scholarly journals ON THE FINE STRUCTURE OF THE CAMBIUM OF FRAXINUS AMERICANA L

1966 ◽  
Vol 31 (1) ◽  
pp. 79-93 ◽  
Author(s):  
Lalit M. Srivastava

The fine structure of ash cambium was studied after glutaraldehyde-osmium tetroxide fixation. The fusiform and ray initials are essentially alike, and both have the basic complement of organelles and membranes typical of parenchyma cells. The varied behavior of the two types of initials and the role of cambium in oriented production of the xylem and phloem are still unexplained phenomena. Actively growing cambial cells are highly vacuolate. They are rich in endoplasmic reticulum of the rough cisternal form, ribosomes, dictyosomes, and coated vesicles. Microtubules are present in the peripheral cytoplasm. The plasmalemma appears to be continuous with the endoplasmic reticulum and produces coated vesicles as well as micropinocytotic vesicles with smooth surfaces. The plastids have varying amounts of an intralamellar inclusion which may be a lipoprotein. The quiescent cambium is deficient in rough ER and coated vesicles and has certain structures which may be condensed proteins.

1965 ◽  
Vol 43 (11) ◽  
pp. 1401-1407 ◽  
Author(s):  
James Cronshaw

Cambial derivatives of Acer rubrum have been examined at stages of their differentiation following fixation in 3% or 6% glutaraldehyde with a post fixation in osmium tetroxide. At early stages of development numerous free ribosomes are present in the cytoplasm, and elements of the endoplasmic reticulum tend to align themselves parallel to the cell surfaces. The plasma membrane is closely applied to the cell walls. During differentiation a complex system of cytoplasmic microtubules develops in the peripheral cytoplasm. These microtubules are oriented, mirroring the orientation of the most recently deposited microfibrils of the cell wall. The microtubules form a steep helix in the peripheral cytoplasm at the time of deposition of the middle layer of the secondary wall. During differentiation the free ribosomes disappear from the cytoplasm and numerous elements of rough endoplasmic reticulum with associated polyribosomes become more evident. In many cases the endoplasmic reticulum is associated with the cell surface. During the later stages of differentiation there are numerous inclusions between the cell wall and the plasma membrane.


1977 ◽  
Vol 55 (9) ◽  
pp. 1530-1544 ◽  
Author(s):  
A. R. Fontaine ◽  
Philip Lambert

The fine structure of amoebocytes, lymphocytes, and morula cells is described and related to their functions. Three morphological phases (bladder, transitional, and filiform) of the amoebocyte are distinguished. Their surface protrusions and activities are based on microtubule and microfilament systems and the transitional-filiform phases are functionally involved in coelomocyte aggregation. The bladder phase is phagocytic; bladder formation and activities are also microfilament based. Morula cells contain spherules composed of acid mucopolysaccharide and protein. Dilated rough endoplasmic reticulum (ER) cisternae apparently synthesize spherule material which is added by accretion. Lymphocytes have little cytoplasm and relatively few organelles, except for abundant rough ER and free ribosomes. Lymphocytes are probably stem cells for amoebocytes and morulas. These cells are compared with the leucocytes of other echinoderms.


1962 ◽  
Vol 12 (1) ◽  
pp. 101-113 ◽  
Author(s):  
Allen C. Enders

Corpora lutea from the period of delayed implantation and from early postimplantation stages of the armadillo, mink, and rat were fixed in buffered osmium tetroxide-sucrose or potassium permanganate. After rapid dehydration, the portions of the corpora lutea were embedded in either methacrylate or epoxy resin. Examination of the lutein cells by electron microscopy revealed the presence, in the better preserved material, of an extensive development of tubular agranular endoplasmic reticulum. Although the membranes of the endoplasmic reticulum are the most striking feature of the lutein cells of both stages of the three animals examined, very numerous large mitochondria with cristae that exhibit a variety of forms tending toward villiform, and protrusions and foldings of the lutein cell margins on the pericapillary space are also characteristic of these cells. Certain minor differences in the lutein cells of the species examined are also noted. No indications of conversion of mitochondria into lipid, of accumulation of lipid in the Golgi area, or of the protrusion of lutein cells into spaces between the endothelial cells, as suggested by other authors, were noted in these preparations. Some of the difficulties inherent in the visualization of the secretory activity of cells producing steroid hormones are briefly discussed.


