analysis.
SINGLE-FIBER DISSECTION
Approximately 40 single muscle fibers ( 1 mm in length) were removed from each PCA and TA muscle sample using a surgical microscope and fine Dumont forceps (Biomedical Research Instruments, Rockville, Md). Each single fiber was placed in a vial containing 30 µL of a sample buffer (6-mg/mL EDTA, 0.06-mol/L Tris, 1% sodium dodecyl sulfate (SDS), 2-mg/mL bromophenol blue, 15% glycerol, 5% [volume per volume]  -mercaptoethanol), heated for 2 minutes at 95°C, and vortexed for 1 minute. The MyHC isoform composition of each individual fiber was then determined using gel electrophoresis.
ELECTROPHORETIC SEPARATION OF MyHC ISOFORMS
Myosin heavy-chain isoforms were separated using a discontinuous gel electrophoresis (SDS-polyacrylamide gel electrophoresis) technique that separated 5 MyHC isoforms in rodent laryngeal muscle (type I, type IIA, type IIX, type IIB, and type IIL).20 The separating gel contained 8% acrylamide, 0.6% bis-acrylamide, 29% glycerol, 0.4% SDS, 0.2 mol/L Tris (hydroxymethyl)-aminomethane (pH 8.8), and 0.1-mol/L glycine. After allowing the solution to degas for 30 minutes, polymerization was initiated by adding N, N, N', N',-tetramethylethylenediamene (TEMED, 0.05% final concentration) and ammonium persulfate (0.1% final concentration). The separating gel was layered with a 10% ethanol solution and allowed to polymerize for 30 minutes. After polymerization of the separating gel, a stacking gel was prepared containing 4% acrylamide, 0.2% bis-acrylamide, 30% glycerol, 70-mmol/L Tris (pH 6.8), 4-mmol/L EDTA, and 4% SDS. This stacking gel was allowed to degas for 15 minutes, with polymerization initiated by adding TEMED (0.05% final concentration) and ammonium persulfate (0.1% final concentration). This gel was then poured on top of the separating gel and allowed to polymerize for 60 minutes. For single-fiber analysis, 1 muscle fiber was loaded into each well. Gels used a running buffer containing 0.1-mol/L Tris, 0.15-mol/L glycine, and 0.1% SDS. Electrophoresis was performed using an SG-200 vertical slab gel system (C.B.S. Scientific, Del Mar, Calif), and gels were run at a constant voltage of 275 V for 24 hours (4°C). Gels were stained using a Silver Stain Plus Kit (Bio-Rad, Richmond, Calif) and scanned wet using a high resolution personal densitometer running Version 5.0 Imagequant software (Molecular Dynamics, Sunnyvale, Calif).
STATISTICAL ANALYSES
All statistical analyses were performed using a computer program (Systat, Evanston, Ill). Heart weights, body weights, and muscle weights were analyzed using a 1-way analysis of variance. The single-fiber distributions from the control, -T3, and +T3 groups were compared with one another using  2 analyses. Only the comparisons that were significant for 2 analyses are discussed. Comparisons were considered statistically significant when P was .05 or smaller.
RESULTS
PHYSICAL DESCRIPTION OF ANIMALS AND MUSCLES
The effects of –T3 and +T3 on animal, heart, and muscle weights are given in Table 1. The mean heart weight of the -T3 group was 35% lower than that of the control group (P<.001). In contrast, the mean heart weight of the +T3 group was approximately 50% greater than that of the control group (P<.001).
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Description of Animal, Heart, and Muscle Weights*
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PCA WHOLE-MUSCLE MyHC ISOFORM COMPOSITION
As shown in Figure 1, the control PCA muscles expressed 5 MyHC isoforms (ie, slow type I, fast type IIA, fast type IIX, fast type IIB, and fast type IIL MyHC). Of these 5, however, the fast type IIX and IIB MyHC isoforms represented approximately 85% of the total MyHC pool (35% and 50%, respectively).
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Figure 1. Histogram illustrating the mean±SE whole muscle myosin heavy-chain (MyHC) isoform expression in the different groups of the posterior cricoarytenoid (PCA) muscle. Muscles from all 3 experimental groups expressed predominantly the type IIX and type IIB MyHC isoforms. When compared with the control muscles, the PCA muscles from the hypothyroid (–T3) group exhibited an up-regulation of the type IIX MyHC isoform and a concomitant down-regulation of the type IIB MyHC isoform. In contrast, PCA muscles from the hyperthyroid (+T3) group showed an up-regulation of the type IIB MyHC isoform and a down-regulation of the type IIX MyHC isoform. A indicates significantly different from the control group; B, significantly different from the –T3 group.
