Cardiac muscle

Summary The ultrastructure of chicken and frog cardiac muscle are compared and then contrasted with the ultrastructure of mammalian cardiac muscle. Both chicken and frog cardiac muscle have no transverse tubules, remarkably few nexuses and no prominent M-lines. M-fibers of both animals are small (2–5 ) in diameter and contain dense granules. Chicken cardiac muscle like mammalian cardiac muscle has very well developed sarcoplasmic reticulum and couplings. The latter do not occur in frog cardiac muscle and the former is poorly developed in that muscle. Morphologic evidence is presented in the frog and chicken heart that would tend to attribute to the sarcoplasmic reticulum a transport function for electron-dense material (presumably proteinaceous) the possible significance of which is discussed. Purkinje fibers were identified in the form of a network on the endocardial surface of both atria and ventricles of chicken hearts. The topography of these fibers corresponds to that of a population of fibers in small mammalian hearts that, and unlike ventricular fibers in those animals, does not have transverse tubules.This investigation was presented, in part, at the 2nd Annual Summer Workshop of the Council on Basic Science of the American Heart Association in Mountain View, California, August 5–8, 1968; at the Gordon Conference on Myocardial Contractility in Holderness, New Hampshire, August 12–16, 1968; and at the 8th Annual Meeting of the American Society for Cell Biology in Boston, Massachusetts, November 11–13, 1968. This research was supported by grant No. 66737 from the American Heart Association, Inc. and by grant No. HE 08620 from the NIH.     

Fine structure of the autonomic nerves of the rabbit myometrium

Summary The fine structure of the preterminal nerve fibers of the rabbit myometrial smooth muscle was studied using potassium permanganate fixation or glutaraldehyde fixation with postosmification. The preterminal fibers were mostly formed by 2–10 axons enveloped by Schwann cells. Two kinds of axons and axon terminals were found. (1) Adrenergic axons, which contained many small, granular vesicles (diameter 300–600 Å) and large granular vesicles (diameter 700–1200 Å) which represented ca. 2% of the total count of the vesicles. (2) Nonadrenergic axons, which contained small agranular vesicles (diameter 300–600 Å) and large granular vesicles (diameter 700–1200 Å). Both types of axons formed preterminal varicosities along their course. The real terminal varicosities, representing the anatomical end of the axons, were usually larger than the preterminal ones and showed close contact to the plasma membranes of the smooth muscle cells. Both adrenergic and nonadrenergic terminals were found close to the smooth muscle cells, but a gap of at least 2000 Å was always present between the two cell membranes. The axons and preterminal varicosities of both types of nerves were in intimate contact with each other within the preterminal nerve fiber. Axo-axonal interactions between the two types of axons are possible in the rabbit myometrium. The relative proportion of the nonadrenergic axons from the total was about one fourth.     

A comparative study on sub-filament organization in primary myofilaments of basalar direct flight and tibial extensor muscles of the lepidopteran,Achalarus lyciades

Summary Primary myofilaments of direct flight muscle fibers are hexagonally arranged, are surrounded by six secondary myofilaments, and are composed of two sub-unit-fibrils, 90–120 Å in diameter, at mid-sarcomere levels. Primary myofilaments are resolvable into electron-densities 15–25 Å in diameter, which number 3–4 in each sub-fibril at mid-sarcomere levels, and number 6–8 elsewhere. Primary myofilaments of tibial extensor muscle are not found in hexagonal arrays, are surrounded by 10–12 secondary myofilaments, and are resolvable into electron densities which are 15–25 Å in diameter similar to primary myofilaments of basalar flight muscle. However, a binary sub-fibril structure at mid-sarcomere levels is lacking in tibial extensor muscle fibers.The functional significance of the two-sub-fibril organization of myofilaments at midsarcomere levels in basalar direct flight muscle is not known, but may be related to the high rate of excitation-contraction cycles in these muscles.Supported by U.S.P.H.S. No. NB-06285. — The author wishes to express his grateful appreciation for the technical assistance given by Mrs. Ann Florendo during the course of this investigation.     

