Intercellular connections between germ cells in the developing human ovary

Summary An electron microscopic examination of human fetal ovaries reveals the presence of intercellular bridges between developing germ cells. The bridges are characterized by a band of electron-dense material beneath the lateral limiting membrane, and cell organelles are seen within the confines of these connections. Their general morphology is similar to that described in ovaries of other species. The possible functional significance of these connections is discussed.This work was supported by grants from the Edward G. Schlieder Educational Foundation, New Orleans, Louisiana State University and HD-03288 from the National Institute of Child Health and Human Development.The authors would like to thank Miss Cathy Chase for her technical assistance.     

The occurrence of intercellular bridges during oogenesis in the mouse

A fine structural analysis of fetal mouse ovaries reveals the presence of intercellular bridges between developing oocytes. These bridges, which connect two or more oocytes, are most frequently seen prior to the dictyate stage of meiotic prophase. The intercellular connections are limited by a tri-laminar membrane which is continuous with the oocyte plasmalemma. A characteristic feature of all bridges is the presence of an electron-dense material on the cytoplasmic side of the limiting membrane. Since this dense material is a constant and conspicuous component of the entire bridge, identification of these connections is possible in all planes of section. In cross section, the bridges are usually cylindrical, while in longitudinal section, a variety of configurations are observed. Oocytes connected by intercellular bridges exhibit a highly developed Golgi complex which is frequently localized in the region of the cytoplasmic continuities. Vesicular elements, apparently derived from the Golgi, are routinely observed within the boundaries of the bridges. Other cytoplasmic organelles, including rough and smooth endoplasmic reticulum, free ribosomes and mitochondria, are also seen in these bridges. The presence of these vesicles and organelles within intercellular bridges suggests that these connections may provide a means for transfer of organelles and other substances from one oocyte to another. It may be, therefore, that intercellular bridges are important for the nourishment and maturation of certain selected oocytes as well as for the synchronization of meiotic events.     

Oogenesis in four species of Piscicola (Hirudinea, Rhynchobdellida)

Piscicola has a pair of elongated sac-shaped ovaries. Inside the ovaries are numerous small somatic cells and regularly spherical egg follicles. Each follicle is composed of three types of cells: many (average 30) germ cells (cystocytes) interconnected by intercellular bridges in clones (cysts), one intermediate cell, and three to five outer follicle cells (envelope cells). Each germ cell in a clone has one intercellular bridge connecting it to the central anucleate cytoplasmic mass, the cytophore. Each cluster of germ cells is completely embedded inside a single huge somatic follicle cell, the intermediate (interstitial) cell. The most spectacular feature of the intermediate cell is its development of a system of intracytoplasmic canals apparently formed of invaginations of its cell membrane. Initially the complex of germ cell cluster + intermediate cell is enclosed within an envelope composed of squamous cells. As oogenesis progresses the envelope cells gradually degenerate. All the germ cells that have terminated their mitotic divisions are of similar size and enter meiotic prophase, but one of the cystocytes promptly starts to grow faster and differentiates into the oocyte, whereas the remaining cystocytes withdraw from meiosis and become nurse cells (trophocytes). Numerous mitochondria, ER, and a vast amount of ribosomes are transferred from the trophocytes via the cytophore toward the oocyte. Eventually the oocyte ingests all the content of the cytophore, and the trophocytes degenerate. Little vitellogenesis takes place; the oocyte gathers nutrients in the form of small lipid droplets. At the end of oogenesis, an electron-dense fibrous vitelline envelope appears around the oocyte, among short microvilli. At the same time, electron-dense cortical granules occur in the oocyte cortical cytoplasm; at the end of oogenesis they are numerous, but after fertilization they disappear from the ooplasm. In the present article we point out many differences in the course of oogenesis in two related families of rhynchobdellids: piscicolids and glossiphoniids.     

