Microscopic anatomy of the thin-walled vessels leaving the heart of the lobster Homarus americanus: anterior lateral arteries

Abstract. The anterior lateral arteries are paired vessels leaving the anterior end of the lobster ( Homarus americanus ) heart and proceeding to the antennae and eyestalks, the stomach and hepatopancreas, the gonads, and the thoracic and branchial muscles. These vessels have a trilaminar organization, consisting of a tunica interna with elastic fibrils, a tunica intermedia represented by a bilayered cell mass, and a tunica externa with collagen fibrils. In the tunica intermedia, cells flanking the tunica interna (light cells) show less affinity for basic dyes and electron stains than those flanking the tunica externa (dark cells). Each light cell exhibits an irregularly shaped stress fiber (a bundle of closely packed microfilaments) in the region adjoining the tunica interna. Collectively, these bundles have a circumferential or slightly oblique orientation relative to the lumen of the vessel. The role of the stress fibers is unresolved. If they are static structures, they might contribute to the non-linear elasticity shown by lobster arteries. If they generate force, and small bundles of microfilaments do diverge from the stress fibers to enter filamentous mats applied to the plasmalemmata, a coordinated contraction of the cells might reduce the luminal diameter and, thus, retard the flow of hemolymph. Coordination of contraction would have to occur in the absence of nerves and without the benefit of communicating (gap) junctions between the light and dark cells.     

Ultrastructural analysis of the apical ectodermal ridge during vertebrate limb morphogenesis: I. The human forelimb with special reference to gap junctions

The fine structure of the human forelimb apical ectodermal ridge of stages 12–19 was examined using techniques of transmission electron microscopy, freeze fracture, and scanning electron microscopy. This paper reports the presence of subcellular structures that distinguish the inductively active apical ectoderm from adjacent dorsal and ventral ectoderms.The apex of the human forelimb begins development with an epithelium of two cell layers (stage 12) which thickens at the distal tip during stages 13 and 14 into a multilayered apical ectodermal ridge. During this transition we have observed that the basal lamina differentiates from a bilayered structure to the definitive single lamina. Some cells in the ectoderm become detached from the basal lamina as stratification begins. At the same time these cells show increased mitotic activity and the developing ridge cells acquire gap junctions. Annular gap junctions are also observed. Gap junctions are not observed in adjacent, presumably noninductive, epithelia. Finally, the ridge cells next to the basal lamina acquire bundles of microfilaments that are oriented in the dorsal-ventral plane in the basal cytoplasm of the cells.The apical ridge reaches its greatest dimensions during stage 15. The number and peripheral extent of gap junctions also appear to be greatest at this same time. At stage 17, cells within the ridge begin to die, and other ridge cells engulf them. By stage 19, gap junctions in the apical epithelium are sparse and are of lesser diameter than in the definitive ridge. In addition, the oriented bundles of microfilaments present at stages 14–17 are absent. Thus, at stage 19 a morphologically distinct apical ectodermal ridge is no longer present. The apex of the limb is covered by two cell layers typical of human embryonic epidermis.     

Electron microscopic observations on the formation of elastic fibres in cultures of aortic medial cells and adventitial cells

The formation of elastic fibres was observed in the cultured cells derived from the tunica media and the tunica adventitia of mouse aorta. Bundles of myofilaments with dense bodies were abundantly observed in the cytoplasm of the cultured medial cells, and numerous bundles of microfibrillar components were present in the intercellular spaces. Fine granules of approximately 50 nm in diameter were observed in the bundles of microfibrillar components. It was supposed that these fine granules of elastin fused with each other and formed elastic aggregates and then formed large elastic clumps. Numerous bundles of microfibrillar components were also present in the intercellular spaces of the cultured adventitial cells. Elastic aggregates were scarcely observed in the bundles of microfibrillar components. However, large elastic clumps as observed in the medial cell culture could not be found in the adventitial cell culture. It is suggested that the formation of large elastic clumps might be related to the sheet structures or lamellae of elastic fibres in the tunica media.     