Muscle remodeling in adult snapping shrimps via fast-fiber degeneration and slow-fiber genesis and transformation

Bilateral asymmetry of the paired snapper/pincer claws may be reversed in adult snapping shrimps (Alpheus heterochelis). Removal of the snapper claw triggers transformation of the contralateral pincer claw into a snapper and the regeneration of a new pincer claw at the old snapper site. During this process the pincer closer muscle is remodeled to a snapper-type, and these alterations have been examined with the electron microscope. There is selective death of the central band of fast fibers, accompanied by an accumulation of electron-dense crysttaline bodies in the degenerating fibers. Two principal types of hemocytes (amebocytes and coagulocytes) invade the area and the degenerating muscle fibers. New myotubes also appear in this central site. The myotubes are characterized by a prolific network of presumptive sarcoplasmic reticulum and transverse tubules, nascent myofibrils, and crystalline bodies. The myotubes are innervated by many motor nerve terminals, and they subsequently differentiate into long-sarcomere (8–12 m), slow muscle fibers. Remodeling of the central band, therefore, occurs by degeneration of the fast fibers and their replacement by new slow fibers. Remnants of the degenerating fast fibers act as scaffolding for the myotubes which originate from adjacent satellite cells. The crystalline bodies may represent protein stores from the degeneration of the fast fibers, recycled for use in the genesis of new fibers. The invading hemocytes appear to play several roles, initially phagocytosing the fast muscle fibers, transporting the crystalline bodies into the new myotubes, and acting as stem cells for the new muscle fibers. Apart from the central band of fibers, the remaining pincer-type slow fibers with sarcomere lengths of 5–7 m are transformed via sarcomere lengthening into snapper-type slow fibers with sarcomere lengths of 7–12 m. Thus, during claw transformation in adult snapping shrimps, the pincer closer muscle is remodeled into a snapper closer muscle by selective death of the fast-fiber band, replacement of the fast-fiber band by new slow fibers, and transformation of the existing slow fibers to an even-slower variety. Note. This paper is dedicated to the fond memory of Professor M.S. Laverack whose enjoyment of biological research and gentle encouragement of such endeavours touched all those who knew him.     

The fine structure of neuromuscular junctions and contact zones between body wall muscle cells of Ascaris lumbricoides (var. suum)

Summary Neuromuscular junctions and close membrane apposition between body wall muscle cells of Ascaris lumbricoides (var. suum) have been examined with the light and electron microscopes. It was found that the body wall muscle cells send out elongate processes from their basal, myofibril containing portion to terminate on dorsal and ventral nerves. When observed with the aid of the electron microscope the neuromuscular junctions were seen to consist of several muscle cell processes in apposition to a single axon. The intersynaptic cleft was approximately 350–500 Å wide. Both the axolemma and sarcolemma were triple layered membranes which were 75–80 Å thick. Electron dense patches were observed at intervals on the apposed membranes which were due to increased thickness of the inner membrane leaflets of axolemma and sarcolemma. Muscle cell membranes, at the level of the neuromuscular junction, were in close apposition resulting in an apparently five-layered membrane complex which was 170–210 Å thick. The sarcolemmata in these regions were separated by 10–50 Å. Presynaptic axons contained mitochondria, microtubules which were 180–270 Å in diameter, and two, morphologically distinct types and sizes of synaptic vesicles. One was 200–600 Å in diameter, with a single, triple-layered membrane bounding a center of low electron density. The other was 600–1200 Å in diameter, with a single, triple-layered membrane bounding a central, electron dense granule of 500–800 Å size.The functional significances of the close membrane appositions between body wall muscle cells and of the two types of synaptic vesicles found at the neuromuscular junctions of Ascaris lumbricoides were discussed with respect to their possible role in neuromuscular physiology.Supported by U.S.P.H.S. Grant No. NB-01528 and Research Career Development Award No. 9-K3-NB-15255. — The author wishes to express his grateful appreciation for the excellent technical assistance given by Miss Gabrielle Rouiller during the course of this investigation.     

Chromosome fibers studied by a spreading technique

Chromosomes and interphase nuclei can be spread on the surface of water in a simplified Langmuir trough. Interphase nuclei of Triturus erythrocytes display fibers with a diameter of about 250–300 Å. Very similar fibers are seen in metaphase chromosomes of cultured human cells. Fibers from grasshopper spermatocyte chromosomes (prophase) are more variable in diameter, and many fibers thinner than 200 Å extend laterally from the chromosome. In the grasshopper spermatocyte, fibers align in parallel to form plates. It is suggested that the 250–300 Å fibers may represent an inactive state of the chromosome material, and that only the thinner fibers are involved in RNA synthesis. The 250–300 Å fibers may result from the folding or coiling of a thinner fiber having the approximate dimensions of the nucleohistone molecule.     

