Differential mitotic rates and patterns of growth in compartments in the Drosophila wing

In the wing disks of Drosophila slowly dividing cells of Minute mutations are progressively eliminated from Minute/Minute⁺ mosaic compartments by a process known as cell competition. From a study of two different Minutes we show here that the intensity of competition is greater in the more extreme Minute with the slowest rate of cell division. The way in which the more rapidly growing Minute⁺ clones grow and overcome the surrounding Minute cells is described and cell competition is shown to be a result of local interactions between slow- and faster-growing cells.     

Structural studies of the apoprotein of the Folch-Pi bovine brain myelin proteolipid : characterization of the CNBr-fragments and of a long C-terminal sequence.

The action of cyanogen bromide on the quite insoluble bovine proteolipid apoprotein allowed the determination of four peptide fragments: two of them constituted a 19 amino acid long C-terminal sequence of the apoprotein. Our results were in favour of the existence of only one subunit presenting a molecular weight closely related to 25,000 for which a schematic representation is given.     

Autoradiographic studies of a glucocorticoid agonist and antagonist: Localization of 3H-corticosterone and 3H-cortexolone in mouse brain

Summary The localization in the mouse brain of corticosterone, the natural glucocorticoid in the mouse, and cortexolone, reported to be a glucocorticoid antagonist, was studied by autoradiography 30 min after in vivo administration of the tritiated compounds.After ³H-corticosterone (³HB) injection, radioactivity was preferentially concentrated in cell nuclei of several structures within the limbic system, and in nuclei of certain neurones of the cerebral cortex and medulla oblongata. This nuclear concentration was abolished after injection of ³H-corticosterone with an excess of unlabelled corticosterone. After ³H-cortexolone (³HS) injection, a diffuse radioactivity was observed throughout the brain. However, a higher concentration of grains was present in the ventral nucleus arcuatus and in the infundibulum. When excess unlabelled cortexolone was administered with ³H-cortexolone this preferential accumulation of grains was abolished.The accumulation of ³H-cortexolone in the medial basal hypothalamic region suggests that cortexolone concentrates preferentially in dexamethasone (DM) target regions, and in addition the autoradiographic results show that the cortexolone-receptor complex does not accumulate in the cell nucleus.

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Résumé La localisation au niveau du cerveau de souris de la corticostérone, qui est le glucocorticoide naturel chez la souris, et de la cortexolone, démontrée comme étant un antagoniste des glucocorticoides, est étudiée par autoradiographie 30 min après injection in vivo des composés tritiés.Après injection de ³H-corticosterone (³HB), la radioactivité se concentre préférentiellement dans des noyaux cellulaires de plusieurs structures du système limbique et dans les noyaux de certains neurones du cortex cérébral et du bulbe rachidien. Cette concentration nucléaire est abolie après injection de ³H-corticostérone en présence d'un excès de corticostérone non radioactive. Après injection de ³H-cortexolone (³HS), une distribution diffuse de la radioactivité est observée dans tout le cerveau, cependant, une concentration plus élevée de grains d'argent est présente dans la partie ventrale du nucleus arcuatus et dans l'infundibulum. Après injection de ³H-cortexolone en présence d'un excès de cortexolone non radioactive, cette accumulation préférentielle des grains est abolie.L'accumulation de la ³H-cortexolone dans la région hypothalamique suggère que la cortexolone se concentre préférentiellement dans la région cérébrale qui contient les sites de liaison de la dexaméthasone et de plus, les résultats autoradiographiques montrent que le complexe cortexolone-récepteur ne s'accumule pas dans le noyau cellulaire.

     

Autoradiographic localization of 3H-glucocorticoids and 3H-cortexolone in mouse pituitary

Summary Autoradiograms of mouse pituitaries were prepared 30 min after injection of ³H-dexamethasone (³HDM), ³H-corticosterone (³HB) and ³H cortexolone (³HS) either alone or in the presence of competing unlabelled steroids. ³H-dexamethasone accumulated in cell nuclei of both the pars distalis and the pars nervosa but not in those of the pars intermedia. This preferential accumulation (nuclear/cytoplasmic grain density, 41) was abolished by the concurrent administration of excess dexamethasone. ³H-corticosterone, to a much less marked extent than ³H-dexamethasone, accumulated in cell nuclei of the pars distalis but not in those of the pars intermedia and the pars nervosa. Excess unlabelled corticosterone diminished nuclear grain density in the pars distalis. After ³H-cortexolone injection, preferential nuclear uptake was not observed. In a second series of experiments, excess dexamethasone (10 x, 100 x), corticosterone (100 x, 300 x) and cortexolone (100 x, 300 x) administered with ³H-dexamethasone were without effect on cytoplasmic grain density but totally abolished preferential nuclear accumulation. Parallel biochemical studies on kidney cytoplasmic preparations from the same animals showed no differences in total cytoplasmic radioactivity between treatments but marked differences in cytoplasmic bound ³H-dexamethasone. The results demonstrate: i) that dexamethasone binds specifically to cell nuclei of the pars distalis and the pars nervosa and that this nuclear concentration is abolished by competing corticosterone and cortexolone as well as dexamethasone; ii) that corticosterone localizes in cell nuclei of the pars distalis but much less markedly than dexamethasone; iii) that cortexolone fullfils the criteria of a glucocorticoid antagonist at the pituitary cell level.