1961 ◽  
Vol 11 (2) ◽  
pp. 419-431 ◽  
Author(s):  
Patricia Harris

The fine structure of cells at different stages of the mitotic cycle was studied in the blastomeres of 6-hour-old embryos of the sea urchin Strongylocentrotus purpuratus. The material was fixed in 1 per cent osmium tetroxide in sea water, buffered with veronal-acetate to pH 7.5, embedded in Araldite, and sectioned with glass knives. The aster, as it forms around the centriole, has the appearance of the endoplastic reticulum, with elements oriented radially from the centrosphere to the periphery of the cell. Anaphase structures described include the kinetochores, with bundles of fine filaments extending toward the centrioles, as well as continuous filaments passing between the chromosomes. Two cylindrical centrioles composed of parallel rods are present in each of the anaphase asters. At late anaphase, elements of the endoplasmic reticulum condense on the surface of the chromosomes to form a double membrane which already at this stage possesses pores or annuli. At telophase bundles of continuous filaments can be seen in the interzonal region. These filaments, as well as those associated with the chromosomes, have a diameter of approximately 15 mµ, and appear physically different from the astral structure.


1972 ◽  
Vol 50 (6) ◽  
pp. 707-711 ◽  
Author(s):  
Sherwin S. Desser

Following penetration through the midgut epithelium of Simulium rugglesi, ookinetes of Leucocytezoon simondi round up beneath the basal lamina and transform into young oocysts. These spherical, walled structures contain a large central core of crystalloid material. Dividing nuclei are seen in the peripheral cytoplasm, which is characterized by several concentric layers of granular endoplasmic reticulum. In a succeeding stage of development the trilaminar plasma membrane appears intermittently doubled, and bud-like outgrowths occur in these thickened areas. At this stage the crystalloid material is dispersed throughout the cytoplasm. A nucleus, an elongate mitochondrion, and some crystalloid material move into each forming sporozoite, which continues to grow at the expense of the residual cytoplasm.


1965 ◽  
Vol 43 (6) ◽  
pp. 747-755 ◽  
Author(s):  
Michael Shaw ◽  
M. S. Manocha

Detached leaves of Little Club wheat were allowed to senesce on water or on kinetin (10 mg/l.) in petri dishes on the laboratory bench. Samples taken at intervals of 24 to 48 hours for 8 to 10 days were fixed in permanganate or osmium tetroxide, embedded, usually in araldite or epon, and examined by electron microscopy. Abnormalities were noted in the endoplasmic reticulum (ER) of the mesophyll cells 2 days after the leaves were detached; ER and cytoplasmic ribosomes were not present after 4 or 5 days. Swelling of the mitochondria and degeneration of the cristae, collapse of the chloroplast grana, and abnormalities in nuclear structure were noted after 3 days. Vacuolar contraction occurred in some cells after 4 days but the plasma membrane usually remained unbroken until the seventh or eighth day, by which time the mitochondria were no longer recognizable and most of the chloroplasts and nuclei had also disintegrated.Kinetin induced an increase in the amount of ER and ribosomes and markedly delayed the degeneration of cellular fine structure.


1965 ◽  
Vol 24 (3) ◽  
pp. 415-431 ◽  
Author(s):  
James Cronshaw ◽  
G. Benjamin Bouck

Differentiating xylem elements of Avena coleoptiles have been examined by light and electron microscopy. Fixation in 2 per cent phosphate-buffered osmium tetroxide and in 6 per cent glutaraldehyde, followed by 2 per cent osmium tetroxide, revealed details of the cell wall and cytoplasmic fine structure. The localized secondary wall thickening identified the xylem elements and indicated their state of differentiation. These differentiating xylem elements have dense cytoplasmic contents in which the dictyosomes and elements of rough endoplasmic reticulum are especially numerous. Vesicles are associated with the dictyosomes and are found throughout the cytoplasm. In many cases, these vesicles have electron-opaque contents. "Microtubules" are abundant in the peripheral cytoplasm and are always associated with the secondary wall thickenings. These microtubules are oriented in a direction parallel to the microfibrillar direction of the thickenings. Other tubules are frequently found between the cell wall and the plasma membrane. Our results support the view that the morphological association of the "microtubules" with developing cell wall thickenings may have a functional significance, especially with respect to the orientation of the microfibrils. Dictyosomes and endoplasmic reticulum may have a function in some way connected with the synthetic mechanism of cell wall deposition.


