Age and changes in the structure of the walls of the intrinsic arteries of the uterus

By means of common histological, histochemical and morphometrical methods age changes in the cushion-like intimal protrusions of the intraorganic arteries have been studied in 176 uteri of women at all ages that died from trauma and other diseases which do not produce any changes in the uterus. Beginning from two years of age, in the uterus segmentary artery wall certain intimal thickenings are revealed; at this age they consist of immature fibrillar and cellular elements of the connective tissue and single myocytes. At the pubertal age an intensive development of the cushion-like protrusions is observed. The amount of myocytes in them increases at the expense of migration from muscular tunic of the vessel; they arrange chaotically. Then the structure of the elastic and collagenous carcass of the protrusions becomes more complex, the myocytes in them are oriented along the course of the artery, or along the sloping spiral. During adolescence and mature age, cyclic changes in the wall structure of the uterus intraorganic arteries are observed, depending on the phase of the menstrual cycle. During the second part of the proliferative phase, certain retruction of the protrusions is observed, and at the end of the secretion phase--maximal increase in their height. The intimal protrusions are specialized structures, playing an important role in ensuring an optimal blood circulation in the uterus during ovulation and in performing menstruation. Reverse development of these structures takes place in elderly and old age.     

Direct Visualization of Lignifying Secondary Wall Thickenings in Zinnia elegansCells in Culture

The lignifying secondary wall thickenings of tracheary elementsthat were differentiating from Zinnia mesophyll cells in suspensionculture were examined by a freeze-etch replica technique. Cellulosemicrofibrils in primary and secondary wall thickenings differedin terms of both width and arrangement. The primary wall wasobserved as a randomly arranged network of microfibrils. Bycontrast to microfibrils in the secondary wall thickenings werehighly organized, with many pores and spaces between them. Numerousfilamentous and granular cross-links were observed in both primarywalls and secondary wall thickenings. As lignifica-tion proceeded,the cellulose microfibrils in secondary wall thickenings becameobscure as a result of the deposition of large numbers of sphericalbodies around and between the microfibrils. This material hadcompletely covered the fibrous matrix by the end of lignification.It might have been composed of the products of the dehydrogenationof monolignols. We also noted that the microfibrils appearedto be slightly irregular or wavy just after the start of lignificationbut were straighter and appeared to be more rigid when lignificationwas complete. (Received July 25, 1996; Accepted April 24, 1997)     

Protochordate immunity. I. Primary immune response of the tunicate Ciona intestinalis to vertebrate erythrocytes

Serum from the tunicate Ciona intestinalis contains a low titer, natural agglutinin for a variety of vertebrate erythrocytes. Primary injections of 8.5 × 10³ human erythrocytes or 7.0 × 10² duck erythrocytes into the tunic tissues or perivisceral cavity were agglutinated and then cleared by phagocytosis within 24 hr. Higher concentrations of human or duck erythrocytes injected into the tunic tissues were encapsulated. Concomitant with clearance or encapsulation, serum agglutinin levels decreased and then returned to normal within 24 hr. Tunicates are classified taxonomically with the vertebrates in the phylum Chordata. Since phagocytosis and encapsulation reactions are typical of most invertebrates, the results of this study suggest that tunicate internal defense mechanisms are more closely allied to invertebrates than to vertebrates.     

Minute protrusions of the cuticle: Fine surface structures of the tunic in ascidians

The fine structure of the cuticular surface of the tunic was studied by scanning and transmission electron microscopy in 25 species belonging to 9 families of ascidians. The cuticular surface is ornamented with numerous minute protrusions in some species, but not in others. The minute protrusions are usually papillate in shape, and less than ～0.05 μm high (in some species of the families Polyclinidae and Polycitoridae), or ～0.1 μm high (in all species of Botryllidae, all colonial species of Styelidae and one solitary species of Pyuridae). In Clavelina miniata (Polycitoridae), the tunic is provided with parallel ridges on the surface of which papillate protrusions are distributed. The minute protrusions of Halocynthia roretzi (Pyuridae) are irregularly shaped, giving an appearance of paving stones. No protrusions are found in the families Didemnidae, Cionidae, Perophoridae, and Ascidiidae, and in one solitary species of Styelidae. At least in some colonial species, the density of the minute protrusions is lower at the edge of the colony than elsewhere. It is very probable that minute protrusions are found shortly after the secretion of tunic, growing larger both in size and in number as the tunic becomes older.     

