Analysis of clotting defects in diseased lobsters—I. Alterations in blood parameters

• 1.1. In gaffkemic lobsters kept at 15°C. drastic declines in the hemocyte number and clotting ability occur.
• 2.2. In animals kept at 10°C, although some clotting defects rapidly occur, a high number of amoebocytes is found. Clotting ability reappears after 5 days.
• 3.3. The proportion of each type of hemocyte changes. Numerous hemocytes show morphologic altered features.
• 4.4. Dorsal hematopoietic tissue is as in control lobsters.
• 5.5. Total protein contents are similar in bacteremic or control lobster hemolymphs.

     

Digestive protease,lipase and amylase activities in stage i larvae of the american lobster,Homarus americanus

• 1.1. Digestive protease, lipase, and amylase of Stage I larvae of the American lobster Homarus americanus are characterized.
• 2.2. A sensitive method for detection of crustacean lipase was developed using an latroscan which combines thin-layer chromatography and flame ionization detection to quantify free fatty acids generated by lipase digestion.
• 3.3. pH optima of the three enzymes occurred at or near the pH of gastric fluid.
• 4.4. A time course study demonstrated slight increases in protease and amylase activities during the first larval stage, regardless of whether the lobsters were fed or not, whereas lipase activity was constant.

     

Rates of heat exchange in the ornate box turtle,Terrapene ornata

• 1.1. Eight ornate box turtles, Terrapene ornata, were heated and cooled in water at 35 and 15°C respectively.
• 2.2. Thermal time constants were calculated and no significant differences were found (t-test; 0.05 level) between warming and cooling rates.
• 3.3. Heart-rate data indicated slightly higher, but non-significant, mean values during warming.
• 4.4. It was concluded that T. ornata is not able to physiologically alter rates of heat exchange in water significantly and must rely on behavioral mechanisms to maintain body temperature.

     

Salt and water balance in selected crabs of madagascar

• 1.1. Salt and water regulation were studied in Cardisoma carnifex, Sesarma meinerti, Varuna litterata and Coenobita cavipes.
• 2.2. The brachyurans, Cardisoma, Sesarma and Varuna show strong osmoregulation in tap water or 150 per cent sea water, the antennary glands being ineffective in the process but able to concentrate magnesium in the urine independently of the magnesium influx from the medium.
• 3.3. The anomuran Coenobita was not studied in immersion experiments but was ssown to control its water balance on land by behavioral means.
• 4.4. When desiccated, Cardisoma can regain water against an osmotic gradient from sea water dampened sand.

     

Effect of bovine milk antigens and egg lysozyme on the binding of 59Fe-lactoferrin to platelet plasma membranes

• 1.1. Platelets bind specifically to lactoferrin. A significant similarity between human lactoferrin and some bovine milk proteins has been established.
• 2.2. Because of the structural homology of lactoferrin and cows milk proteins they are able to influence lactoferrins regulatory function on the level of its binding to membrane receptors on platelets.
• 3.3. An inhibitory effect of bovine α-lactalbumin and of β-lactoglobulin on lactoferrin-receptor interaction was shown.
• 4.4. Bovine α-lactalbumin competes with lactoferrin for the binding sites.
• 5.5. Scatchard plot analysis of data shows one binding site for lactoferrin in the presence of α-lactalbumin with an affinity constant, Ka = 0.46 × 10⁹ mol/1 and 335 receptors/cell.
• 6.6. The inhibitory effect of β-lactoglobulin reaches 62% and is different for the common fraction ⨿-lactoglobulin and the genetic variants β-lactoglobulin A and B.
• 7.7. β-lactoglobulin does not compete with lactoferrin for the membrane receptors.
• 8.8. Bovine casein and egg lysozyme stimulate ⁵⁹Fe-lactoferrin binding to the receptors. The mechanism of these effects is still unknown.
• 9.9. Tested alimentary antigens are able to interact with lactoferrin and also with some platelet membrane structures.
• 10.10. Established changes in lactoferrin binding to the platelet membrane might be in relation to lactoferrins regulatory function and (or) eliminating mechanisms of these alimentary antigens.

     

Evolution of LDH isozymes during programmed cell death

• 1.1. Lactic dehydrogenase dehydrogenase isozymes and other respiratory enzymes were studied in degenerating intersegmental muscles of Manduca sexta and Antheraea polyphemus.
• 2.2. Total activities of the different enzymes (isocitric dehydrogenase, malic dehydrogenase, catalase, lactic dehydrogenase) decline at varying rates, starting before the rapid phase of involution.
• 3.3. One isozyme of LDH, an M-type isozyme, increases several-fold during the final three days prior to the emergence of the insect.
• 4.4. The same isozyme appears very transiently or not at all in muscles which do not break down, and is present in degenerating silk glands at the time of their most rapid involution.
• 5.5. The data suggest that limitation of oxidative metabolism plays a role in the involution of the muscles.

