scholarly journals Visualization of particle complexes in the plasma membrane of Micrasterias denticulata associated with the formation of cellulose fibrils in primary and secondary cell walls.

1980 ◽  
Vol 84 (2) ◽  
pp. 327-339 ◽  
Author(s):  
T H Giddings ◽  
D L Brower ◽  
L A Staehelin

Highly ordered arrays of intramembrane particles are observed in freeze-fractured plasma membranes of the green alga Micrasterias denticulata during the synthesis of the secondary cell wall. The observable architecture of the complex consists primarily of a precise hexagonal array of from 3 to 175 rosettes, consisting of 6 particles each, which fracture with the P-face. The complexes are observed at the ends of impressions of cellulose fibrils. The distance between rows of rosettes is equal to the center-to-center distance between parallel cellulose fibrils of the secondary wall. Correlation of the structure of the complex with the pattern of deposition indicates that the size of a given fibril is proportional to the number of rosettes engaged in its formation. Vesicles containing hexagonal arrays of rosettes are found in the cytoplasm and can be observed in the process of fusing with the plasma membrane, suggesting that the complexes are first assembled in the cytoplasm and then incorporated into the plasma membrane, where they become active in fibril formation. Single rosettes appear to be responsible for the synthesis of microfibrils during primary wall growth. Similar rosettes have now been detected in a green alga, in fern protonemata, and in higher plant cells. This structure, therefore, probably represents a significant component of the cellulose synthesizing mechanism in a large variety of plant cells.

1992 ◽  
Vol 101 (1) ◽  
pp. 93-98 ◽  
Author(s):  
TAKASHI MURATA ◽  
MASAMITSU WADA

The preprophase band (PPB) of microtubules (MTs), which appears at the future site of cytokinesis prior to cell division in higher plant cells, disappears by metaphase. Recent studies have shown that displacement of the endoplasm from the PPB region by centrifugation delays the disappearance of the PPB. To study the role of the endoplasm in the cell cycle-specific disruption of the PPB, the filamentous protonemal cells of the fern Adiantum capilius-veneris L. were centrifuged twice so that the first centrifugation displaced the endoplasm from the site of the PPB and the second returned it to its original location. The endoplasm, including the nucleus of various stages of mitosis, could be returned by the second centrifugation to the original region of the PPB, which persists during mitosis in the centrifuged cells. When endoplasm with a prophase nucleus was returned to its original location, the PPB was not disrupted. When endoplasm with a prometa-phase telophase nucleus was similarly returned, the PPB was disrupted within 10 min of termination of centrifugation. In protonemal cells of Adiantum, a second PPB is often formed near the displaced nucleus after the first centrifugation. In cells in which the endoplasm was considered to have been returned to its original location at the prophase/prometaphase transition, the second PPB did not disappear even though the initial PPB was disrupted by the endoplasm. These results suggest that cell cycle-specific disruption of the PPB is regulated by some factor(s) in the endoplasm, which appears at prometaphase, i.e. the stage at which the PPB is disrupted in non-centrifuged cells.


1969 ◽  
Vol 40 (2) ◽  
pp. 446-460 ◽  
Author(s):  
G. Benjamin Bouck

Mastigonemes (Flimmer) from the sperm of Ascophyllum and Fucus were found to consist of a tripartite structure—a ca. 2000-A tapered basal region, a closed microtubular shaft, and a group of terminal filaments. Each of these regions appears to be constructed of globular subunits with a center-to-center distance of about 45 A. The mastigoneme microtubule is of smaller diameter (170–190 A) than cytoplasmic microtubules in these or other plant cells. During the initial stages of flagellar ontogeny, structures similar to mastigonemes (presumptive mastigonemes) are found within membrane-limited sacs in the cytoplasm or within the perinuclear space. Mastigonemes at this time are generally not found on the flagellar surface. Later, when the anterior flagellum acquires mastigonemes, the presumptive mastigonemes are absent from the cytoplasm. The regularity of attachment of mastigonemes to the flagellar surface suggests that specific attachment sites are constructed on the plasma membrane during flagellar ontogeny. No evidence for penetration of the mastigoneme through the plasma membrane was obtained. The origin and structure of mastigonemes are discussed in relation to reports of the origin and structure of other microtubular systems.


2011 ◽  
Vol 1808 (6) ◽  
pp. 1728-1736 ◽  
Author(s):  
Lars H. Wegner ◽  
Bianca Flickinger ◽  
Christian Eing ◽  
Thomas Berghöfer ◽  
Petra Hohenberger ◽  
...  

1969 ◽  
Vol 47 (12) ◽  
pp. 1873-1877 ◽  
Author(s):  
L. C. Fowke ◽  
George Setterfield

Applied auxin caused cells of artichoke tuber slices to expand and deposit significant amounts of new wall material while cells in slices held on water remained essentially inert in both respects. Cells in all physiological treatments showed multivesicular structures at the plasma membrane (plasmalemmasomes, lomasomes), within the cytoplasm and within the central vacuoles. The number of plasmalemmasomes was considerably greater in cells not depositing wall than in cells treated with auxin to stimulate wall synthesis. Multivesicular structures showed no relation to Golgi bodies, which increase in number and apparent activity in response to auxin treatment. It is concluded that plasmalemmasomes are not involved in cell wall deposition. Multivesicular structures in plant cells could have several origins and it is suggested that some may represent artifactual reorganization of plasmalemma and tonoplast membranes during cytological processing. Such reorganization would presumably be sensitive to the physiological state of the tissue.


1981 ◽  
Vol 59 (6) ◽  
pp. 1021-1025 ◽  
Author(s):  
Larry C. Fowke ◽  
Harvey J. Marchant ◽  
Peter M. Gresshoff

Protoplasts from will carrot (Daucus carota) cell cultures were fused with protoplasts of the filamentous green alga Stigeoclonium sp. using polyethylene glycol. Following fusion of the algal and higher plant plasma membranes, intact Stigeoclonium chloroplasts, nuclei, and centrioles were observed within the carrot cytoplasm. Other algal organelles were not distinguishable in the fusion products.


1977 ◽  
Vol 55 (18) ◽  
pp. 2383-2393 ◽  
Author(s):  
Pyoyun Park ◽  
Mitsuya Tsuda ◽  
Yoshiharu Hayashi ◽  
Tamio Ueno

AM-toxin I (4 μg/ml), a host-specific toxin of Alternaria mali, caused permeability changes in susceptible apple and Nijisseiki pear leaves within 5 min of treatment. The first effect of the toxin appeared on plasma membranes of susceptible apple cells. One hour after toxin treatment, slight invaginations were evident in plasma membranes near plasmodesmata. Six hours after treatment, the spaces between cell wall and invaginated plasma membrane contained lomasome-like vesicles, membranous fragments, and desmotubules extending from plasmodesmata. The membranous materials appeared to originate from the plasma membrane. Thirty-one hours after treatment, necrotic cells of susceptible leaves showed the general disruptions of cellular membranes which might be caused by secondary effects of the toxin. The similar changes of plasma membrane and plasmodesmata also were found in Nijisseiki pear cells treated with AM-toxin I (4 μg/ml) for 1 h and 6 h. The invaginations of the plasma membrane at plasmodesmata were the first ultrastructural modifications in the toxin-treated Nijisseiki cells. AM-toxin I did not affect the ultrastructure of resistant apple and Chojuro pear cells. These results indicate that the initial sites for the toxin may be on the plasma membrane of the susceptible apple cells. Furthermore, the results suggest that the plasma membrane modifications are associated with permeability changes in the toxin-treated, susceptible plant cells except for original host cells treated with the toxin.


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