Ultrastructure and some other properties of inverted thyroid follicles in suspension culture

Separated thyroid follicles in suspension culture invert in 5% serum. In some, the inversion is not complete in that a small normal follicle persists completely in the interior of an inverted follicle. In inverted follicles the lumens are distended and electron lucent. The bounding epithelial cells are stretched, have relatively few microvilli on the surface toward the medium but they have bundles of oriented microfilaments usually located near the lumen. The cells are connected together by tight junctions. When inverted follicles are punctured, the lumen shrinks, the cells retract and become cuboidal and microvilli reappear. Microfilaments persist at the luminal surface but no longer in oriented bundles. No appreciable extracellular matrix is present at the basal cell surface in contact with the lumen, but matrix is occasionally observed between cells. Since bundles of microfilaments like stress fibers are observed in the cells in suspension culture, the presence of stress fibers in cells in monolayer culture is probably not dependent on attachment but might be a reflection of the spreading of the attached cells.     

Distribution of actin-filament bundles in myoid cells,Sertoli cells,and tunica albuginea of rat and mouse testes

Summary Frozen sections of the rat and mouse testes were stained with either FITC-phalloidin or NBD-phallacidin and viewed with conventional fluorescence and confocal laser microscopes in order to demonstrate the arrangment of actin-filament bundles in myoid cells, Sertoli cells and tunica albuginea. Myoid cells are rich in actin-filament bundles crossing at right angles. These bundles running in different directions can also be visualized by means of electron microscopy. Nerve fibers occur in the vicinity of myoid cells, suggesting a neural control of the cell. At Sertoli cell junctions actin filaments occur at the circumference of the cell, where they show a honeycomb pattern. The ratio of the number of Sertoli cells per myoid cell can be calculated by means of confocal microscopy; this technique may provide a new parameter for determining spermatogenic activity. In the tunica albuginea of the juvenile mouse testis, actin filaments are arranged in an alternate fashion.     

Organelle movement and fibrillar elements of the cytoskeleton in the angiosperm pollen tube

Summary Continuous observation of organelles and other cytoplasmic inclusions in the older stretches of living pollen tubes of Iris pseudacorus shows that in the more attentuated parts of the protoplast they move along single, mainly longitudinally oriented fibrils, corresponding to those previously isolated from other species and shown to contain bundles of uniformly polarised actin microfilaments. The traffic associated with each fibril is unidirectional, but organelles move along them independently, sometimes with conspicuously different velocities. Larger columns of cytoplasm passing along the tube are associated with several such fibrils, as revealed in occasional discontinuities and also in columns isolated from the tube in suitable medium without fixation. The dimensions of the individual fibrils suggest that the bundles of actin microfilaments are not likely to be enclosed in a unit membrane corresponding to a tonoplast. If so, the nature of the continuous cavities traversed by numerous fibrils in the older parts of the pollen tube requires reappraisal, since these are more likely to be volumes of attentuated cytoplasm comparable with that of the central cavity of the sieve tube than vacuoles of the normal plant-cell type.     

Extracellular and Intracellular Correlates of Organ Initiation in the Embryonic Chick Thyroid

Apical and basal bundles of microfilaments have been suggestedas intracellular structures which might cause cellular contractionsleading to bending movements during organogenesis. Microfilamentbundles may have a different role in some organ primordia. Theembryonic chick thyroid develops as an evagination of the pharyngealfloor at the level of the anterior attachment of the heart.The developing thyroid is confined to a pocket surrounded bythe developing aortic arches, ventral aorta, and truncus arteriosus.Initiation of thyroid evagination is accompanied by the formationof grooves as two concentric rings in the basal surface of theplacode near its margins. The cells surrounding the groovescontain longitudinally oriented bundles of microfilaments andmicrotubules. Other microfilament bundles are present at thecell apices and bases. The primordium almost doubles in volumeduring the period of evagination, but the area of pharyngealfloor that it occupies undergoes virtually no increase. A modelis presented which describes the role of microfilament bundlesduring thyroid evagination as stabilizing cellular dimensions.The bending movements are thought to result from cell elongation,increase in cell numbers, and confinement of the thyroid toa limited space by the developing truncus arteriosus and itsbranches.     