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Relative to the control group, -T3 decreased the proportion of fast type IIB MyHC isoform (P<.05) and increased the relative amounts of the fast type IIA and IIX MyHC isoforms (P<.05) (Figure 1). In contrast, +T3 increased the proportion of the fast type IIB MyHC isoform (P<.05) and concomitantly reduced the fast type IIX MyHC isoform (P<.05) relative to the control group.
TA WHOLE-MUSCLE MyHC ISOFORM ANALYSES
Whole-muscle MyHC isoform compositions for the TA muscles from the control, -T3, and +T3 groups are shown in Figure 2. Unlike the control PCA muscles that expressed all 5 MyHC isoforms, the control TA muscles expressed only the fast type IIX, IIB, and IIL isoforms. Of these 3 MyHC isoforms, the type IIB represented approximately 65% of the total MyHC pool. Hypothyroidism, compared with the control group, produced relatively small but significant changes in the relative amounts of the fast type IIX, IIB, and IIL. As seen in the PCA muscle, +T3 produced effects that were opposite those of –T3, increasing the proportion of the fast type IIB MyHC isoform and concomitantly decreasing the relative amount of the fast type IIX MyHC isoform (Figure 2).
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Figure 2. Histogram illustrating the mean ±SE whole muscle myosin heavy-chain (MyHC) isoform expression in the different groups of the thyroarytenoid muscle. Muscles from all 3 experimental groups expressed predominantly the type IIB MyHC isoform, with smaller expression of the type IIX and type IIL MyHC isoforms. No significant differences were found between the whole muscle MyHC isoform expressions of the control, hypothyroid (-T3), and hyperthyroid (+T3) groups. A indicates significantly different from the control group; B, significantly different from the –T3 group.
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PCA SINGLE-FIBER MyHC ISOFORM COMPOSITION
The PCA single-fiber MyHC isoform compositions for each of the 3 experimental groups are shown in Figure 3 and Figure 4. There were approximately 12 or 13 different fiber types in the PCA muscle. Most of the fibers from the control group (80% of the total population of fibers) fell into 3 distinct pools: fast type IIX fibers (15%), fast type IIB fibers (30%), and polymorphic IIX/IIB fibers (35%).
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Figure 3. Representative gels illustrating separation of myosin heavy-chain (MyHC) isoforms found in single fibers taken from posterior cricoarytenoid muscles of the control, hypothyroid (-T3), and hyperthyroid (+T3) groups. Some lanes (control, 1 and 13; -T3, 1 and 9; and +T3, 1 and 10) represent a reference solution containing all 5 MyHC isoforms found in rodent laryngeal muscle.
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Figure 4. Histogram illustrating the distribution of myosin heavy-chain (MyHC) isoform combinations found in single fibers of the posterior cricoarytenoid muscle. Approximately 200 fibers were sampled from each group (control, n=204; hypothyroid [-T3], n=225; and hyperthyroid [+T3], n=197). The 31 possible combinations for the 5 laryngeal MyHC isoforms are listed along the x-axis. Each bar depicts an individual fiber type with color scheme representing relative expression of each MyHC isoform found within a given population of fibers. A majority of the fibers in the control group were either fast type IIB or polymorphic IIX/IIB fibers. Application of –T3 resulted in a reduction of fast type IIB fibers and an increase in the proportion of polymorphic IIX/IIB/IIL fibers. Most of the fibers in the +T3 group were fast type IIB fibers.
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Relative to the control group, -T3 produced a significant reduction in the proportion of fast type IIB fibers and an increase in the proportion of polymorphic IIX/IIB/IIL fibers (Figure 3 and Figure 4). In contrast, +T3 produced a large increase in the proportion of fast type IIB fibers and a concomitant decrease in the proportion of IIX/IIB fibers (Figure 3 and Figure 4).
TA SINGLE-FIBER MyHC ISOFORM ANALYSES
The TA single-fiber MyHC isoform compositions of the 3 groups are shown in Figure 5 and Figure 6. The control TA muscles were composed of 5 fiber types (Figure 5). However, approximately 85% of the total population of fibers were represented by just the IIB/IIL (65%) and IIX/IIB/IIL (25%) fibers.
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Figure 5. Representative gels illustrating separation of myosin heavy-chain (MyHC) isoforms in single fibers taken from thyroarytenoid muscles of the control, hypothyroid (-T3), and hyperthyroid (+T3) groups. Lanes 1 and 12 in each gel represent a reference solution containing all 5 MyHC isoforms found in rodent laryngeal muscle.
