Lipid accumulation in oöcytes of Locusta migratoria migratorioides

Oöcytes of Locusta migratoria accumulate lipids during vitellogenesis by acylation of haemolymph diacylglyerols and by de novo synthesis from free fatty acids and glycerol. This was shown by following the incorporation of lipids in vivo after injecting (1-¹⁴C)-palmitate to vitellogenic females and in vitro by incubation of isolated oöcytes with (1-¹⁴C)-palmitate, (1,3-¹⁴C)-glycerol and (¹⁴C)-labelled male and female haemolymph. Both the lipid and protein components of diacylglycerol carrier protein were taken up by isolated locust oöcytes incubated in vitro.Triacylglycerols were preferentially synthesized in vitro by isolated oöcytes incubated in the presence of labelled haemolymph, while phospholipids were the major component synthesized by incubating with (1-¹⁴C)-palmitate.     

β-Cyclodextrin and permeability to water in the bladder of Bufo arenarum

We measured the effect of β-cyclodextrin (BCD, a cholesterol scavenger) on water flow across the isolated toad bladder exposed to an osmotic gradient (J(w)) by a gravimetric technique. BCD, when present in the solution bathing the apical side of the bladder, inhibited the increase in J(w) caused by nystatin, a polyene antibiotic that acts by directly binding apical membrane cholesterol. When present in the basolateral bath, BCD inhibited the increase in J(w) caused by basolateral exposure to oxytocin (which binds membrane receptors and stimulates the synthesis of cAMP), but did not alter the response to theophylline (which inhibits hydrolysis of cAMP by cyclic nucleotide phosphodiesterase). The present data are consistent with the notion that agents that increase J(w) by interacting with membrane receptors, which appear to be clustered in cholesterol-rich domains of the basolateral membrane, are altered by cholesterol depletion, whereas agents that do not interact with receptors or other basolateral membrane components are not affected by this treatment. In either case, cholesterol depletion of the apical membrane does not affect the increase in J(w) brought about by an increase in intracellular cAMP concentration.     

β-adrenergic control of the water permeability of the skin during rehydration in the toad Bufo arenarum

1. Toads dehydrated to 80% of their standard weight (% SW) were rehydrated during 3 hr in distilled water.2. Water permeability of the skin was positively correlated with the degree of dehydration in the range 80–100% SW.3. Systemic administration of the β-adrenergic agonist isoproterenol (5 mg/kg) 90 min after rehydration started (animals fully hydrated) increased skin permeability to the values observed in 80% SW dehydrated animals.4. The administration of the β-adrenergic blocker propranolol (5 mg/kg) 15 min before rehydration started produced a long-lasting decrease in water permeability during the 3 hr of rehydration.5. The results are consistent with the hypothesis of a β-adrenergic control of the water permeability of the skin during rehydration.     

The formation of “Accessory Nuclei” and annulate lamellae in the oöcytes of the flour moth anagasta kühniella

Summary Oöcytes in various stages of maturation were studied with the electron microscope. Stacks of annulate lamellae were found attached to large ribosome studded vesicles. The outer nuclear membrane was found to form blebs and it is considered that these produce the large vesicles. It is suggested that mRNA enters the cytoplasm in membraneous vesicles which collapse, liberating the mRNA, and thus produce annulate lamellae which may later form E.R. Oöcyte nuclei were examined in the E.M. as a potential source of accessory nuclei. Membrane bound organelles containing granules were found in the periphery of the nucleus. The granules were shown to be extruded from the oöcyte nucleolus. The timing of the disappearance of these organelles from the nucleus, together with their structure, suggests that they are precursors of accessory nuclei.The author is indebted to Miss Audrey Taylor, Mr. A. W. Morison, and Mr. M. Craig for technical assistance. The Science Research Council provided a grant for the purchase of equipment with the author gratefully acknowledges.     

