Influence of adult food on the reproduction of virgin females of anAcanthoscelides obtectus strain originating from Colombian altiplanos

Summary The reproductive activity of virgin females of anAcanthoscelides obtectus strain originating from the high Colombian plateau was variable. Some females did not synthesize vitellogenin during imaginal life while others produced mature oocytes. In the case of virgin females without reproductive activity, the supply of pollen in the adult diet did not stimulate synthesis and incorporation of vitellogenin. On the other hand, the supply of pollen always induced a higher vitellogenin titre in the haemolymph of females which produced oocytes, and stimulated ovarian production.     

Vitellogenin synthesis induced in locust fat body by juvenile hormone analog in vitro

Summary Fat bodies from adult females ofLocusta migratoria continue to synthesize vitellogenin and other proteins when cultured in vitro. A strong secondary induction of vitellogenin synthesis was obtained in fat bodies cultured in the presence of methoprene, and a weaker but significant primary induction was also obtained using higher doses (>100 g) of methoprene.This work was carried out in Dr G.R. Wyatts Laboratory and I thank him for helpful discussions. I also thank Dr G. Staal (Zoecon Corp.) for supplying the methoprene and Pfizer Inc. for rimocidin sulfate. This research was supported by grants from the US NIH (HD 02176) and Canada NSERC.     

Induction of vitellogenin by estradiol and androgens in a teleostean fish: Gobius niger L]

At any point in the sexual cycle of both males and females, oestradiol benzoate induces synthesis of plasmatic vitellogenin, identifiable by a specific immunserum. Pharmacological doses of purified testosterone and dihydrotestosterone also induce synthesis of this yolk precursor. Although a partial aromatisation of testosterone into oestrogen is possible, our results show that there must also be interaction between the androgens and the oestrogens receptors in the liver.     

The selective accumulation of vitellogenin in the locust oocyte

Summary The selectivity of vitellogenin absorption by the locust oocyte was examined by comparing the uptake of vitellogenin and a haemolymph protein of similar molecular weight (MHP). Though both proteins occurred in the haemolymph at approximately the same concentration there occurred a 500-fold difference in accumulation of vitellogenin over MHP during a 24-h period. Surprisingly MHP did not accumulate in the oocyte during vitellogenesis.     

Vitellogenin and lipovitellins inOrchestia gammarellus (pallas) (Crustacea,Amphipoda); labelling of subnuits after in vivo administration of3H-leucine

Summary The distribution of³H-leucine between the various polyopeptide components ofOrchestia gammarellus vitellogenin and lipovitellins, separated by SDS-PAGE, has been stdied after in vivo injection of this amino-acid. The results corroborate the view that, the heaviest components, or native polypeptide subunits of vitellogenin, are progressively transformed into lighter ones.     

Is vitellogenin a cuticular component of the female locust?

Summary One major antigen, present in female cuticle, female blood and eggs, is revealed by the antiserum against soluble cuticular proteins of adults locusts, and by all the antisera against vitellin or vitellogenin. It is not revealed by the specific antiserum against diglyceride-binding lipoprotein. The presence of this major antigen in the cuticle depends on the presence of vitellogenin in the blood.     

Immunochemical identification of vitellogenin in the serum of the newtTriturus cristatus

Summary The hematic yolk precursor — vitellogenin — has been identified immunochemically in the serum of estrogenized females of the newtTriturus cristatus by employing an antiserum prepared against yolk proteins.     

Relationship between the absolute configuration and the biological activity of juvenile hormone III

Summary The activity of the pure 10R (=natural) and 10S enantiomers of juvenile hormone III (JH III) was determined in 3 different bioassays, and the relative binding affinity of the 2 enantiomers to the haemolymph JH-binding protein of the cockroachNauphoeta cinerea was measured. In theGalleria wax test, a local morphogenetic assay, the 10R enantiomer was 5240 times more active than, the 10S enantiomer, 1Galleria unit corresponding to 0.42 pg of 10R-JH III as compared to 2.2 ng for 10S-JH III. In a systemic morphogenetic assay with the cockroachNauphoeta cinerea 380 times less 10R enantiomer was necessary in order to induce detectable juvenilisation (58 ng 10R and 22 g 10S) and in a systemic gonadotropic assay withNauphoeta cinerea 255 times less 10R was needed to induce vitellogenin synthesis in 50% of the insects (6.7 ng 10R and 1710 ng 10S). In the JH-binding protein assay 10R-JH III had an affinity for the JH-binding protein (lipophorin) which was approximately 46 times higher than that of 10S-JH III.     