     

Studies on prolonged spermatozoa survival in chiroptera—II. The role of zinc in the spermatozoa storage phenomenon

• 1.1. The mean annual Zn content of the sperm storage organs (uterus and epididymis) in Myotis velifer and M. lucifugus is two to three times higher than in corresponding tissues of other mammals.
• 2.2. The content of Zn in the sperm storage organs and male accessory glands has an annual cyclic pattern. Significant increases are recorded at prehibernation insemination (September) and posthibernation conception (April/May).
• 3.3. Zinc is present in the storage organs of bats throughout the spermatozoa storage phase of the reproductive cycle.
• 4.4. Zinc, due to its regulatory effects on spermatozoa (maturation, metabolism, motility) may be important in sperm storage in hibernating bats.

     

Serological and histochemical studies on the Achatina fulica galactan

• 1.1. Glycoconjugates in the albumin glands of Achatina fulica have been fractionated by combination of organic solvents, salt precipitation and chromatography on specific agarose-lectin beads.
• 2.2. A galactan consisting only of galactosyl residues was isolated from an agarose peanut-lectin matrix. It gave single precipitin arcs with many heterophile lectins in agar-gel electrophoresis.
• 3.3. The galactan exhibited selective serological reactivity with some galactose-specific lectins, (PNA, RCA, Tridacnins).
• 4.4. Histochemical studies with fluorescein-labelled lectins demonstrated the topochemical distribution of this galactan within the snail's albumin gland.

     

Proteomics of Asrij Perturbation in Drosophila Lymph Glands for Identification of New Regulators of Hematopoiesis

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Highlights

• •First report on the quantitative proteomic profiling of Drosophila lymph glands.
• •Comparative proteomic analysis under conditions of perturbed blood cell homeostasis.
• •Resource for identifying new regulators of insect and vertebrate hematopoiesis.

     

Analysis of clotting defects in diseased lobsters—II. Immunochemical study of blood proteins

• 1.l. In gaffkemic lobsters kept at 15°C, the plasma coagulogen amount rapidly decreases and the gelation of hemolymph is prevented.
• 2.2. In animals kept at 10°C, the available plasma coagulogen amount is always normal even when coagulation appears impaired or prevented.
• 3.3. Extended clotting times as well as damaged coagulation cannot be correlated with coagulogen concentration.
• 4.4. The site of synthesis of this factor is discussed.

     

Collagenaceous,thiol-containing proteins of cnidarian nematocysts: A comparison of the chemistry and protein distribution patterns in two types of cnidae

• 1.1. Nematocyst structural proteins (NSP) from the sea anemones Aiptasia pallida and Metridium senile and the siphonophore Physalia physalis are primarily low molecular weight collagens linked by disulfide bonds.
• 2.2. NSP patterns resolved by SDS-PAGE revealed a common, major collagen species (40 kDa) in each nematocyst type, together with other collagens and non-thiol-containing proteins.
• 3.3. For each cnidarian, NSP glycosylation profiles were significantly different.
• 4.4. Monoclonal antibodies against Aiptasia NSP demonstrated a differential distribution between capsule wall and thread.
• 5.5. NSP differences would account for the diversity of morphologic and functional types.

     

Role of arginase transferred from the vesicula seminalis during mating and changes in amino acid pools of the spermatophore after ejaculation in the silkworm,Bombyx mori

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• 1.1. Ejaculation of seminal fluid into the spermatophore formed inside the female bursa copulatrix terminates 20 min after the beginning of copulation of Bombyx mori. The amounts of amino acids transferred are small, but the amounts of amino acids in the spermatophore continue to increase after this time due to protein degradation and amino acid interconversions.
• 2.2. Arginase, which has high activity in the vesicula seminalis, is transferred to the spermatophore without loss of activity during ejaculation. During mating, ornithine and much urea are formed in the spermatophore, indicating activity of the transferred arginase.
• 3.3. In the spermatophore, marked increase of alanine with low concentrations of ornithine and glutamate suggests the presence of a pathway for the active formation of 2-oxoglutarate with pyruvate via glutamate from arginine. During mating, proline and glutamine also increase, but at low rates.
• 4.4. Of the exocrine glands in the male reproductive system, the vesicula seminalis secretes the highest concentration of glutamate (30% of the total amino acids); serine is the amino acid present at highest concentration in secretions of other glands (20–30%). No urea was found in the secretions of any of the glands.

     

Relative bioavailability and DNA adduct formation of benzo[a]pyrene and metabolites in the diet of the winter flounder

• 1.1. Radiolabeled metabolites of the carcinogenic polycyclic aromatic hydrocarbon benzo[a]pyrene (BaP) were shown to be absorbed through the diet of the winter flounder, Pseudo pleuronectes americanus.
• 2.2. Oral bioavailability of a mixture of naturally produced metabolites was significantly less than that of the parent BaP.
• 3.3. Oral bioavailability of a pure metabolite, BaP-7,8-dihydrodiol (7,8-D) was found to be similar to that of BaP.
• 4.4. Both metabolites and BaP formed DNA adducts in liver.

