scholarly journals THE NATURE OF HYPOTHALAMO-NEUROHYPOPHYSEAL NEUROSECRETION IN THE RAT

1974 ◽  
Vol 60 (3) ◽  
pp. 554-570 ◽  
Author(s):  
Christine Kent ◽  
M. A. Williams
Keyword(s):  
Amino Acids ◽  
Electron Microscope ◽  
Great Majority ◽  
Time Of Arrival ◽  
Neural Lobe ◽  
Ether Anesthesia ◽  
Light Microscope Level ◽  
Dense Cores ◽  
Intraventricular Injections ◽  
Tritiated Amino Acids

The nature of hypothalamo-neurohypophyseal neurosecretion was examined in the rat by means of intraventricular injections of tritiated amino acids. Quantitation of autoradiographs was used at the light microscope level to study the sites of synthesis of proteins and their time of arrival in the neural lobe. Electron microscope autoradiographs were used to study the labeling of neural lobe tissue. It was concluded that the great majority of the labeled material was translocated inside dense-cored granules and was probably composed mostly of neurophysins. The effect of ether anesthesia was also examined. It was found to remove the dense cores from about 20% of the granules in the neural lobe tissue, a process accompanied by the loss of most of their labeled material. The mechanism of the ether effect is discussed and compared to the normal secretion process.

scholarly journals SYNTHESIS AND STORAGE OF MICROTUBULE PROTEINS BY SEA URCHIN EMBRYOS

1971 ◽  
Vol 50 (2) ◽  
pp. 516-528 ◽  
Author(s):  
Rudolf A. Raff ◽  
Gerald Greenhouse ◽  
Kenneth W. Gross ◽  
Paul R. Gross
Keyword(s):  
Amino Acids ◽  
Sea Urchin ◽  
Messenger Rna ◽  
Binding Activity ◽  
Total Soluble Protein ◽  
Cell Stage ◽  
Lytechinus Pictus ◽  
Sea Urchin Embryos ◽  
Tritiated Amino Acids ◽  
Vinblastine Sulfate

Studies employing colchicine binding, precipitation with vinblastine sulfate, and acrylamide gel electrophoresis confirm earlier proposals that Arbacia punctulata and Lytechinus pictus eggs and embryos contain a store of microtubule proteins. Treatment of 150,000 g supernatants from sea urchin homogenates with vinblastine sulfate precipitates about 5% of the total soluble protein, and 75% of the colchicine-binding activity. Electrophoretic examination of the precipitate reveals two very prominent bands. These have migration rates identical to those of the A and B microtubule proteins of cilia. These proteins can be made radioactive at the 16 cell stage and at hatching by pulse labeling with tritiated amino acids. By labeling for 1 hr with leucine-3H in early cleavage, then culturing embryos in the presence of unlabeled leucine, removal of newly synthesized microtubule proteins from the soluble pool can be demonstrated. Incorporation of labeled amino acids into microtubule proteins is not affected by culturing embryos continuously in 20 µg/ml of actinomycin D. Microtubule proteins appear, therefore, to be synthesized on "maternal" messenger RNA. This provides the first protein encoded by stored or "masked" mRNA in sea urchin embryos to be identified.

A histological examination of the holding sacs and glandular scent organs of some bat species (Emballonuridae, Hipposideridae, Phyllostomidae, Vespertilionidae, and Molossidae)

2000 ◽  
Vol 78 (4) ◽  
pp. 613-623 ◽  
Author(s):  
William MR Scully ◽  
M B Fenton ◽  
A SM Saleuddin
Keyword(s):  
Electron Microscope ◽  
Sexual Dimorphism ◽  
Sebaceous Glands ◽  
Microscope Examination ◽  
Scent Gland ◽  
Light Microscope Level ◽  
Histological Techniques ◽  
Saccopteryx Bilineata ◽  
The Face ◽  
Scanning Electron

Using histological techniques at the light-microscope level, we examined and compared structure and sexual dimorphism of the wing sacs and integumentary glandular scent organs of 11 species of microchiropteran bats. The antebrachial wing sacs of the Neotropical emballonurids Peropteryx macrotis, Saccopteryx bilineata, and Saccopteryx leptura differed in size and location but lacked sudoriferous and sebaceous glands, confirming that they were holding sacs rather than glandular scent organs. Glandular scent organs from 11 species consisted of sebaceous and (or) sudoriferous glands in emballonurids (P. macrotis, S. bilineata, S. leptura, Taphozous melanopogon, Taphozous nudiventris), hipposiderids (Hipposiderous fulvus, Hipposiderous ater), the phyllostomid Sturnira lilium, the vespertilionid Rhogeessa anaeus, and molossids (Molossus ater and Molossus sinaloe). Glandular scent organs were located on the face (H. fulvus, H. ater), gular region (S. bilineata, P. macrotis, T. melanopogon, M. ater, M. sinaloe), chest (T. nudiventris), shoulder (S. lilium), or ears (R. anaeus). Glandular scent organs showed greater similarities within than between families, and typically were rudimentary or lacking in females. Scanning electron microscope examination revealed that the hairs associated with glandular areas of male T. melanopogon were larger and had a different cuticular-scale pattern than body hairs. These were osmetrichia, hairs specialized for holding and dispersing glandular products. In S. lilium, hairs associated with the shoulder scent-gland area were larger than body hairs but similar in cuticular-scale pattern.

