Ultrastructural study on nuclear-cytoplasmic relationships in oocytes of the African lungfish,Protopterus aethiopicus

Summary Growing oocytes of Protopterus, like those of some amphibians and teleosts, show an impressive development of the nucleolar apparatus. Numerous nucleolus-like bodies establish close spatial relationships with the nuclear envelope by extending pedicels and streams of finely dispersed material towards the inner membrane.At such contact points, gaps in the perinuclear cistern are more frequent than elsewhere along the nuclear boundary. Expansion of the outer nuclear membrane gives rise to blebs, with or without visible content, and these become pinched off to form small vesicles in the perinuclear cytoplasm.Small, electron dense aggregates, indistinguishable from nucleolar material occur on both sides of the nuclear envelope opposite to each other, some being connected by a slender portion of the same material within a nuclear pore. Such accumulations are interpreted as detached parts of nucleolar bodies in transit to cytoplasmic sites where they presumably participate in the biogenesis of ribosomes. At the height of nucleolar emission, nucleoplasm and perinuclear cytoplasm are so rich in small electron dense particles that they are almost indistinguishable from each other.At this stage of massive transport, the route provided by the nuclear pores seems to be insufficient and another, more spacious, gateway may be in operation. The latter involves direct passage of material across the nuclear membranes preferentially where these form blebs.This view is supported not only by the overt spatial relationships between nucleolar pedicels and blebs, but by the occurrence within perinuclear lacunae and blebs of particles that seem to be derived from nucleolar bodies. Furthermore, frequent interruptions in the nuclear membranes preferentially located where they expand into outpocketings suggest that at these sites temporary gateways may exist in the living cell that permit easy access of intranuclear components to the cytoplasm.Supported by grants AM-3984, NB-00840, and NB-05219 from the U.S.P.H.S.     

Electron Microscope Studies of Nuclear Extrusions in Pancreatic Acinar Cells of the Rat

This paper describes "blebs" protruding from the surface of the nucleus into the cytoplasm. The "blebs" are separated from the cytoplasm by 2 membranes which are continuous with the outer and inner nuclear membranes. The "blebs" contain 3 structurally distinct substances. Two of these substances (β and γ substances) are similar to extranucleolar karyoplasm and nucleolar material. The other substance (α substance) is present in every "bleb," but it cannot be readily compared to a recognizable nuclear structure. Cytoplasmic vesicles are described that are apparently different from the Golgi vesicles or the vesicular component of the ergastoplasm. It is suggested that these vesicles may be of nuclear "bleb" origin. A dark karyoplasmic zone extending from the region of the nucleolus into the nuclear "bleb" is shown. This zone may be similar in some respects to the preformed pathway ("Leitbahn") described by Altmann (3) and Hertl (28) and could reflect movement of nuclear material from the nucleolar region into the cytoplasm. The "blebs" are thought to be homologous to structures described by many light microscopists, but they are considerably larger than the nuclear "blebs" described previously by electron microscopists.     

Electron microscopic studies on the foraminiferAllogromia laticollaris arnold mitosis in agamonts

Summary During mitosis in multinucleated agamonts ofAllogromia laticollaris the nucleolar substance cannot be demonstrated in the nuclei, but only in the cytoplasm as large opaque bodies, some of which are surrounded by two membranes. Only a few smaller bodies are still present within vacuoles of young agamonts formed subsequent to the dividing state. Since the nuclear envelope persists during karyokinesis, the division spindle is localized intranuclearly. The component continuous microtubules, which prefer the nuclear periphery, are mostly visible as bundles, whereas the microtubules running to the chromosomes appear single and less numerous. Centrosomes can be noticed not only at elongated but also at ovoid or irregularly shaped nuclei. These centrosomes represent round or elliptic bodies surrounded by a membrane and consist of granular and fibrillar material. They occur within the perinuclear space and are restricted to the state of karyokinesis.     

