Relation between corpus allatum and haemolymph proteins in Sphaerodema rusticum Fabr.

The active and inactive stages of the corpora allata have been described on the basis of size and nucleo-cytoplasmic ratio. The polyacrylamide gel disc electrophoresis of the haemolymph has been done in the males and different stages of reproducing females. A protein fraction with a value 14 less than or equal to Rm less than 16 has been observed only in females. Out of 8 protein fractions, 5 showed oscillations in their concentration at the time of vitellogenesis. Finally active stages in the corpora allata are correlated with the fluctuations in haemolymph protein concentration.     

Formation of protein yolk in the eggs of a parasitoid hymenopteran,Nasonia vitripennis (Walker) (Pteromalidae: Hym)

Summary Electron micrograph profiles of developing yolk inclusions in the oöcytes and comparative electrophoresis of the haemolymph of males and females and of mature oöcytes, indicates that a fraction is present in the haemolymph of the females, which does not occur in the haemolymph of the males. Changes occur to the protein fractions from the haemolymph which are passed into the egg. This suggests that the egg synthesises some of its own yolk and does not have a synthetically passive role during vitellogenesis.We would like to thank Professor E. W. Knight-Jones in whose Department the work was done.     

Studies on the proteins of Poekilocerus pictus. II--changes taking place in the haemolymph protein during maturation of female

In all, 7 protein fractions have been detected in the haemolymph of Poekilocerus pictus by the polyacrylamide gel disc electrophoresis. Out of seven protein fractions, four fractions i.e.3,4,5 and 6 take major role in the vitellogenesis. These fractions are accumulated in the ovariectomised female insect. No yolk is deposited in the allatectomised female ovary. The protein fractions 4, 5 and 6 show high concentration of protein in the allatectomised female as compared to the show operated female. It is concluded that the synthesis of protein fraction 3 is controlled by the corpora allata while the fractions 4, 5 and 6 are controlled by the neurosecretory cells.     

Studies on the proteins of Poecilocera picta. I-changes taking place in the haemolymph protein during moulting

The haemolymph proteins of the 6th nymph of P. picta were fractioned by the polyacrylamide gel disc electrophoresis. A total of seven proteins fractions have been detected from the haemolymph. The chemical nature of different protein fractions have been examined by histochemical methods. The changes taking place in the cuticle and epidermal cells have been examined during the transformation of 6th nymph into adult. The fat body proteins have been electrophoretically fractioned and the changes in the concentration of different protein fractions have been examined. It is suggested that the protein fraction 3 of the haemolymph is utilized in the formation of new cuticle. It is concluded by the histochemical observations that proteins of the band 3 are synthesized in the fat body.     

Vitellogenesis by the American cockroach: Electrophoretic and antigenic characterization of haemolymph and oöcyte proteins

Several peptides have been found in the haemolymph which are antigenically similar to peptides found in the terminal oöcyte during vitellogenesis. There appear to be two major peptides. labeled A and D, in the oöcyte with a stoichiometry of A₂D₁. These two proteins are also found in the haemolymph. Several other prominent proteins found in the haemolymph during the six day cycle are not found to be immunochemically similar to yolk antisera.The possibility of a precursor protein found in both the haemolymph and terminal oöcyte with a molecular weight of 189,000 is discussed.     

Changes taking place in the electrophoretic haemolymph protein pattern during metamorphosis of Polytela gloriosae (Lepidoptera)

The haemolymph proteins of the larva, pupa and adult of Polytela gloriosae have been fractioned by Polyacrylamide gel disc electrophoresis. In the haemolymph of the fifth instar larval stage a total of ten protein fractions have been detected. The concentration of the protein fractions 2, 3, 4, 9 and 10 shows oscillations in their concentration in the early fifth instar, middle fifth instar and late fifth instar larval stage. In all 11 protein fractionswere detected in the haemolymph of different stages of the pupa. The protein bands 1, 7 and 10 of the pupa appear newly in the haemolymph as these bands were not found in the haemolymph of the larvae. The protein fraction 9 of larva was not found in the pupa. In the haemolymph of adult insect sexual difference was observed in the haemolymph protein pattern. In the haemolymph of adult female a total of 10 protein fractions were detected while from the male haemolymph a total of 8 protein fractions were detected. The pupal band 7 was not found in the adults of both the sexes. In the haemolymph of larva and adult one pigmented protein fraction was observed. No pigmented protein fraction was found in the haemolymph of pupa. Iron - containing protein fraction and the acid mucopolysaccharides were not found in the haemolymph. The protein fractions 3, 4, 5, 6 and 7 of adult haemolymph were darkly stained by the Schiff reagent and, thus, they are the fractions of glycoprotein. One protein fraction of lipoprotein was also found in the haemolymph.     