Oocytes develop from interconnected cystocytes in the panoistic ovary of Nemoura sp. (Pictet) (Plecoptera : Nemouridae)

The 2 ovaries of Nemoura sp. (Plecoptera : Nemouridae) are comb-like and house about 60–70 ovarioles each. By ultrathin serial sections through a whole ovariole of a last-larval instar, we gathered information on its ultrastructure and 3-dimensional architecture. The germarial region contains several clusters of interconnected oogonia or oocytes. The intercellular bridges (ring canals) are filled with fusomes. Most of the fusomes assemble to polyfusomes and some of the intercellular bridges move together and their cells assemble to rosettes. Results indicate that existence of polyfusomes is not sufficient for rosette formation. The oogonia or oocytes of each cluster develop synchronously. Oocytes detach from clusters next to intercellular bridges. A transdetermination of oogonia to nurse cells does not occur. Thus, the stone flies remain true panoists.     

Fine structure of spermatogonia and intercellular bridges in Macaca nemestrina

Spermatogonia of the monkey, Macaca nemestrina, were studied with the electron microscope. The spermatogonial nucleus is characterized by dense homogeneous chromatin and an eccentric nucleolus with a prominent surrounding clear zone. Cytoplasm consists chiefly of free ribosomes and vesicular endoplasmic reticulum. Scattered mitochondria with closely spaced transverse cristae are arranged singly and in pairs separated by thin electron-dense bands. Binucleated spermatogonia resemble other spermatogonia in their ultrastructural characteristics, but contain an increased number of lysosome-like structures and degenerating mitochondria. Spermatogonial interconnections are of two types: broad cytoplasmic connections and narrow intercellular bridges. Connected cells are always identical in appearance and stage of maturation. Multiple connections occur. Interconnection of spermatogonia provides a syncytial type of arrangement which allows synchronization of differentiation and results in similar apperance of adjoining cells. Similarity of regressive changes in adjacent degenerating cells is explained by the presence of intercellular bridges.     

Intercellular bridges between oocytes in the chicken ovary

Summary Fine structural analysis of the functional (left) ovary of the newly-hatched chick reveals the presence of true intercellular bridges between developing oocytes in the early stages of the meiotic prophase. These structures are characterized by: 1) cytoplasmic continuity between the participating oocytes, 2) a dense, fibrillar material beneath the lateral limiting membrane and 3) numerous cellular organelles within their confines. In addition, microtubular elements, parallel to the long axis of the bridge, are routinely observed. This latter finding suggests that intercellular bridges originate through incomplete cytokinesis of mitotically active oogonia and that the dense material beneath the limiting membrane may represent the cortical microfilaments associated with the contractile ring. Functionally, these structures may serve as channels for transfer of nutrients and organelles between oocytes although the possibility that certain oocytes function as nurse cells, in the sense that these cells exist in invertebrate ovaries, seems unlikely. In addition, intercellular bridges may be responsible for both restriction of oogonial mitoses and meiotic synchrony.Partial support for this study was provided by grant DE-00241 from the National Institute for Dental Research administered by Dr. Melvin Hess. We gratefully acknowledge his support of the initial aspects of this study. We are pleased to express our appreciation to Mrs. Cindy G. Wilcox, Mr. Lloyd Thibodeau and Mr. Don Driscoll for their expert technical assistance.     

Early oogenesis in the short-tailed fruit bat Carollia perspicillata: transient germ cell cysts and noncanonical intercellular bridges

The ovaries of early embryos (40 days post coitum/p.c.) of the bat Carollia perspicillata contain numerous germ-line cysts, which are composed of 10 to 12 sister germ cells (cystocytes). Variability in the number of cystocytes within the cyst and between the cysts (defying the Giardina rule) indicates that the mitotic divisions of the cystoblast are asynchronous in this bat species. Serial section analysis showed that the cystocytes are interconnected via intercellular bridges that are atypical, strongly elongated, short-lived, and rich in microtubule bundles and microfilaments. During slightly later stages of embryonic development (44-46 days p.c.), somatic cells penetrate the cyst, and their cytoplasmic projections separate individual oocytes. Separated oocytes surrounded by a single layer of somatic cells constitute the primordial ovarian follicles. The oocytes of C. perspicillata are similar to mouse oocytes and are asymmetric. In both species, this asymmetry is clearly recognizable in the localization of the Golgi complexes. The presence of germ-line cysts and intercellular bridges (although noncanonical) in the fetal ovaries of C. perspicillata suggest that the formation of germ-line cysts is an evolutionarily conserved phase in the development of the female gametes in a substantial part of the animal kingdom.     