THE NUCLEAR ENVELOPE : ITS STRUCTURE AND RELATION TO CYTOPLASMIC MEMBRANES

An electron microscope study of thin sections of interphase cells has revealed the following:— Circular pores are formed in the double nuclear envelope by continuities between the inner and outer membranes which permit contact between the nucleoplasm and the cytoplasm unmediated by a well defined membrane. The pores, seen in sections normal to the nuclear envelope, are profiles of the ring-shaped structures described by others and seen in tangential section. The inner and outer nuclear membranes are continuous with one another and enclose the perinuclear space. The pores contain a diffuse, faintly particulate material. A survey of cells of the rat derived from the embryonic ectoderm, mesoderm, and endoderm, and of a protozoan and an alga has revealed pores in all tissues examined, without exception. It is concluded that pores in the nuclear envelope are a fundamental feature of all resting cells. In certain cells, the outer nuclear membrane is continuous with membranes of the endoplasmic reticulum, hence the perinuclear space is continuous with cavities enclosed by those membranes. There are indications that this is true for all resting cells, at least in a transitory way. On the basis of these observations, the hypothesis is made that two pathways of exchange exist between the nucleus and the cytoplasm; by way of the perinuclear space and cavities of the endoplasmic reticulum and by way of the pores in the nuclear envelope.     

The nuclear envelope; its structure and relation to cytoplasmic membranes

An electron microscope study of thin sections of interphase cells has revealed the following:- Circular pores are formed in the double nuclear envelope by continuities between the inner and outer membranes which permit contact between the nucleoplasm and the cytoplasm unmediated by a well defined membrane. The pores, seen in sections normal to the nuclear envelope, are profiles of the ring-shaped structures described by others and seen in tangential section. The inner and outer nuclear membranes are continuous with one another and enclose the perinuclear space. The pores contain a diffuse, faintly particulate material. A survey of cells of the rat derived from the embryonic ectoderm, mesoderm, and endoderm, and of a protozoan and an alga has revealed pores in all tissues examined, without exception. It is concluded that pores in the nuclear envelope are a fundamental feature of all resting cells. In certain cells, the outer nuclear membrane is continuous with membranes of the endoplasmic reticulum, hence the perinuclear space is continuous with cavities enclosed by those membranes. There are indications that this is true for all resting cells, at least in a transitory way. On the basis of these observations, the hypothesis is made that two pathways of exchange exist between the nucleus and the cytoplasm; by way of the perinuclear space and cavities of the endoplasmic reticulum and by way of the pores in the nuclear envelope.     

Impairment of nuclear pores in bovine herpesvirus 1-infected MDBK cells

Herpesvirus capsids originating in the nucleus overcome the nucleocytoplasmic barrier by budding at the inner nuclear membrane. The fate of the resulting virions is still under debate. The fact that capsids approach Golgi membranes from the cytoplasmic side led to the theory of fusion between the viral envelope and the outer nuclear membrane, resulting in the release of capsids into the cytoplasm. We recently discovered a continuum from the perinuclear space to the Golgi complex implying (i) intracisternal viral transportation from the perinuclear space directly into Golgi cisternae and (ii) the existence of an alternative pathway of capsids from the nucleus to the cytoplasm. Here, we analyzed the nuclear surface by high-resolution microscopy. Confocal microscopy of MDBK cells infected with recombinant bovine herpesvirus 1 expressing green fluorescent protein fused to VP26 (a minor capsid protein) revealed distortions of the nuclear surface in the course of viral multiplication. High-resolution scanning and transmission electron microscopy proved the distortions to be related to enlargement of nuclear pores through which nuclear content including capsids protrudes into the cytoplasm, suggesting that capsids use impaired nuclear pores as gateways to gain access to the cytoplasmic matrix. Close examination of Golgi membranes, rough endoplasmic reticulum, and outer nuclear membrane yielded capsid-membrane interaction of high identity to the budding process at the inner nuclear membrane. These observations signify the ability of capsids to induce budding at any cell membrane, provided the fusion machinery is present and/or budding is not suppressed by viral proteins.     