Neuroendocrine control of vitellogenesis in the dragonfly, Orthetrum chrysis (Selys) (Odonata: Libellulidae).

1. Histological correlative studies on the cerebral neurosecretory cells, the corpora allata and the oocyte development strongly suggest the involvement of cerebral NSM mostly produced by the A cells of pars intercerebralis and the CA hormone in the vitellogenesis. 2. Biochemical studies reveal the incorporation of haemolymph proteins and lipids in the yolk during vitellogenesis. 3. Exogenous administration of the extract of the brain-CC and FME demonstrates, to some extent, the stimulation of protein synthesis during vitellogenesis in the haemolymph by the cerebral NSM and the CA hormone, while the lipid metabolism lies, mostly, under the control of juvenile hormone.     

The neuro-endocrine control of protein metabolism in the migratory grasshopper, Melanoplus sanguinipes

In normal females, distinct fluctuations in the protein content of the fat body and haemolymph are evident during each gonotrophic period. These fluctuations partly reflect changes in the protein requirements of the developing oocytes. Almost one half of the total protein deposited in the mature ovary is sequestered during the final stages of vitellogenesis when protein accumulated in the fat body and haemolymph is rapidly depleted. Although similar amounts of protein are deposited in the ovary during the first and subsequent gonotrophic periods, significantly less extraovarian protein is present throughout the latter periods.The accumulation of large amounts of protein in the fat body and haemolymph of ovariectomized females suggests that most yolk protein is of extraovarian origin. As the total protein content of these insects is comparable to that of vitellogenic females, ovariectomy apparently has no immediate effect on protein synthesis.Allatectomy or cautery of the median neurosecretory cells (mNSC) prevents vitellogenesis. Although protein gradually accumulates in the fat body and haemolymph of allatectomized females, the total protein content of these insects is significantly lower than that of controls. Treatment of allatectomized females with juvenile hormone analogue leads to a temporary but significant increase in the protein content of the fat body. However, the subsequent decline in fat body protein is paralleled by a pronounced increase in the protein content of the ovary. These findings suggest that the corpora allata (CA) stimulate both yolk protein synthesis in the fat body and its uptake into the ovary. The total protein content of mNSC-cauterized females is less than that of allatectomized females. This observation supports the proposal that the mNSC have not only an allatotropic effect but also a direct effect on protein synthesis.     

Variations in protein levels in the hemolymph, hepatopancreas and ovary of Penaeus schmitti during ovarian maturation (Crustacea, Decapoda, Peneidae)

Variations of protein concentrations in the haemolymph, hepatopancreas and ovaries were studied during the ovarian maturation of the shrimp Penaeus schmitti. The main variations observed during this physiological process are the increase of protein and the decrease of water contents in the ovary, more pronounced at the first stages of gonadosomatic index (GSI:0-4). During ovarian maturation, water content of the ovaries and hepatopancreas decrease from 10.7 and 3.9% respectively. In relative values, protein content increases from about 40.0% in the ovary, 47.5% in the haemolymph and 15.4% in the hepatopancreas. In absolute values, the protein concentrations of the hepatopancreas showed no significant variation. In the opposite, ovary protein content is 14.7 fold higher at the end than the early stages of vitellogenesis. Relations between haemolymph, hepatopancreas and ovary with eventual transfers of protein material are discussed.     

Immunological analysis of lipophorin in the haemolymph,ovaries, and testes of the fall webworm,Hyphantria cunea (Drury)

