A new device for electron microscope autoradiography of whole cultured cells

1980 ◽  
Vol 36 (6) ◽  
pp. 689-689
Author(s):  
T. Katsumoto ◽  
A. Takagi ◽  
A. Hirano ◽  
T. Kurimura
Keyword(s):  
Electron Microscope ◽  
Cultured Cells ◽  
Electron Microscope Autoradiography ◽  
New Device ◽  
Microscope Autoradiography

scholarly journals THE LABELING OF CULTURED CELLS OF ACER WITH [14C]PROLINE AND ITS SIGNIFICANCE

1974 ◽  
Vol 60 (3) ◽  
pp. 695-701 ◽  
Author(s):  
F. C. Steward ◽  
H. W. Israel ◽  
M. M. Salpeter
Keyword(s):  
Cell Wall ◽  
Electron Microscope ◽  
Cell Walls ◽  
Cultured Cells ◽  
The State ◽  
The Other ◽  
Electron Microscope Autoradiography ◽  
Cells In Culture ◽  
Microscope Autoradiography ◽  
The Status

The distribution of the radioactivity from [14C]proline that is bound in cultured cells of Acer has been determined by electron microscope autoradiography. In this way proline may be related to the cell wall as a morphological entity rather than as a fraction in a biochemical separation of a heterogeneous crop of cells. The cells in culture may vary greatly. Some are active growing, turgid cells, with thin protoplasts tightly pressed against their walls; in others the protoplasts may spontaneously withdraw from the wall; in still others the protoplasts disorganize, and walls thicken and become sculptured as the cells differentiate and even senesce. Different culturing practices may affect the status of the cells, and this, in turn, affects the distribution of radioactivity from proline in the cells. Cells which are actively growing, turgid, and nucleated have the highest grain density in their protoplasts and nuclei; as the protoplasts of such cells withdraw from their walls, they retain the bulk of the radioactivity. On the other hand, in cells which have thickened walls and sparse protoplast contents, the radioactivity is accumulated in their walls. A high content of proline and hydroxyproline-rich protein is, therefore, not a necessary or invariable feature of the cell walls of cultured Acer cells but depends on the state of development of these cells.

Incorporation of Cholesterol into Peripheral Nerve Myelin

1972 ◽  
Vol 30 ◽  
pp. 334-335
Author(s):  
Frank A. Rawlins
Keyword(s):  
Electron Microscope ◽  
Sciatic Nerve ◽  
Electron Microscope Autoradiography ◽  
Myelin Sheaths ◽  
Microscope Autoradiography ◽  
Grain Distribution ◽  
Sciatic Nerves ◽  
Autoradiographic Analysis ◽  
Old Mice ◽  
Short Times

Several speculations exist as to the site of incorporation of preformed molecules into myelin. The possibility that an autoradiographic analysis of cholesterol-1,2-H3 incorporation at very short times after injection might shed some light in the solution of that problem led to the present experiment.Cholesterol-1,2-H3 was injected intraperitoneally into 24 tenday old mice. The animals were then sacrificed at 10,20,30,40,60,90,120 and 180 min after the injection and the sciatic nerves were processed for electron microscope autoradiography. To analyze the grain distribution in the autoradiograms of cross and longitudinal sections from each sciatic nerve myelin sheaths were subdivided into three compartments named: outer 1/3, middle 1/3 and inner 1/3 compartments.It was found that twenty min. after the injection of cholesterol -1.2-H3 (Figs. 1 and 2), 55% of the total number of grains (t.n.g) found in myelin were within the outer 1/3 compartment, 9% were within the middle 1/3 and 36% within the inner 1/3 compartment

Synthesis and Localization of Sulphated Mucopolysaccharide in Megakaryocytes and Platelets of the Rat, An Analysis by Electron-Microscope Autoradiography

1972 ◽  
Vol 10 (3) ◽  
pp. 705-717
Author(s):  
G. G. MacPHERSON
Keyword(s):  
Electron Microscope ◽  
Golgi Apparatus ◽  
Blood Platelets ◽  
Total Activity ◽  
Electron Microscope Autoradiography ◽  
Dense Granules ◽  
Level Of Activity ◽  
Microscope Autoradiography ◽  
Almost All