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Résumé La localisation au niveau de l'hypophyse de souris de la ³H-dexaméthasone (³HDM), de la ³H-corticostérone (³HB) et de la ³H-cortexolone (³HS) est étudiée par autoradiographie 30 min après l'injection des composés tritiés seuls ou en présence de stéroides compétiteurs non radioactifs. La ³H-dexaméthasone s'accumule dans des noyaux cellulaires de la pars distalis et de la pars nervosa mais pas dans des noyaux de la pars intermédia. Cette accumulation préférentielle (densité des grains d'argent nucléaire/cytoplasmique: 4/1) est abolie par l'injection de ³H-dexaméthasone en présence de dexaméthasone non radioactive. La ³H-corticostérone se concentre avec une intensité beaucoup plus faible que la ³H-dexaméthasone uniquement dans certains noyaux de la pars distalis. Un excès de corticostérone non radioactive diminue la densité nucléaire des grains d'argent des cellules de la pars distalis. Après injection de ³H-cortexolone, aucune accumulation préférentielle de grains d'argent n'est observée dans les noyaux cellulaires. Dans une seconde série d'expériences, la ³H-dexaméthasone est injectée soit en présence d'excès de dexaméthasone (10x, 100x) ou de corticostérone (100x, 300x) ou de cortexolone (100 x, 300 x). Dans ces conditions, la densité cytoplasmique des grains d'argent n'est pas différente de celle observée après injection de ³H-dexaméthasone seule mais l'accumulation préférentielle de la radioactivité dans les noyaux cellulaires est abolie. Des études biochimiques parallèles effectuées sur des préparations cytoplasmiques de rein des mêmes animaux montrent que la radioactivité cytoplasmique totale ne varie pas tandis que la liaison cytoplasmique de la ³H-dexaméthasone diffère suivant les traitements. Ces résultats montrent i) que la dexaméthasone se fixe spécifiquement dans des noyaux cellulaires de la pars distalis et de la pars nervosa et que cette fixation nucléaire est abolie aussi bien par des excés de corticostérone ou de cortexolone que par des excès de dexaméthasone, ii) que la corticostérone se localise dans des noyaux cellulaires de la pars distalis mais beaucoup moins intensément que la dexaméthasone, iii) que la cortexolone se comporte comme un antagoniste des glucocorticoides au niveau de la cellule hypophysaire.

     

Restrictive antibiotherapy after renal transplantation.

Forty-two patients were followed up after 44 renal transplantations in an effort to evaluate possible benefits from the following protocol: systematic microbiologic and clinical surveillance, early and aggressive research for the cause of suspected infections, refusal to use prophylactic antibiotherapy, and selection of treatment according to the established cause of the infection. During 18,030 days of follow-up 124 infections were recorded, of which 110 were bacterial, 11 viral and 3 protozoal. Eighty originated in the urinary tract, 17 in skin wounds and 10 in the lower respiratory tract. Septicemia occurred three times, and one death due to infection was recorded. In the treatment of bacterial infections patients received antibiotics for 2486 days. Ampicillin (given for 816 days) and "minor" drugs such as sulfonamides and urinary antiseptics (given for 1036 days) were used 74.5% of the time, whereas gentamicin was used only 2.6% of the time (64 days). Combined antibacterial therapy was needed 1.2% of the time (29 days). A restrictive policy regarding anti-biotherapy seems to be beneficial to renal transplant recipients.     

Molecular data on urinary glycoproteins with human leucocyte antigen (HLA) activity

Two glycoproteins characterized by their serological activities (HLA-A9 and HLA-B12), their isoelectric points and their molecular weights were purified from urine from a patient suffering from tubular proteinuria (cystinosis). Their physicochemical properties as well as an important increase of their specific activities during the different purification steps suggested that they behave as human leucocyte antigens (HLA) which had been excreted into urine. Their amino acid compositions and N-terminal sequences were different to those described for HLA solubilized from cultured human lymphoblast cell lines. The N-terminal sequences of the two serologically active glycoproteins were identical to the N-terminal sequence of another recently purified human urinary glycoprotein called human complex-forming glycoprotein. The relationship between HLA, human complex-forming glycoprotein and the serologically active urinary glycoproteins is discussed.     

Prediction of the conformation of the cow and sheep kappa-caseins

The secondary structures of cow and sheep kappa-caseins were established according to the predictive rules of Chou and Fasman. The diagrams derived from this treatment allowed us to study the chymosin sensitive bond (milk-clotting process), as well as the glycosylation and phosphorylation sites, found to be situated in beta-turns. Despite a high variability between the primary structures of the COOH-terminal part (caseinoglycopeptide) of cow, sheep, and also other caseins, the secondary structures of the biologically important sites were found to be conserved.     

Large scale preparation of purified exocellular DD-carboxypeptidase–transpeptidase of Streptomyces strain R61

The exocellular DD -carboxypeptidase–transpeptidase that Streptomyces R61 excretes during growth has been produced in large fermentation units of 15 m³ total capacity. The yield from 15,000 liter culture filtrate was 1.080 g purified enzyme (92% purity) with a total recovery of 29% and at least a 2000-fold increased specific activity.