Lipophorin (LP) was purified from haemolymph in last instar larvae of Hyphantria cunea (Drury) by KBr density gradient ultracentrifugation and gel filtration. LP is composed of Apo-LP I and Apo-LP II with molecular weights of 230 kDa and 80 kDa, respectively. The level of haemolymph LP in early pupae was somewhat greater than in last instar larvae. In males, this LP concentration is maintained throughout pupal development, whereas the level of haemolymph LP decreases in female pupae beginning at day 7, coincident with the onset of vitellogenesis in the fall webworm. In both male and female adults, haemolymph LP concentrations were dramatically increased in comparison to their pre-adult levels. Actually, LP was found in the ovary by immunodiffusion, tandem-crossed immunoelectrophoresis, and Western blotting. Location of LP in the ovary was also traced by immunogold labelling. Also, LP appeared in small amounts in protein yolk bodies of the ovary at an early stage of vitellogenesis, when nurse cells are bigger than the oocyte, but in greater amounts at those stages when the oocyte is larger than nurse cells—that is, when vitellogenesis is actively taking place. This fact clearly reveals that LP is synthesized by fat body and released into the haemolymph, and then taken up by the growing ovary during vitellogenesis. Also, LP was detected in testes by immunological analysis. Western blotting showed that LP was present in testicular fluid but not in the peritoneal sheath and cysts. To test whether LP is also synthesized in testes, testes and fat body tissues were cultured in vitro, indicating that fat body synthsizes LP but testes do not. The result showed that the haemolymph LP itself is taken up into the testes. © 1994 Wiley-Liss, Inc.     

Gene-controlled incorporation of haemolymph protein into the ovaries of Bombyx mori

The haemolymph protein concentration in Bombyx mori decreases normally by about one-fourth during pharate adult development. In females homozygous for the small egg gene, the concentration of haemolymph protein remained constant throughout the pupal and pharate adult stages. The sm gene does not influence the synthesis of vitellogenic female protein of pupal and pharate adult haemolymph (FP). Normal ovaries transferred to the haemocoele of sm females undergo normal vitellogenesis. In the absence of normal alleles of sm, the ovaries encounter difficulties in the incorporation of FP into their oöcytes from pharate adult haemolymph. These results suggest that an active translocation mechanism is involved in the transfer of haemolymph protein into the ovaries.     

Côntrole neuroendocrine des protéines sanguines vitellogenes d'Anacridium aegyptium sain et parasite

The changing patterns of haemolymph proteins were followed in male and female adults of normal and parasitized Anacridium aegyptium during diapause (autumn, winter) or during activity (spring) of their endocrine system without or with electrostimulations of the pars intercerebralis (PI).The haemolymph protein concentration is high in winter and decreases in spring. It is comparatively depleted in locusts infected by the fly Metacemyia calloti. However, the depletion is significant only in ‘castrated’ females.Fifteen protein fractions were resolved by polyacrylamide disk gel electrophoresis in haemolymph of normal and infected locusts during diapause and activity. Some fractions decrease in quantity during activity in males, normal females, and parasitized females with complete ovarian development. One fraction disappears in females with mature eggs and seems correlated with formation of the eggshell. Eight others protein fractions exhibit electrophoretic mobility identical to the 7 protein fractions of homogenates of eggs. There is little doubt that these haemolymph protein fractions are involved in yolk synthesis and are thus ‘vitellogenic’. One of these ‘vitellogenic’ fractions (band 6) is larger in yolk than in blood.Five protein fractions were demonstrated by electrophoresis of homogenates of parasites. Their electrophoretic mobilities are similar to those of 5 of the 8 haemolymph ‘vitellogenic’ fractions of the host. There is little doubt that these 5 haemolymph protein fractions (one of them is the band 6) are involved in the nutritional requirements of the parasite.Electrostimulation of the PI, during diapause and activity, increase the haemolymph protein concentration and chiefly the protein concentration of the blood band 6. Thus, the median neurosecretory cells of the brain (M-NSC) regulate protein synthesis and chiefly the synthesis of ‘vitellogenic’ proteins.In parasitized females, the increase of the haemolymph protein concentration after electrostimulations of the PI is associated with an enhancement of ovarian development. The depletion of the haemolymph protein concentration in ‘castrated’ females is thus involved in the inability of the oöcytes to sequester available proteins from the haemolymph. The haemolymph protein deficiency may be attributed to (1) an impairment of protein synthesis, attendant upon the hypoactivity of the M-NSC, and (2) the nutritional requirements of the parasite.     

Vitellogenin accumulation in the fat body and haemolymph of Locusta migratoria in relation to egg maturation

Vitellogenins first appear in the fat body of Locusta migratoria during subphase I of vitellogenesis and increase to a constant level during subphase II. A second increase occurs shortly before the oöcyte attains maximal size. Vitellogenin content of fat body subsequently returns to that of subphase I, appropriate to the size of the subterminal oöcyte. The absolute amount of vitellogenin in the fat body is low compared to that found in the haemolymph. Fat body and haemolymph vitellogenins have immunological properties similar to oöcyte yolk proteins—when challenged with oöcyte protein antiserum. They exhibit similar electrophoretic mobility in polyacrylamide gel electrophoresis and are complex glyco-lipoproteins.     