Transport of ribosomal RNA into the oöcytes of the milkweed bug, Oncopeltus fasciatus

The accumulation of detectable amounts of newly synthesized ribosomes has been shown to be prevented by ligaturing the nutritive cords between the oöcytes and the trophic syncytium of the Oncopeltus ovary. Unligatured control oöcytes on the opposite side of the same bug accumulated normal quantities of newly synthesized ribosomes under the same conditions. It is concluded that the oöcytes are inactive in the synthesis of ribosomes, this function being entirely the province of the trophic syncytium. Evidence is presented which supports the contention that the oöcytes are synthesizing transfer RNA as well as a high molecular weight, polydisperse, fraction which may be the maternal messenger RNA of the egg.     

Yolk deposition in Douglas-fir beetle oöcytes: Possible rôle of RNA synthesis in the follicular epithelium

RNA synthesis and morphological changes in the follicular epithelial cells of oöcytes of Douglas-fir beetle, Dendroctonus pseudotsugae were studied during the reproductive phase. Inhibition of synthesis of DNA dependent RNA by actinomycin D injections blocked yolk deposition in the oöcytes as well as oviposition within the normal period. A mixture of radioactively labelled haemolymph and ovarial proteins was deposited as yolk proteins in the oöcytes of normal beetles. Such proteins were not deposited in the oöcytes of females injected with actinomycin D; the blockage of yolk deposition persisted even when such females were treated extraneously with juvenile hormone.     

Uptake of vitellogenin into developing oöcytes of Locusta migratoria

The selective incorporation of vitellogenin into developing locust oöcytes was studied using ¹²⁵I-vitellin. Vitellogenin incorporation does not start before the oöcytes are 1.5 mm in length. It increases rapidly up to a maximum at 4.7 mm oöcyte length and decreases steadily until the eggs are fully developed (6.5 mm). Concentrations of serum proteins and vitellogenin in the haemolymph show parallel changes, vitellogenin titre reaching a maximum of 7.5 mg/ml. Incorporation rates for vitellogenin increase from 1.5 μg/hr/oöcyte (2.2 mm) up to 13.8 μg/hr/oöcyte (4.7 mm). In this range incorporation per unit surface area increases 4-fold. While the vitelline and chorionic membranes are being formed, the incorporation rates as well as the protein concentrations in the haemolymph decrease steadily until the second gonotrophic cycle starts. The hormonal basis for oögenesis and the mechanism for selective uptake of locust vitellogenin are discussed.     

The ultrastructure of oösorption in Locusta migratoria migratorioides

Summary The changes in the ultrastructure of the oöcyte and associated follicle cells during oösorption in Locusta migratoria migratoroides are described.Throughout the process the follicle cells act in a phagocytic manner and invade the oöplasm. Localizatio of acid phosphatase activity indicates that at the start of resorption the Golgi complexes of the follicle cells begin to produce lysosomes on a large scale, and that these are utilised in the breakdown of yolk spheres which have been taken up from the oöcyte. Partly degraded yolk spheres are collected together along with other cell organelles into cytolysomes.The significance of large numbers of microtubules within the follicle cells and of microvillar borders between the cells in late stage resorbing bodies is discussed.     

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.     

The dual localization of β-glucuronidase in rat thyroid

Summary After 20 days of treatment with propylthiouracil, a two-fold increase in the amount of -glucuronidase per gram of rat thyroid was noted. This change was manifested cytochemically by both an increase in the number of -glucuronidase containing granules and an enhancement of the generalized cytoplasmic activity. The results are discussed in relation to the dual localization of -glucuronidase.     

Oöcytes degeneration in the queen honey bee after infection by Nosema apis

Terminal o?cytes containing yolk in both healthy and nosema infected queen honey bees were studied. In the healthy queens the terminal o?cytes exhibited a layer of follicular cells which were covered by a smooth-surfaced ovariole sheath. In the o?plasm were numerous electron-dense yolk granules and lipid yolk droplets. The elecron-dense yolk granules exhibited a crystalline structure. Stacks of endoplasmic reticulum were observed in the yolk granules throughout the o?plasm. Numerous mitochondria possessing well defined cristae were also observed. O?cytes in the ovary of queen honey bees appeared degenerated after 7 days of infection by Nosema apis. The ovariole sheath was wrinkled. In the o?plasm, yolk granules were broken down into small spheres and granular substances. Numerous ribosomes without stacks of endoplasmic reticulate were observed. Lysosomes were abundant and numerous electron-dense materials surrounded by a membrane were detected. The o?cytes appeared to be extensively autolysed. The significance of these observations is discussed.     