Tendon development requires regulation of cell condensation and cell shape via cadherin-11-mediated cell-cell junctions

The ability of tendon to transmit forces from muscle to bone is directly attributable to an extracellular matrix (ECM) containing parallel bundles of collagen fibrils. Although the biosynthesis of collagen is well characterized, how cells deposit the fibrils in regular parallel arrays is not understood. Here we show that cells in the tendon mesenchyme are nearly cylindrical and are aligned side by side and end to end along the proximal-distal axis of the limb. Using three-dimensional reconstruction electron microscopy, we show that the cells have deep channels in their plasma membranes and contain bundles of parallel fibrils that are contiguous from one cell to another along the tendon axis. A combination of electron microscopy, microarray analysis, and immunofluorescence suggested that the cells are held together by cadherin-11-containing cell-cell junctions. Using a combination of RNA interference and electron microscopy, we showed that knockdown of cadherin-11 resulted in cell separation, loss of plasma membrane channels, and misalignment of the collagen fibrils in the ECM. Our results show that tendon formation in the developing limb requires precise regulation of cell shape via cadherin-11-mediated cell-cell junctions and coaxial alignment of plasma membrane channels in longitudinally stacked cells.     

Occurrence of cell junctions and microfilaments in osteoblasts

Osteoblasts in the diaphysis of the tibia during endochondral ossification in young rats are attached to one another by nexus, by "adhaerens" junctions, and by simple appositions. "Adhaerens" junctions and nexus also occur between preosteoblasts and osteoblasts. Furthermore, to osteoblasts exhibit a network of microfilament bundles in the cell periphery overlying the osteoid. From this network bundles extend into the cell processes which protrude into the unmineralized matrix. The mean diameter of individual microfilaments is 5.9 +/- 0.06 nm. A possible role of nexus and microfilaments in controlled bone growth and differentiation is discussed.     

Organization of rat mesenteric artery after removal of cells or extracellular matrix components

Summary Rat mesenteric arteries, perfusion fixed in relaxed or contracted conditions, were digested with acid and elastase, bleach (sodium hypochlorite), or alkali to selectively remove collagen, elastin, or cells. Scanning electron microscopy was used to study the three-dimensional organization of the remaining cells or extracellular components. Smooth muscle cells of the tunica media were elongated and circumferentially oriented. Superior mesenteric artery cells had an irregular surface with numerous projections and some ends were forked. Small mesenteric artery cells were spindle shaped with longitudinal surface ridges, and showed extensive corrugations upon contraction. Elastin was present both as laminae and as an interconnected fibrous meshwork. Collagen was arranged in an irregular network of individual fibrils and small bundles of fibrils that formed nests around the cells in both arteries. This irregular arrangement persisted, with no apparent reordering or loss of order, upon contraction. The lack of an ordered arrangement or specialized organization at the cell ends suggests mechanical coupling of the cells to elastin or collagen throughout the length of the cell, allowing for force transmission in a number of directions. The tunica media is thus a composite material consisting of cells, elastin, and collagen. The isotropic network of fibers is well suited for transmitting the shearing forces placed on it by contraction of smooth muscle cells and by pressure-induced loading.     

Orientation of adhering junctions between bovine pulmonary fibroblasts

The ultrastructure and orientation of microfilament-attaching junctions between pulmonary fibroblasts (also known as myofibroblasts or contractile interstitial cells) of bovine lung septa were investigated by transmission electron microscopy. Adhering junctions similar to the fascia adherens of the intercalated disc, but of a macular design, link microfilament bundles of adjacent fibroblasts. The bundles of microfilaments joined by junctions were usually aligned perpendicularly to the axis of the alveolar wall. Gap junctions were located in close proximity to the adhering junctions, presumably to co-ordinate the contraction of the cells. The data indicate that fibroblasts are able to form multicellular contractile units within healthy, mature lung parenchyma.     