     

DNase-I-like enzyme from the carp liver—Inhibition by muscle and endogenous actin

• 1.1. DNase-I-like activity occurs in the carp (Cyprinus carpio) liver cytosol (supernatant 105,000g).
• 2.2. The enzyme resembles DNase I from bovine pancreas in respect to the molecular mass (~31 kDa), pH (7.4) and ion requirements (Mg²⁺, Ca²⁺) and the ability to degrade native as well as denatured DNA.
• 3.3. As judged by comparison of DNase zymograms obtained after native- and SDS-PAGE, the enzyme occurs in the three molecular forms of similar molecular weight and different charges.
• 4.4. All these forms are inhibited by rabbit skeletal muscle actin as well as by endogenous actin isolated from the carp liver cytosol.
• 5.5. DNase from the carp liver cytosol does not interact with the antibodies directed against DNase I from bovine pancreas and against DNase I from the rat and bovine parotid glands.

     

Isolation of collagen granules from the foot of the sea mussel,Mytilus californianus

• 1.1. Membrane bound granules were isolated from homogenates of the foot of Mytilus californianus and shown to correspond to the ellipsoid collagen granules described by Tamarin & Keller (1972).
• 2.2. Protein was extracted from the purified granules by standard procedures for preparation of collagen and its amino acid composition was compared with that of vertebrate collagen and different parts of the byssus secreted by glands in the mussel's foot.
• 3.3. Hydrolysates of collagen extracted from granules contained approximately 8 mole % hydroxyproline and 33 mole % glycine and were similar in composition to byssus threads.
• 4.4. Analyses of other parts of the byssus indicated that they contained collagen in addition to other protein components.

     

Fluorescence studies on the interaction of muscle M-line proteins,creatine kinase and the 165,000 dalton component,with each other and with myosin and myosin subfragments

• 1.1. The binding of 8-anilino-l-naphthalene sulfonate (ANS) by M-line creatine kinase (CPK) and the 165,000 dalton protein component was studied by fluorescence.
• 2.2. One mole of ANS binds to a mole of each M-protein and the binding site on these two M-proteins is hydrophobic in nature.
• 3.3. M-line proteins labeled with ANS were used to demonstrate their interaction with myosin and myosin subfragments 1 and 2.
• 4.4. A unique finding of this study, that labeled M-line CPK binds to subfragment 2 of myosin, is of significance from a structural view point, since only the rod portions of myosin molecules are exposed at the M-line and therefore able to interact with CPK.
• 5.5. The use of a sulfhydryl fluorescent probe, N-(2-iodoacetyl)-N-(5-sulfo-l-napthyl) ethylene diamine, (1,5-AEDANS), has shown that the essential sulfhydryl group on CPK is very important for its interaction with both myosin and the 165,000 dalton M-line protein component.

     

Temperature regulation and metabolic rhythms in populations of the house sparrow,Passer domesticus

• 1.1. The house sparrow, Passer domesticus, has a circadian rhthym of metabolism and body temperature.
• 2.2. Evolutionary adaptation to a hot and humid climate is reflected in the lower metabolism and greater insulation of the Houston population than observed in populations from Ann Arbor, Michigan; Boulder, Colorado and Syracuse, New York.
• 3.3. There are no significant differences in either body temperature or evaporative water loss of all four populations.
• 4.4. The Houston population is able to survive higher ambient temperatures than is found in the Ann Arbor, Michigan or Boulder, Colorado population.

     

1H NMR study of metabolic alterations in the small intestine of rats infected with Hymenolepis diminuta

• 1.1. 1H NMR spectra of the duodenum, jejunum and ileum tissues of the small intestine of a rat showed metabolic gradients.
• 2.2. The concentrations of metabolites in these gut regions were altered by the presence of the tapeworm Hymenolepis diminuta.
• 3.3. In the infected duodenum there was significantly less glycogen, glucose and phosphocreatine/creatine, but significantly more lactate than in the corresponding controls.
• 4.4. Infected jejunum contained significantly less betaine but significantly more succinate, alanine and lactate.
• 5.5. Infected ileum had significantly less glycogen and taurine but significantly more alanine and lactate.

     

Amino acid composition and the protein form of procarboxypeptidase a purified from the pancreas of the sei whale Balaenoptera bolealis

• 1.1. Procarboxypeptidase (W-PCPA) was purified from the pancreas of the sei whale Balaenoptera bolealis.
• 2.2. W-PCPA was obtained as a homogeneous protein in polyacylamide gel disc electrophoresis.
• 3.3. W-PCPA has a molecular weight of 75,000.
• 4.4. Amino acid composition of W-PCPA was compared with that of bovine procarboxypeptidase as A S5 (PCPA-S5).
• 5.5. W-PCPA may be two subunits, and the aggregate form may resemble PCPA-S5.