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Figure 6. Histogram illustrating the distribution of myosin heavy-chain (MyHC) isoform combinations found in thyroarytenoid single-muscle fibers. Approximately 200 fibers were analyzed from each group (control, n=233; hypothyroid [-T3], n=322; and hyperthyroid [+T3], n=211). The 31 possible combinations for the 5 laryngeal MyHC isoforms are listed along the x-axis. Each bar depicts an individual fiber type with color scheme representing relative expression of each MyHC isoform found within a given population of fibers. Most of the fibers from the control group were either polymorphic IIB/IIL fibers or polymorphic IIX/IIB/IIL fibers. Application of –T3 resulted in a reduction in the number of polymorphic IIB/IIL fibers and an increase in polymorphic IIX/IIB/IIL fibers. Most of the fibers in the +T3 group were polymorphic IIB/IIL fibers.
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Relative to the control group, -T3 produced a substantial reduction in the proportion of IIB/IIL fibers that was accompanied by an increase in the proportion of IIX/IIB/IIL fibers (Figure 5). In contrast, +T3 produced an opposite effect, increasing the proportion of IIB/IIL fibers and reducing the proportion of IIX/IIB/IIL fibers.
COMMENT
No studies have directly examined the MyHC isoform composition of single fibers from rodent laryngeal muscle. In this context, there were 3 unique findings of this study. First, most of the fibers in both the PCA and TA muscles of rodents exhibited polymorphic expression of MyHC isoforms. The patterns of single-fiber MyHC polymorphism were, however, unique to each muscle. Second, the fast type IIL MyHC isoform was expressed in both the PCA and TA muscles. However, the fast type IIL MyHC isoform was always coexpressed with other MyHC isoforms; hence, neither the PCA nor TA muscles seem to contain so-called type IIL fibers (ie, fibers that only express the fast type IIL MyHC isoform). Finally, the patterns of single-fiber MyHC isoform expression in both the PCA and TA muscles were influenced by thyroid state. Transitions in MyHC isoform expression were primarily confined to the relative proportions of the fast type IIX and IIB MyHC isoforms.
SINGLE FIBERS FROM THE PCA AND TA MUSCLES EXHIBIT A HIGH DEGREE OF MyHC POLYMORPHISM
The plethora of studies using histochemical adenosine triphosphatase techniques to determine fiber types has created the impression that individual fibers express only 1 MyHC isoform. However, electrophoretic and immunohistochemical work has shown that polymorphic expression of MyHC isoforms within a fiber occurs under both normal and perturbed conditions (V.J.C., unpublished data, 1999).13-14,17, 21-26 In this context, we recently observed the presence of polymorphic fibers in the canine laryngeal muscle.9-10 This observation raised the possibility that single-fiber MyHC polymorphism might be a "common motif" among mammalian laryngeal muscle. As shown in our study, single-fiber MyHC polymorphism seems to be a common feature not only of canine but also rodent laryngeal muscle. The degrees and patterns of polymorphism, however, seem to be both muscle and region specific within both rodent and canine laryngeal muscle. Within this context, the patterns of single-fiber MyHC polymorphism were clearly different between the PCA and TA muscles. Within the PCA muscle, there were 13 different types of fibers (as defined by MyHC isoform composition), and 9 of these exhibited a polymorphic profile. The dominant fiber type in the PCA muscle was the IIX/IIB fiber (40% of the total population). In contrast, the TA muscle was composed of just 5 different fiber types, with the IIB/IIL fibers representing approximately 65% of the total population of fibers.
Few studies have examined the MyHC isoform composition of laryngeal muscle. DelGaudio et al11 used a combination of adenosine triphosphatase histochemical and immunohistochemical analysis to determine the MyHC isoform composition of muscle fibers in rodent laryngeal muscle. These investigators found, however, that it was difficult to categorize fibers in the TA and PCA muscles using this approach. Based on the findings of the current study, the difficulty encountered by DelGaudio et al11 might have been due, in part, to (1) the highly polymorphic nature of single-fiber MyHC isoform expression in these 2 rodent muscles; and (2) the pH lability of the fast type IIL MyHC isoform.
RODENT LARYNGEAL MUSCLES DO NOT CONTAIN PURE IIL FIBERS
In 1995, 2 independent research groups reported the existence of a MyHC isoform in laryngeal muscle different from that typically occurring in the hind limb musculature of mammals.6, 11 Lucas et al,6 studying rabbit laryngeal muscle, reported that this additional isoform was EOM. In contrast, DelGaudio et al11 studied rodent laryngeal muscle and classified this additional isoform as the fast type IIL MyHC. More recently, Jung et al5 reported that the DNA sequence of the additional isoform found in rodent laryngeal muscle matched that of the EOM MyHC isoform. Based on this most recent evidence, it would seem that the so-called fast type IIL MyHC isoform found in rodent laryngeal muscle is really the EOM MyHC isoform.