The formation of intercellular spaces in the cotyledons of developing and germinating pea seeds

Summary Electron microscopic observations have shown that the intercellular spaces in the storage parenchyma of the cotyledons of pea (Pisum sativum L.) seeds arise schizogenously. The wall segments adjoining future intercellular spaces display a triple zonation and contain regions with electron-dense material. Space formation starts at the central point of contact between several cells and spreads then further up to the electron-dense, intra-wall structures. As a result of this the electron-dense material is found again in the corners of intercellular spaces. It is proposed that the intra-wall structures may have an important function in limiting the schizogenous process. The localization of the intercellular spaces is thus predetermined. The amount of electron-dense material in their corners increases considerably during further development of the embryo. During germination wall segments between two intercellular spaces diverge resulting in a fusion of several spaces.     

Actin localization in male germ cell intercellular bridges in the rat and ground squirrel and disruption of bridges by cytochalasin D

Filaments about 6-7 nm in diameter were seen associated with germ cell intercellular bridges in detergent-permeabilized cells treated with tannic acid. Approximately 40-50 filaments were present subjacent to the bridge density. Filaments encircled the bridge channel in a manner similar to contractile ring actin filaments of dividing cells. NBD-phallacidin and myosin S-1 subfragments were employed to demonstrate that the filaments observed at intercellular bridges are actin. Intratesticular injection of a single dose of cytochalasin D, a specific inhibitor of actin filaments, caused certain intercellular bridges of spermatids to open within 3 hr after injection, leading to the production of symplasts. During bridge opening, remnants of bridge densities were gradually incorporated into the lateral aspect of the plasma membrane of the symplast. Thus actin, present in bridge structures, appeared to participate in maintaining certain intercellular bridges. A model of intercellular bridge structure is presented.     

The linear clusters of oogonial cells in the development of telotrophic ovarioles in polyphageColeoptera

Summary During the premetamorphic development of coleopteran telotrophic ovaries the culsters of sister oogonial cells, in which the differentiation of nurse cells and oocytes occurs, are arranged in linear chains. This results from a series of mitoses with the consistent orientation of the spindle parallel to the long axis of the ovariole. As a result of incomplete cytokinesis, the oogonial cells in each sibling cluster are linked to each other by intercellular bridges occupied by fusomes. As a rule, at each cluster division the basal cell (i.e. the oocyte progenitor) starts to divide first. From this cell a wave of mitoses spreads toward the anterior end of the cluster, resulting in a mitotic gradient. It is suggested that the failure of the fusomes in adjacent cells to fuse into one continuous fusome (i.e. polyfusome) allows the spindles to orientate with their long axes parallel to the long axis of the sibling cluster. This would explain why the oogonial divisions in coleopteran telotrophic ovaries generate linear chains of cells rather than the cyst-like arrangement which is typical for polytrophic sibling clusters. Dividing sibling clusters within ovarioles are arranged in bundles. The presence of intercellular bridges between sibling clusters seems to be the underlying cause of this nonrandom distribution of the mitotically active clusters. The transverse bridges have been found to occur between the basal cells as well as between the cells located more anteriorly in adjacent sibling clusters. The transverse bridges are filled with typical fusomes, which in more anterior parts of sibling clusters may fuse with the fusomes of adjacent sister oogonial cells into polyfusomes. The transverse bridges between the basal cells are incorporated in the oocytes. The pattern of sibling cluster formation described in this paper apparently occurs widespread in polyphagous Coleoptera, since it has been found in three relatively distantly related families.     