Spindle membranes and calcium sequestration during meiosis ofDysdercus intermedius (Heteroptera)

The fate of intracellular membranes stained by the osmium ferricyanide (OsFeCN) procedure was followed from premeiotic interphase to interkinesis inDysdercus intermedius. During diakinesis the centrioles forming primary cilia attach temporarily with their proximal ends to the nuclear envelope which is stretched from pole to pole. Breakdown of the nuclear envelope is preceded by deep indentations with microtubules from growing asters. Vesicles of smooth endoplasmic reticulum which accumulate gradually in the course of prophase contribute to the ensheathment of the chromosomes with membranes. When the nuclear envelope breaks down, the polar parts of the formerly perinuclear membranes follow the ingrowth of the spindle microtubules towards the cell equator where the seven bivalents are arranged in a circle with the X₁X₂ sex chromosomes in the centre. The metaphase I spindle thus contains longitudinally oriented membranes between the poles, membranous envelopes around all chromosomes and radial connections from the autosomes to the sex chromosomes in the centre. At anaphase the homologues leave their common sheath and a microtubular stembody surrounded by membranes appears between the receding dyads. In the interkinetic nucleus the gonosomes are separated from the autosomes by a common membranous sheath which may be instrumental in their joint assignment to only one pole in the second meiotic division. Calcium sequestering sites visualized by oxalate precipitation are the Golgi lamellae and vesicles derived from them that surround the whole spindle body.     

Ultrastructural Features of Mitosis in Anisonema sp. (Euglenida)1

The fine structure of stages in mitosis in a colorless euglenoid, Anisonema sp., reveals that chromosomes remain condensed throughout the life cycle and are attached to the nuclear envelope at interphase. The onset of mitosis is marked by the anterior migration of the nucleus towards the base of the reservoir and by elongation of the nucleolus. The nuclear envelope persists throughout mitosis. Microtubules are generated in the peripheral nucleoplasm adjacent to the envelope and attach to the chromosomes while they are still associated with the envelope. The region of microtubular contact develops into a distinct layered kinetochore as the developing spindle with attached chromosomes separates from the nuclear envelope and moves into the nucleoplasm. The mature spindle consists of a number of subspindles each containing about 8–10 microtubules and a few associated chromosomes. Both chromosomal and non-chromosomal microtubules are present in each subspindle and extend towards the envelope terminating at or near the nuclear pores. Chromosomal segregation is concomitant with nuclear elongation. By late division, an interzonal spindle develops in the dumbbell-shaped nucleus and nucleolar separation occurs. Continued invagination of the nuclear envelope in the region of the interzonal spindle eventually separates the daughter nuclei. A remnant of the interzonal spindle persists in the cytoplasm until cytokinesis.     

ELECTRON MICROSCOPIC STUDIES ON THE OOGENESIS OF DRAGONFLY AND CRICKET WITH SPECIAL REFERENCE TO THE PANOISTIC OVARIES

The successive ultrastructural changes during oogenesis in Sympetrum frequens (Odonata, Libellulidae) and Gryllus yemma (Orthoptera, Gryllidae) were studied.
The structures of the terminal filament and boundary between the terminal filament and the germarium differed from each other in these 2 species; in Sympetrum the boundary between the terminal filament and the germarium was a special acellular transverse septum, whereas that in Gryllus was composed of several flattened cells which seemed to be similar to the prefollicular cells in the germarium.
During the previtellogenesis, the nucleolar extrusions and emissions of the outer nuclear envelope were observed frequently in young oocytes. In Sympetrum , electron dense masses were observed in the oocyte cytoplasm, which seemed to be "yolk nuclei" or "Balbiani bodies" and were composed of aggregated small particles (about 200 A in diameter). They were gradually dispersed in the cytoplasm until the onset of vitellogenesis.
In both Sympetrum and Gryllus , yolk precursors seemed to be incorporated into oocytes by micropinocytosis as observed in various animals.
The egg membranes, viz. , the vitelline membrane and the chorion, seemed to be formed by products from follicle cells which developed rough-surfaced endoplasmic reticulum and Golgi bodies. Thus, both of these egg membranes were assumed to be the secondary egg membranes.     

