A comparative study of the regeneration of the striated and smooth-muscle tissues of the esophagus]

By means of electron microscopy and observational histological techniques, using a similar experimental model, regeneration of the striated and smooth muscle tissues of the esophagus has been studied in rats. During early periods after lesion in both muscle tissues destructive-necrotic changes develop. Beginning from the 2nd-3d days regeneration processes are observed. The course and periodicity of the regenerative processes are specific for the types of the muscle tissues studied. Each of the muscle tissues of the esophagus has its own source of regeneration. For the smooth muscles those are myoblasts, that convert into smooth myocytes, for the striated ones--myosatellites, which after activation get out of the muscle fiber. During the restorative process of the muscular membrane no tissue interconnections are observed. This also proves certain specificity of the striated and smooth muscle tissues of the esophagus.     

Ultrastructure of striated muscle fibers in the middle third of the human esophagus

Striated muscle fibers and their spatial relationship to smooth muscle cells have been studied in the middle third of human esophagus. Biopsies were obtained from 3 patients during surgery. In both the circular and longitudinal layers, the muscle coat of this transition zone was composed of fascicles of uniform dimension (100-200 microns of diameter); some of these bundles were made up of striated muscle fibers, others were pure bundles of smooth muscle cells and some were of the mixed type. Striated muscle fibers represented three different types, which were considered as intermediate, with certain structural features characteristic of the fast fiber type. Of these, the most frequently-found fibers were most similar to the fast fiber type. Satellite cells were numerous; in mixed fascicles they were gradually replaced by smooth muscle cells. The gap between striated muscle fiber and smooth muscle cells was more than 200 nm wide. It contained the respective basal laminae and a delicate layer of amorphous connective tissue. No specialized junctions were formed between consecutive striated muscle fibers, or between striated muscle fibers and smooth muscle cells. Interstitial cells of Cajal were never situated as close to striated muscle fibers as to smooth muscle cells.     

Changes in myosatellitocytes in response to injuries of the muscles of the esophagus

Processes occurring in the striated muscle tissue in the rat oesophagus have been studied light- and electron-microscopically under various lesions of the oesophageal muscles. Stages of the regenerative process are described. The muscle tissue in the oesophagus is revealed to possess the ability of myosatellitogenesis. Ultrastructural peculiarities of various types of myosatellitocytes are reported. Segregation of nucleo-sarcoplasmic segments from some injured muscle fibers is demonstrated. Owing to these data, it is possible to consider the striated muscle tissue in the oesophagus as one of the varieties of the somatic muscle tissue.     

Postnatal changes in vagal control of esophageal muscle contractions in rats

AimsReplacement of smooth muscles by striated muscles occurs in the esophagus during the early postnatal period. The aim of this study was to clarify postnatal changes in vagal control of esophageal muscle contractions in rats.Main methodsAn isolated segment of the neonatal rat esophagus was placed in an organ bath and the contractile responses were recorded using a force transducer.Key findingsElectrical stimulation of the vagus trunk evoked a biphasic contractile response in the neonatal esophageal segment. The first and second components of the contractions were inhibited by α-bungarotoxin and atropine, respectively. Ganglion blockers, hexamethonium and mecamylamine, did not affect vagally mediated contractions. The first component gradually enlarged with age in days, whereas the second component declined during the first week after birth. Application of d-tubocurarine or acetylcholine caused an apparent contraction in the esophageal striated muscle at postnatal day 0, but responses to these drugs were not observed at 1 week after birth. The neonatal esophagus expressed the γ-subunit of nicotinic acetylcholine receptors. In contrast, the ε-subunit was dominantly expressed in the adult esophagus.SignificanceThe vagus nerves directly innervate both the esophageal striated muscles and smooth muscles in the early neonatal period. During the process of muscle rearrangement, the property of the striated muscles is altered substantially. The specific features of striated muscles in the neonatal rat esophagus might compensate for immature formation of neuromuscular junctions. Unsuccessful conversion of the striated muscle property during postnatal muscle rearrangement would be related to disorders of esophageal motility.     

Sarcosin (Krp1) in skeletal muscle differentiation: gene expression profiling and knockdown experiments

SARCOSIN, also named Krp1, has been identified as a protein exclusively expressed in striated muscle tissue. Here we report on the role of SARCOSIN in skeletal muscle development and differentiation. We demonstrate, by means of whole-mount in situ hybridization, that Sarcosin mRNA is expressed in the myotome part of the mature somites in mouse embryos from embryonic day 9.5 onwards. Sarcosin is not expressed in the developing heart at these embryonic stages, and in adult tissues the mRNA expression levels are five times lower in the heart than in skeletal muscle. SARCOSIN protein partially co-localizes with the M-band protein myomesin and between and below laterally fusing myofibrils in adult skeletal muscle tissue. RNA interference mediated knock-down of SARCOSIN in the C2C12 myoblast cell line appeared to be stimulatory in the early phase of differentiation, but inhibitory at a later phase of differentiation.     