Selenium deficiency in Crustacea

Summary The effect of selenium deprivation onDaphnia magna was examined under controlled rearing conditions in a synthetic culture medium. After three generations, fertility was significantly reduced in deprived (Se^–) animals. Growth and mortality of parent daphnids and development of parthenogenetic eggs were not affected during this period. In the fourth generation Se^– daphnids rejected parts of their second antennae. At the ultrastructural level antennal muscle tissue was severely affected. Animals deprived of selenium had mitochondria and sarcoplasmic reticulum with myelin-like alterations. Giant lysosomes were present and complete lysis of muscle fibrils was observed in antennal muscle cells. These alterations are characteristic features of peroxidic damage in tissues. This interpretation is consistent with the function of selenium as a constituent of the enzyme glutathione peroxidase which protects cells from peroxidation. Selenium should be included in synthetic culture media for daphnids.Abbreviations GSH-Px selenium dependent glutathione peroxidase - Se⁺/Se^– selenium supplemented (control)/selenium deprived animals - SOD Superoxide dismutase - SR sarcoplasmic reticulum     

A COMPARATIVE STUDY ON THE FINE STRUCTURE OF THE BASALAR MUSCLE OF THE WING AND THE TIBIAL EXTENSOR MUSCLE OF THE LEG OF THE LEPIDOPTERAN ACHALARUS LYCIADES

Basalar and tibial extensor muscle fibers of Achalarus lyciades were examined with light and electron microscopes. Basalar muscle fibers are 100–150 µ in diameter. T-system membranes and sarcoplasmic reticulum make triadic contacts midway between Z lines and the middle of each sarcomere. The sarcoplasmic reticulum is characterized by a transverse element situated among myofilaments halfway between Z lines in every sarcomere. The morphology of Z lines, hexagonal packing of thin and thick myofilaments, and thin/thick myofilament ratios are similar to those of fast-acting insect muscles. Tibial extensor muscle fibers are 50–100 µ in diameter. Except for a lack of the transverse element, the T system and sarcoplasmic reticulum are similar to those of basalar muscle. Wavy Z lines, lack of a hexagonal packing of myofilaments, and larger thin/thick myofilament ratios are similar to those of other postural muscles of insects. The morphology of basalar and tibial extensor muscle is compared to that of other insect muscle with known functions, and reference is made to the possible contribution of the transverse element of sarcoplasmic reticulum in basalar flight muscle to speed and synchrony in this muscle.     

Electron microscopical observation of polyglucose synthesized from glucose-1-phosphate by the phosphorylase activity in rat skeletal muscles

Summary An improved demonstration of polyglucose synthesized histochemically from glucose-1-phosphate by the phosphorylase activity in rat skeletal muscle was made by use of electron histochemical techniques.New polyglucose was found in the sarcoplasmic matrix among various organelles in muscle fibers embedded with epoxy resin. This polyglucose stained less densely with lead, forming amorphous aggregates or finer particulates with 100 to 150 Å in diameter, different from native glycogen which was separately observed in the same section.     

SPECIFIC GRANULES IN ATRIAL MUSCLE CELLS

Large populations (up to 600/cell) of spherical, electron-opaque granules ~0.3 to 0.4 µ in diameter are characteristically found in muscle fibers of mammalian atria. They are absent in muscle fibers of the ventricles. The granules are concentrated in the sarcoplasmic core and occur in lesser numbers in the sarcoplasmic layers between myofibrils and under the plasma membrane. Their intimate association with a central voluminous Golgi complex and the frequent occurrence of material reminiscent of the granular content within the cisternae of the Golgi complex suggest that the latter is involved in the formation of the atrial granules. Atrial granules are larger and more numerous in smaller species (rat, mouse), and generally smaller and less numerous in larger mammals (dog, cat, human); they are absent from the atrial fibers of very young fetuses (rat) but are present in those of newborn animals. A small population of bodies containing glycogen particles and remnants of the endoplasmic reticulum and mitochondria occurs in the sarcoplasmic cores of atrial as well as ventricular muscle fibers in the rat; they contain acid phosphatase and thus appear to be residual bodies of autolytic foci. Their frequency increases with the age of the animal. Typical lipofuscin pigment granules, which are known to contain acid phosphatase and are found in the sarcoplasmic cores in old animals (cat, dog and human), are presumed to arise by progressive aggregation and fusion of small residual bodies.     

