Elektronenmikroskopische Untersuchungen über die Eizellbildung und Eizellreifung des Lebermooses Sphaerocarpus donnellii Aust.

1965 ◽  
Vol 20 (8) ◽  
pp. 795-801 ◽  
Author(s):  
Lothar Diers
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Phase Contrast ◽  
Lipid Droplets ◽  
Unit Membrane ◽  
Light Phase ◽  
Lamellar System ◽  
Small Bodies ◽  
Canal Cell ◽  
Ventral Canal

The formation and maturation of the egg of the liverwort, Sphaerocarpus donnellii, was investigated by light, phase contrast and particularly by electron microscopy. The division of the central cell into the egg and the ventral canal cell, and the maturation of the egg, is completed within four days. All stages of this formation and maturation were examined under the electron microscope after fixation in KMnO4 or OsO4. — In the maturing egg there always occur the endoplasmic reticulum, well recognisable plastids with a poorly developed lamellar system, numerous mitochondria and dictyosomes, a rising number of lipid droplets, unknown small bodies limited by a unit membrane, and numerous ribosomes. During maturation the nucleus considerably enlarges and forms evaginations into the cytoplasm. Starch is increasingly deposited in the plastids. A degeneration of plastids has not been found.

Phase-contrast and electron-microscopic observations on a membranous complex in primary spermatocytes of the mouse

1975 ◽  
Vol 18 (1) ◽  
pp. 1-17
Author(s):  
A. Pleshkewych ◽  
L. Levine
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Phase Contrast ◽  
Cultured Cells ◽  
Light And Electron Microscopy ◽  
Cytoplasmic Inclusion ◽  
Electron Microscopic ◽  
Secondary Spermatocyte ◽  
Living Mouse ◽  
Circular Contour

A prominent cytoplasmic inclusion present in living mouse primary spermatocytes has been observed by both light and electron microscopy. It began to form at prometaphase and continued to increase in thickness and length as the cells developed. By metaphase it was a distinct sausage-shaped boundary that enclosed a portion of the cytoplasm between the spindle and the cell membrane. At the end of metaphase, the inclusion reached its maximum length. At telophase, it was divided between the daughter secondaries. The inclusion persisted as a circular contour in the interphase secondary spermatocyte. Electron microscopy of the same cultured cells that were previously observed with light microscopy revealed that the inclusion was a distinctive formation of membranes. It consisted of agranular cisternae and vesicles, and was therefore a membranous complex. Many of the smaller vesicles in the membranous complex resembled those found in the spindle. The cisternae in the membranous complex were identical to the cisternal endoplasmic reticulum of interphase primary spermatocytes. Nevertheless, the organization of vesicles and cisternae into the membranous complex was unique for the primaries in division stages, since such an organization was not present in their interphase stages.

scholarly journals A conserved family of proteins facilitates nascent lipid droplet budding from the ER

2015 ◽  
Vol 211 (2) ◽  
pp. 261-271 ◽  
Author(s):  
Vineet Choudhary ◽  
Namrata Ojha ◽  
Andy Golden ◽  
William A. Prinz
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Lipid Metabolism ◽  
Caenorhabditis Elegans ◽  
Lipid Droplet ◽  
Lipid Droplets ◽  
De Novo ◽  
Fat Storage ◽  
Higher Eukaryotes ◽  
Er Membrane

Lipid droplets (LDs) are found in all cells and play critical roles in lipid metabolism. De novo LD biogenesis occurs in the endoplasmic reticulum (ER) but is not well understood. We imaged early stages of LD biogenesis using electron microscopy and found that nascent LDs form lens-like structures that are in the ER membrane, raising the question of how these nascent LDs bud from the ER as they grow. We found that a conserved family of proteins, fat storage-inducing transmembrane (FIT) proteins, is required for proper budding of LDs from the ER. Elimination or reduction of FIT proteins in yeast and higher eukaryotes causes LDs to remain in the ER membrane. Deletion of the single FIT protein in Caenorhabditis elegans is lethal, suggesting that LD budding is an essential process in this organism. Our findings indicated that FIT proteins are necessary to promote budding of nascent LDs from the ER.