Ultrastructure of the striated muscle tissue of the iris of birds]

Heteromorphism of the contractile elements of the iris muscular tissue in chick embryos and in chickens has been studied by means of electron microscopical investigation. The leading contractile tissue of the iris is the striated muscular tissue, which is formed as a cellular-simplastic system with its own cambium-myosatellitocytes. Some cells, containing myofilaments in their cytoplasm, are related to myofibroblastic and smooth muscle differons, which functions remain to be studied. A hypothesis is proposed on existence of two sources for development of the iris muscular elements. The first-stem cells for the striated muscular tissue; at early stages of embryonal development they are included into composition of ectomesenchyme of the neural crest and migrate into the area of the muscle anlages. The second-cells migrating from the ocular cup margins and developing into the smooth myocytes of the iris.     

Role of calcineurin in striated muscle: development, adaptation, and disease

Striated muscles, cardiac and skeletal muscles, use calcium as a second messenger to respond and adapt to environmental stimuli. Elevations in intracellular calcium activate calcineurin, a serine/threonine phosphatase, resulting in expression of a set of genes involved in remodeling striated muscle. Activation of calcineurin in hearts produces cardiac hypertrophy, and in skeletal muscle promotes cell differentiation and transforms fiber type specificity. In this review we discuss the effects of calcineurin activity on development, adaptation, and disease of striated muscle.     

Proteomic analysis of striated muscle

The techniques collectively known as proteomics are useful for characterizing the protein phenotype of a particular tissue or cell as well as quantitatively identifying differences in the levels of individual proteins following modulation of a tissue or cell. In the area of striated muscle research, proteomics has been a useful tool for identifying qualitative and quantitative changes in the striated muscle protein phenotype resulting from either disease or physiological modulation. Proteomics is useful for these investigations because many of the changes in the striated muscle phenotype resulting from either disease or changes in physiological state are qualitative and not quantitative changes. For example, modification of striated muscle proteins by phosphorylation and proteolytic cleavage are readily observed using proteomic technologies while these changes would not be identified using genomic technology. In this review, I will discuss the application of proteomic technology to striated muscle research, research designed to identify key protein changes that are either causal for or markers of a striated muscle disease or physiological condition.     

Electron Microscopy of Peripheral Nerves and Neuromuscular Junctions in the Wasp Leg

The peripheral nerve branch innervating the femoral muscles of the common yellow jacket (Vespula carolina) has been found to possess a thick lemnoblast basement membrane and a complex mesaxon. The term "tunicated nerve" is proposed to designate the type of peripheral nerve in which one or several axons are loosely mantled by meandering, cytoplasm-enclosing membranes of the lemnoblast. The peripheral axon courses longitudinally in a groove in the muscle fiber between the plasma membrane of the muscle fiber and a cap formed by lemnoblast and tracheoblast. The junction is characterized by apposition of plasma membranes of axon and muscle fiber, abundant mitochondria, and synaptic vesicles in the axon, and aggregates of "aposynaptic granules" plus mitochondria and endoplasmic reticulum on the muscle side of the synapse. Unlike the vertebrate striated muscle fiber, no complex infolding of the synapsing plasma membrane of the muscle fiber occurs. The "connecting tissue" of the insect is formed by tracheoblasts, their basement membranes, and the basement membranes of other cells. Further mechanical support is given by the ramifying tracheoles. The physiologic roles of the specialized structures are considered.     

Mathematical modeling of capillary density

Capillary density is important as a determinant for total oxygen transport to tissue. Because both capillary morphology and fiber composition vary considerably from muscle to muscle, measurement of capillary morphology and fiber composition vary considerably from muscle to muscle, measurement of capillary density alone cannot provide the detailed information necessary for analyzing physical phenomena. In this report we consider the capillary:fiber ratio, fiber types, fiber diameters, and fiber composition as components of a unit to express capillary density. We have applied the hexagonal fiber array model to calculate capillary density in cat and dog striated muscle and compared this with experimental data in the literature. The results indicate that this model may be useful for predicting capillary densities from simple biopsy procedures.     

Insights from diploblasts; the evolution of mesoderm and muscle

The origin of both mesoderm and muscle are central questions in metazoan evolution. The majority of metazoan phyla are triploblasts, possessing three discrete germ layers. Attention has therefore been focused on two outgroups to triploblasts, Cnidaria and Ctenophora. Modern texts describe these taxa as diploblasts, lacking a mesodermal germ layer. However, some members of Medusozoa, one of two subphyla within Cnidaria, possess tissue independent of either the ectoderm or endoderm referred to as the entocodon. Furthermore, members of both Cnidaria and Ctenophora have been described as possessing striated muscle, a mesodermal derivative. While it is widely accepted that the ancestor of Eumetazoa was diploblastic, homology of the entocodon and mesoderm as well as striated muscle within Eumetazoa has been suggested. This implies a potential triploblastic ancestor of Eumetazoa possessing striated muscle. In the following review, I examine the evidence for homology of both muscle and mesoderm. Current data support a diploblastic ancestor of cnidarians, ctenophores, and triploblasts lacking striated muscle.     

