Memoirs: A Cytological Study of the Gregarine Parasites of Tenebrio Molitor, using the Ultra-Centrifuge

1938 ◽  
Vol s2-80 (318) ◽  
pp. 293-319
Author(s):  
MARGARET I. DANIELS

A. Three gregarine species are found to inhabit the mid-gut of the mealworm larvae used: Gregarina cuneata Stein, Gregarina polymorpha Hamm, and Gregarina steini Berndt. The often described Steinina ovalis is probably seldom or never found. They live only in the mid-gut of larvae. They are never found in pupal or adult forms. Gregarines have been seen moving when in a stratified condition. B. The gregarine cytoplasm has five important inclusions, each having a characteristic position in a centrifuged animal (Text-fig. 2). 1. Paraglycogen.--This gives a dark brown colour with iodine, a pinkish general colour with the acid fuchsin of the Feulgen technique, and often a red colour with Bauer's reaction. It occupies the centrifugal pole of the centrifuged cell and is in the form of disc-like granules of varying size. 2. In young centrifuged Gregarina steini chromidial granules are seen in the paraglycogen area, and have, therefore, approximately the same specific gravity. They arise by karyosomic budding with the subsequent extrusion of these buds into the cytoplasm. They stain with iron alum haematoxylin, like the karyosome, and both give a negative result with the Feulgen test for thymonucleic acid. They probably correspond to Joyet-Lavergne's ‘albuminoid reserves’, but do not have the mitochondrial‘cap’ he describes. 3. Mitochondria.--These are usually granular, but sometimes rod-like. They are seen between the ‘alveoli’ formed by the paraglycogen granules. They lie distally to the paraglycogen in a centrifuged parasite; they stain by the iron alum haematoxylin long method, after Benoit, Champy, or Altmann fixation, also with Altmann's fuchsin picric acid stain and the Bensley Cowdry modification of it. 4. The Nucleus is karyosomic, and the karyosome is moved to the centrifugal pole by pressure as is the nucleolus of metazoan cells. The nucleus shows budding of the karyosome. There is plasmatic as well as chromatic material in the karyosome, as shown by centrifuging. The nucleus gives a negative result with Feulgen's nuclear reaction, but chromatin may exist in a very dispersed condition. 5. Golgi Material.--This lies at the centripetal end of the nucleus. It is best shown by Weigl fixation. The large and regular Golgi elements are slightly heavier than the granular Golgi material, which may be compared with that of young oocytes. 6. Fatty Material lies at the extreme centripetal pole of the cell, in globules of varying size. It becomes brown or black after treatment with osmium tetroxide, and vivid cherry red with Sudan IV. It gives a negative result with the Schultz reaction for cholestrol. C. Large globules are seen in the protomerite of Gregarina steini , eosinophile, sometimes fuchsinophile, and also staining with methylene blue. These move towards the centrifugal pole. Methylene blue preparations show blue granules among the paraglycogen granules in the centrifuged animal. They are remarkably resistant to dilute sulphuric acid. They are possibly allied to volutin or chromidia. Tests for the presence of Vitamin C yielded negative results. Only the inclusions of the gregarines in the gut lumen were studied, and the complete life-cycles of the species were not followed out.

Development ◽  
1966 ◽  
Vol 16 (1) ◽  
pp. 29-39
Author(s):  
J. B. Lloyd ◽  
F. Beck

Although the potency of trypan blue as a teratogenic agent in rodents has been known for almost twenty years the mechanism of its action remains obscure. The dye produces a variety of biological effects (see review by Beck & Lloyd, 1966) and most of these have at some time been suggested as possibly relevant to its teratogenicity. The investigation of such correlations would clearly be assisted by determining whether the biological effects of the dye are individually modified by small changes in its chemical structure, particularly if these changes also result in differences in its teratogenicity. The first teratological study of dyes related to trypan blue was made by Gillman, Gilbert, Spence & Gillman (1951), who obtained negative results in rats with six dyes (methylene blue, trypan red, Sudan IV, Bismarck brown, Niagara blue and sky blue), but gave no experimental details of their investigation.


Author(s):  
Larry F. Lemanski ◽  
Eldridge M. Bertke ◽  
J. T. Justus

A recessive mutation has been recently described in the Mexican Axolotl, Ambystoma mexicanum; in which the heart forms structurally, but does not contract (Humphrey, 1968. Anat. Rec. 160:475). In this study, the fine structure of myocardial cells from normal (+/+; +/c) and cardiac lethal mutant (c/c) embryos at Harrison's stage 40 was compared. The hearts were fixed in a 0.1 M phosphate buffered formaldehyde-glutaraldehyde-picric acid-styphnic acid mixture and were post fixed in 0.1 M s-collidine buffered 1% osmium tetroxide. A detailed study of heart development in normal and mutant embryos from stages 25-46 will be described elsewhere.


1966 ◽  
Vol 12 (4) ◽  
pp. 625-639 ◽  
Author(s):  
D. H. Evans

Twenty-three substrains representing colonial variants of 11 strains of Actinabacillus mallei were examined for their ability to attack carbohydrates. Tests conducted in a basal liquid complex medium, containing yeast extract and proteose peptone No. 3 with bromcresol purple as indicator, showed that all strains tested produced acid from arabinose, glucose, fructose, galactose, mannose, and trehalose, while five substrains gave positive results with lactose, one with sucrose, and two with maltose. Eosin methylene blue agar of the same basal composition gave positive results for most of the strains grown on arabinose, glucose, fructose, galactose, mannose, and trehalose, and negative results for all strains grown on xylose, lactose, sucrose, and maltose. In a chemically defined medium containing ammonium chloride as nitrogen source and bromcresol purple as indicator, acid was produced by eight substrains of five of these strains from glucose, galactose, mannose, and trehalose, and by several strains from fructose and sucrose. The ability of these five selected strains to utilize carbohydrates as sole carbon sources for growth was tested in a chemically defined medium containing ammonium citrate as nitrogen source. All strains were able to grow on glucose, galactose, mannose, and trehalose, and most were able to grow on fructose. Arabinose, xylose, lactose, sucrose, and maltose did not support the growth of any of the strains tested.