Conidiogenesis in Termitaria snyderi (Fungi Imperfecti)

1973 ◽  
Vol 51 (12) ◽  
pp. 2307-2314 ◽  
Author(s):  
Saeed R. Khan ◽  
Henry C. Aldrich
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Lipid Droplets ◽  
Light And Electron Microscopy ◽  
Cross Wall ◽  
Transverse Septum ◽  
Conidiogenous Locus ◽  
Oriented Parallel ◽  
Fungi Imperfecti

Termitaria snyderi Thaxter forms small discoid lesions on the exoskeleton of different species of termites. Its conidiogenesis has been studied by light and electron microscopy. The phialides are oriented parallel in a closely packed sporodochium. The conidia are produced endogenously in basipetal succession from a fixed conidiogenous locus and are liberated when the tip is broken off the phialide as a result of the force applied by the formation of new conidia. The area of the phialide beyond the locus forms a tubular collarette. The conidium initial buds out at the locus and after it has received its organelles and reached a certain size it is delimited by a centripetally growing transverse septum. The region of the growing septum has many vesicles which may be involved in cross wall synthesis. Conidia are cylindrical, uninucleate, and double-walled. They have mitochondria, endoplasmic reticulum (ER), conspicuous lipid droplets, and vacuoles. Each conidiophore has long mitochondria, elongate nuclei, and much endoplasmic reticulum. The plasmalemma of the conidiophore is highly convoluted.

Structure of Cultured Fibroblasts from Dermatosparaxic Calves

1975 ◽  
Vol 12 (1) ◽  
pp. 16-31 ◽  
Author(s):  
J. A. Yaeger ◽  
R. L. Church ◽  
M. L. Tanzer
Keyword(s):  
Electron Microscopy ◽  
Tissue Culture ◽  
Endoplasmic Reticulum ◽  
Cell Lines ◽  
Lipid Droplets ◽  
Cultured Fibroblasts ◽  
Fibrillar Material ◽  
Golgi Region ◽  
Clonal Cell Lines ◽  
Extracellular Fibrils

Clonal cell lines from the dermis of a dermatosparaxic calf were grown in tissue culture. After fixation in a mixture of glutaraldehyde and osmium, they were prepared for electron microscopy. Most cells contained a well-developed Golgi region, lysosomes, mitochondria, and dilated cisternae of rough endoplasmic reticulum. They also contained numerous, large bundles of intracellular filaments, many lipid droplets and extensive arrays of vesicles. Cultures accumulated substantial amounts of extracellular fibrillar material. The fibrils were loosely packed and indistinctly cross-banded. Bundles of intracellular filaments were commonly parallel in adjacent cells and also parallel to extracellular fibrils. These cytoplasmic features may result from the inability of the secreted collagen to form normal fibrils.

SPERMATOCYTE GRANULES IN DROSOPHILA MELANOGASTER

1969 ◽  
Vol 11 (1) ◽  
pp. 153-168 ◽  
Author(s):  
John Erickson ◽  
A. B. Acton
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Drosophila Melanogaster ◽  
Host Cell ◽  
Acridine Orange ◽  
Meiotic Drive ◽  
Adult Males ◽  
Unit Membrane ◽  
The Third ◽  
The Individual

Granular inclusions are found in testes from a cn bw stock of Drosophila melanogaster, and maternally derived lines, such as SD. In late larval and early pupal stages, these granules show a polarized distribution within primary spermatocytes corresponding to the polarity basic to the type of meiotic drive where certain homologues reach that pole of the spermatocyte leading to functional sperm. In adult males, the granules are found in intercellular patches in the testes. Electron microscopy shows the spermatocyte granules to be spheroids of about 0.7 μ; dividing, or double forms resulting from division, are about 1.8 μ long. They contain numbers of ribosome-like particles and fine strands presumed to be DNA. The acridine orange test for nucleic acids was positive. Each granule is surrounded by two layers of unit membrane and a third such membrane envelopes the individual or the pair of granules, as the case may be. The third membrane layer (and additional membranes sometimes seen) is thought to be due to entrance of the granules into the host cell through the cisternae of the endoplasmic reticulum. Transmission of the granules is strictly maternal and independent of chromosome constitution. Transmission by contagion was not found. Spermatocyte granules are not requisite to the effectiveness of the SD meiotic drive system, which regularly carries them. A slightly lowered fertility of females carrying the granules was found but no similar effect is produced in males. The evidence suggests that they are parasitic organisms, probably Rickettsiae.

scholarly journals Ultrastructure of rhesus monkey renomedullary interstitial cells

1979 ◽  
Vol 13 (2) ◽  
pp. 75-80 ◽  
Author(s):  
David J. Lewis ◽  
David E. Prentice
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Fine Structure ◽  
Rhesus Monkey ◽  
Rough Endoplasmic Reticulum ◽  
Lipid Droplets ◽  
Stellate Cells ◽  
Interstitial Cells ◽  
Prominent Feature

Summary The fine structure of rhesus monkey renomedullary interstitial cells was studied by electron microscopy. These stellate cells contained variable numbers of lipid droplets, moderate numbers of mitochondria, moderate amounts of rough endoplasmic reticulum, and prominent Golgi zones. In rare instances, apparent release of lipid droplets into the interstitium was observed. The most prominent feature of the interstitial cells was large nuclear pseudoinclusions which were observed in a high proportion of the animals examined.