Wood anatomy of Elaeagnaceae, with comments on vestured pits, helical thickenings, and systematic relationships

The secondary xylem of Elaeagnus, Hippophae, and Shepherdia is described and illustrated in detail. Shrubs and small trees of Elaeagnaceae have ring-porous or semi-ring-porous wood with simple perforation plates, vascular tracheids, fiber-tracheids, diffuse or rarely paratracheal axial parenchyma, and uni- or biseriate rays in Hippophae and Shepherdia, but wider rays in Elaeagnus. Walls of vessel elements, especially narrow ones, tracheids, or fiber-tracheids sometimes show helical thickenings; in a few instances these intergrade with small bud-like protrusions associated with pits. Scanning electron microscopy illustrates that small to vestigial vestures are present in all species studied, although nonvestured pits are also common. The analogous nature of vestures and helical thickenings is considered. Comparative wood anatomy suggests a rather isolated position of the family Elaeagnaceae; affinities with Rhamnaceae, Proteaceae, and Thymelaeaceae are discussed.     

Ascidian tunic cells: morphology and functional diversity of free cells outside the epidermis

Abstract. Tunic cells are free cells distributed in the tunic, the integumentary matrix of tunicates. In ascidians, various types of tunic cells have been described both in solitary and in colonial species. Many of them are functionally specialized and are related to the protection of the animal, such as phagocytosis to prevent infection, acid storage to avoid predation, and pigmentation to protect against solar radiation. While some tunic cells are known to play a role in colonial allorecognition, bioluminescence, and algal symbiosis, the functional roles of many cell types still remain to be determined. The composition of tunic-cell types varies among ascidian species, most likely reflecting the functional requirements of the tunic in each species. Although some cell types, e.g., tunic net cells and tunic bladder cells, are restricted to particular taxa of ascidians, tunic phagocytes are found in all known ascidians. Therefore, tunic phagocytes are hypothesized to be basal and shared with ancestral tunicates. In some ascidians, phagocytic cells are involved in other functions, such as pigmentation, intracellular photosymbiosis, and bioluminescence. These specialized phagocytic cells are hypothesized to be derived from tunic phagocytes, suggesting that tunic cells have a high potential to diversify and evolve a wide variety of cellular functions.     

Ontogeny of the appendicularian <Emphasis Type="Italic">Oikopleura dioica</Emphasis> (Tunicata,Chordata) reveals characters similar to ascidian larvae with sessile adults

Appendicularians have always occupied a central role in considerations of tunicate and chordate evolution. Two hypotheses have been proposed – one holds that appendicularia represents the sister taxon to the remaining tunicates, the other suggests that appendicularians were derived from an ascidian-like ancestor. In the present study I report results from electron microscopic investigation of larval tunicates including the first electron microscopic investigation of the tail of the early ontogenetic appendicularian “Streckform” and discuss their phylogenetic implications. The early “Streckform” of Oikopleura dioica Fol, 1872 is invested with an extracellular covering that consists of an inner electron-light layer and an electron-dense outermost layer. In addition, the extracellular covering forms fin blades. Because these traits are shown to be similar to the tunic of different ascidian larvae, the extracellular covering in early appendicularian embryos is suggested to be homologous to the larval tunic of ascidian larvae. Overall, the tail of early developmental stages of appendicularians consists of a mosaic of apomorphic and plesiomorphic features. The straight, continuous endodermal strand was inherited from a common chordate ancestor whereas the finlets of larvae, consisting of extracellular material, were inherited from a common tunicate ancestor. The horizontal orientation of the tail as a whole was inherited from the last common ancestor of appendicularians and aplousobranch ascidians, and the discovered floating extension at the posterior tip of the tail is unique to the holoplanktonic Oikopleura dioica. These findings support the hypothesis that Appendicularia is derived from a sessile, ascidian-like ancestor.     