As shown in Figure 1 and Figure 2, the fast type IIL MyHC isoform represents a relatively small proportion of the total MyHC isoform pool in both the PCA and TA muscles of the rodent. In this regard, however, the TA muscle clearly has a larger proportion of fast type IIL MyHC isoform than the PCA muscle. These observations are consistent with those made previously.8 As shown in Figure 4 and Figure 6, none of the fibers in either the PCA or TA muscles expressed exclusively the fast type IIL MyHC isoform. Within both the PCA and TA muscles, the fast type IIL MyHC isoform was found primarily in IIB/IIL and IIX/IIB/IIL fibers. Note that the fast type IIL MyHC isoform was never the dominant isoform within any given fiber type (Figure 4 and Figure 6). On this basis, it can be concluded that the rodent PCA and TA muscles do not contain so-called type IIL fibers (ie, fibers that only express this isoform).
In rabbit laryngeal muscle, there seems to be a large variation in the expression of the fast type IIL MyHC isoform.6 Immunohistochemical analyses have shown that the rabbit TA muscle contains a large proportion of fibers that stain positive for the fast type IIL MyHC isoform. In contrast, rabbit cricothyroid muscle seems to be void of fibers expressing this MyHC isoform.6 Clearly, a broader survey of laryngeal muscle is needed to fully appreciate the significance of this isoform.
LARYNGEAL MUSCLES ARE INFLUENCED BY –T3 AND +T3 IN A MyHC ISOFORM-SPECIFIC MANNER
In a simplistic view, one might assume that the effect of thyroid hormone on all skeletal muscle would be similar. However, studies have shown that the thyroid hormone acts in a muscle-specific manner.15-16,19 Our study is the first to determine the effect of thyroid hormone on rodent laryngeal muscle MyHC isoform composition. Clearly, the whole-muscle and single-fiber shifts in MyHC isoform expression produced by –T3 and +T3 were not equivalent in the PCA and TA muscles, indicating that thyroid hormone also acts in a muscle-specific manner within rodent laryngeal muscle.
In the PCA muscle, thyroid state affected the relative amounts of the fast type IIA, IIX, and IIB MyHC isoforms. Of these 3 MyHC isoforms, the fast type IIB MyHC isoform seemed the most sensitive (Figure 1) to thyroid state. At the single-fiber level, most of the fast type IIB MyHC isoform in the control group was found in the IIB and IIX/IIB fibers (Figure 4). Hypothyroidism down-regulated the fast type IIB MyHC isoform primarily by reducing the proportion of fast type IIB fibers. In contrast, +T3 produced an increase in the relative amount of the fast type IIB MyHC isoform by producing a dramatic increase in the proportion of IIB fibers and reducing the proportion of IIX/IIB fibers. In the TA muscle, -T3 reduced the proportion of IIB/IIL fibers and increased the proportion of IIX/IIB/IIL fibers. Hyperthyroidism produced an opposite effect.
With respect to MyHC isoform plasticity, Pette and Staron,1 Aigner et al,21 Staron and Pette,23 and Termin et al25 proposed a simple sequential scheme of MyHC that can be summarized as follows: IIA/IIB. Currently, it is not clear whether such a model pertains to rodent laryngeal muscle. If such a model is applicable, then a modification of this scheme is required to account for the presence of the type IIL isoform. While the whole-muscle data in the current study create the impression that transitions occurred between the fast type IIX and IIB MyHC isoforms, the manifestation of such transitions at the single-fiber level was clearly more complex than this. Also, recent studies have shown that the IIA/IIB scheme may not apply to all rodent skeletal muscles or conditions.13-14,17, 26 For instance, rodent muscles such as the diaphragm and plantaris contain fibers inconsistent with this scheme (V.J.C., unpublished data, 1999). Additionally, altered thyroid and mechanical states have been shown to produce patterns of single-fiber MyHC polymorphism that cannot be explained by this model (V.J.C., unpublished data, 1999).13-14,26
SUMMARY
In summary, the findings of this study demonstrate that the mechanisms regulating the expression of MyHC isoforms in laryngeal muscle are highly complex. This is exemplified by the finding that a large proportion of fibers in both the PCA and TA muscles exhibit polymorphic expression of MyHC isoforms. Within this context, manipulation of thyroid state proved to be a useful tool in exploring the plasticity of single-fiber MyHC isoform composition.
AUTHOR INFORMATION
Accepted for publication December 12, 1999.
Reprints: Vincent J. Caiozzo, PhD, Medical Sciences I, B-152, Department of Orthopedics, University of California, Irvine, CA 92697 (e-mail: vjcaiozz{at}uci.edu).
From the Departments of Otolaryngology–Head and Neck Surgery (Drs Wu and Crumley), Orthopedics (Mr Baker and Dr Caiozzo), and Physiology and Biophysics (Dr Caiozzo), College of Medicine, University of California, Irvine.
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26. Talmadge RJ, Roy RR, Edgerton VR. Distribution of myosin heavy chain isoforms in non-weight bearing rat soleus muscle fibers. J Appl Physiol. 1996;81:2540-2546.
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