Expression of connexin 43 mRNA and protein in developing follicles of prepubertal porcine ovaries

A major form of cell-cell communication is mediated by gap junctions, aggregations of intercellular channels composed of connexins (Cxs), which are responsible for exchange of low molecular weight (<1200 Da) cytosolic materials. These channels are a growing family of related proteins. This study was designed to determine the ontogeny of connexin 43 (Cx43) during early stages of follicular development in prepubertal porcine ovaries. A partial-length (412 base) cDNA clone was obtained from mature porcine ovaries and determined to have 98% identity with published porcine Cx43. Northern blot analysis demonstrated a 4.3-kb mRNA in total RNA isolated from prepubertal and adult porcine ovaries. In-situ hybridization revealed that Cx43 mRNA was detectable in granulosa cells of primary follicles but undetectable in dormant primordial follicles. The intensity of the signal increased with follicular growth and was greatest in the large antral follicles. Immunohistochemical evaluation indicated that Cx43 protein expression correlated with the presence of Cx43 mRNA. These results indicate that substantial amounts of Cx43 are first expressed in granulosa cells following activation of follicular development and that this expression increases throughout follicular growth and maturation. These findings suggest an association between the enhancement of intercellular gap-junctional communication and onset of follicular growth.     

Ultrastructure of the cells of the ovarian interstitial gland in hypophysectomized rats

Summary The fine structure of the interstitial gland of the ovary was studied in hypophysectomized rats and in hypophysectomized rats after denervation of the ovary or stimulation of the ovarian plexus. Hypophysectomized rats were used to eliminate gonadotropic influences on interstitial cells. In hypophysectomized rats, there was a large amount of intercellular space and cells had irregularly shaped nuclei and a large nuclear-cytoplasmic ratio. Prominent cytoplasmic features included small mitochondria with an electron-dense matrix, rough and smooth endoplasmic reticulum, polysomes and large osmiophilic lipid droplets. Interstitial cells from stimulated ovaries had reduced intercellular space and a reduced nuclear-cytoplasmic ratio. Mitochondria had tubular cristae; smooth endoplasmic reticulum-surrounded lipid droplets, and large polysomes were present. After section of the ovarian plexus, intercellular space was increased and filopodia were numerous. Cytoplasmic features included mitochondria with a dense matrix and indistinct cristae, large electronlucent lipid droplets, and variously sized multivesicular structures. These observations suggest that stimulation of the ovarian plexus in hypophysectomized rats causes regressed cells to assume the fine structural features of active steroidogenic cells. In contrast, interruption of the ovarian nerve supply causes a qualitative and quantitative increase in ultrastructural features characteristic of regressed steroidogenic cells. These responses of interstitial gland cells to denervation and stimulation provide morphological evidence for a functional role for the adrenergic nerves to this ovarian compartment.     

The formation of intercellular bridge coating in the hairy whirligig beetle,Orectochilus villosus

Summary The ultrastructure of the intercellular bridges in the ovaries of Orectochilus villosus has been studied. In young egg chambers the inner filamentous coating of the bridge is thin. Characteristic vesicles are observed in close contact with this coating. The inner coating of the vitellogenic chambers is fully developed although vesicles are only sporadically associated with it. These observations suggest that the vesicles are involved in the formation of the filamentous coating.This work was supported by Government Problem Grant MR II, 1.6.4.     

Clonal development of interconnected germ cells in the rat and its relationship to the segmental and subsegmental organization of spermatogenesis.

Segments and subsegments are the smallest unit of synchrony thus far described within longitudinal sections of seminiferous tubules. It is known that cells in a clone joined by intercellular bridges are at the same phase of development and are also thought to be units of synchrony. This study was designed to determine if it is possible that the synchrony seen in cells joined by intercellular bridges is the same as that cataloged along the long axis of the seminiferous tubule. In the present study, the maximum number of rat spermatids joined by intercellular bridges (a clone) was obtained. It was hypothesized that if the clone size were larger than the smallest known units of synchrony (segments or subsegments) in the long axis of the seminiferous tubule, then intercellular bridges would most likely govern the synchronous development of segments or subsegments (or finer subdivisions thereof). If the clone size is smaller than the number of cells present in a segment or subsegment, then other factors must govern synchrony in the longitudinal aspect of the tubule. In the determination of spermatid clone size, rat testes were injected with cytochalasin D which opens intercellular bridges of a spermatid clone to produce large symplasts. The number of nuclei in the symplasts was determined from serially sectioned tissue, by drawing nuclei with a camera-lucida, and by counting nuclei. After extensive examination of tubules, the number of spermatids found in the suspected five largest clones observed was determined to be 650, 607, 338, 240, and 177.(ABSTRACT TRUNCATED AT 250 WORDS)     