Cellular components and tunic architecture of the solitary ascidian Styela canopus (Stolidobranchiata, Styelidae)

Cell distribution and tunic morphology in the ascidian Styela canopus were examined by electron microscopy. The observations showed that the outer covering is composed of a thin sinuous cuticle with several protrusions and a deep layer of ground substance. The fibrous component and its arrangement in the tunic were demonstrated: elementary fibrils exhibit a 'microtubular' structure and an elliptical cross-sectional shape. Four types of cells were described: clear vesicular tunic granulocytes, tunic microgranulocytes, unilocular tunic granulocytes, and globular tunic granulocytes. Morphofunctional aspects of the tunic tissue and certain phylogenetic relationships are discussed.     

The identification and localization of two intermediate filament proteins in the tunic of Styela plicata (Tunicata, Styelidae)

The intermediate filament (IF) proteins Styela C and Styela D from the tunicate Styela (Urochordata) are co-expressed in all epidermal cells and they are thought to behave as type I and type II keratins. These two IF proteins, Styela C and Styela D, were identified in immunoblots of proteins isolated from the tunic of Styela plicata. The occurrence and distribution of these proteins within the tunic of this ascidian was examined by means of immunofluorescence and immunoperoxidase techniques, using anti-Styela C and anti-Styela D antibodies. In addition, immuno-electron microscopy of the tunic showed that the two proteins are located in the cuticle layer and in the tunic matrix. These results represent the first data about the presence of IF proteins in the tunic of adult ascidian S. plicata. The possible involvement of these IF proteins in reinforcing the integrity of the tunic, that represents the interface between the animal body and the external environment, is discussed.     

Dispersed lignin in tracheary elements treated with cellulose synthesis inhibitors provides evidence that molecules of the secondary cell wall mediate wall patterning

Mesophyll cells of Zinnia elegans var. Envy that had been induced to differentiate into tracheary elements (TEs) in suspension culture were treated with the cellulose synthesis inhibitor 2,6-dichlorobenzonitrile (DCB). The deposition of cellulose into the patterned secondary cell wall thickenings typical of TEs was inhibited as demonstrated by reduced incorporation of [¹⁴C]glucose into acetic/nitric insoluble material and absence of cellulose detectable by fluorescence after staining with Tinopal LPW, polarization optics, or labeling with a specific cellulase. Respiration as indicated by release of ¹⁴CO₂ was inhibited to a much lesser extent, supporting a selective mechanism of action of DCB on the cellulose biosynthetic pathway. Patterned secondary cell wall thickenings were deposited in DCB-treated TEs, but these were smaller and less regularly shaped than those of control TEs. These cellulose-depleted thickenings lacked another abundant component of normal thickenings, the hemicellulose xylan, as indicated by absence of labeling with a specific xylanase or an antibody to xylan. DCB-treated TEs also showed dispersed lignin after staining with phloroglucinol, whereas control TEs contained lignin specifically localized to the secondary cell wall thickenings. Isoxaben, another recently described inhibitor of synthesis of acetic/nitric insoluble cell wall material (putatively cellulose), caused the same absence of detectable cellulose and xylan in the thickenings and dispersed lignin. These data suggest that: (i) the localization of lignin is ultimately dependent on the localization of cellulose; (ii) normal patterned wall assembly in TEs occurs in a self-perpetuating cascade in which some molecules of the secondary cell wall mediate patterning of others.     

BARINOPHYTON CITRULLIFORME (BARINOPHYTALES INCERTAE SEDIS,BARINOPHYTACEAE) FROM THE UPPER DEVONIAN OF PENNSYLVANIA

Barinophyton citrulliforme is definitely proven to be a tracheophyte. The vascular cylinder of the main axis is an exarch protostele composed of tracheids having a continuous secondary wall folded into protrusions into the cell lumen. These protrusions delineate the position of annular thickenings which were deposited earlier than the continuous secondary wall. Between successive protrusions, the later-deposited secondary wall is interrupted by minute pitlike structures. It is suggested that the secondary walls of the tracheids were laid down in a two-phase depositional sequence. The fertile system of B. citrulliforme consists of a main axis bearing spirally arranged strobili. The strobilus consists of an axis that bears two alternate rows of sporangiferous appendages. The sporangiferous appendages are borne laterally along the strobilar axis and recurve abaxially around the axis. The sporangia are attached along the inside curve of the appendages, one sporangium per appendage, each containing both microspores and megaspores. This species thus exhibits sporangial heterospory which is considered to be an adaptation to an aquatic habit and the sporangia are considered to be functional analogs of the sporocarps of Marsilea. The interpretation of the strobilus is morphologically identical to Ananiev's interpretation of the strobilus of Pectinophyton bipectinatum; consequently P. bipectinatum is here transferred to Barinophyton as B. robustius comb. nov.     