FERTILIZATION IN OEDOGONIUM. III. KARYOGAMY

Karyogamy is described in Oedogonium cardiacum from ultrastructural studies. Close proximity of the two gamete nuclei in the fusion cell is established by plasmogamy, whereas karyogamy appears to be initiated by multiple contacts formed between the outer membranes of the adjoining nuclear envelopes. Blebs of endoplasmic reticulum (ER) originate from the outer membrane of each nuclear envelope; these ER blebs presumably contact and fuse with the outer membrane of the nuclear envelope of the opposing nucleus. This is followed by the fusion of the inner membranes of the opposing nuclear envelopes, thereby resulting in a series of small connective bridges between the two gamete nuclei. It is estimated that in this manner 30–50 bridges are formed, perhaps many more. Several of these bridges enlarge relative to the others; one presumably becomes the major connection between the fusing nuclei. As it continues to enlarge, any organelles positioned between the fusing nuclei are pushed aside. There is also evidence, particularly in later stages of karyogamy, that the smaller connective bridges fuse to form larger ones. Temporary cytoplasmic channels often result at the juncture of fusion. In other instances, isolated inclusions of cytoplasm may be delimited by remnants of nuclear envelope deep within the developing zygote nucleus; these inclusions disappear with subsequent development. Throughout karyogamy the contribution of the male gamete nucleus is readily recognized by the characteristic appearance of its highly condensed chromatin. Ultimately, however, this distinction is lost and the content of the mature zygote nucleus assumes a more uniform appearance very similar to that of an egg nucleus. The complete process of fertilization in Oedogonium may occur within 15 min of mixing the spermatozoids with eggs.     

Synthesis, transport and incorporation into the nuclear envelope of A-type lamins and inner nuclear membrane proteins

The mammalian NE (nuclear envelope), which separates the nucleus from the cytoplasm, is a complex structure composed of nuclear pore complexes, the outer and inner nuclear membranes, the perinuclear space and the nuclear lamina (A- and B-type lamins). The NE is completely disassembled and reassembled at each cell division. In the present paper, we review recent advances in the understanding of the mechanisms implicated in the transport of inner nuclear membrane and nuclear lamina proteins from the endoplasmic reticulum to the nucleus in interphase cells and mitosis, with special attention to A-type lamins.     

Nucellar degeneration inCortaderia (Gramineae)

Summary Vigorous degradation of nucellar tissue in the apomictic grassCortaderia jubata is associated with early degeneration of the megaspore mother cell and the subsequent enlargement of several cells to form somatic embryo sacs. Nucellar degeneration is recognised by the separation of the nuclear membranes, at first along only small sectors of the nucleus, and the appearance within the enlarging perinuclear space of vesicles formed by blebbing of both the inner and outer membranes of the nuclear envelope. Invaginations of the bounding membrane of the dilating RER are responsible for many single-membrane-bound vesicles lying in cisternae throughout the cytoplasm. Eventually the nucleus, enclosed mainly in the inner nuclear membrane, and the cytoplasm, are subject to extensive vesicularization. An electron opaque substance is present in the perinuclear space, in the ER, in vacuoles, and outside the plasmalemma adjacent to the degenerating cell wall, and is similar to a substance which appears on the inner and outer membrane surfaces of mitochondria during later stages of cell degeneration. It is suggested that the genesis and growth of embryo sacs inC. jubata are linked with a programmed nucellar cell autolysis.     

Development of a nuclear polyhedrosis virus in midgut cells and penetration of the virus into the hemocoel of the armyworm,Pseudaletia unipuncta

The development of a nuclear polyhedrosis virus (NPV) in larval midgut cells of the armyworm, Pseudaletia unipuncta, is similar to that of other NPV. In the nucleus, the envelopes around the nucleocapsids seem to be derived de novo or from the inner layer of the nuclear envelope wich forms cisternae, blebs, or infoldings. The nucleocapsids are also enveloped by synhymenosis during passage through the nuclear membrane, the cell membrane, or the endoplasmic reticulum membrane. Both enveloped and unenveloped nucleocapsids may enter the cytoplasm through the nuclear pore or budding through the nuclear membrane. From the cytoplasm the virions may enter the hemocoel through the basal cell and basement membranes or through the endoplasmic reticulum, intercellular space, and the basement membrane.     