Response of actin microfilaments during phytochrome-controlled growth of maize seedlings

Summary In seedlings of maize (Zea mays L. cv. Percival), growth is controlled by the plant photoreceptor phytochrome. Whereas coleoptile growth is promoted by continuous far-red light, a dramatic block of mesocotyl elongation is observed. The response of the coleoptile is based entirely upon light-induced stimulation of cell elongation, whereas the response of the mesocotyl involves light-induced inhibition of cell elongation. The light response of actin microfilaments was followed over time in the epidermis by staining with fluorescence-labelled phalloidin. In contrast to the underlying tissue, epidermal cells are characterized by dense longitudinal bundles of microfilaments. These bundles become loosened during phases of rapid elongation (between 2–3 days in irradiated coleoptiles, between 5–6 days in dark-grown coleoptiles). The condensed bundles re-form when growth gradually ceases. The response of actin to light is fast. If etiolated mesocotyls are transferred to far-red light, condensation of microfilaments can be clearly seen 1 h after the onset of stimulation together with an almost complete block of mesocotyl elongation. The observations are discussed in relation to a possible role of actin microfilaments in the signal-dependent control of cell elongation.     

The autonomous innervation of the buffalo (Bubalus bubalis) testis. An immunohistochemical study

The innervation pattern in the buffalo testis was determined by using histochemical and immunohistochemical methods. Nerves were concentrated in the tunica albuginea and septula testis, and did not show an uniform distribution. The tunica albuginea at the lateral and medial sides and at the free border of the testis is most densely innervated than at the epididymal border. At the cranial pole thick nerve bundles were observed between albugineal vessels and muscle bundles. Rare parenchymal nerves were found in perivascular position between seminiferous tubules and their occurrence is confined to lobules at the cranial and caudal testicular poles. An intense NPY immunoreactivity occurred in nerve bundles and in solitary varicose fibres. Nerves were concentrated in the tunica albuginea at the lateral and medial side and at the free border of the testis, and in the lobules at the cranial and caudal testicular poles. Sub P immunoreactivity was occasionally detected in some thicker nerve bundles and solitary fibers, in the tunica albuginea and in the wall of blood vessels, showing a similar distribution but less intensity and density than NPY immunoreactivity. TH immunoreactivity stained nerve fibers in the buffalo testis with a distribution pattern similar to that obtained with general neuronal markers. The histochemical reaction for AchE was negative, so cholinergic fibers cannot be detected in the buffalo testis. The histochemical NADPHd reaction stained rare nitrergic nerve bundles and solitary fibers. The majority of NADPHd activity was confined to the vascular endothelium, and rarely to the interstitial Leydig cells, whereas the Sertoli and germ cells did not show any reaction.     

Cytoskeletal changes in the endothelial cells of the rat aorta in the early periods of postnatal ontogeny]

The cytoskeleton of endothelial cells is a modulator of all the cell reactions. The formation of a definitive structure of the bearing-contracting apparatus of the rat aorta endothelium is finished in the postnatal development (up to the age about 3 months after birth), passing through some qualitative changes. Using the transmission and scanning electron microscopy of detergent extracting preparations, the structuring pattern (saturation) of the aorta endothelial cell cytoskeleton of newborn animals. From 10 days to 1 month after birth, the most important period takes place within peripheral dense microfilament bundles are formed responsible for the cell monolayer integrity for the contractility of cell boundaries (it is most important in recombination of endothelial monolayer in the processes of cell proliferation and vessel growth) and also for the integrity of longitudinal bundles of microfilaments, i.e. fibres of tightening. The increase in anisotropy of cytoskeleton frame during its maturation evidences on the establishment of orientation of microfibril bundles, whose main function being the opposition to haemodynamic loading.     