Exotesta morphology of the Gardenieae — Gardeniinae (Rubiaceae)

Persson, C. 1995. Exotesta morphology of the Gardenieae-Gardeniinae (Rubiaceae). -Nord. J. Bot. 15: 285–300. CGpenhagen. ISSN 0107–055X.
Exotesta morphology of 68 species in 59 genera of the Gardeniinae were examined with the aid of scanning and light microscopy. The shape of the exotesta cells in surface is either isodiametrical or elongate and both shapes occur among New World and Old World genera. All genera, except for Monosalpinx, Posoqueria and Macrosphyra , are provided with secondary thickenings in the cell walls of the exotesta. The majority of the genera has a thickened radial wall. In the Asian genera Catunaregam, Deccania, Tamilnadia and the mainly Pacific genera, Atractocarpus and Trukia thickenings of the radial wall are very low or absent. In nearly half the genera the inner tangential wall is provided with thickenings, usually in the shape of a continuous plate. However, in four African genera, Atractogyne, Didymosalpinx, Mitriostigma and Sherbournia , the wall is provided with elongate anastomosing ribs. Atractocarpus differs markedly from the rest of the Gardeniinae by its ring-like thickenings in the inner tangential wall. Thickenings, in the shape of a continuous plate, in the outer tangential wall is restricted to three neotropical genera, Alibertia, Amaioua and Borojoa . Presence of distinct knobs is common in palaeotropical genera, whereas in neotropical genera this feature is only present in Casasia and Kotchubaea . It is concluded that data on exotesta morphology alone does not support any of the previously proposed informal groups, but may still be an important character to deduce phylogenetic relationships, primarily on a level just above the genus.     

Pathological studies on corynebacterial ulcerative entero-colitis in rats treated with ACTH (author's transl)]

Ulcerative entero-colitis was developed in 6-week-old male Sprague-Dawley rats treated daily with ACTH (4 mg/kg. s. c.) as well as necrotic purulent lesions in liver, kidney, lung or heart. Incidence of ulcerative lesions was 6.3% in Farm-A rats and 56% in Farm-B rats. Although ulcerative lesions were mostly observed in cecum, the similar lesions were also detected in distal ileum or proximal colon in some cases. Histologically, the lesions were characterized by focal necrosis demarcated from surrounding normal tissue containing a number of clumps of bacteria and cellular debris. Bacteriological examination revealed that provocation of Coryne-bacterium kutscheri by ACTH-treatment resulted in appearance of the lesions. By means of intravenous or intraperitoneal inoculation with the strain isolated from lesion similar lesions were produced in the cecum of inoculated rats under the ACTH-treatment.     

Wound-induced and naturally occurring regenerative differentiation of xylem in Zea mays L.

The regenerative differentiation of xylem, both around a wound in the stem and at the root junction was studied in seedlings of maize. The regeneration of vessels around a wound was very small, being limited to the very young internodes and sharply declining basipetally. There were more regenerative vessel elements and they differentiated faster above the wound than below it. The regenerative vessel elements around the wound were characterized by helical or annular pattern of secondary wall thickenings. Wounding also resulted in the development of additional vascular anastomoses in the leaf immediately above the wound, and in differentiation of discontinuous vessels in adjacent bundles. Regenerative vessel elements were very common where the adventitious roots connected with the stem internodes, and exhibited pitted or reticulated secondary wall thickenings.     