Bioactive fractions containing methyl eugenol-derived sex pheromonal components in haemolymph of the male fruit fly Bactrocera dorsalis (Diptera: Tephritidae)

Sex pheromonal components of the tephritid fruit fly Bactrocera dorsalis (Hendel), 2-allyl-4,5-dimethoxyphenol and (E)-coniferyl alcohol, are biosynthesized from a highly potent male attractant, methyl eugenol, then sequestered and stored in the rectal gland prior to their release during courtship at dusk. These sex pheromonal components have been detected in the haemolymph and crop organ. Hence, attempts were made to separate and identify the haemolymph fractions which contained the sex pheromonal components. Identification of these bioactive fractions in methyl eugenol-fed male flies using gel filtration column chromatography and biodetection using live male flies showed two fractions as highly attractive to conspecific males. These fractions show a significant increase in protein absorbance in the elution profile of haemolymph from methyl eugenol-fed males compared with that from methyl eugenol-deprived males. The molecular mass of these bioactive fractions as determined by using gel filtration was in the peptide range of 3.3 to 5.5 kDa. Subsequent gas chromatography-mass spectrometry analyses further confirmed the presence of the pheromonal components in the bioactive fractions. The presence of these methyl eugenol-derived sex pheromonal components in specific haemolymph fractions suggests the involvement of a sex pheromone binding complex.     

The dynamics of yolk deposition in the desert locust Schistocerca gregaria

Injection of the protein dye Fast Green or the fluid-phase probe fluorescein dextran into the haemolymph of vitellogenic female desert locusts (Schistocerca gregaria) resulted in their incorporation into oocytes. We used Fast Green to study the physical dynamics of yolk deposition during vitellogenesis. Timed maternal injections of Fast Green reveal that yolk deposition and oocyte growth are inextricably linked during vitellogenesis, and that little or no yolk movement occurs within oocytes prior to embryogenesis. The yolk granules laid down early during vitellogenesis lie at the centre of the egg, with yolk granules deposited later packed around these, such that they lie progressively closer to the eventual egg surface. In contrast, during early embryogenesis yolk granules migrate in a manner that closely resembles the movement of early cleavage nuclei. We find fluorescein dextran to be a clear, robust and developmentally inert marker for the timing of maternal injections relative to vitellogenesis in S. gregaria, and we propose its use in parental RNAi or morpholino knockdown experiments. With such experiments in mind, we show that fluorescein-labelled DNA oligonucleotides are internalized within oocytes during vitellogenesis. However, neither Fast Green, fluorescein dextran nor fluorescein-labelled DNA oligonucleotides are detectably transferred from yolk granules to embryonic cells during embryogenesis, and our initial attempts at parental RNAi using maternal injections of dsRNA targeted to late vitellogenesis have proved unsuccessful.     

Vitellogenin fluctuations in haemolymph and fat body and dynamics of uptake into oöcytes during the reproductive cycle of Diploptera punctata

Haemolymph and fat body soluble protein titres have been examined during the reproductive cycle of Diploptera punctata, with particular emphasis on the occurrence of vitellogenin and its uptake into the developing oöcytes. Vitellogenin was first detected in the haemolymph of mated females 2 days after adult eclosion at about the same time that vitellin deposition in basal oöcytes began. Peak haemolymph titres of vitellogenin occurred on day 6, correlated with the completion of yolk uptake. Thereafter vitellogenin levels declined and were generally undetectable throughout most of gestation, rising again shortly before parturition in association with the second gonotrophic cycle. Total haemolymph protein levels were not correlated with vitellogenesis.Soluble fat body vitellogenin titres of mated females remained low during the first oöcyte growth period but then rose several-fold at its completion and remained high throughout pregnancy and the second gonotrophic cycle. Total fat body soluble proteins decline after adult eclosion in association with oöcyte growth.Vitellin accumulation in basal oöcytes was related linearly to increase in volume until the onset of chorion formation. Thus no post-vitellogenic growth period was detected.     

