scholarly journals STUDIES ON THE GOLGI APPARATUS BY ELECTRON MICROSCOPY WITH PARTICULAR REFERENCE TO AOYAMA'S TECHNIQUE

1956 ◽  
Vol 2 (4) ◽  
pp. 395-402 ◽  
Author(s):  
Dennis Lacy ◽  
Cyril E. Challice

1. Aoyama's silver impregnation method for the Golgi apparatus has been used on exocrine cells of the pancreas of the mouse and studied by electron microscopy in order to determine as precisely as possible where the silver is deposited. Similar cells have also been fixed in buffered osmium tetroxide solution and compared with cells treated by the silver technique. 2. Examination of the Aoyama preparations usually revealed a light deposition of silver in the cytoplasm (hyaloplasm or matrix) and a heavy deposition of silver around a series of closely apposed vacuoles. The heavy deposition of silver was regarded as revealing the chromophilic region of the Golgi apparatus while the vacuoles were identified as the chromophobic component. 3. Comparison of the silver preparations with those fixed in buffered osmium tetroxide solution showed that the silver was primarily deposited in the region of the Golgi membranes.

1962 ◽  
Vol s3-103 (63) ◽  
pp. 287-296
Author(s):  
S. K. MALHOTRA

The effect of fixation with osmium tetroxide solution, made alkaline by the addition of potassium acetate, was studied by electron microscopy. Exocrine cells of the pancreas and the cells of the first (‘proximal’) convoluted tubules of the kidney of the mouse were used as test-objects. Partially prepolymerized methacrylate was used for embedding. The preservation of the various cell inclusions was similar to what is generally produced after fixation with Palade's buffered osmium tetroxide.


1962 ◽  
Vol s3-103 (61) ◽  
pp. 5-15
Author(s):  
S. K. MALHOTRA

The effect of fixation with a simple solution of osmium tetroxide in distilled water was studied by electron microscopy. Exocrine cells of the pancreas and cells of the proximal tubule of the kidney of the mouse were used as test-objects. Partially prepolymerized methacrylate was used for embedding. There did not appear to be any marked disorganization of the cell inclusions. The appearance of the inclusions in the electron micrographs was similar to what is generally seen after fixation with the buffered osmium tetroxide solution of Palade.


1965 ◽  
Vol s3-106 (73) ◽  
pp. 15-21
Author(s):  
JOHN R. BAKER

The exocrine cells of the mouse pancreas were fixed in potassium dichromate solution, embedded in araldite or other suitable medium, and examined by electron microscopy. Almost every part of these cells is seriously distorted or destroyed by this fixative. The ergastoplasm is generally unrecognizable, the mitochondria and zymogen granules are seldom visible, and no sign of the plasma membrane, microvilli, or Golgi apparatus is seen. The contents of the nucleus are profoundly rearranged. It is seen to contain a large, dark, irregularly shaped, finely granular object; the evidence suggests that this consists of coagulated histone. The sole constituent of the cell that is well fixed is the inner nuclear membrane. The destructive properties of potassium dichromate are much mitigated when it is mixed in suitable proportions with osmium tetroxide or formaldehyde.


2000 ◽  
Vol 6 (S2) ◽  
pp. 844-845
Author(s):  
O.J. Castejón ◽  
R. P. Apkarian ◽  
H. V. Castejón

Samples of albino mice cerebellar cortex were processed by the cryofracture method for scanning electron microscopy and examined with the field emission scanning electron microscope (FESEM). Albino mouse cerebellar cortex was excised, cut into 1-2 mm slices and inmersed in 4% glutaraldehyde in O. l M phosphate buffer solution, pH 7.4, for 24h at 4°C; and postfixed for 1 h in a similarly buffered 1% osmium tetroxide solution. Specimens were dehydrated in a graded serie of ethanol (30, 50, 70, 80, 90 2x100%) prior to wrapping individual tissue pieces in preformed absolute ethanol filled parafilm cryofracture packets. Rapid freezing of packets was performed by plunging into LN2. First, the packet was transferred from the LN2 storage vessel with LNT chilled forceps in order to avoid themial damage. Secondly, the cooled fracture blade was removed from the LN2, the packet was orientated under the blade, and immediately struck with a heavy tool.