Inhibition of phenylalanine ammonia-lyase activity causes the depression of lignin accumulation of secondary wall thickening in isolatedZinnia mesophyll cells

Summary Isolated mesophyll cells ofZinnia elegans L. cv. Canary Bird differentiate into tracheary elements in differentiation (D) medium. These elements develop lignified secondary wall thickenings. The influence of 2-aminoindan-2-phosphonic acid (AIP), an inhibitor of phenylalanine ammonia-lyase (PAL), on lignification ofZinnia tracheary elements was examined. The mesophyll cells were cultured in D and AIP media. The latter medium, in which 100 M AIP was added to the D medium, inhibited PAL activity, though the differentiation proceeded. Morphological differences of secondary wall thickenings cultured in these two types of media were investigated under an UV microscope and a transmission electron microscope. The secondary wall thickenings at 96 h in the D medium showed strong UV absorption. The fibrillar structure of the thickenings observed clearly at 72 h was covered with electron opaque materials by 96 h. The secondary wall thickenings at 96 h in the AIP medium showed weak UV absorption. The thickenings at 96 h had a cracked appearance. Furthermore, the thickenings showed a little irregular or wavy arrangement of cellulose microfibrils and had many pores and spaces between microfibrils. From these results, the role of lignin accumulation in the formation of secondary wall thickenings was discussed.Abbreviations AIP 2-aminoindan-2-phosphonic acid - PAL phenylalanine ammonia-lyase     

Evidence for the role of the glomerulocyte in cellulose synthesis in the tunicate,Metandrocarpa uedai

Summary The tunicate,Metandrocarpa uedai, contains a large quantity of cellulose; however, it is not known how and where the cellulose is synthesized. Based on evidence from electron diffraction and conventional thin-sectioning for electron microscopy, this study shows that the glomerulocyte is involved in the synthesis of cellulose. The bundles of microfibrils in the glomerulocyte as well as the tunic were identified as cellulose I using selected area electron diffraction analysis. The diffraction pattern of cellulose in the glomerulocyte was similar to that from the tunic, suggesting that the crystallization of cellulose already is initiated in the glomerulocyte. The diameter of cellulose microfibrils, both in the glomerulocyte and the tunic was the same, about 16 nm. These results suggest that the glomerulocyte is the most probable site for the synthesis of cellulose in the tunic ofM. uedai. Using thin-sectioning techniques, a series of observations showed that individual microfibrils are primarily assembled in structures tentatively identified as vacuole-like structures, then they are bundled by a tapering region within the vacuole-like structures. These bundles of microfibrils are deposited in a continuously circular arrangement. The microtubules are oriented parallel to the bundles of microfibrils at the tapering vacuole-like structure, and they may be involved in the tapering of these structures (perhaps controlling the shape). This study also provides the first account for the involvement of a vacuole-like structure in the synthesis of cellulose microfibrils among living organisms.     

Ultrastructure of cardiocyte degeneration and myocardial calcification in the dystrophic hamster

The myocardium of the Bio 14.6 cardiomyopathic hamster was examined with the electron microscope to identify cellular and organelle changes during the acute lesioning stage, a period typified by concomitant cardiocyte destruction and calcium elevation. Most cardiocytes retained their normal histologic and ultrastructural features, but scattered foci of altered and necrotic cells were observed in association with degenerative calcifying lesions. Prenecrotic alterations of myocytes included cellular edema; varying degrees of distension of sarcoplasmic reticulum and T-tubules; contraction bands and other myofibrillar abnormalities; mitochondrial clustering and hyperplasia; a wide spectrum of mitochondrial changes such as altered sizes, shapes, and cristal patterns, and increases in the number and size of osmiophilic matrix inclusions. Morphologic features consistent with substantial calcium excess were not observed in most altered but prenecrotic cells. Instead, calcium deposition within extruded mitochondria and upon degenerating organelle debris was observed only after cardiocyte disruption. Some calcifying cell remnants were phagocytized by macrophages, whereas large calcified plaques and other deposits remained in the interstitium. Mitochondrial calcification in vascular smooth muscle cells and fibroblasts was evident in highly calcified lesions. These observations suggest that most of the morphologically identifiable calcium deposition present in this cardiomyopathy results from secondary calcification subsequent to sarcolemmal disruption.     