scholarly journals POLYRIBOSOMES AND CISTERNAL ACCUMULATIONS IN ROOT CELLS OF RADISH

1965 ◽  
Vol 27 (2) ◽  
pp. 423-432 ◽  
Author(s):  
Howard T. Bonnett ◽  
Eldon H. Newcomb
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Raphanus Sativus ◽  
Phase Contrast ◽  
Animal Cells ◽  
Root Cells ◽  
Common Component ◽  
Raphanus Sativus L ◽  
Root Hair Formation ◽  
Hair Formation

The zone of root hair formation of seedling radish roots, Raphanus sativus L., was studied by phase-contrast and electron microscopy. Localized dilations of the endoplasmic reticulum, which contained a moderately dense proteinaceous material, were found to be a common component of the cytoplasm in cells of the epidermis and cortex. The surfaces of these dilations were covered with polyribosomes in discrete coils commonly composed of 15 to 17 ribosomes. The function of these structures and the fate of the material accumulated in them are unknown. Their similarity to structures described in some types of animal cells is discussed.

The Morphology of Normal and Abberrant Murine Type Leukemia Virus and Its Relationship to Ribosomes

1972 ◽  
Vol 30 ◽  
pp. 274-275
Author(s):  
T. N. Tahmisian ◽  
E. J. Ainsworth
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Rough Endoplasmic Reticulum ◽  
Intraperitoneal Injection ◽  
Leukemia Virus ◽  
X Rays ◽  
Type Virus ◽  
Unit Membrane ◽  
Viral Membrane ◽  
Viral Development

Studies are in progress to characterize a transmissible leukemia and the causal agent which is presumably viral. The neoplasm, originally isolated from an aged irradiated B6CF1, mouse, has been transmitted in irradiated (200 R; 250 kVp X rays) weanling mice by intraperitoneal injection of millipore filtered (0.45μ) supernatant from spleen cell suspensions. At 22 days after filtrate injection in syngeneic mice, spleen, lymph nodes, and thymus were removed and prepared for electron microscopy to determine the presence of virus and morphology of viral development.The ultrastructure of cells from the above organs showed viral infection by a murine type leukemia virus with many “C” type buds 90 to 110nm formed in the cisternae of the rough endoplasmic reticulum (Fig. 1). The limiting membrane of the “C” type virus, apparently isolating it from the cytoplasm, is the unit membrane from the rough endoplasmic reticulum. The viral membrane is not invariably intact.

The Unit Membrane, the Endoplasmic Reticulum, and the Nuclear Pores are Artefacts

Perception ◽  
1977 ◽  
Vol 6 (6) ◽  
pp. 667-673 ◽  
Author(s):  
Harold Hillman ◽  
Peter Sartory
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Living Cells ◽  
Unit Membrane ◽  
Nuclear Pores ◽  
Solid Geometry

It is shown on the basis of solid geometry that the trilaminar appearance of membranes described by Robertson must be an artefact, although the membranes themselves are not. However, considerations of solid geometry as well as observations on living cells indicate that the endoplasmic reticulum and nuclear pores are artefacts resulting from preparation for electron microscopy. Suggestions for their genesis are proposed.

scholarly journals Morphological and Histochemical Studies of the Leukemic Cells from a Patient with Atypical Myeloblastic Leukemia with Special Reference to Intracytoplasmic Mucopolysaccharide Vacuoles and Fibrillar Formation

Blood ◽  
1960 ◽  
Vol 16 (3) ◽  
pp. 1253-1267 ◽  
Author(s):  
G. ADOLPH ACKERMAN ◽  
JOSEPH A. GRASSO ◽  
RALPH A. KNOUFF
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Chemical Composition ◽  
Special Reference ◽  
Phase Contrast ◽  
Leukemic Cells ◽  
Study Phase ◽  
Bright Field ◽  
Structural Alterations ◽  
Altered Metabolism

Abstract A detailed study (phase contrast, bright field and electron microscopy) of the primitive leukemic cells from a patient with atypical myeloblastic leukemia has been presented. An unusual mucopolysaccharide-containing vacuole has been observed and characterized both morphologically and histochemically. In addition, this study has yielded considerable information concerning the structure and chemical composition of the fibrillar formations, fat droplets and the alterations in erythrocytes following their ingestion by the leukemic cells. Intramitochondrial structural alterations have been observed and characterized in many of the primitive myeloblasts. Changes in the mitochondria and endoplasmic reticulum may reflect impaired or altered metabolism in these abnormal leukemic cells.

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