Etude tridimensionnelle du complexe sécréteur plastes–réticulum endoplasmique dans les poils glandulaires d'Hygrophila difformis (Acanthacées)

1980 ◽  
Vol 58 (17) ◽  
pp. 1859-1871 ◽  
Author(s):  
René Rohr ◽  
Jean Dexheimer ◽  
Mariette Kieffer

The general organisation and functioning of the secretory cells of the glandular hairs of Hygrophila difformis show some analogies with previously studied glandular systems of the same type; they differ from the latter, however, in the complexity of organisation of the reticulum – plastid complex.In the undifferentiated cell the plastids have a simple rounded, slightly elongated form; they display no special relationship with the endoplasmic reticulum which, at this stage, is represented by irregularly enlarged cisternae containing a dense substance of fibrous appearance.During the secretory phase, on the contrary, the ultrastructures of the plastids and of the endoplasmic reticulum undergo considerable changes; the latter appears in the form of small tubes arranged parallel to each other and in close contact with the plastids. The plastids themselves take on shapes which, until now, have never been observed in this type of cell and which can only be shown clearly by a three-dimensional reconstruction. This technique, which involves making a series of thin sections, has been applied to secretory plastids for the first time. It gives a faithful picture of their original morphology and the various modes of association possible between the plastids of a given reticulum – plastid complex.

Author(s):  
Robert Glaeser ◽  
Thomas Bauer ◽  
David Grano

In transmission electron microscopy, the 3-dimensional structure of an object is usually obtained in one of two ways. For objects which can be included in one specimen, as for example with elements included in freeze- dried whole mounts and examined with a high voltage microscope, stereo pairs can be obtained which exhibit the 3-D structure of the element. For objects which can not be included in one specimen, the 3-D shape is obtained by reconstruction from serial sections. However, without stereo imagery, only detail which remains constant within the thickness of the section can be used in the reconstruction; consequently, the choice is between a low resolution reconstruction using a few thick sections and a better resolution reconstruction using many thin sections, generally a tedious chore. This paper describes an approach to 3-D reconstruction which uses stereo images of serial thick sections to reconstruct an object including detail which changes within the depth of an individual thick section.


Author(s):  
S. Cusack ◽  
J.-C. Jésior

Three-dimensional reconstruction techniques using electron microscopy have been principally developed for application to 2-D arrays (i.e. monolayers) of biological molecules and symmetrical single particles (e.g. helical viruses). However many biological molecules that crystallise form multilayered microcrystals which are unsuitable for study by either the standard methods of 3-D reconstruction or, because of their size, by X-ray crystallography. The grid sectioning technique enables a number of different projections of such microcrystals to be obtained in well defined directions (e.g. parallel to crystal axes) and poses the problem of how best these projections can be used to reconstruct the packing and shape of the molecules forming the microcrystal.Given sufficient projections there may be enough information to do a crystallographic reconstruction in Fourier space. We however have considered the situation where only a limited number of projections are available, as for example in the case of catalase platelets where three orthogonal and two diagonal projections have been obtained (Fig. 1).


2013 ◽  
Vol 288 (23) ◽  
pp. 16460-16475 ◽  
Author(s):  
Linda J. Olson ◽  
Ramiro Orsi ◽  
Solana G. Alculumbre ◽  
Francis C. Peterson ◽  
Ivan D. Stigliano ◽  
...  

Here we report for the first time the three-dimensional structure of a mannose 6-phosphate receptor homology (MRH) domain present in a protein with enzymatic activity, glucosidase II (GII). GII is involved in glycoprotein folding in the endoplasmic reticulum. GII removes the two innermost glucose residues from the Glc3Man9GlcNAc2 transferred to nascent proteins and the glucose added by UDP-Glc:glycoprotein glucosyltransferase. GII is composed of a catalytic GIIα subunit and a regulatory GIIβ subunit. GIIβ participates in the endoplasmic reticulum localization of GIIα and mediates in vivo enhancement of N-glycan trimming by GII through its C-terminal MRH domain. We determined the structure of a functional GIIβ MRH domain by NMR spectroscopy. It adopts a β-barrel fold similar to that of other MRH domains, but its binding pocket is the most shallow known to date as it accommodates a single mannose residue. In addition, we identified a conserved residue outside the binding pocket (Trp-409) present in GIIβ but not in other MRHs that influences GII glucose trimming activity.