Cytochemical investigations on tunic morphogenesis in the sea peach Halocynthia papillosa (Tunicata, Ascidiacea) 2: demonstration of proteins

In a previous paper, cellulose fibres were demonstrated in the larval, the metamorphosing, and the juvenile tunics. In this paper we used cytochemical methods and X-ray microanalysis to obtain additional information on tunic morphogenesis in Halocynthia papillosa. The chemical composition of the tunic evolves with its structural complexity. The larval and juvenile fibres are shown to be structurally and chemically different. While neither proteins nor glycosaminoglycans seem to be associated with the larval fibres, the juvenile fibres consist of a cellulose core wrapped in a sheath of tannophilic proteins. Patches of glycosaminoglycans line their longitudinal axes. In the course of metamorphosis, the cuticle undergoes profound modifications in regions of spine morphogenesis. Granular material that was previously called fibro-granular material (Lübbering et al., 1993) is essential to the formation of cuticular plates and spines. During metamorphosis, this material accumulates in epidermal granules and is discharged into the tunic. It crosses the fundamental layer of the tunic and reaches the cuticle. Our results strongly suggest that this material consists of proteins rich in cysteine and hydrophobic amino acids.     

Study of color variation in the solitary ascidian Halocynthia roretzi, collected in the Inland Sea of Japan

In the vicinity of Yashiro Island in the Inland Sea of Japan, the solitary ascidian (tunicate) Halocynthia roretzi with tunics of various colors were collected. Samples of these animals were sorted into three groups on the basis of visual observation of tunic color. The red group includes animals with dark-red, light-red, or orange tunics. The pink group includes animals with tunic colors ranging between red and white. The white group includes only animals with completely white tunics. Animals in the white group lacked color internally, with the exception of the hepatopancreas and the gonads in breeding season; the epidermis and gill basket were white. In contrast, animals of both the red group and the pink group were colored internally, with red-orange epidermis and yellow gill basket. Alloreactivity was tested by mixed-hemocyte incubation between different animals belonging to the same color group and between animals belonging to different color groups. Alloreactivity between animals of the white group was 56.3%, between animals of the pink group was 60.0%, and between animals of the red group was 69.3%. The relatively high frequency of compatible combinations among the white animals is discussed.     

Keratinized squamous cells in fine needle aspiration of the brain. Cytopathologic correlates and differential diagnosis

OBJECTIVE: To analyze the differential diagnosis when keratinized squamous cells are found in a brain aspirate. STUDY DESIGN: Twenty cases of brain aspirates with keratinized squamous cells were retrieved (1982-2001). Diagnoses included craniopharyngioma (CP) (n = 11), metastatic squamous cell carcinoma (SCC) (n = 5), epidermoid cyst (EC) (n = 3) and Rathke cleft cyst (RCC) (n = 1). Aspirates were obtained under stereotactic radiologic (CT) guidance. Smears were stained with Diff-Quik or Papanicolaou stain, and cell block sections were stained with hematoxylin and eosin. Radiologic and histopathologic correlation with subsequent resection specimens was performed in selected cases. RESULTS: CP showed cellular smears with numerous keratinized squamous cells in a background of degenerated cellular and keratinaceous debris. Also noted were clusters of anucleate squamous cells, multinucleated giant cells, histiocytes, calcified debris and characteristic fragments of basaloid epithelial cells. Metastatic SCC showed single cells and tissue fragments of markedly atypical and focally keratinized cells with enlarged, hyperchromatic nuclei; prominent pleomorphism in a background of necrotic cellular debris and acute inflammatory exudate. EC showed numerous isolated keratinized squamous cells often with prominent keratohyaline granules and occasional parakeratotic cells in a relatively clean background. RCC showed single cells and aggregates of benign-appearing squamous cells admixed with numerous anucleate squames and hemosiderin-laden macrophages. Glandular-type epithelium was present only rarely. CONCLUSION: Squamous cell-containing lesions in the brain present a spectrum of pathologic entities. Although they all display the common morphologic denominator of keratinizing squamous cells, subtle cytomorphologic differences exist in these lesions, permitting an accurate cytopathologic diagnosis. Clinicardiologic features and anatomic location of the tumor in the brain are additionally helpful.