Excitation-calcium release uncoupling in aged single human skeletal muscle fibers

The biological mechanisms underlying decline in muscle power and fatigue with age are not completely understood. The contribution of alterations in the excitation-calcium release coupling in single muscle fibers was explored in this work. Single muscle fibers were voltage-clamped using the double Vaseline gap technique. The samples were obtained by needle biopsy of the vastus lateralis (quadriceps) from 9 young (25–35 years; 25.9 ± 9.1; 5 female and 4 male) and 11 old subjects (65–75 years; 70.5 ± 2.3; 6 f, 5 m). Data were obtained from 36 and 39 fibers from young and old subjects, respectively. Subjects included in this study had similar physical activity. Denervated and slow-twitch muscle fibers were excluded from this study. A significant reduction of maximum charge movement (Q_max) and DHP-sensitive Ca current were recorded in muscle fibers from the 65–75 group. Q_max values were 7.6 ± 0.9 and 3.2 ± 0.3 nC/F for young and old muscle fibers, respectively (P < 0.01). No evidences of charge inactivation or interconversion (charge 1 to charge 2) were found. The peak Ca current was (–)4.7 ± 0.08 and (–)2.15 ± 0.11 A/F for young and old fibers, respectively (P < 0.01). The peak calcium transient studied with mag-fura-2 (400 m) was 6.3 ± 0.4 m and 4.2 ± 0.3 m for young and old muscle fibers, respectively. Caffeine (0.5 mm) induced potentiation of the peak calcium transient in both groups. The decrease in the voltage-/ Ca-dependent Ca release ratio in old fibers (0.18 ± 0.02) compared to young fibers (0.47 ± 0.03) (P < 0.01), was recorded in the absence of sarcoplasmic reticulum calcium depletion. These data support a significant reduction of the amount of Ca available for triggering mechanical responses in aged skeletal muscle and, the reduction of Ca release is due to DHPR-ryanodine receptor uncoupling in fast-twitch fibers. These alterations can account, at least partially for the skeletal muscle function impairment associated with aging.This work was supported by Grant-in-Aid from the American Heart Association (National) and Muscular Dystrophy Association, and National Institutes of Health (2-P60AG18484-06)     

Effect of chronic hypoxia on the capillarity of dog skeletal muscle

Capillarity and fiber composition were studied by the ATPase technique in frozen samples of sternothyroid muscle of dogs from sea level (SL) and high altitude (3,300–4,300 m) (HA). Capillary density (CD), capillary to fiber ratio (C:F) and fiber cross sectional area (FCSA) were measured. The mean CD was 791/mm² at SL and 743/mm² at HA. CD was linearly related to FCSA in the SL animals (CD=1112.8–0.10 FCSA; r=–0.63). In both SL and HA animals, C:F was linearly and positively correlated with FCSA. There was no significant difference between the two regression lines; therefore, only one line represents all the data (C:F=0.78+(5.19×10^–4) FCSA; r=0.77). Thus, at a given FCSA the C:F was the same for SL and HA dogs. Two types of fibers were identified: type I (slow twitch) (42%) and type II (fast twitch) (58%). No differences in fiber composition or FCSA were observed between the SL and HA dogs. These results indicate that moderate levels of hypoxia do not affect the capillarity of dog skeletal muscle.     

Ultrastructure of the human chromosome fiber

Summary Human chromosomes and their fibers were studied by electron microscopy as whole mounts in metaphase and interphase after surface spreading and critical point drying and as thin sections after fixation and embedding. Chromosomes and interphase nuclei were composed of irregularly coiled fibers measuring about 200 to 300 Å in width. Thinner and straighter chromosome fibers were produced by stretching or NaCl extraction. Thin sections of metaphase chromosomes showed 200 Å wide granular outlines containing regularly coiled 70–80 Å wide fibrils. These smaller substructures appeared hollow with a 20 Å thick electron dense wall. The possible arrangement of the DNA molecule as a tertiary coil in the chromosome fiber of living cells is suggested.