Electron-microscope autoradiography has been used to investigate the synthesis and localization of sulphated mucopolysaccharide in megakaryocytes and blood platelets. Following 10-min incubation of bone marrow with 35S-sulpahte in vitro the majority of the activity in megakaryocytes was associated with the Golgi apparatus, but a substantial proportion was associated with other cytoplasmic organelles, suggesting either rapid transport or sulphation of mucopolysaccharide outside the Golgi apparatus. Three hours after the intravenous injection of 35SO4 only a small proportion of the total activity was associated with the Golgi apparatus, most being associated with demarcation membranes and dense granules, while 12 h after injection almost all the activity was associated with demarcation membranes and granules. A rising proportion of activity localized solely on the demarcation membranes suggested that they may possess some activity of their own. Autoradiographs of blood platelets prepared 72 h after the injection of 35SO4 were analysed. It was shown that most of the activity was associated with the α-granules, but there was strong evidence that the platelet membrane possessed a low level of activity.

Timing of nucleolar DNA replication in Amoeba proteus

1976 ◽  
Vol 22 (3) ◽  
pp. 521-530
Author(s):  
I. Minassian ◽  
L.G. Bell
Keyword(s):  
Electron Microscope ◽  
Dna Replication ◽  
Dna Synthesis ◽  
Central Region ◽  
Thymidine Incorporation ◽  
Tritiated Thymidine ◽  
Amoeba Proteus ◽  
Electron Microscope Autoradiography ◽  
Microscope Autoradiography ◽  
G2 Phase

Light- and electron-microscope autoradiography have been used to follow the incorporation of [3H]thymidine at different stages during the interphase of synchronously growing populations of Amoeba proteus. Two main patterns were found for tritiated thymidine incorporation, i.e. DNA synthesis. The major incorporation was in the central region of the nucleus, but a lesser degree of incorporation occurred in the nucleolar region. The bulk of this nucleolar DNA was found to be late replicating, i.e. it replicated during the G2 phase.

Studies on the Synthesis and Composition of Extracellular Mucilage in the Unicellular Red Alga Rhodella

1974 ◽  
Vol 16 (1) ◽  
pp. 1-21
Author(s):  
L. V. EVANS ◽  
MAUREEN E. CALLOW ◽  
ELIZABETH PERCIVAL ◽  
V. FAREED
Keyword(s):  
Electron Microscope ◽  
Uronic Acid ◽  
Red Alga ◽  
Electron Microscope Autoradiography ◽  
Golgi Bodies ◽  
Microscope Autoradiography ◽  
Reducing Substances

35SO42- has been used to investigate the production of extracellular mucilage by log-phase cells. Uptake of isotope occurs most rapidly in the light, when cells are actively dividing. The mucilage comprises about 50% carbohydrate, 16% protein and 10% sulphate. The major sugar is xylose; uronic acid, a small amount of galactose, glucose (trace) and 2 reducing substances are also present. Methylation studies have established the major linkages. Electron-microscope autoradiography shows that the mucilage is packaged in the Golgi bodies, passing to the plasmalemma in large vesicles. Sulphation of the mucilage occurs in the Golgi cisternae.

scholarly journals Resolution of electron microscope autoradiography. IV. Application to analysis of autoradiographs.

1978 ◽  
Vol 76 (1) ◽  
pp. 127-145 ◽  
Author(s):  
M M Salpeter ◽  
F A McHenry ◽  
E E Salpeter
Keyword(s):  
Electron Microscope ◽  
Electron Microscope Autoradiography ◽  
Microscope Autoradiography ◽  
Cross Scatter ◽  
Best Fit ◽  
Subsequent Comparison ◽  
Complex Cases

The previous publications of this series described the expected grain distributions around model radioactive structures in EM autoradiographs as a function of the specimen resolution. This family of expected distributions was called the "universal curves". In the present study, experiments on 14C-sources were compared, significant differences were found depending on the energy of the isotope. These differences were primarily in the tails of the distributions, and are therefore important in correcting for cross-scatter when analyzing electron microscope autoradiographs. Using the universal curves unique for 125I, 3H, and 14C, we designed three sets of transparent overlays, or "masks", one set for each of these isotopes. The masks can be used by an investigator in a manner similar to that suggested by Blackett and Parry to generate grain distributions in autoradiographs on the basis of any desired hypothesis regarding the levels of radioactivity in different structures. A subsequent comparison between these generated distributions and those obtained from the observed grains in these autoradiographs leads to a determination of the most likely levels of radioactivity in the tissue. A computer (described in an Appendix by Land and Salpeter) can be used to find the "best fit" levels of radioactivity in complex cases. The accuracy of the masks was checked on generated line sources for each of the three isotopes.

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