Primary envelopment of pseudorabies virus at the nuclear membrane requires the UL34 gene product

Primary envelopment of several herpesviruses has been shown to occur by budding of intranuclear capsids through the inner nuclear membrane. By subsequent fusion of the primary envelope with the outer nuclear membrane, capsids are released into the cytoplasm and gain their final envelope by budding into vesicles in the trans-Golgi area. We show here that the product of the UL34 gene of pseudorabies virus, an alphaherpesvirus of swine, is localized in transfected and infected cells in the nuclear membrane. It is also detected in the envelope of virions in the perinuclear space but is undetectable in intracytoplasmic and extracellular enveloped virus particles. Conversely, the tegument protein UL49 is present in mature virus particles and absent from perinuclear virions. In the absence of the UL34 protein, acquisition of the primary envelope is blocked and neither virus particles in the perinuclear space nor intracytoplasmic capsids or virions are observed. However, light particles which label with the anti-UL49 serum are formed in the cytoplasm. We conclude that the UL34 protein is required for primary envelopment, that the primary envelope is biochemically different from the final envelope in that it contains the UL34 protein, and that perinuclear virions lack the tegument protein UL49, which is present in mature virions. Thus, we provide additional evidence for a two-step envelopment process in herpesviruses.     

Cytological Studies of Large Nucleus-Like Structures Formed by Exogenously-Injected Linear and Circular DNAs in Fertilized Eggs of Xenopus laevis

Relatively large amounts of linear or circular DNAs were injected into the animal or vegetal cytoplasm of fertilized eggs of Xenopus laevis and the nature of large nucleus-like structures formed by the injected DNAs was studied cytologically and electron microscopically. Results of fluorescent microscopic examination combined with immunohistochemical analysis strongly suggested that the injected DNAs were assembled into the nucleus-like structures probably after being complexed with maternal histones. The assemblage of nucleus-like structures preferentially took place in the animal most region of the egg, and the size of the nucleus-like structures formed depended on the amount of the injected DNA. The nucleus-like structures were surrounded by double membranes equipped with nuclear pore complexes, but there were at least two abnormal features in their ultrastructures. First, nucleus-like structures contained cytoplasmic particulate materials, most probably ribosomes and/or glycogen granules. Secondly, many of the nuclear pore complexes on the "nuclear envelope" appeared to be incomplete, with blebs formed from inner leaflet and protruded into the perinuclear space. Injected circular plasmid DNAs were also assembled into large nucleus-like structures in the animal most region, and appeared to be partitioned into descendant cells during the cleavage.     

Herpes simplex virus 1 envelopment follows two diverse pathways

Herpesvirus envelopment is assumed to follow an uneconomical pathway including primary envelopment at the inner nuclear membrane, de-envelopment at the outer nuclear membrane, and reenvelopment at the trans-Golgi network. In contrast to the hypothesis of de-envelopment by fusion of the primary envelope with the outer nuclear membrane, virions were demonstrated to be transported from the perinuclear space to rough endoplasmic reticulum (RER) cisternae. Here we show by high-resolution microscopy that herpes simplex virus 1 envelopment follows two diverse pathways. First, nuclear envelopment includes budding of capsids at the inner nuclear membrane into the perinuclear space whereby tegument and a thick electron dense envelope are acquired. The substance responsible for the dense envelope is speculated to enable intraluminal transportation of virions via RER into Golgi cisternae. Within Golgi cisternae, virions are packaged into transport vacuoles containing one or several virions. Second, for cytoplasmic envelopment, capsids gain direct access from the nucleus to the cytoplasm via impaired nuclear pores. Cytoplasmic capsids could bud at the outer nuclear membrane, at membranes of RER, Golgi cisternae, and large vacuoles, and at banana-shaped membranous entities that were found to continue into Golgi membranes. Envelopes originating by budding at the outer nuclear membrane and RER membrane also acquire a dense substance. Budding at Golgi stacks, designated wrapping, results in single virions within small vacuoles that contain electron-dense substances between envelope and vacuolar membranes.     

