Moniliformis dubius: uptake of leucine and alanine by adults

Uptake of ¹⁴C-leucine by Moniliformis dubius in 2-min incubations was not linear with respect to substrate concentration and appeared to involve a combination of diffusion and mediated transport. During a 90-min incubation in 1 mM¹⁴C-leucine, the total pool of free leucine increased from an initial concentration of 0.46–12.21 mM; less than 2% of the absorbed leucine was metabolized during this time period. The concentrations of leucine in the pseudocoelomic fluid and extracts of body walls, measured before and after incubation, were the same in either case. Uptake of ¹⁴C-leucine was insensitive to the external concentration of Na⁺, Ca²⁺, Mg²⁺, K⁺, and Tris(hydroxymethyl) aminomethane.Uptake of ¹⁴C-alanine also appeared to be mediated, however, the alanine pool was not altered after a 30-min incubation in 1 mM¹⁴C-alanine. Following a 30-min incubation in ¹⁴C-alanine, only 38% of the absorbed radioactivity was present as labeled alanine; the remaining radioactivity was detected in aspartic acid, cysteic acid, taurine, and urea.     

Glycolytic enzymes in polyamine-treated bovine retina

The retina is characterized by glycolysis under aerobic conditions, mediated by lactate dehydrogenase isoenzyme-5 (LDH-5) as well as by the soluble isoenzyme of malate dehydrogenase. Bovine retina LDH and MDH isoenzymes and their activities were studied after polyamine treatment. Our results showed that LDH-5 isoenzyme presented the highest activity in untreated as well as in putrescine-treated retina. Decreased activity was present when the retina was treated with spermidine or spermine. It was demonstrated that retinic LDH-5 had a high affinity for lactate which enabled the isoenzyme to be more effective than the other LDH isoenzymes in the conversion of NADH to NAD. Therefore, the putrescine enhancing LDH-5 activity appeared to be capable of stimulating NAD-mediated rhodopsin regeneration. Putrescine induced a marked increase of both MDH isoenzymes--soluble (s-MDH) and mitochondrial (m-MDH), while spermine and spermidine mostly affected the soluble form of the enzyme. Putrescine induced a three-fold increase in s-MDH and m-MDH activities, while spermine and spermidine induced a four to five-fold increase in s-MDH. These results document the differential effects of polyamine treatment on LDH and MDH isoenzyme activities.     

The structure of the ovarian ball and oogenesis in Moniliformis dubius (Acanthocephala)

Seven to nine days after infection of the definitive host (rat) by cystacanths, the genital primordium of the female acanthocephalan is transformed from a fragmented mass of cells into discrete ovarian balls. This is accomplished by envelopment of free germinal cells by somatic tissue which originates from the ligament sac primordium. Germinal cell nuclei then undergo repeated mitoses until about 21 days of development, with concurrent formation of oogonial syncytia which occupy the interior of the ovarian balls. Oocytes, derived from these oogonia, move to the periphery of the germinal syncytia for differentiation, growth, fertilization, shell formation, and release from the ovarian ball. After oogonial proliferation ceases, continued growth of the ovarian ball apparently results from increase in size of already present cells. Free-floating mature ovarian balls are found in the dorsal ligament sac; each consists of germ cells in various developmental stages, enveloped and pervaded by a multinucleate matrix syncytium of somatic origin, which functions as a follicle. Spermatozoa pass through the matrix cell for the internal fertilization of mature oocytes. Myelinated structures of an undetermined nature were found to correspond to previously reported polar bodies. After 100 days post-infection, the somatic matrix syncytium begins to manifest the degenerative effects of aging. The germinal tissue exhibits no subcellular signs of senescence by 154 days, but decreases in amount in older worms.     

The absorptive surface of Moniliformis dubius (Acanthocephala). II. Functional aspects

The functional nature of the acanthocephalan absorptive surface was further elucidated by a series of morphological and cytochemical studies with the electron microscope. The use of lanthanum nitrate and ruthenium red in fixatives and Thorotrast staining en bloc and on epoxy thin sections provided information about the surface coat and the surface crypts. Acid phosphatase was localized in the lumina of the crypts and in the five lysosomal types. In vitro studies utilizing ferritin, Thorotrast and horseradish peroxidase implicated the surface crypts in the digestion and/or uptake of large molecules. A consideration of the evidence suggests that these crypts are highly selective and specific in their function.     

The absorptive surface of Moniliformis dubius (Acanthocephala). I. Fine structure

The fine structure of the syncytial epidermis of Moniliformis dubius (Acanthocephala) was examined with emphasis on the Streifenzone. Numerous crypts elaborate the area of the absorptive surface. Surface architecture is supported by a tripartite filamentous terminal web consisting of a 100 Å sheet underlying the plasma membrane, a more extensive and diffuse inner region surrounding the crypts and a differentiated cytoplasmic annulation encircling each crypt neck. Inclusions and organelles described include filaments, microtubules, glycogen, lipid droplets, vesicles, mitochondria, Golgi complexes, endoplasmic reticulum and five lysosomal types. The eutelic nuclei contain little beterochromatin and have unusual nucleolar features.