Radiation Damage to Polypeptides and Proteins in the Solid State: Changes in Amino Acid Composition *

1981 ◽  
Vol 36 (3-4) ◽  
pp. 310-318 ◽  
Author(s):  
J. Seredynski ◽  
T. Söylemez ◽  
W. Baumeister
Keyword(s):  
Amino Acids ◽  
Electron Microscope ◽  
Amino Acid ◽  
Solid State ◽  
Trypsin Inhibitor ◽  
Concanavalin A ◽  
Thin Layers ◽  
Aminobutyric Acid ◽  
Sensitivity Pattern ◽  
State Changes

Thin layers of synthetic homopolypeptides (poly-α-Ala, -Arg, -Asn, -Asp, -Glu, -His, -Lys and -Tyr) and proteins (myoglobin, concanavalin A, trypsin-inhibitor) were irradiated under solid state conditions in an electron microscope with 100 keV electrons. Radiolytic changes were investigated by amino acid analysis. The results are discussed in terms of the relative radiosensitivities of the constituent amino acids, and possible topochemical effects on the sensitivity pattern emerging. An attempt is also made to trace at least some of the predominant pathways of amino acid transformation, namely the production of alanine and a-aminobutyric acid

scholarly journals THE CHEMICAL NATURE OF KERATOHYALIN GRANULES OF THE EPIDERMIS

1970 ◽  
Vol 47 (3) ◽  
pp. 593-603 ◽  
Author(s):  
A. Gedeon Matoltsy ◽  
Margit N. Matoltsy
Keyword(s):  
Amino Acids ◽  
Electron Microscope ◽  
Citric Acid ◽  
Column Chromatography ◽  
Chemical Nature ◽  
Newborn Rats ◽  
Amorphous Precursor ◽  
Native Form ◽  
Cell Content

Keratohyalin granules were isolated in the native form from the epidermis of newborn rats by the use of citric acid and a detergent. The isolated granules revealed a fine granular substructure in the electron microscope similar to that seen in situ. Analyses of amino acids by automated column-chromatography showed that proline and cystine are present in large proportions whereas histidine is present in a small amount. Accordingly, it was concluded that keratohyalin represents a sulfur-rich amorphous precursor of the horny cell content, rather than a sulfur-poor side product of the keratinization process, or a unique histidine-rich protein as proposed by in situ histochemical and radioautographic studies.

scholarly journals FINE STRUCTURAL AND RADIOAUTOGRAPHIC OBSERVATIONS ON DENSE PERINUCLEAR CYTOPLASMIC MATERIAL IN TADPOLE OOCYTES

1971 ◽  
Vol 49 (1) ◽  
pp. 90-108 ◽  
Author(s):  
E. M. Eddy ◽  
Susumu Ito
Keyword(s):  
Amino Acids ◽  
Nucleic Acids ◽  
Fibrous Material ◽  
Actinomycin D ◽  
Cytoplasmic Material ◽  
Germ Cell Differentiation ◽  
Dense Bodies ◽  
Perinuclear Cytoplasm ◽  
Tritiated Amino Acids ◽  
Silver Grains

Dense fibrous material is first seen in association with mitochondria in tadpole oogonia but is most prominent in oocytes during the extended first meiotic prophase when it aggregates into dense bodies in the perinuclear cytoplasm. The origin of this material has been attributed to 350-A nuclear granules which form cytoplasmic streamers of fibrous material upon passage through nuclear pores. This has commonly been interpreted as the transfer of ribonucleoprotein to the cytoplasm for storage. However, cytochemical reactions for nucleic acids have indicated an absence of detectable RNA in this dense material, and the results of radioautographic studies with labeled uridine, thymidine, or actinomycin D argue against the presence of nucleic acids. When sites of incorporation of tritiated amino acids were radioautographically localized, an appreciable number of silver grains were present over the dense bodies. Uptake of certain amino acids occurs fairly promptly but the degree of labeling levels off after about 6 hr, suggesting a rapid turnover of the material in the dense bodies. Attention is drawn to the similarity of the dense bodies to structures present in germ cells of a number of other species, and possible functions of the dense bodies in germ cell differentiation are considered.

scholarly journals Glutamate and Aspartate Do Not Modify the Ataxic Gait of Acrylamide Treated Animals

1982 ◽  
Vol 9 (2) ◽  
pp. 179-180
Author(s):  
G. De Michele ◽  
F.B. Jolicoeur ◽  
A. Barbeau
Keyword(s):  
Amino Acids ◽  
Ataxic Gait ◽  
Intraventricular Injections

SUMMARY:The purpose of this experiment was to examine the effects of intraventricular injections of glutamate and aspartate on the gait of animals rendered ataxic by the administration of acrylamide. Contrary to their previously reported corrective Influence on ataxia induced by 3-acetyl pyridine, these amino acids did not modify the ataxic gait of acrylamide treated animals. This suggests that glutamate and aspartate can act in cerebellar but not in peripheral types of ataxia in animals.

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