Endocrine control of oögenesis in the housefly,Musca domestica vicina

The endocrine system involved in the control of oögenesis in the housefly, Musca domestica vicina, was investigated. Allatectomy, decapitation, and starvation of newly emerged females resulted in inhibition of oögenesis, showing a close relationship between enlargement of the corpus allatum and growth of follicles during the first oögenesis. Histological observation of sexually matured females showed active secretion of the corpus allatum and the medial neurosecretory cells of pars intercerebralis. Topical application of juvenile hormone analogues (JHA) to the allatectomized fly induced the growth of ovary, and critical doses of methoprene and methyl-7, 11-diethyl-juvenate for the maturation of the ovary were determined. JHA stimulated initiationof oögenesis in the starved or decapitated flies as well as vitellogenesis in the sugar-fed one; subsequently it was found that juvenile hormone acted not only as a gonadotropin but also as a regulator of vitellogenesis. Furthermore, JHA stimulated cell lysis in pupal fat body of female flies, indicating a possible influence of juvenile hormone upon the process of releasing vitellogenin.     

The localization and the isoenzymes of α- and β-Galactosidases in root tips

The localization was studied of α- and β-galactosidases in frozen sections of Ca-formol fixed root tips using simultaneous azocoupling reaction. In all species studied (Allium cepa,Cucurbita maxima, Lupinus albus, Pisum sativum, Vicia faba, Zea mays) positive results were obtained, the localization being ubiquitous (according to localization typology given here). InVicia faba andZea mays the isoenzymes of α- and β-galactosidases were revealed by means of acrylamide gel electrophoresis, using authors’ modification of Reisfeld method, in whole root tips, particular growth zones and separately in cortex and central cylinder. No differences were observed comparing stele and cortex. Whereas characteristic isoenzyme patterns were found in individual growth zones in maize, no differences appeared in broad bean. A comparison was made of thein situ localization and of the isoenzyme patterns of α- and β-galactosidases with α- and β-glucosidases. In the case of galactosidases, positive results appear with both α- and β-galactoside. The rising of pH to neutrality leads to considerable decrease in the activity of both galactosidases.     

The properties of “active” Cl transport across the cornea of the toad Bufo marinus

• 1.1. Active Cl transport occurs from the endothelial to epithelial side of the cornea of Bufo marinus. Na transport is much less and is in the opposite direction.
• 2.2. The rate of Cl transport is not saturable and is linearly related to the Cl concentration on the endothelial side.
• 3.3. Active efflux (endo to epi) of Cl is reduced (50%) by CN and abolished by IAA. Ouabain and Na-free solutions on the endothelial side also reduce Cl efflux.
• 4.4. O₂ consumption or lactate production are also decreased by ouabain or Na-free solutions. However, metabolism was not inhibited by Cl-free solutions or a specific Cl blocking drug bumetanide.
• 5.5. Cl transport exhibits some rather unusual characters and a model is proposed to account for them which involves an exchange of Cl for metabolically produced organic anions.