Geology ◽  
2020 ◽  
Author(s):  
Faye Walker ◽  
Nick Schofield ◽  
John Millett ◽  
Dave Jolley ◽  
Simon Holford ◽  
...  

The nature and growth of magmatic plumbing systems are of fundamental importance to igneous geology. Traditionally, magma chambers have been viewed as rapidly emplaced bodies of molten rock or partially crystallized “magma mush” connected to the surface by a narrow cylindrical conduit (referred to as the “balloon-and-straw” model). Recent data suggest, however, that magma chambers beneath volcanoes are formed incrementally through amalgamation of smaller intrusions. Here we present the first high-resolution three-dimensional reconstruction of an ancient volcanic plumbing system as a large laccolithic complex. By integrating seismic reflection and gravity data, we show that the ~200 km3 laccolith appears to have formed through partial amalgamation of smaller intrusions. The complex appears to have fed both surface volcanism and an extensive sill network beneath the volcanic edifice. Numerous sills are imaged within the volcanic conduit, indicating that magma stalled at various levels during its ascent. Our results reveal for the first time the entire multicomponent plumbing system within a large ancient shield volcano.


Nature ◽  
1984 ◽  
Vol 310 (5975) ◽  
pp. 285-291 ◽  
Author(s):  
Kenneth A. Taylor ◽  
Mary C. Reedy ◽  
Leonidas Córdova ◽  
Michael K. Reedy

1994 ◽  
Vol 68 (3) ◽  
pp. 647-654 ◽  
Author(s):  
A. Kemp

Skull bones of Gosfordia truncata Woodward, 1891, from the Lower Triassic Hawkesbury Sandstone of New South Wales, Australia, are described for the first time. The skull roofing pattern suggests possible affinities between G. truncata and Paraceratodus germaini (Triassic, southwest Madagascar). A three-dimensional reconstruction of the skull of Ceratodus formosus Wade, 1935, based on the holotype, found in a Lower Triassic deposit at Brookvale in New South Wales, is included. This reconstruction indicates that this species is not closely related either to the recent Australian lungfish, Neoceratodus forsteri, or to the Triassic Ceratodus (Tellerodus) sturii from Nord Alpen in Austria, and it has no close affinities with G. truncata. A new genus, Ariguna, is therefore proposed to receive Ceratodus formosus Wade, 1935. Without associated tooth plate material, G. truncata and A. formosa cannot be defined more precisely.


1961 ◽  
Vol 11 (2) ◽  
pp. 333-347 ◽  
Author(s):  
Susumu Ito

An electron microscopic survey has been made of the gastric parietal or oxyntic cell of the human, cat, beaver, dog, hamster, rat, mouse, and bat, and of the corresponding cell type in two species of frog, two species of toad, and the horned lizard. A feature consistently found in the parietal cells of the mammals or their equivalent in the lower vertebrates is the agranular endoplasmic reticulum, which takes the form of branching and anastomosing small tubules approximately 200 to 500 A in diameter, sometimes expanded into flattened cisternae. In mammalian parietal cells this form of the endoplasmic reticulum is found only in limited amounts, but in the corresponding secretory cells of the amphibia and reptilia the tubular agranular reticulum is abundant. It is believed to comprise a more or less continuous system of channels, but owing to their tortuous course only short profiles are seen in thin sections. Immediately subjacent to the plasmalemma at the free surface, the cytoplasm is relatively free of organelles but is occasionally traversed by the agranular reticulum, which appears to be continuous at some points with the cell surface. The possible participation of the agranular endoplasmic reticulum in hydrochloric acid secretion is discussed.


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