Development of terminal filaments and ovariole envelopes in Thermobia domestica (Insecta, Zygentoma) larvae

The 3rd instar female larvae of Thermobia domestica have five pairs of gonad primordia, each enclosed within a basal lamina (tunica propria). At the end of the 3rd instar some somatic cells scattered on the outer surface of the lamina are seen. During the 4th larval instar the gonad primordia start to form the ovarioles. Each ovariole is elongated and polarized, having anterior and posterior ends. The anterior group of outer somatic cells proliferate to form the terminal filament. At the 6th larval stage the ovarioles are already formed. The terminal filament is separated from the germarium by a thick basal lamina (transverse septum). There are three types of cell building the terminal filament. 1/Basal cells with numerous fingerlike projections; 2/Cells with electron lucent cytoplasm and large nuclei, and 3/Cells with darker cytoplasm containing bundles of fibers and more compact nuclei. The outer surface of the filament is covered by a thick, fibrous basal lamina. The somatic cells that in the previous stages were scattered on the tunica propria as distinct cells, in the 6th larval stage form a cellular envelope (tunica externa). This envelope is formed by a layer of flat cells, and contains numerous tracheae.     

Structure of the trophic chamber (germarium) in virginoparae of the vetch aphid,Megoura viciae Buckton (Homoptera : Aphididae)

The structure of the germaria in the ovaries of the viginoparous morph of the vetch aphid, Megoura viciae Buckton (Homoptera : Aphididae) is described and compared to other insects, including aphids. Each consists of a syncytium of trophocytes and resting oocytes arranged around a trophic core. Trophocytes contain mitochondria, ribosomes, vacuoles and some membrane-bounded material. Golgi complexes were not found. Each trophocyte has a single spherical nucleus with “nuage-like” material confluent between nucleoplasm and cytoplasm via numerous nucleopores. The surrounding monolayer of somatic epithelial sheath cells are bounded externally by an acellular tunica propria. These cells continue into the prefollicular tissue in the base of each germarium. Cells from the prefollicular tissue envelop each oocyte as it is released from a germarium. The “previtellogenic” growth phase of oocytes is relatively short, and vitellogenesis is absent. Virginoparae are reproductively precocious, and newly born larvae have up to 3 oocytes undergoing development in their anterior ovarioles. Interovariole ovulation is asynchronous within, and partially synchronous between, the 2 ovaries.     

Ultrastructure of the ovary of Dermatobia hominis (Diptera: Cuterebridae). I. Development during the 3rd larval instar

The ultrastructure and distribution of gonial and somatic cells in the ovary of Dermatobia hominis was studied during the 3rd larval instar. In larvae weighing between 400 and 500 mg, the ovary is partially divided into basal and apical regions by oblong somatic cells that penetrate from the periphery; these cells show ovoid nucleus and cytoplasm full of microtubules. In both regions, gonial cells with regular outlines, large nucleus and low electron-density cytoplasm are scattered among the interstitial somatic cells. These later cells have small nucleus and electrondense cytoplasm. Clear somatic cells with small nucleus and cytoplasm of very low electron-density are restrict to the apical region of the gonad. Degenerating interstitial somatic cells are seen in the basal portion close to the ovary peduncle. During all this larval period the morphological features of the ovary remain almost the same. At the end of the period there is a gradual deposition of glycogen in the cytoplasm of the somatic cells, increase in the number and density of their mitochondria plus nuclear modification as membrane wrinkling and chromatin condensation in masses.     

Response to cryptorchidism of the testis and epididymis of the opossum (Didelphis virginiana).

Adult male opossums, Didelphis virginiana, were rendered hemicryptorchid for 35 days. The cyrptorchid testis exhibited a significant reduction in weight, while the contralateral testis had a compensatory weight gain compared with testes of untreated animals. Histological changes in the cryptorchid testis included fibrosis of the tunica propria, involution of the seminiferous tubules and an apparent increase in the interstitial tissue. Many seminiferous tubules were empty and germinal cells were absent. Some Sertoli cells persisted, but the cytoplasm was vacuolated. Cryptorchid testes were characterized by mononuclear leucocytic invasion around the tubules, and some eosinophils were observed. Cryptorchidism in the opossum may induce a reaction similar to experimental orchitis.     

Ultrastructure of peritubular tissue in association with tubular hyalinization in human testis.