     

The redox state of free nicotinamide–adenine dinucleotide phosphate in the cytoplasm of rat liver

1. The concentrations of the oxidized and reduced substrates of the ;malic' enzyme (EC 1.1.1.40) and isocitrate dehydrogenase (EC 1.1.1.42) were measured in freeze-clamped rat livers. By assuming that the reactants of these dehydrogenase systems are at equilibrium in the cytoplasm the [free NADP(+)]/[free NADPH] ratio was calculated. The justification of the assumption is discussed. 2. The values of this ratio obtained under different nutritional conditions (well-fed, 48hr.-starved, fed with a low-carbohydrate diet, fed with a high-sucrose diet) were all of the same order of magnitude although characteristic changes occurred on varying the diet. The value of the ratio fell on starvation and on feeding with the low-carbohydrate diet and rose slightly on feeding with the high-sucrose diet. 3. The mean values of the ratio were calculated to be between 0.001 and 0.015, which is about 100000 times lower than the values of the cytoplasmic [free NAD(+)]/[free NADH] ratio. 4. The differences in the redox state of the two nicotinamide-adenine dinucleotide couples can be explained on a simple physicochemical basis. The differences are the result of equilibria that are determined by the equilibrium constants of a number of highly active readily reversible dehydrogenases and transaminases and the concentrations of the substrates and products of these enzymes. 5. The decisive feature is the fact that the NAD and NADP couples share substrates. This sharing provides a link between the redox states of the two couples. 6. The application of the method of calculation to data published by Kraupp, Adler-Kastner, Niessner & Plank (1967), Goldberg, Passonneau & Lowry (1966) and Kauffman, Brown, Passonneau & Lowry (1968) shows that the redox states of the NAD and NADP couples in cardiac-muscle cytoplasm and in mouse-brain cytoplasm are of the same order as those in rat liver. 7. The determination of the equilibrium constant at 38 degrees , pH7.0 and I 0.25 (required for the calculation of the [free NADP(+)]/[free NADPH] ratio), gave a value of 3.44x10(-2)m for the ;malic' enzyme (with CO(2) rather than HCO(3) (-) as the reactant) and a value of 1.98x10(-2)m(-1) for glutathione reductase.     

The effects of cyanide plus β-hydroxybutyrate on changes in mitochondrial absorbancy and ultrastructure induced by hypotonicity and inorganic phosphate

Summary Absorbancy measurements and electron microscopy of isolated rat liver mitochondria show that simple osmotic swelling is not prevented by cyanide plus -hydroxybutyrate. Similarly, electron microscopy shows that these two agents do not prevent the swelling induced by inorganic phosphate. However, the absorbancy decrease induced by inorganic phosphate is inhibited by cyanide plus -hydroxybutyrate.These findings cast doubt on the validity of the absorbancy method as an index of mitochondrial morphology. The evidence also indicates that both simple osmotic swelling and that induced by inorganic phosphate are independent of respiration. An osmotic mechanism is proposed as an alternative.Dedicated to Prof. Berta Scharrer on her 60^th birthday.This study was supported by Research Grants GM-08900, NB-02145, NB-05219 from the U.S.P.H.S. and a Lederle Medical Faculty Award. Fine technical assistance was provided by Mrs. Cynthia Jones, Miss Ursula Moeller and Mr. Stanley Brown.     

Autoradiographic localization of α-bungarotoxin-binding sites in the carotid body of the rat

Summary Radioiodinated -bungarotoxin (-Bgt) was used to localize -Bgt-acetylcholine receptors in the carotid body of the rat. The gamma spectrometer analyses indicated a high uptake of [¹²⁵I] -Bgt in carotid bodies incubated in vitro (1.51 fmole per organ). Incorporation of the isotope was effectively blocked by pretreatment of carotid bodies with d-tubocurarine and unlabeled -Bgt, but not by atropine. Light microscopic autoradiography showed a heavy labeling of some parenchymal cells. Electron-microscopic autoradiography revealed that labeling was localized along the interface between parenchymal cells, especially where their cytoplasmic processes engage in complex interdigitations. The silver grain counts on electron-microscopic autoradiographs suggest that labelings are preferentially associated with the plasma membrane of certain Type I cells. It is suggested that these Type I cells in the rat's carotid body probably are provided with nicotinic acetylcholine receptors on their plasma membranes.This research was partly supported by a grant from the Edward G. Schleider Foundation of New Orleans.The authors extend appreciation to Drs. Akira Arimura, Dept. of Medicine, for supplying a part of the radioisotope and to James Fisher, Dept. of Pharmacology, Tulane Medical School, for use of the gamma spectrometer. Appreciation also is extended to Mrs. Lia Pedroza for technical assistance     