Germ cell cluster in the panoistic ovary of Thysanoptera (Insecta)

Summary Germ cell clusters are found in the germarial region of ovarioles of Parthenothrips dracenae. Cluster mitoses are synchronized, at least initially. The intercellular bridges are filled with fusomal material, which can fuse to form polyfusomal aggregates which in turn form small rosettes. All cells develop into oocytes. Oocytes become isolated by a secondary detachment process. Intercellular bridges, together with fusomal material and cell membranes, survive for some time as isolated bodies. Phylogenetic consequences are discussed. The data provide strong evidence for a secondary panoistic ovary in thysanopterans, since cluster formation in ovaries of primary panoists has not been shown.     

Stable intercellular bridges in development: the cytoskeleton lining the tunnel

A wide variety of intercellular junctions that are involved with cell adhesion or signal transduction have been described in recent years. A widespread but less well-characterized type of intercellular junction is the stable intercellular bridge. Several organisms use stable intercellular bridges as cytoplasmic connections, probably to allow rapid transfer of information and organelles between cells. Here, the authors take a detailed look at the assembly of intercellular bridges called ring canals in the Drosophila germline and discuss how examination of mutants that disrupt Drosophila ovarian ring canal assembly indicates that these bridges are required for intercellular transport of cytoplasm.     

Cytonemes and tunneling nanotubules in cell-cell communication and viral pathogenesis

Cells use a variety of intercellular structures, including gap junctions and synapses, for cell-cell communication. Here, we present recent advances in the understanding of thin membrane bridges that function in cell-cell signaling and intercellular transport. Cytonemes or filopodial bridges connect neighboring cells via mechanisms of adhesion, which enable ligand-receptor-mediated transfer of surface-associated cargoes from cell to cell. By contrast, tunneling nanotubes establish tubular conduits between cells that provide for the exchange of both cell-surface molecules and cytoplasmic content. We propose models for the biogenesis of both types of membrane bridges and describe how viruses use these structures for the purpose of cell-to-cell spread.     

Identification and characterization of RBM44 as a novel intercellular bridge protein

Intercellular bridges are evolutionarily conserved structures that connect differentiating germ cells. We previously reported the identification of TEX14 as the first essential intercellular bridge protein, the demonstration that intercellular bridges are required for male fertility, and the finding that intercellular bridges utilize components of the cytokinesis machinery to form. Herein, we report the identification of RNA binding motif protein 44 (RBM44) as a novel germ cell intercellular bridge protein. RBM44 was identified by proteomic analysis after intercellular bridge enrichment using TEX14 as a marker protein. RBM44 is highly conserved between mouse and human and contains an RNA recognition motif of unknown function. RBM44 mRNA is enriched in testis, and immunofluorescence confirms that RBM44 is an intercellular bridge component. However, RBM44 only partially localizes to TEX14-positive intercellular bridges. RBM44 is expressed most highly in pachytene and secondary spermatocytes, but disappears abruptly in spermatids. We discovered that RBM44 interacts with itself and TEX14 using yeast two-hybrid, mammalian two-hybrid, and immunoprecipitation. To define the in vivo function of RBM44, we generated a targeted deletion of Rbm44 in mice. Rbm44 null male mice produce somewhat increased sperm, and show enhanced fertility of unknown etiology. Thus, although RBM44 localizes to intercellular bridges during meiosis, RBM44 is not required for fertility in contrast to TEX14.