Fasting-induced changes of tyrosine transaminase activity in rat tissues

Tyrosine transaminase activity in liver, kidney, intestine, stomach, skin, adipose tissue, striated muscle and brain in fed and 24-hour fasted rats, has been studied. Maximal activity has been found in liver, with only fractional activity in the other tissues. 24 hour fasting induced significant decrease in liver and adipose tissue activity, while no changes have been detected in the other tissues. The possible implications of these facts are discussed.     

Mitochondrial network of skeletal muscle fiber

Highly specialized muscle fibers require a unique spatial organization of the mitochondrial network. Mitochondrial morphology is largely determined by the fusion and fission of these organelles. This review summarizes the current concepts of mitochondrial dynamics mechanisms and structural features of the mitochondrial network in striated muscle tissue. The role of mitochondria and their dynamics in muscle fiber physiology are also discussed.     

The transformational potential of striated muscle in hydromedusae.

Isolated striated muscle tissue of the Anthomedusa Podocoryne carnea participates in the regeneration of a functional manubrium (the feeding organ of medusae) when it is combined homoclonally with endodermal cells of the medusa umbrella. The morphogenetic potential of striated muscle cells in this regeneration process was evaluated by combining nuclear labeled striated muscle cells with some unlabeled endoderm cells. Histological and autoradiographical results demonstrate that transformation of striated muscle cells into smooth muscle cells of the ectoderm and also into endoderm cells must have occurred in the regenerate. The potential for cell transformation of isolated striated muscle cells of Podocoryne carnea is discussed and it is postulated that under appropriate conditions all cell types necessary for the regeneration of a manubrium can be formed from striated muscle cells.     

The mammalian testicular capsule and its muscle elements

This study of the testicular capsule of rat, dog, cat and human has confirmed the presence of three layers, viz., the tunica vaginalis, the tunica albuginea proper and an innermost tunica vasculosa. Smooth muscle cells are present in the tunica albuginea of all four species and are more prominent at the posterior pole of the testis where the capsule merges with the mediastinum testis. In the rat and the dog, a few striated muscle fibers also are present. While the tunica albuginea is to be considered as a dense connective tissue, the arrangement of the collagen bundles and the presence of a relatively high content of elastic fibers probably permits changes in size of the testis following spontaneous contractions of the muscle elements, which are known to occur. The role of the testicular capsule in sperm transport is discussed in relation to other factors, the spontaneous contractions of the capsule presumably having a “pumping” action and aiding the movement of non-motile spermatozoa from the testis to the epididymis. The presence of striated muscle fibers in two species is of interest and, while these may function in a similar manner to the smooth muscle, they may represent simply an unusual differentiation of embryonic myoblasts.     

肌细胞发育过程中间隙连接的变化

The appearance and changes of gap junctions during the development of striated muscle cells of Cynops orientalis have been studied by paraffin section, ultrathin-section and freeze-etching techniques. Gap junctions first appear between the somitic mesoderm cells in the late gastrula. A marked increase of the number of gap junctions occurs at the end of gastrulation. The number of gap junctions remains at a high level from neural plate stage up to nasal pit stage. After the stage of muscle contraction, the number of gap junctions decreases. Gap junctions do not disappear until muscle cells have attained their final differentiation and neuromuscular junctions have fully developed. The changes of size of gap junctions parallel with the changes in number. In addition, the number and size of gap junctions are both at the high level before cell fusion. Therefore, it is possible to conclude that cell communication is closely correlated with the development of striated muscle cells. The role of communications in cell determination and differentiation and in cell fusion of muscle cells are discussed.     

Muscle development in squid: Ultrastructural differentiation of a specialized muscle fiber type

The ultrastructural differentiation of two muscle fiber types of the squid Sepioteuthis lessoniana was correlated with development of prey-capture behavior. Transmission electron microscopy was used to document the differentiation of the fast-contracting cross-striated muscle cells of the tentacles and the obliquely striated muscle cells of the arms of specimens sampled at one week intervals from hatching to 5 weeks. By using high-speed video recordings, the ultrastructural differentiation was correlated with changes in prey-capture behavior that occur during development and growth. The ultrastructural analysis focused on the muscle cells of the transverse muscle of the tentacles and the transverse muscle of the arms. For the first 2 weeks after hatching, the tentacle transverse muscle fibers do not show the adult ultrastructure and are indistinguishable from the obliquely striated fibers of the transverse muscle of the arms. Transverse striation of the tentacle muscle cells appears at approximately three weeks and adult ultrastructure is present by 4–5 weeks after hatching. The high-speed video recordings show correlated behavioral changes. During the first 2–3 weeks after hatching, the animals use a different prey-capture mode from the adults; they jet forward and capture the prey with splayed arms and tentacles rather than employing the rapid tentacular strike. © 1996 Wiley-Liss, Inc.