Microfilament-associated adhering junctions (6 nm F-maculae adherentes) connect bovine pulmonary fibroblasts in vivo

Fibroblasts in the pulmonary alveolar septa of neonatal and mature cattle form spot-shaped intercellular junctions with each other where 6 nm microfilaments adhere to the plasma membranes. The junctions have variable cleft widths (10-20 nm) and a diffuse periodic intracleft substance. Impinging 6 nm microfilaments and plaque specializations were present in thin sections of junctions ranging from 0.4 to 0.6 micron in length. The microfilaments involved in junctions are parts of either cortical cytoplasmic webs or highly organized bundles. Two or more fibroblasts may form one complex of junctions and multiple junctions may occur between two fibroblasts. It is proposed that the in vivo fibroblast junction be named a 6 nm F-macula adherens, based on size of the associated microfilaments and type of junctional specialization.     

An ultrastructural study of cell junctions and the cytoskeleton in epithelial cells of the molluscan integument

Cell junctions and the cytoskeleton of integumental epidermal cells from six bivalves, four gastropods, and two cephalopods were studied by transmission electron microscopy. In all species examined, the junctions in supporting cells presented the following similar pattern: an apical-lateral adhesion belt (occluding junctions were not observed); (b) a lateral complex of septate junctions and smooth septate junctions, with interdigitations between adjacent cells while the gap junctions were not constantly present, and a basal complex with hemidesmosomes, focal contacts, and sometimes basolateral adherent junctions. Desmosomes were never observed. Microfilamentous and microgranular material were present throughout the cells, as bundles of microfilaments within microvilli and the terminal web, within interdigitations, and as cytoplasmic plaques forming part of the adherent junctions, hemidesmosomes, and focal contacts. Bundles of intermediate filaments that originated from basal hemidesmosomes were located close to and oriented parallel with the lateral plasma membrane and terminated within the terminal web. In cells of Aplysia depilans, intermediate filaments converged apically to terminate in hemidesmosome-like structures at the bases of the microvilli. In the cephalopods, hemidesmosomes were never observed and intermediate filaments made direct contact with the basal cell membrane. Some functional interpretations and hypotheses were also discussed.     

The structure of epidermal feet during their development

Epidermal cells in Calpodes and other insects form basal processes or feet that at first extend axially and later shorten at the same time as the larval segment shortens to the pupal shape. The feet grow into spaces at the surfaces of other cells to make a basal interlacing meshwork of cellular extensions that are combined mechanically by their desmosomal attachments to cell bodies above and to the basal lamina below. Microtubules and microfilaments are linked to these junctions by a reticular fibrous matrix. Gap junctions on the feet may couple cells that are several cell bodies removed from one another. The meshwork is also a sieve separating the hemolymph from the spaces between cells to form an intercellular compartment. Entry to the intercellular compartment is through the sieve made by the negatively charged basolateral cell surfaces that can prevent the entry of positively charged molecules such as cationic ferritin. As the cells become columnar, coincident with the metamorphic change in segment shape, the feet shorten and pack more densely together. At this time the basal lamina buckles axially as if responding to contraction of the feet. Segment shape change involves cell rearrangement and relative cell movement, necessitating the transient loss of plasma membrane plaque attachments to the cuticle apically and the loss of junctions laterally. Gap junctions involute in characteristic vacuoles. The metamorphic reduction in cell surface area coincides with the loss of basolateral membrane in smooth tubes and vesicles and the turnover of the apical surface in multivesicular bodies. New apical plasma membrane plaques and new lateral and basal junctions stabilize the cells in their pupal positions.     