Testicular peritubular tissue, also known as the tunica propria, surrounds the seminiferous tubules and is responsible for contractile, paracrine and transport functions. The aim of the present report is to describe the pathomorphology of peritubular tissue in association with tubular hyalinization in human testis. Twenty-seven testicular biopsies from 21 subfertile and infertile men were studied with the electron microscope. Biopsies from five patients showed complete or nearly complete tubular hyalinization. In addition to changes described earlier, the following new ultrastructural features were observed: 1. loss of polarity and configuration of myoid cells; 2. protrusion of myoid cells towards the tubule and evagination of basal lamina surrounding the tubule towards the interstitial direction leading to 'bridge' formation. These 'bridges' of myoid cells often created completely separated small compartments within the tunica propria; 3. vacuolization and fragmentation of myoid cell nuclei; 4. a balloon-like swelling of myoid cell containing phagolysosomes and lipid droplets. We conclude that disorganization and loss of vital functions of the extracellular matrix and myoid cells contribute to the pathogenesis of tubular hyalinization.     

Structure and development of ovaries in the weevil, Anthonomus pomorum (Coleoptera, Polyphaga). I. Somatic tissues of the trophic chamber

In developing ovarioles of Anthonomus pomorum (Coleoptera, Polyphaga, Curculionidae) the trophic chambers (tropharia) are relatively large and consist of clusters (clones) of germ cells and various somatic tissues. Each ovariole is enclosed within an outer epithelial sheath (tunica externa). Throughout the pupal phase, the growth of this sheath is accelerated and precedes the development of the rest of the ovariole. As a result, the epithelial sheath proliferates anteriorly and forms an elongated "sleeve" that during the later stages of development becomes gradually filled by the growing tropharium. In the early pupal stage, a few terminal filament cells are observed in contact with the anterior end of the tropharium. These cells are separated from the rest of the trophic chamber by a transverse septum, which maintains continuity with the basal lamina. Beneath the basal lamina there is a layer of inner sheath cells, whereas inside the tropharium there are interstitial cells. These two types of cell differ morphologically in a mature ovary but they retain, until the end of the imago-B stage, a similar ultrastructure testifying to their common origin. At the posterior end of the tropharium, from the imago-B stage on, many young oocytes, surrounded by prefollicular cells, are observed. This is the so-called neck region of the tropharium. Extraction with Triton X-100 detergent showed that in a mature trophic chamber there are only individual microtubules arranged along the projections of interstitial cells. This indicates that the cytoskeleton elements (microfilaments and microtubules) participate only to a very limited extent in the spatial organisation of the tropharium in A. pomorum.     

Differentiation and function of the ovarian somatic cells in the pseudoscorpion,Chelifer cancroides (Linnaeus, 1761) (Chelicerata: Arachnida: Pseudoscorpionida)

Pseudoscorpion females carry fertilized eggs and embryos in specialized brood sacs, where embryos are fed with a nutritive fluid produced and secreted by somatic ovarian cells. We used various microscopic techniques to analyze the organization of the somatic cells in the ovary of a pseudoscorpion, Chelifer cancroides. In young specimens, the ovary is a cylindrical mass of internally located germline cells (oogonia and early previtellogenic oocytes) and two types of somatic cells: the epithelial cells of the ovarian wall and the internal interstitial cells. In subsequent stages of the ovary development, the oocytes grow and protrude from the ovary into the hemocoel (opisthosomal cavity). At the same time the interstitial cells differentiate into the follicular cells that directly cover the oocyte surface, whereas some epithelial cells of the ovarian wall form the oocyte stalks – tubular structures that connect the oocytes with the ovarian tube. The follicular cells do not seem to participate in oogenesis. In contrast, the cells of the stalk presumably have a dual function. During ovulation the stalk cells appear to contribute to the formation of the external egg envelope (chorion), while in the post-ovulatory phase of ovary function they cooperate with the other cells of the ovarian wall in the production of the nutritive fluid for the developing embryos.     