1991 ◽  
Vol 69 (2) ◽  
pp. 336-341 ◽  
Author(s):  
Tommy C. Sewall ◽  
Jeffrey C. Pommerville

The Chytridiomycete Allomyces macrogynus generates new membranes for cleavage furrow and nuclear-cap formation during gametogenesis and zoosporogenesis. Transmission electron microscopy after impregnation with a mixture of zinc iodide and osmium tetroxide clearly demonstrated changes in the endoplasmic reticulum. Endoplasmic reticulum was intensely stained but did not appear to contribute to the formation of the unstained flagellar membranes or cleavage furrows. However, the relative cytoplasmic volume of endoplasmic reticulum decreased as positively stained nuclear-cap membrane formed. These observations are consistent with the hypothesis that flagellar membranes and cleavage furrows are derived from trans-Golgi equivalents, whereas the nuclear-cap membrane is derived from the endoplasmic reticulum. Key words: Allomyces macrogynus, Chytridiomycetes, endoplasmic reticulum, gametogenesis, zoosporogenesis.


The retinae of the posterior eyes of pisaurid spiders in the genus Dolomedes are described.They resemble those of Lycosidae, but the receptors are much larger, and proximal to the strips of tapetum upon which they rest the receptor axons are grossly dilated. Each receptive segment contains two rhabdomeres, and pairs of rhabdomeres belonging to adjacent receptors are contiguous. Prolonged (6 h) illumination at physiological levels causes the rhabdomeres to diminish in volume by loss of membrane which is restored on return to darkness. W hen spiders are kept in darkness for 4-5 d, the rhabdomeres grow by the orderly addition of membrane to the microvilli until they completely fill the receptive segments, and such novel membrane is subsequently disassembled when the retina is illuminated. It is proposed that under normal conditions there is a balance maintained between the growth and destruction of rhabdomere membrane. The paired rhabdomeres are flanked by the processes of supportive cells which exhibit much membrane amplification, and the supportive cell system extends below the tapetum completely to ensheath the swollen receptor axons, which are some 70-80 pm long. In dark-adapted retinae the supportive processes are shrunken; illumination causes them to swell, and the extracellular space between the interdigitations fills with electron-dense material derived from the breakdown of rhabdom ere membrane. The material is passed basally and reintroduced into the receptor axons via an extensive system of endocytotic pleats. The tips of pleats often enclose pigment granules from the supporting system, and identical granules in various states of lysis are found within the axoplasm after exposure to light, thus implying that the pleats burst rather than merely transport material across their membranes. There is evidence that pleats may become detached. Exposure of retinae to infrared radiation also evokes breakdown of rhabdomere membrane, but the extracellular route is not employed. The swollen axons are filled with whorls of rough endoplasmic reticulum, abundant Golgi bodies, and mitochondria. After long periods of darkness, all these systems are depleted, and the space they occupied becomes highly vacuolated. Light adaptation from dim light on a normal diurnal cycle evokes dilation of the cisternae of the endoplasmic reticulum, which pinch off smooth vesicles, and the Golgi bodies become highly active and produce coated vesicles in abundance. The relations between smooth vesicles and microvilli are ambiguous; precedents exist for supposing that smooth vesicles in the inter-rhabdom eral cytoplasm are pinocytotic and have been pinched off from the bases of the microvilli, but in Dolomedes there is some evidence to suggest that they may be identical with those manufactured by the endoplasmic reticulum and are also fusing with rhabdomere membrane. Multivesicular and multilamellar bodies are the product of membrane fragments which have broken off from the rhabdomeres during light adaptation, and of coated vesicles produced by pinocytosis; they are transported within the receptors to the swollen axons where they undergo lysis. It is proposed that in Dolomedes the role of the endoplasmic reticulum is to synthesize materials for the repair of rhabdomere membrane, and that the bulk of precursors to sustain this process is obtained by recycling the products of rhabdom ere breakdown via the supportive cell system. The hypothesis is discussed in terms of current information about invertebrate retinae, and analogous processes which are well established for those of vertebrates. Dolomedes do not move retinal pigment granules to modulate the shielding of their receptors, and it is likely that manipulation of the properties of photoreceptor membrane is the only strategy of adaptation available to them.


Author(s):  
John J. Wolosewick ◽  
John H. D. Bryan

Early in spermiogenesis the manchette is rapidly assembled in a distal direction from the nuclear-ring-densities. The association of vesicles of smooth endoplasmic reticulum (SER) and the manchette microtubules (MTS) has been reported. In the mouse, osmophilic densities at the distal ends of the manchette are the organizing centers (MTOCS), and are associated with the SER. Rapid MT assembly and the lack of rough ER suggests that there is an existing pool of MT protein. Colcemid potentiates the reaction of vinblastine with tubulin and was used in this investigation to detect this protein.


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