1996 ◽  
Vol 51 (1) ◽  
pp. 116-120 ◽  
Author(s):  
Katsukuni Fujimoto ◽  
Maki Murakami-Hisaichi ◽  
Chikako Tokuda ◽  
Fumihiko Kajiya

1940 ◽  
Vol s2-81 (324) ◽  
pp. 595-617
Author(s):  
J. BRONTÉ GATENBY ◽  
J. D. SMYTH

1. In Chilomonas paramecium the contractile vacuole is surrounded by a cortical substance (Golgi apparatus) which has the power of reducing osmium tetroxide solution and thus impregnating black (Nassonow). 2. This cortex blackens thus in over 99 per cent, of individuals in a culture which has not been dividing. In a culture in which the individuals have been rapidly dividing, the percentage of unimpregnated contractile vacnoles increases considerably, up to about 5 per cent. 3. During division of Chilomonas in about 70 per cent. of cases the osmiophile substance is very equally divided between the daughter cells. The dividing cortex comes away from the contractile vacuole, which eventually collapses, new contractile vacuoles arising in the site of the divided osmiophile material. In about 25 per cent, of division stages osmication of the cortex fails to a greater or lesser degree. There is always a very distinct tendency for this failure to take place even in the best of preparations. 4. In some cases (about 3 per cent.), during division, the entire contractile vacuole and its cortex goes over whole to one individual. A new vaeuole, apparently without cortex, arises spontaneously in the other individual. It is unlikely that all of these cases are due to failure of impregnation in one of the individuals, though this possibility cannot be roled out completely. 5. The behaviour of the original contractile vacuole cavity before separation of the daughter cells is as follows. The lipoid, having partially retreated from the vacuole, becomes separated into two parts, and the centrally placed vacuole disappears (figs. 4 and 6, Pl. 36; figs. 10 and 15, Pl. 37). New vacuoles appear in the site of the lipoid bodies in each daughter cell (fig. 5, Pl. 36). 6. Two ellipsoidal accessory bodies or pyrenoids lie on a level with the vestibule. In older cultures the two bodies are often exactly the same size and colour (corrosive osmic followed by neutral red or haematoxylin), but in rapidly dividing cultures, one body may be of normal size, whereas the other may be absent or much smaller. During cell division, one body is carried across to each daughter. No exception to this was ever found. 7. Identification of the smaller Peranemidae is in a confused state. Probably several species, and possibly even genera, have been described by various authors as Scytomonas (Copromonas) subtilis.


1969 ◽  
Vol 17 (2) ◽  
pp. 102-106 ◽  
Author(s):  
BERNARD P. LANE ◽  
EUGENE MARTIN

Electron microscopy of Epon-embedded mouse vas deferens eipthelium treated with buffered potassium pyroantimonate-osmium tetroxide solution revealed precipitates in the lamina propria and along the apical plasma membrane. Electron microprobe elemental analysis of adjacent sections demonstrated that the deposits contained sodium and antimony. Other cations noted to precipitate pyroantimonate in vitro were not present in large amounts compared to controls, and were randomly distributed.


Author(s):  
Richard M. Eakin ◽  
Jean L. Brandenburger

Friend and Murray found that long osmification of mouse epididymis revealed localized osmium reduction in epithelial cells; in this instance, in only the outer cisternae and vesicles of the Golgi apparatus. Although many substances reduce osmium, aldehydes and compounds with multiple double bonds are particularly active. Knowing that retinaldehyde (vitamin A aldehyde) is a highly unsaturated aldehyde we applied their technique to eyes of tadpoles of two amphibians (Xenopus laevis and Hyla regilla) and to adult eyes of one pulmonate snail (Helix aspersa). Eyes were extirpated, immersed in unbuffered 2% aqueous osmium tetroxide for two or three days at 40°C, and prepared for electron microscopy by rapid dehydration with ethanol, embedment in Epon, and examination of ultrathin sections without further staining.


1963 ◽  
Vol s3-104 (65) ◽  
pp. 123-127
Author(s):  
S. K. MALHOTRA

The effect of fixation with acidified solutions of osmium tetroxide (pH 1.5 to 3.5 has been studied on the first (proximal) convoluted tubule cells of the kidney and the pancreatic exocrine cells of the mouse, by electron microscopy. Partially prepolymerized methacrylate was used for embedding. The various membranous structures and the ribosomes retain their individuality even after prolonged fixation in solutions containing 5% acetic acid (pH 1.5). However, the mitochondrial matrix and the ground cytoplasm are not preserved; the zymogen granules are also partially washed out.


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