The localization of the relaxed form of plasminogen activator inhibitor type 2 in human gingival tissues

The plasminogen activating system is important in extracellular proteolysis. Plasmin degrades tissues and activates proteases. Plasminogen activators (tissue type; t-PA and urokinase type; u-PA) and plasminogen activator inhibitors (PAI-1, PAI-2) are found in high concentrations in gingival crevicular fluid (GCF). Previous findings indicate the significance of PAI-2 in gingival inflammation. When PAI-2 inhibits a plasminogen activator its conformation relaxes and neoepitopes can be detected with a monoclonal antibody (#2H5). Our aim was to study if and where in the gingival region PAI-2 has acted as an inhibitor. Methodological studies were performed on GCF with western blotting. Frozen sections of human gingiva were studied immunohistochemically. The methodological studies showed that our antibody #2H5 selectively detects relaxed low molecular weight non-glycosylated PAI-2. Total PAI-2 and relaxed PAI-2 were found in all gingival epithelia with a honeycomb-like staining. Relaxed PAI-2 showed the most pronounced staining in the cell layers near the surface of the epithelium and no staining in the suprabasal layers, while total PAI-2 was found throughout the epithelium, often more pronounced suprabasally. The results showed that PAI-2 indeed has acted as an inhibitor of a protease in gingival tissues, primarily in the epithelia. The results also suggest primarily an intracellular localization and thus the interaction of PAI-2 with a protein other than t-PA.     

Redistribution of phosphate deposits in the algaScenedesmus quadricauda deprived of exogenous phosphate—an ultra-cytochemical study

Summary The green algaScenedesmus quadricauda (Turp.) Bréb. was cultivated in the presence or absence of orthophosphate and synchronized daughter or mother cells were cytochemically stained. Forin situ capturing of water soluble phosphates Ca²⁺ and Mg²⁺ ions were added to the ice-cold glutaraldehyde fixative to form a polymeric metal-phosphate complex which was equivalent to the energy-rich condensed polyphosphates in staining by alkaline lead acetate. The X-ray microanalysis of the extensive stained deposits proved the presence of phosphorus. In orthophosphate-supplied daughter cells cytoplasmic vacuoles contained round stained bodies; a layer of phosphate-containing paracrystals encompassing some starch grains and a fine stained layer delineating the chloroplast envelope were also observed. In the equivalent mother cells only the material inside theloculi of stacked thylakoids was stained. In orthophosphate starved daughter cells filamentous phosphate-containing paracrystals filled extensive cytoplasmic vacuoles. A stained layer covered the chloroplast envelope and continuous stained layers appeared inside theloculi of stacked thylakoids. Mother cells that develop from these daughter cells were filled with starch grains and showed only peripheral stained deposits. The results are compared with the biochemical evidence of phosphate turnover in algal cells.Abbreviations ADP adenosine diphosphate - ATP adenosine triphosphate - ATPase adenosine triphosphatase - EDAX energy dispersive analysis of X-rays - Pi orthophosphate - PPi pyrophosphate - PP polyphosphate - PhAR photosynthetic active radiation - TCA trichloroacetic acid     

Control of oötheca formation and oviposition in Blattaria

The brain is not required for oviposition in five species of Blaberidae; the control centre for formation, 90° counterclockwise rotation, and retraction of the oötheca lies in the abdomen. A similar centre controls oötheca formation and 90° clockwise rotation in Blattella germanica (Blattellidae). It is suggested that during oviposition, abdominal proprioceptors or musculature contribute nervous information to the last abdominal ganglion. Nerve impulses are presumably integrated in the last abdominal ganglion and transmitted to the colleterial glands, oviducts, and ovipositor. In Periplaneta americana (Blattidae), the brain is needed for initiating egg case formation, but it is unnecessary once the process has begun. The results suggest a divergence of control centres for oviposition between the Blaberoidea and Blattoidea.