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Zusammenfassung Menschliche Chromosomen und-Fäden in Meta- und Interphase wurden als Totalpräparate nach Oberflächenspreitung und Kritischer-Punkt-Trocknung und als Dünnschnitte nach Fixierung und Einbettung mit dem Elektronenmikroskop untersucht. Metaphase-Chromosomen und Interphase-Kerne fanden sich als aus unregelmäßig gewundenen Fäden von 200–300 Å Dicke bestehend. Durch Dehnung und NaCl-Extraktion wurden diese Chromosomenfäden dünner und gerader. Dünnschnitte der Metaphase-Chromosomen zeigten 200 Å breite granuläre Fadenkonturen, die regelmäßig gewundene, spiralig angeordnete 70–80 Å breite Fibrillen enthielten. Diese fibrillären Unterstrukturen erschienen hohl mit einer 20 Å dicken elektronendichten Wand. Die mögliche Anordnung des DNA-Moleküls als Tertiärschraube im Chromosomenfaden lebender Zellen wird diskutiert.

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Supported by a grant (La 185/3) of the Deutsche Forschungsgemeinschaft.     

Cell contacts and smooth muscle bundle formation in tissue transplants into the anterior eye chamber

Summary Segments of the taenia coli from guinea-pig were transplanted into the anterior chamber of the eye. Depending on such factors as the total volume of the transplant and the presence or absence of ganglion cells degeneration was either very extensive (90% or more of the total number of muscle cells) or localized (alternating regions of degenerating and normal structure). During days 1–2 muscle cells lost their plasma membranes so that their cytoplasmic contents were dispersed into the intercellular spaces. Many cells produced numerous small processes which were pinched off and dispersed in a similar manner. Following a period of intense mitotic activity (3–8 days) numerous cells with the characteristics of embryonic smooth muscle cells were evident. Within 10–14 days these differentiating cells produced bulbous protrusions and assumed more irregular outlines than at 3–8 days. The protrusions formed close contacts (50–100Å intercellular space) and tight junctions between adjacent muscle cells. Aggregation of muscle cells into bundles was under way between 14–28 days. At approximately 4–6 weeks these developing muscle groups were invaded by nerve fiber bundles. The pattern of the innervation and the form and size of the muscle bundles simulated the normal. These findings are discussed in relation to the possible functions of the intercellular contacts and cellular protrusions which characterise various periods of regeneration.This work was supported by the Australian Research Grants Committee. The transplants were carried out by Dr. T. Malmfors assistant, Miss Ulla Enberg.     

Ultrastructural comparison of smooth muscle from ovarian follicle and oviduct of the golden hamster

Summary Ultrastructural characteristics of smooth muscle taken from ovarian follicles and oviducts of hamsters are compared. Differences between the two muscle types are more quantitative than qualitative, thus confirming that follicular muscle is a true smooth muscle with no unique characteristics. While both muscle types contain 50–80 Å filaments, -glycogen deposits, and organelles characteristically found in smooth muscle, the oviductal cells have substantially more sacs, tubular structures, sarcoplasmic reticulum, and mitochondria. Another difference concerns the cellular junctions; the oviductal cells exhibit nexuses, whereas the follicular cells show desmosomelike junctions. Based on ultrastructural differences, follicular smooth muscle seems to be a relatively toneless muscle suited for short, infrequent contractions, whereas oviductal smooth muscle is probably involved in more active tonic contractions.Supported by an Institutional Research Grant from Texas Women's University, by NIH Grant HD 12988, and by the Department of Anatomy at Wright State University     

A quantitative electron histochemical estimation of ruthenium red binding to heparin in mast cell granules

Summary Mast cell granules were shown to contain an apparently branched meshwork of fibers, which had a diameter of about 240 Å and a denser core of about 20–30 Å. Mast cell granules from rats were found to have a median weight of 39×10^–14 g after critical-point drying. Their dry mass increased 23% when stained with ruthenium red at pH 5.0. The staining reaction was found to be stoichiometric, and the bulk of the stain appeared to be taken up by heparin in a molar relationship of one ruthenium red cationic complex per sulfate group of heparin. The uptake of the stain was largely localized to the cores of the granule fibers, which after staining appeared double contoured. These findings suggest that mast cell heparin is integrated into the fibrous structure of the mast cell granules.This project was supported in part by Grant No. P-259-H from the American Cancer Society.The opinions or assertions contained herein are the private views of the author and are not to be construed as official or as reflecting the views of the Department of the Army or the Department of Defense.     