Determination of the molecular weight of vitellogenin and of lipovitellins of Orchestia gammarella, Crustacea, Amphipoda]

Vitellogenin and lipovitellins of Orchestia gammarella, tested by electrophoresis on gels of different acrylamide concentrations, following the procedure of Hedrick and Smith (1968), displays a migration pattern identical to that of proteins of respectively congruent to 4 x 10(5) (vitellogenin), congruent to 3,5 x 10(5) (lipovitellins I and I') and congruent to 5 x 10(5) (lipovitellin II) molecular weights.     

Correlation between ovarian growth,vitellogenin titer,and yolk polypeptide pattern in the haemolymph ofCalliphora vicina

Summary During the first egg maturation cycle ofCalliphora vicina changes in the vitellogenin titer and yolk polypeptide pattern of the haemolymph are correlated with the intensity of follicular growth, and the rate of yolk deposition.Acknowledgments. Support from The Danish Natural Science Research Council (grant: 11-0423) and access to facilities at the laboratory of Dr Bente L. Hansen (Institute of Medical Microbiology) is gratefully acknowledged.     

Adenylate storage,metabolism and utilization in coelomic cells of the polychaeteNereis virens (Annelida,polychaeta)

Eleocytes are specialized coelomic cells in nereid annelids which assume a central role during germ cell development. They may contain extremely high concentrations of both adenosine monophosphate (AMP) and adenosine diphosphate (ADP) (each >10 mol/ml of cell vol.), whereas the adenosine triphosphate (ATP) content is comparatively low (0.8 mol/ml cell vol.).³¹P nuclear magnetic, resonance (NMR) studies of living eleocytes suggest the compartmentalization of both AMP and ADP in the large acidic vacuole characteristic for this cell type. Eleocytes are thus capable of storing high concentrations of ADP and AMP without inhibiting energy metabolism, by sequestering these compounds in a separate compartment. The high concentrations of both AMP and ADP in the eleocytes decrease in both males and females during the course of maturation. In eleocytes of male animals, the decline of the high nucleotide concentrations was accompanied by a transient increase of two intracellular nucleosides, inosine and guanosine. This suggests the degradation and further metabolism of nucleotides to the corresponding nucleosides. In culture, eleocytes release both inosine and guanosine into the medium. Both nucleosides are also present in the coelomic fluid, the common compartment for both eleocytes and germ cells. Both male and female germ cells incorporate¹⁴C-labelled inosine and guanosine in culture. For oocytes, the further incorporation of [¹⁴C]inosine into the RNA fraction could be demonstrated. The large adenylate pools in the eleocytes may be regarded as a store for purine compounds for later use by the growing germ cells to supplement nucleic acid synthesis. The supply of nucleic acid precursors seems to be another specific function of eleocytes related to gametogenesis, in addition to their known synthesis of vitellogenin.     

Development of an enzyme linked immunosorbent assay (ELISA) for measurement of vitellogenin concentrations in cockroaches

Summary A competitive enzyme linked immunosorbent assay was developed for the quantification of a large lipoprotein, namely the yolk protein vitellogenin, in the haemolymph of cockroaches (Nauphoeta cinerea). This assay was found to be specific, reproducible and it has a high sensitivity (approximately 10 ng).Acknowledgments. We would like to express our thanks to Prof. H. Fey and Ms H. Pfister, Veterinary Bacteriological Institute, University of Berne, for introducing us into the ELISA methodology, to P. Beyeler for technical assistance and to M. Kaltenrieder for drawing the graphs. We also thank the Sandoz Foundation for a fellowship to M. Dumas and the Swiss National Science Foundation (grant No. 3. 188-0.77) for financial support.     

Tamoxifen ‘sex reverses’ alligator embryos at male producing temperature,but is an antiestrogen in female hatchlings

Summary Tamoxifen is an anticancer drug widely used in the treatment of estrogen-dependent breast cancer. In hatchling alligators it acts as a pure antiestrogen in that it completely blocks the effect of estradiol-induced oviductal hypertrophy and completely blocks the estradiol-induced hepatic vitellogenin secretion. Paradoxically, when injected into alligator eggs incubated at 33°C, a temperature which would normally result in 100% male hatchlings, tamoxifen sex reverses the embryos into apparently normal female hatchlings.     