Ontogenesis of the ovary in a moth midge,Tinearia alternata Say (Diptera: Psychodidae)

In a psychodid, Tinearia alternata, the initial differentiation of the polytrophic ovary occurs during the early larval stages. Early in development, each ovary anlage is a solid organ subdivided into three distinct zones: the cortex houses germ cells and somatic interstitial tissue, while two other somatic regions will give rise to the oviduct calyx and anterior part of the lateral oviduct. Germ cell cluster formation precedes the development of ovarioles. Each ovariole houses only one functional egg chamber. All ovarioles within paired ovaries are developmentally synchronized. In the larval ovaries, the newly formed egg chambers and then the ovarioles are intermingeled with and surrounded by the somatic interstitial tissue of the ovary cortex. The interstitial cells give rise to all the somatic elements of the ovarioles. In the pupal ovaries, the remaining interstitial tissue degenerates; thus, the ovarioles protrude into the body cavity. The ovaries in psychodids develop relatively large and swollen oviduct calyxes that are equivalent to receptaculum seminis (spermatheca). The morphological differentiation of germ cells within the egg chambers starts during late larval/early pupal stages. Nurse cell nuclei contain prominent nucleoli and polytene chromosomes. Oocyte growth results from accumulation of yolk and then, in the final stages of oogenesis, from an inflow of cytoplasm from the nurse cells. J. Morphol. 236:167–177, 1998. © 1998 Wiley-Liss, Inc.     

Histological and ultrastructural investigation of the female reproductive system of Argulus bengalensis Ramakrishna, 1951 (Crustacea: Branchiura)

In order to understand branchiuran reproductive biology, it is imperative to know the sites of oogenesis and oocyte maturation, locate the accessory reproductive glands, and identify the fertilization site with the present knowledge of the sperm transfer mechanism of the genus Argulus. With these objectives, we attempted to describe the female reproductive system of Argulus bengalensis using serial histological sections through the ovaries and associated ducts in the transverse, longitudinal, and sagittal planes. The reproductive organs include a median ovary, one pair of ovarian lumina, a median oviduct, and a pair of collateral accessory glands. A duct from each of the collateral accessory glands leads into the proximal part of the median oviduct, which opens to the exterior through a genital opening at the distal end. The glandular secretion presumably contributes to the jelly coat of the egg. The ovary is bound with a tunica propria which extends further diametrically inside the ovary forming the paired lumina. The lumina are confluent into the median oviduct. Two distinct areas, the germarium and differentiating zones, are clearly distinguishable within the ovary. The tunica propria itself houses the oogonia within a matrix, serving as the germarium. Transmission electron micrograph reveals that the matrix is made of collagen. The collagen matrix confers elasticity to the tunica propria to accommodate the postvitellogenic oocytes within the ovarian lumen. The differentiating zone is situated in between the germarium: dorsally it is covered with a chromatophore layer. The ovary is ensheathed by a circum ovarian striated muscle. The presence of spermatophores in the ovarian lumen indicates the fertilization site. J. Morphol. 277:707–716, 2016. © 2016 Wiley Periodicals, Inc.     

Morphological characteristics and developmental changes of the ovary in the tick Haemaphysalis longicornis Neumann

Haemaphysalis longicornis (Ixodida: Ixodidae) is an important vector of transovarially transmitted parasites of the genus Babesia (Piroplasmida: Babesiidae). In the present study, we investigated the morphological characteristics and developmental changes of the ovary of H. longicornis. We show that the ovary of H. longicornis has a single tubular structure and is surrounded by a tunica propria. There is a longitudinal groove along one side of the ovary. During feeding and after engorgement, great changes can be observed in the ovary of H. longicornis and two rapid growth phases can be detected. The number of major protein bands of the ovary is significantly increased from day 3 of feeding and reaches a maximum on the day of engorgement. Therefore, the great diversity of proteins in the ovaries of H. longicornis can facilitate the identification of new targets for vaccine development.     

Symbionts in the oocytes of Blattella germanica (L.) (Dictyoptera : Blattellidae): Their mode of transmission

In Blattodea, the transmission of symbionts from one generation to the next is of transovarial type. The symbionts in Blattella germanica (L.) (Dictyoptera : Blattellidae) reach the ovary inside bacteriocytes in the 5-day-old nymphal instar, and are located among the ovarioles. Between the 11th and 17th day, the symbionts leave the bacteriocytes, cross the ovariole sheath, the tunica propria, and the follicular epithelium, and reach the space between the latter and the oocyte. In 17-day-old nymphs, the symbionts are in contact with the microvilli of the oocyte, remaining in this position until the end of the vitellogenic phase, when the microvillar border is progressively reduced. At this stage, the symbionts are actively phagocytosed by the oocyte before chorion formation.     