The fine structure of muscle in a marine turbellarian

Summary The fine structure of the myofibers of Notoplana acticola as studied by electron microscopy indicates that they are composed of thick myofilaments about 200 Å wide with tapering ends and thin myofilaments about 50 Å wide, arranged alongside each other parallel to the long axis of the cell. There is no orderly transverse arrangement of filaments; instead they appear staggered in the fiber. In cross sections 6 to 10 thin filaments form an orbit around one thick filament with possible cross-linkage between the two types of filaments.Dense bodies are associated with the sarcolemma and with the sarcoplasmic reticulum, and appear to serve as attachments for the thin filaments. Dense bodies are compared to elements forming a fragmented Z-disc.Mitochondria, situated in the periphery or the center of fibers, are associated with granules interpreted as glycogen.The sarcoplasmic reticulum consists of: sacs or cisternae in close proximity to the sarcolemma, longitudinal tubular elements between and parallel to the myofilaments, and a tubular network around the filaments. There is no well-defined sarcolemmal-derived transverse tubule system as described in striated muscles. It is hypothesized that in these muscles, the functional equivalent of the T system may be the area of sarcolemma in contact with the cisternae of the sarcoplasmic reticulum.This work was supported by Grant No. GM 10292 from the U. S. Public Health Service to Professor Richard M. Eakin, Department of Zoology at the University of California, Berkeley, USA, where this investigation was conducted during the author's sabbatical leave of absence from the University of Illinois.I wish to thank Professor Eakin for valuable discussions and for his kind hospitality in extending the facilities of his laboratory and the use of the electron microscope to me, and the John Simon Guggenheim Memorial Foundation for the Fellowship which I held during 1964–65.     

Molecular Mechanisms of Regulation of the Activity of Sarcoplasmic Reticulum Ca-Release Channels (Ryanodine Receptors), Muscle Fatigue, and Severin''s Phenomenon

In this short review of the literature and our own data the characteristics of structural organization of sarcoplasmic reticulum Ca-release channels (ryanodine receptors) in different types of muscles, the participation of other sarcoplasmic reticulum proteins in excitation–contraction coupling and Ca-release channel operation, and the regulation of the channel activity by endogenous low molecular weight compounds are analyzed. Special attention is given to changes that occur in muscle cells during exhausting work and to the role of sarcoplasmic reticulum Ca-release channels in the loss of muscle contractile activity during the development of fatigue. It is concluded that the protection of muscle fibers against fatigue in the presence of the histidine-containing dipeptide carnosine, called in the literature Severin's phenomenon, is primarily connected with modulation of sarcoplasmic reticulum Ca-release channel activity by carnosine.     

Vesicle and granule content of sympathetic ganglion cells during limb regeneration of the newt Triturus

Summary Fine structural observations were made on the vesicle and granule content of ganglion cells in the posterior subclavian ganglion and peripheral nerve fibers of the upper forelimb of the newt Triturus. The populations of vesicles and granules in normal ganglion cells and nerve fibers were compared with those observed after limb transection. In normal neurons, clear vesicles range in size from 250 to 1000 Å in diameter, but are most frequently 400–500 Å. Vesicles with dense contents (granules) also vary greatly in size, but most are 450–550 Å in diameter and correspond to dense-core vesicles. Large granules that contain acid phosphatase activity are thought to be lysosomes. During limb regeneration, in both the ganglion cells and peripheral nerves, the ratio of dense vesicles to clear vesicles increases. There is a large increase in number of dense granules with a diameter over 800 Å, particularly in the peripheral regenerating fibers. This study shows that regenerating neurons differ from normal in their content of vesicular structures, especially large, membrane-bounded granules.This work was supported by grants from the National Science Foundation (GB 7912) and from the National Cancer Institute (TICA-5055), National Institutes of Health, United States Public Health Service.     

Weitere Untersuchungen zur Feinstruktur und Innervation des Pinealorgans von Passer domesticus L.

