Répartition de l'activité phosphatasique acide dans les cellules gonadotropes de la Grenouille au cours de leur cycle sécrétoire

Résumé Dans les cellules de l'hypophyse de la Grenouille, Rana temporaria, produisant l'hormone gonadotrope, nous avons analysé la localisation et l'évolution de l'activité phosphatasique acide au cours du cycle sécrétoire.Durant l'élaboration des sécrétions, l'activité enzymatique est essentiellement localisée au niveau de l'ergastoplasme, des saccules et des vésicules golgiennes, avec quelques accumulations plus importantes dans les grains juxta-golgiens et dans certains grains de diamètre plus important. A ce stade, quelques vésicules du réticulum endoplasmique lisse et un petit nombre de formations globuleuses présentent également une réaction positive. Ces images pourraient être en relation d'une part avec un processus de formation des lysosomes, d'autre part avec le fonctionnement normal de l'appareil de Golgi.Dans les cellules en phase de stockage et en cours d'excrétion, aucune activité n'est décelable dans la région golgienne. On note, par contre, la présence d'un grand nombre de corpuscules lytiques dispersés parmi les grains de sécrétion. Dans la matrice de ces corpuscules on distingue parfois des formations granulaires qui pourraient être en voie de résorption.Ces formations qui interviennent dans le processus de résorption intracellulaire des produits de sécrétion non excrétés pourraient également à certains moments du cycle cellulaire jouer un rôle, dans le processus de libération de l'hormone.

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Localization of phosphatasic acid activity in gonadotrophs of the frog during their secretory cycle

Summary The localization and evolution of acid phosphatase activity during the secretory cycle of the gonadotropic cells of Rana temporaria are described.During the secretory phase of the cells the enzymatic activity is demonstrable in the rough endoplasmic reticulum, the Golgi saccules or vesicles and in granules of different diameters. Some vesicles of the smooth endoplasmic reticulum and a few number of globular formations contain also acid phosphatase. This picture corresponds to the normal function of Golgi zone or to the first step of the formation of lysosomes.During the phases of accumulation and excretion of secretory granules acid phosphatase activity is concentrated in lytic bodies which sometimes contain secretory granules. This picture may be interpreted as an intracellular digestion of secretory products. At this time the Golgi zone lacks acid phosphatase activity.From these findings it may be concluded that in gonadotropic cells lysosomes act in the regulation of secretory process, specially the resorption of accumulated secretory granules, but a role in the hormone releasing process cannot be excluded.

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Avec la collaboration technique de Mme R.-O. Clauss.     

Isolation and characterization of glycolipids from some photosynthetic bacteria

Glycosyl glycerides have been found in substantial amounts in Chloropseudomonas ethylicum but could not be detected in two strains of Rhodopseudomonas palustris. Rhodospirillum molischianum possibly contains small amounts of monoglycosyl diglyceride. The glycolipids of C. ethylicum have been separated into two components. One of these, glycolipid I, is a monogalactosyl diglyceride. Glycolipid II, upon acid hydrolysis, yields galactose, rhamnose, and a third, unidentified sugar. The glycolipids or total lipids of the photosynthetic bacteria examined contained saturated and monounsaturated, but none of the more highly unsaturated, fatty acids.     

The Distribution of Acidic and Neutral Peptidases in Barley and Wheat Kernels

The activity of barley and wheat peptidases which hydrolyze alpha-N-benzoyl-dl-arginine-p-nitronnilide (BAPA) and alpha-N-benzoyl-l-arginine ethyl ester (BAEE) has been measured in proximal and distal portions of ungerminated grain and in these tissues during 6 and 7 day incubations. The proximal portion of ungerminated barleys contained the major part of both the acidic (BAPA-ase and acidic BAEE-ase) and neutral (neutral BAEE-ase) peptidases. In ungcrminated wheat these acidic and neutral peptidases were nearly evenly distributed between the proximal and dislal portions. Commercial wheat embryo was very high in acidic peptidase but contained no neutral peptidase. During the germination of both wheat and barleys, acidic and neutral peptidase activity in the seedlings increased with time. No such consistent increase was observed for aleurone and starchy endosperm tissue for any of these grains. Aleurone and starchy endosperm tissue incubated in the absence of the proximal portion of the kernel showed reduced peptidase activities.     

Stimulation of root and somatic embryo production in Euonymus europaeus L. by an inhibitor of polyamine biosynthesis

In vitro formation of roots and somatic embryos is obtained from cotyledon explants of a Spindle tree (Euonymus europaeus L.) cultured on two different media: a medium inducing callus formation and the production of roots, and a medium inducing callus formation, root and somatic embryo production. We studied the effects of -difluoromethylornithine (DFMO), a specific, irreversible inhibitor of ornithine decarboxylase (ODC) on root and somatic embryo production, growth and titers of putrescine in Euonymus explants and explant-derived calli. Early changes in putrescine levels were detected in both cultures before the visible emergence of roots or somatic embryos. DFMO rapidly inhibited putrescine accumulation and growth in non-embryogenic calli and highly stimulated rooting activity. DFMO partially inhibited putrescine accumulation in embryogenic calli. This inhibition had no effects on callus growth but significantly reduced the time of emergence of roots and highly stimulated somatic embryo production. The relationship among putrescine, putrescine metabolism, growth, root and somatic embryo formation is discussed.     

Histone differentiation and nuclear activity

When fast green and eosin are used in combination to stain histones, nuclei display different affinities toward the dyes, some binding fast green exclusively, others binding eosin exclusively, and still others, both stains. In a given tissue, the frequencies of nuclei exhibiting the different colors remain fairly constant over a wide range of staining conditions. Nuclei of cells of the same type may stain differently, but when they are in the same stage of development or state of activity they tend to stain alike. Xenopus erythrocyte nuclei stain bright pink. Condensed mitotic and meiotic chromosomes stain purple. In the grasshopper spermatocyte, the main body of the interphase nucleus stains bright green, but the condensed chromosome stains purple. The mole crab sperm contains several distinct histone-like proteins, that differ in their amino acid compositions, within separate areas of the cell. In these sperms, the lysine-rich histones bind eosin, while the protamine-like protein and arginine-rich histone bind fast green. In general, the eosin and fast green bind preferentially to the lysine and arginine rich histones respectively, when the dyes are permitted to compete with one another. In several systems, including spermiogenesis and erythropoiesis, the aquisition of an eosinophilic component by the nuclei accompanies the slowing of RNA synthesis, and it is suggested that there may be a causal relationship between the two events, the eosinophilic histone effecting RNA synthesis within the nucleus as a whole.     

Sterol effects on phospholipid biosynthesis in the yeast strain GL7

Cells of the yeast sterol auxotroph GL7 were grown on either ergosterol or cholesterol to mid-logarithmic phase and total membrane fractions prepared. Activities of phospholipid biosynthetic enzymes in the two cell types were determined. The rates of phosphatidyl-ethanolamine-phosphatidyl-choline-N-methyl transferase and acyl-CoA-alpha-glycerol-3-phosphate transcylase were significantly greater in ergosterol-grown than in cholesterol-grown cells. These reactions were also inhibited by the polyene antibiotic filipin. By contrast the activities of long-chain fatty acyl-CoA synthetase, CTP-phosphatidate-cytidyl transferase, phosphatidylserine decarboxylase and of phosphatidylinositol synthetase were identical in the two (ergosterol and cholesterol) cultures and unaffected by filipin. The ergosterol effect on phosphatidyl-ethanolamine N-methyl transferase was greatest in cells harvested in early log phase, intermediate in the mid-log phase cells, and not significant in stationary phase cells.