The myotendinous junction of the smooth feather muscles (mm. pennati)

Summary Smooth feather muscles (mm. pennati) consist of bundles of smooth muscle cells which are attached to the feather follicles by short elastic tendons. In addition, some muscle bundles are interrupted by elastic tendons. The elastic tendon is composed of longitudinally arranged elastic fibers which branch and wavy bundles of collagen fibrils. Smooth muscle cells of the muscle bundles are attached to each other by desmosome-like junctions and by fusion of the basal laminae. The cytoplasm of the muscle cells is characterized by conspicuous thick filaments and abundant thin and intermediate filaments. These are attached to band-like dense patches (dense bands) at the plasma membrane which are particularly broad at the tapering end of the muscle cell. The contact surface between smooth muscle cells and their elastic tendon is considerably increased (i) by deep finger-like invaginations and indentations located at the tapering muscle end, and (ii) by branching of the coarse elastic fibers into slender processes, which are attached to the richly folded surface of the muscle cell endings by peripheral microfibrils. This intimate interlocking closely resembles the myotendinous junctions in skeletal muscle. In addition to fibroblasts and fibrocytes, the myotendinous junction of the young growing chicks contains numerous so-called myofibroblasts, which are suggested to represent smooth muscle cells differentiating into fibroblasts of the developing tendon.Dedicated to Professor Dr. Helmut Leonhardt on the occasion of his 60th birthdaySupported by a grant from the Deutsche Forschungsgemeinschaft (Dr. 91/1)     

Electron microscopic structure and innervation of the carotid baroreceptor region in the rock hyrax (Procavia capensis).

Semi-thin plastic sections reveal that the carotid baroreceptor region in the rock hyrax comprising the origin of the internal carotid artery has a preponderantly elastic structure and a thick tunica adventitia. In contrast, the common carotid artery has a musculoelastic structure, whereas the cranial segment of the internal carotid artery (immediately distal to the baroreceptor areas) shows the features of a muscular artery. Electron microscopy discloses the presence of sensory nerve endings within the parts of the tunica adventitia adjoining the preponderantly elastic zone of the internal carotid artery. These nerve endings are characterized by varicose regions containing a large quantity of mitochondria. Bundles of collagen fibers in the tunica adventitia form convolutions or whorls around the nerve terminals and often terminate on the surface of the elastic fibers or into the basement membranes of the neuronal profiles. The large content of elastic tissue in the tunica media of the baroreceptor region may render the vessel wall highly distensible to intraluminal pressure changes. This, in turn, would facilitate the transmission of the stimulus intensity to the sensory nerve terminals located in the tunica adventitia. It is suggested that the stretching of elastic fibers may form the main mechanical event leading to the distortion of the associated nerve terminals. However, a change in the geometrical configuration of the bundles of collagen under the influence of the elastic fibers may provide a better insight into the mechanisms of distortion of the baroreceptors related to and/or in contact with collagen fibers.     

Ultrastructure of the ookinetes of Haemoproteus meleagridis (Haemosporina: Haemoproteidae)

Ookinetes of Haemoproteus meleagridis were structurally similar to kinetes of other apicomplexan parasites and possessed a polar ring complex (PRC) composed of an electron-lucent polar ring with 25 supporting tines. Fifty subpellicular microtubules were anchored in a circle to the inner surface of the polar ring. A bilayered electron-dense canopy was continuous with the inner layer of the pellicle and formed a caplike cover over the PRC. Embedded rings of actin-sized microfilaments completely encircled each layer of the canopy. Numerous micronemes, 2 smaller preconoidal rings, and a conoid composed of approximately 6 spirally wound, electron-dense tubules were also present. Other organelles were similar to those reported in previous studies of haemosporidian ookinetes. Mature ookinetes of H. meleagridis developed in the midguts of engorged specimens of Culicoides edeni (Diptera: Ceratopogonidae) within 24 hr after a blood meal. Most parasites were found beneath, or embedded within, a peritrophic membrane composed of fine granules and fibrils. The observation of actin-sized microfilaments within the canopy is a previously unrecognized modification of the pellicle that probably supports the anterior end of ookinetes during penetration of the peritrophic membrane.