Zusammenfassung Im Parenchym der Epiphysis cerebri von Passer domesticus kommen Nervenzellen vor. Ihre Neuriten ziehen im langgestreckten Epiphysenstiel zur Commissura habenularum. Im proximalen Endabschnitt des Epiphysenstiels wird ein Teil dieser Fasern myelinisiert. Zwischen die Nervenfasern schieben sich zahlreiche Pinealocytenausläufer; synaptische Bänder helfen die letzteren eindeutig zu identifizieren. Im Bereich der synaptischen Bänder liegen: 1. 300 Å Vesikel, 2. 300 Å Vesikel und 800–1200 Å Granula, 3. nur 800–1200 Å große granulierte Vesikel. Die Tatsache, daß in Pinealocytenausläufern nebeneinander synaptische Bänder und Granula vorkommen, und daß apikal in zilientragenden Zellen ebenfalls Granula nachweisbar sind, spricht dafür, daß bei Passer domesticus ein Pinealzelltyp sensorische und sekretorische Strukturmerkmale besitzen kann. Außerdem werden Kontaktsynapsen beobachtet; ihre praesynaptischen Fasern enthalten die gleichen Strukturelemente wie die Fasern mit synaptischen Bändern. Die Zahl der Mikrofibrillen und Mikrotubuli variiert in den Pinealocytenausläufern, in den postsynaptischen Dendriten und in den Neuriten so stark, daß es mitunter schwierig ist, diese Fortsatztypen einwandfrei zu unterscheiden und die Zahl der zum Gehirn ziehenden Neuriten exakt zu ermitteln.Efferente sympathische Nervenfasern dringen in die Bindegewebssepten der Epiphyse ein. Sie enthalten Granula mit einem Durchmesser von 300–500 Å und 800–1200 Å. Nach Injektion von Nialamid zeigen beide Granulatypen einen elektronendichten Kern. Mikrospektrographisch ist Serotonin und Noradrenalin in diesen Nervenfasern nachweisbar. Das Material dieser Studie enthält keinen fluoreszenzmikroskopischen oder elektronenmikroskopischen Hinweis darauf, daß die sympathischen Nervenfasern durch die Basalmembran in den Zellverband des Epiphysenparenchyms eintreten. Im elektronenmikroskopischen Bild haben manche Pinealocytenausläufer eine Ähnlichkeit mit autonomen Nervenfasern.Die funktionelle Bedeutung der Vogelepiphyse als photo-neuro-endokrines Organ wird diskutiert.

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Further investigations on the structure and innervation of the pineal organ of Passer domesticus L.

Summary The pineal organ of Passer domesticus contains nerve cells within its parenchyma. Axons of the nerve cells run within the elongated stalk of the pineal organ to the habenular commissure. At the proximal end of the stalk, some axons become myelinated. In the stalk, the axons intermingle with pinealocyte processes containing synaptic ribbons. The synaptic ribbons are in contact with (1) vesicles with a diameter of 300 Å; (2) 300 Å diameter vesicles and 800–1,200 Å diameter dense-core granules; or (3) the dense-core granules only. Dense-core granules are also present in pinealocytes with 9+0 type cilia. These results suggest that sensory and secretory structures are present in the same pineal cell type. Furthermore, conventional synapses are present between receptor and nerve cells: The presynaptic fibers have the same structure as the fibers containing synaptic ribbons. The numbers of microfibrils and microtubules vary among postsynaptic fibers (dendrites), the pinealocyte processes, and the neurites. Thus it is difficult to obtain an exact count of the number of axons running to the brain.Efferent sympathetic nerve fibers enter the pineal organ associated with the connective tissue surrounding blood vessels. The fibers show granules of 300–500 Å diameter or 800–1,200 Å diameter. After nialamide injection, both types of granules contain a dense core. Microspectrographically serotonin and noradrenaline are demonstrated in the sympathetic nerve fibers. There is no evidence found in the material of this study to suggest that sympathetic nerve fibers perforate the basement membrane and enter the parenchymal cell complexes of the pineal organ. Pinealocyte processes and sympathetic nerve fibers often show a very similar ultrastructural pattern.The role of the avian pineal organ in photo-neuro-endocrine regulation is discussed.

Mit Unterstützung durch die Deutsche Forschungsgemeinschaft.