Origin and differentiation of the endocrine cells of the ovary

A large proportion of the somatic cells of the developing ovaries of mouse, human and rabbit stems from the mesonephric tissue. In the immature mouse ovary and in the 19-day-old fetal rabbit ovary, the first steroid-producing cells differentiate among the mesonephric-derived cells within the ovary. In the fetal human ovary, the first steroid-producing cells arise in the inner part of the cortex and differentiate concomitantly with the formation of small follicles. The origin of the early steroid-producing cells in the human ovary is still uncertain. During early ovarian development, formation and further differentiation of the steroid-producing interstitial cells seem to continue only in areas devoid of free viable germ cells.     

Gene expression during gonadal differentiation in the rat: A two-dimensional gel electrophoresis investigation

Gonadal protein patterns were studied during development in the rat by two-dimensional micro-gel electrophoresis. Specific proteins were detected in both the male and the female sex at the morphologically indifferent state (two female- and one male-specific) and during differentiation. At the onset of gonadal differentiation (day 14) two additional sex-specific proteins were discovered in the male and two in the female. These proteins remained expressed during further development. One testicular protein was restricted to the cytosol of the tunica albuginea. The other one was absent from the tunica. In the female gonad, the two proteins were membrane-specific, one present in germ cells, the other in somatic cells. In the testis, one additional protein was discovered at postnatal day 1. Thus according to biochemical criteria there is no indifferent state of gonadal development. The testis and ovary express sex-specific genes both before and after the onset of gonadal differentiation.     

Morphology and ultrastructure of the somatic cells in Astacus leptodactylus ovary

We defined the somatic environment in which female germinal cells develop, and performed ultrastructural analyses of various somatic cell types, with particular reference to muscle cells and follicle cells, that reside within the ovary at different stages of oogenesis. Our findings show that ovarian wall of the crayfish is composed of long muscle cells, blood cells, blood vessels and hemal sinuses. The follicle and germinal cells lie within a common compartment of ovarian follicles that is defined by a continuous basal matrix. The follicle cells form branching cords and migrate to surround the developing oocytes. A thick basal matrix separates the ovarian interstitium from ovarian follicles compartment. Transmission electron microscopy shows that inner layer of basal matrix invaginates deeply into the ovarian compartment. Our results suggest that before being surrounded by follicle cells to form follicles, oogonia and early previtellogenic oocytes reside within a niche surrounded by a basal matrix that separates them from ovarian interstitium. We found coated pits and coated vesicles in the cortical cytoplasm of previtellogenic and vitellogenic oocytes, suggesting the receptor mediated endocytosis for transfer of material from the outside of the oocytes, via follicle cells. The interstitial compartment between the inner muscular layer of the ovarian wall and the basal matrix of the ovarian follicle compartment contains muscle cells, hemal sinuses, blood vessels and blood cells. Granular hemocytes, within and outside the vessels, were the most abundant cell population in the ovarian interstitium of crayfish after spawning and in the immature ovary. J. Morphol. 277:118–127, 2016. © 2015 Wiley Periodicals, Inc.     

Differentiation of the gonad rudiment into ovary and testis in the solitary ascidian, Ciona intestinalis

In the early juveniles of Ciona intestinalis, primordial germ cells arise on the degenerated mass of the resorbed tadpole tail, and assemble to form a discrete gonad rudiment. The present study elucidated the morphological sequences during differentiation of the gonad rudiment into the testis and ovary. In 11- to 12-day juveniles, the gonad rudiment, an elongate sac, divided into the testicular and ovarian rudiments. The testicular rudiment separated as a round vesicle from the thickened wall of the elongate sac. The original sac, after separation of the round vesicle, developed into the ovary. In the testicular rudiment, germ cells formed a continuous central mass without association of somatic cells, while in the ovarian rudiment, each germ cell was associated with somatic cells within the epithelium composing the wall of the rudiment. In 13- to 15-day juveniles the testicular rudiment changed into branched tubes ending in club-shaped follicles. Cells characterized by many flattened cisternae of rough endoplasmic reticulum (distal cells) constituted the distal wall of each follicle. Spermatogenic cells were freely present in the follicular lumen, but the largest spermatogonia were in contact with the distal cells. Both in the testicular and ovarian rudiments, germ cells entered meiosis in 18-day juveniles. A novel body (periesophageal body) was found just beneath the ventral margin of the esophageal opening. It comprised irregular follicles made up of one cell type whose cytoplasm, filled with round vesicles and Golgi complexes, was suggestive of an endocrine function. Fragments derived from the periesophageal body were present around the developing ovary.     