The ultrastructure of the rabbit oocyte at the bilaminar follicle stage]

The electron microscope study of the nucleus and organoids of the rabbit oocytes cytoplasm during growth showed nucleoluslike bodies (RNP-granules) on the lampbrushen chromosomes to reach their maximal size at the stage of bilaminar follicle. The RNP-granules differ from the nucleoli by the time of their occurrence cytochemical characteristics, and by their ultrastructural pattern. Throughout the bilaminar follicle stage four components may be seen in the oocyte nucleolus: a dense fibrillar framework around the vacuoles, islets of the granular mass loosely dispersed, and electron dense fibrillar elements filling up the numberous electrontransparant vacuoles. The nucleolus-like bodies are round in shape and have no vacuoles, consisting to two components only: distinctly outlined granules, and weakly developed fibrillar component. The nuclear envelope is seen blebbing. Separation of two nuclear membranes forms a pocket-like enlargements of the perinuclear space. The pockets are limited by small regions between the adjacent nuclear pores. The outer membrane may bulge producing lacuma and large channels in the cytoplasm, which are interconnected making a closed branched network extending inside of the cytoplasm. The nuclear envelope is suggested to be involved in formation of the endoplasmic reticulum through the blebbing process.     

An ultrastructural study of oogenesis in a marine triclad

The ultrastructural features of oocyte differentiation were studied in the marine triclad Cercyra hastata. Oocytes at several stages of maturation, each surrounded by follicle cell projections, are present within each of the two ovaries. A pre-vitellogenic and a vitellogenic stage have been detected in the oogenesis of C. hastata. The pre-vitellogenic stage is mainly characterized by an increase in the nuclear and nucleolar volume and activity, and the appearance and development of cortical granule precursors which are elaborated by the Golgi complex. In early phases of the vitellogenic stage, intense delamination and blebbing of the nuclear envelope occurs which probably contributes to an increase in number of cytoplasmic membranes and to transfer of nuclear material to the cytoplasm. The rough endoplasmic reticulum is extensively developed and often assumes a ‘whorl’ array. Several areas of yolk precursor formation appear in the whorls. Numerous 2–5 μm protein yolk globules are subsequently formed which appear surrounded by a double membrane (cisternae of the smooth endoplasmic reticulum) and become randomly distributed throughout the cytoplasm of mature oocytes. The peripheral ooplasm is occupied by a monolayer of electron-dense cortical granules. Finally, the evolutionary significance of the autosynthetic mechanism of yolk production is discussed.     

Atg39 links and deforms the outer and inner nuclear membranes in selective autophagy of the nucleus

In selective autophagy of the nucleus (hereafter nucleophagy), nucleus-derived double-membrane vesicles (NDVs) are formed, sequestered within autophagosomes, and delivered to lysosomes or vacuoles for degradation. In Saccharomyces cerevisiae, the nuclear envelope (NE) protein Atg39 acts as a nucleophagy receptor, which interacts with Atg8 to target NDVs to the forming autophagosomal membranes. In this study, we revealed that Atg39 is anchored to the outer nuclear membrane via its transmembrane domain and also associated with the inner nuclear membrane via membrane-binding amphipathic helices (APHs) in its perinuclear space region, thereby linking these membranes. We also revealed that autophagosome formation-coupled Atg39 crowding causes the NE to protrude toward the cytoplasm, and the tips of the protrusions are pinched off to generate NDVs. The APHs of Atg39 are crucial for Atg39 crowding in the NE and subsequent NE protrusion. These findings suggest that the nucleophagy receptor Atg39 plays pivotal roles in NE deformation during the generation of NDVs to be degraded by nucleophagy.     

Nucleolus disassembly in mitosis and apoptosis: dynamic redistribution of phosphorylated-c-Myc, fibrillarin and Ki-67

The nucleolus may undergo disassembly either reversibly during mitosis, or irreversibly in apoptosis, thus allowing the redistribution of the nucleolar proteins. We investigated here by immunocytochemistry the fate of three representative proteins, namely phosphorylated c-Myc, fibrillarin and Ki-67, and found that they behave independently in both processes: they relocate in distinct compartments during mitosis, whereas during apoptosis they may either be cleaved (Ki-67) or be extruded into the cytoplasm with a different kinetics and following an ordered, non chaotic program. The separation of these nucleolar proteins which occurs in early apoptotic nuclei continues also in the cytoplasm, and culminates in the final formation of apoptotic blebs containing different nucleolar proteins: this evidence confirms that the apoptotic bodies may be variable in size, content and surface reactivity, and include heterogeneous aggregates of nuclear proteins and/or nucleic acids.