Haemolymph protein patterns during the spinning stage and metamorphosis of Rhynchosciara americana

An acrylamide gel electrophoretical analysis of the haemolymph proteins of R. americana was carried out at different stages of development. In mature larvae there are about 14 haemolymph protein fractions from which one stains heavily and two others faintly for lipoprotein, while three fractions stain for glycoprotein. The haemolymph protein fraction with Rm 0·25 decreases remarkably in mass during spinning, while the others decrease to a lesser extent. The protein fractions could be used in cocoon spinning since previous work suggests that haemolymph proteins are a major pool of cocoon protein precursors. The finding of a protein fraction in the salivary glands with an electrophoretical mobility similar to that of the haemolymph fraction with Rm 0·25 reinforces our hypothesis.     

Änderungen im muster der Haemolymphproteine von adulten Königinnen der Hummelart Bombus terrestris

The soluble proteins of haemolymph during the life cycle from adult bumblebee queens (Bombus terrestris) were separated by disk electrophoresis on polyacrylamide gels. Twenty-three fractions stainable with amido black were detected. Every phase of the bee's adult life is characterized by a specific pattern of haemolymph proteins.Newly emerged queens have a low haemolymph protein concentration which increases in the first 5 days to a maximum. The high concentration is probably connected with the synthesis of hibernation reserves. Before the beginning of hibernation the concentration of some protein fractions seems to decrease; the concentration of these fractions is low also after hibernation.During the spring the first oöcytes begin to grow and the activity of corpora allata, hypopharyngeal glands, and wax glands reaches a maximum at the time of starting nests. A large increase in the concentration of haemolymph proteins is correlated with the activity of these glands. This high concentration does not change during the whole egg-laying period; however, the concentration decreases to a minimum in old queens with degenerating ovaries.In the protein pattern of ovary homogenate we detected three fractions with an RF identical to haemolymph fractions. Investigations on queens parasitized with the nematode Sphaerularia bombi confirmed that these fractions are yolk material (vitellogenin) taken up by ovaries. In parasitized queens oöcytes do not grow and the fractions are of a much lower concentration than in nonparasitized queens with maturing eggs. Therefore it appears that the parasite injures primarily the corpora allata known to stimulate the synthesis of yolk protein.     

Effects of farnesyl methyl ether on the haemolymph and ovarian proteins of the tent caterpillar, Malacosoma americanum

The mode of antigonadotropic action of farnesyl methyl ether (FME) on Malacosoma americanum was investigated by studying the haemolymph and ovarial proteins during vitellogenesis. Low doses of FME which permitted apparently normal adult development but inhibited ovarian development were used.As indicated by the incorporation of ¹⁴C-glycine, FME treatment had no effect on the protein biosynthetic activity by the fat body. However, it resulted in significant accumulation of several haemolymph proteins apparently caused by their reduced uptake by the ovarioles.Radioassay of individual proteins revealed that all the haemolymph proteins had incorporated ¹⁴C-glycine. However, proteins G and H, and to some extent protein B of the treated females, showed significantly higher incorporation of the labelled glycine. It is concluded that the antigonadotropic action of the JH mimic was due to reduced incorporation of various sex-specific and non-specific haemolymph proteins into the ovarioles.     

Disk electrophoresis fractionation of hemolymph proteins during the metamorphosis of different castes and sexes of Formica pratensis

Using polyacrylamide electrophoresis the proteins of the haemolymph of the different developmental stages can be separated into eight strong and nine weak coloured fractions during the cocoon period of Formica pratensis. The proteins were stained with aniline black and measured quantitatively by a Chromoscan densitometer. The values were compared with those maintained with bovine serum albumin.The total protein content of the haemolymph was calculated as the sum of the different fractions; at maximum it amounts to 2·1 per cent (w/v). The maximum is reached during the pharate pupal stage and during the pigmentation of the eyes; the minimum can be observed at the end of pupal ecdysis. At the beginning of body pigmentation in all the forms the protein content of the haemolymph was very much reduced, especially in workers and females.All fractions change independently resulting in a different composition of the haemolymph proteins in pharate pupae, eclosed pupae, and pharate adults. The slow-running fractions f1, f3, f5, and f6 and the mean bands f8 and f11 are reduced weakly until body pigmentation, and from the eleventh day strongly in both castes. All fractions are reduced during the cocoon period, but mostly the slow-running ones. Only the front band f14 increases to nearly twice that of the protein content. The importance of the changes in the protein fractions for development of different organs and for the synthesis of the haemolymph proteins and the influence of hormones are discussed.