Discovery of a gonad-specific IGF subtype in teleost

Distinct from the conventional IGFs (IGF-1 and IGF-2), here we report the identification of a novel IGF (herein called IGF-3) encoded by a separate gene from teleost species. The IGF-3 cDNA sequences were cloned from tilapia and zebrafish, and predicted from the medaka genome and EST databases. Similar to IGF-1 and IGF-2, IGF-3 is also comprised of five domains (B, C, A, D, E) with a similar tertiary protein structure, despite a low sequence homology among them. Phylogenetic analysis reveals that the IGF-3 sequences from different teleosts cluster to form a distinctive clade separate from IGF-1 and IGF-2. The expression of this novel IGF-3 is gonad-specific and starts early in fish development. In situ hybridization revealed that IGF-3 is expressed in the somatic cells and later in granulosa cells of the ovary, and in the interstitial cells of the testis. These findings highlight the importance of this novel IGF in teleost gonadal development and reproduction.     

On the structure of intestine and presence of endocytic cells in the lamina propria of platy and black tetra (Teleostei)

The structure of the intestine in platy (Xiphophorus maculatus) and black tetra (Gymnocorymbus ternetzi) and the capability of cells within the intestinal wall to endocytose intraperitoneally injected horse-spleen ferritin, are described. The intestinal epithelial layer has about the same thickness in both species, but the width of the lamina propria and tunica muscularis in black tetra was only about 1/5 of that in platy. Ferritin was taken up by numerous cells within the lamina propria throughout the entire length of the platy intestine. The uptake was demonstrated as large and strongly coloured intracellular Prussian blue granules in sections treated with acid ferrocyanide. There was no such uptake by the lamina propria in black tetras. We suggest that the high numbers of endocytic cells within the intestinal lamina propria of platies provide a local defence against foreign cells and particles. Such a functional role may to some extent compensate for the lack of an HCl-based defence in the digestive system of this stomach-less species.     

Some aspects of the reproductive biology of perch Perca fluviatilis L. A histological description of the reproductive cycle

Histological changes in the perch ovary during development are described and related to changes in gonad weight and to a macroscopic scale of maturity stages after Kesteven (1960). A single organ formed by the fusion of two primordial ovaries, a central internal oviduct, and an extremely thick chorion surrounding oocytes are characteristic features of the perch ovary. Resting oocytes can be differentiated from developing oocytes which are larger and possess a granulosa layer which permits formation of the chorion and yolk acquisition. In the maturing ovary, oocyte diameter increases rapidly and the chorion, which possesses four layers, the tunica propria, two middle zones forming a fine network, and the zona radiata, also expands. The spent ovary is disorganized with follicles and tunica wall contracted, and a number of residual oocytes may be apparent. There was no evidence of pre-ovulatory degeneration although autolysis of a small number of residual oocytes was observed. The gonadosomatic index was highest for males in September and at a maximum in females immediately prior to spawning. After spawning the index fell rapidly with lowest values recorded in June and July. Variations in the gonadosomatic index are related to developmental stages in females.     

Binding sites for gonadotropins in the ovary of immature and adult mice

Binding sites for gonadotropins in the mouse ovary were studied using the immunohistochemical technique. Binding sites for LH were localized in the interstitial cells and theca as well as granulosa cells of large follicles. Binding sites for FSH were demonstrated in the interstitial cells and granulosa cells of small follicles. In immature mice very few binding sites for both the gonadotropins were observed until day 21 of age. An intense staining reaction for peroxidase was observed in the ovary of 24-day old mouse. In adult mice, maximum number of binding sites for FSH were demonstrated in the ovary in estrus and metestrus stage of the cycle, respectively. A good correlation between the circulating levels of gonadotropins and binding sites for them in the ovary could be noted in the cycling but not in the prepubertal mice.     

Evidence for the existence of substance P in the prepubertal rat ovary. II. Immunocytochemical localization

Nerve fibers containing substance P (SP) were localized in ovaries from juvenile and peripubertal rats by immunofluorescence. These fibers were closely associated with the theca externa of antral follicles, as well as being in the interstitial tissue and within the tunica adventitia of small blood vessels, mostly arterioles. Consistently, the greatest amount of SP immunoreactivity was observed surrounding the ovarian vasculature. Substance P was not detected in cells or within the corpora lutea (CL). Additionally, the peripubertal animals seemed to have a greater concentration of ovarian SP than the juvenile animals. Possible functional roles for this peptide in the ovary are discussed.