Receptor-mediated transport and deposition of complement component C3 into developing chicken oocytes

Immunological resistance of the chick embryo is dependent upon IgG present in the yolk of the layed egg. Here we show that complement factor 3 (C3), a key component of the humoral complement system, is a yolk component of chicken eggs. C3 is transported into oocytes by LR8-mediated endocytosis. LR8 also binds and transports other major yolk components such as vitellogenin, very-low-density lipoprotein, and α₂-macroglobulin. Expression studies of LR8 during chicken development and oocyte maturation, in combination with studies on the uptake of individual yolk components, suggest the following model for oocyte maturation in the chicken: all oocytes present in the ovary contain high levels of LR8 mRNA and protein long before the onset of oocyte maturation. Selected oocytes gain access to yolk precursors, and LR8 binds, internalizes, and deposits the major yolk components in the ratio of their relative abundance in the accessible pool.Received 9 May 2005; received after revision 6 June 2005; accepted 13 June 2005     

Protein synthesis in vivo in muscles of the growing lamb]

The relationship between incorporation of intravenously injected 14C lysine and specific radio-activity of precursor was used to estimate protein synthesis in muscle of growing lambs. The rate of protein synthesis per unit of muscle weight in Supraspinatus and Extensor digitorum longus decreased strongly from one week of age to puberty (10 weeks); afterwards it decreased in supraspinatus and increased slightly in Extensor digitorum longus. The rate of protein synthesis increase in muscle protein weight was constant during the whole experiment (1 week-16 weeks). In preruminant Lambs )1 week-5 weeks) the rate of protein synthesis per unit of muscle weight decreased; however, due to the increase in muscle weight, the rate of protein synthesis in whole muscle remained relatively constant. In order Lambs the rate of protein synthesis in whole muscle decreased. The turnover time of protein increased with age. These results give some explanation on muscular development of Lambs.     

Relationship between DNA and cholesterol synthesis in kidney after refeeding

Summary DNA and cholesterol synthesis were investigated in the kidneys of fasted-refed rats. Refeeding resulted in an increase in kidney DNA synthesis, as measured by³H-thymidine incorporation, starting at 72 h. The increase in DNA synthesis was accompanied by a stimulation of cholesterol synthesis, as measured by¹⁴C-acetate incorporation into cholesterol.     

Cellular control of the tick-borne virus antigen production in persistently infected cell culture

Summary The influence of inhibition or stimulation of cellular DNA synthesis on tick-borne virus antigen production in persistently infected cell culture was studied. Either mitomycin C or cytosine-arabinoside caused cessation of antigen-containing cell number increase. Stimulation of cellular DNA synthesis by growth medium change increased the level of antigen-containing cells. When HEp-2-Sof culture was synchronized, a correlation was observed between the entrance of cells into DNA synthesis phase and the increase of proportion of antigen-containing cells.     

Differential sensitivity to ethidium bromide of replicative DNA synthesis and bleomycin-induced unscheduled DNA synthesis in permeable mouse sarcoma cells

Replicative DNA synthesis in permeable mouse sarcoma cells was more sensitive to ethidium bromide (EtBr) than bleomycin-induced unscheduled DNA synthesis (UDS). A similar difference in sensitivity to EtBr was observed between DNA polymerases alpha and beta. The difference in sensitivity to EtBr of replicative DNA synthesis and UDS in the present system seems to reflect mainly the sensitivity difference between DNA polymerases alpha and beta.     

Cellular control of the tick-borne virus antigen production in persistently infected cell culture.

The influence of inhibition or stimulation of cellular DNA synthesis on tick-borne virus antigen production in persistently infected cell culture was studied. Either mitomycin C or cytosine-arabinoside caused cessation of antigen-containing cell number increase. Stimulation of cellular DNA synthesis by growth medium change increased the level of antigen-containing cells. When HEp-2-Sof culture was synchronized, a correlation was observed between the entrance of cells into DNA synthesis phase and the increase of proportion of antigen-containing cells.     

Contrasting effects of RNA and protein synthesis blocking on natural and lectin-dependent cell-mediated cytotoxicity against adherent HEp-2 cells

In this study, earlier observations concerning the independence of both natural (NCMC) and lectin-dependent cell-mediated cytotoxicity (LDCC) from DNA synthesis have been confirmed. In addition, blocking of RNA synthesis by actinomycin D and of protein synthesis, reversibly by puromycin (PM) and irreversibly by emetine (EM) had different effects on NCMC and LDCC against 3H-thymidine-prelabeled HEp-2 target cells. Similarly to the Con A-induced proliferation of lymphocytes, LDCC activity was also inhibited by blocking of RNA and protein synthesis. NCMC to HEp-2 target cells was not affected by blocking of RNA synthesis, while both PM and EM strongly enhanced NCMC activity.