1970 ◽  
Vol 16 (11) ◽  
pp. 1041-1044 ◽  
Author(s):  
W. E. McKeen

Osmiophilic bodies appear in parts of the colonial growth of Erysiphe graminis DC. f. sp. hordei Em Marchal culture CR3 growing on the susceptible commercial Keystone variety of barley. They are readily observed by the light and electron microscope after osmium tetroxide staining and are abundant in conidiophores, conidia, and mycelium except in haustorial mother cells, in which they are usually absent. The metabolism of haustorial mother cells is distinct and the fine structure of adjoining cells is frequently different. Osmiophilic bodies are absent from the growing hyphal tip, but gradually increase in number and size further back in the terminal cell. Electron micrographs show that they are intracytoplasmic, intravacuolar, and up to 1 μ in diameter. When the colony is washed with acetone or alcohol rather than with aqueous buffer, after glutaraldehyde fixation, before osmium tetroxide fixation, the osmiophilic bodies are removed, indicating that they are lipids. Fat stains, Sudan black B, and Sudan IV stain these bodies. Perhaps the water needs of the germinating conidium are met in part by the oxidation of fats.


2019 ◽  
Vol 07 (02) ◽  
pp. 051-055 ◽  
Author(s):  
Himanshu Singh ◽  
Kundendu Arya Bishen ◽  
Deepti Garg ◽  
Hemani Sukhija ◽  
Dheeraj Sharma ◽  
...  

AbstractFixation is considered as physiochemical process where cells or tissues are fixed chemically. Fixatives perform various functions such as prevention of autolysis and tissue putrefaction. Various fixative agents include formaldehyde, glutaraldehyde, osmium tetroxide, glyoxal, picric acid, and so on. A detailed search on PubMed, Google scholar, and Scopus database showed very few articles on “fixation” and “fixative.” Keeping this fact in mind, a comprehensive review on fixation and fixatives was prepared. The main aim of this review is to make pathologists and laboratory technicians familiar with the basic aspects and different types of fixatives.


1958 ◽  
Vol 4 (5) ◽  
pp. 593-602 ◽  
Author(s):  
Ned Feder ◽  
Richard L. Sidman

Freeze-substitution is based on rapid freezing of tissues followed by solution ("substitution") of ice at temperatures well below O°C. A 1 to 3 mm. specimen was thrown into 3:1 propane-isopentane cooled by liquid nitrogen to -175°C. (with precautions). The frozen tissue was placed in substituting fluid at -70°C. for 1 week to dissolve ice slowly without distorting tissue structure. Excess substituting agent was washed out, and the specimen was embedded, sectioned, and stained conventionally. For best morphological and histochemical preservation, substituting fluids should in general contain both chemical fixing agent and solvent for ice, e.g., 1 per cent solutions of osmium tetroxide in acetone, mercuric chloride in ethanol, and picric acid in ethanol. Preservation of structure was poorer after substitution in solvent alone. Evidence was obtained that the chemical agent fixes tissue at low temperatures. The chemical mechanisms of fixation are probably similar to those operating at room temperature: new chemical cross-linkages, which contain the fixing agent, join tissue constituents together. This process is distinguished from denaturation by pure solvents. Freeze-substitution has many advantages, particularly the preservation of structure to the limit of resolution with the light microscope, and the accurate localization of many soluble and labile substances.


Author(s):  
Thomas Caceci ◽  
Terry C. Hrubec

The black mollie (Poecilia spp.) is a teleost fish found in Central American estuaries, and taxonomically related to the carps and goldfish. The common strains sold in pet stores are hybrids of P. mexicana and P. sphenops. The ultrastructure of its digestivetract has not previously been described.As with other Cyprinidontiforms, the gut is anatomically simple, consisting of a relatively undifferentiated tube from esophagus to anus. The tube is lined with a simple columnar epithelium and has an external wall composed of two layers of smooth muscle. A serosal investment covers this external muscular tunic. Six intestines were examined by scanning and transmission EM. The fish were anesthetized by chilling and opened on the left side. The gut was removed, unwound, and fixed intact in a 3.0% glutar-aldehyde/ 2.0% formaldehyde/ 2.5% picric acid mixture at RT and buffered with cacodylate at pH 7.4. After primary fixation, each intestine was arbitrarily divided into a cranial, middle, and caudal segment, and four specimens were post-fixed in osmium tetroxide, dehydrated, and embedded for TEM examination. Two specimens for SEM examination were washed, treated with 1.0% tannic acid, then post-fixed in osmium tetroxide, dehydrated, and critical-point dried through CO2.


1969 ◽  
Vol 61 (1) ◽  
pp. 111-116 ◽  
Author(s):  
Svend G. Johnsen

ABSTRACT By means of iron haematoxylin staining carefully differentiated by either picric acid or iron alum, Sertoli cells may be differentiated into two types, one (type A) containing unstained nuclei and the other (type B) intensely stained nuclei. No intermediate forms appear to be present. The two types are most easily found in the Sertoli-cell-only syndrome but they are present in the testes with spermatogenesis although type B is rare. The immature (pro-) Sertoli cells in infantile testes also display the two types. The two types of Sertoli cells differ in their degree of binding between nucleic acids and nucleic protein. The significance of the existence of these two types is discussed.


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