Induction of cell fusion by a factor released by the cellular slime mold Polysphondylium pallidum

Heterokaryons and hybrid cells, which are extremely useful for research in cell biology, can be produced artificially by treating cells with either polyethylene glycol or certain inactivated viruses that alter the plasma membrane. We report here a novel cell-fusion inducing factor secreted by CK-8 strain cells of cellular slime mold Polysphondylium pallidum. Treatment of other strains or other species of cellular slime molds, such as NC-4 of Dictyostelium discoideum with the diluted fraction, containing molecules larger than 50 kDa, of the conditioned medium of CK-8 cell culture induces cell fusion at high frequency and produces multinucleated large cells. This cell fusion is inducible between cells of either a single strain or of two different strains of cellular slime molds.Abbreviations BSS Bonner's salt solution - CM conditioned medium - EDTA ethylenediaminetetraacetic acid - F2 fraction containing cell-fusion induction factor - Mr molecular mass     

Achene morphology and slime structure in some taxa of Artemisia L. and Neopallasia L. (Asteraceae)

We have examined slime cell distribution on the surface of the achenes of some Artemisia and Neopallasia taxa, as well as slime composition, envelope formation during the hydration, and slime relation to different morphological features and environmental factors. The results of the studies show a characteristic pattern of slime cells distribution, which could differ between taxa. The slime in the taxa studied belongs to the cellulose type and consists of two components i.e., pectins and cellulose. Although all fruits contain slime cells, not all of them show the slime envelope formation. Plants occurring in dry habitats (such as A. barrelieri) or annual species (such as A. annua) are characterised by a large amount of slime and a fast process of slime envelope formation. Slime production has not been observed in some polyploid populations (A. campestris and A. campestris ssp. sericea) and in two species occurring in relatively fertile habitats (A. verlotiorum, A. vulgaris). A reason for this may be either the immaturity of polyploid fruits leading to the production of a scarce, not detectable slime amount or, alternatively, the occurrence of not functional slime cells. Slime facilitates and stimulates the germination, as well as the adherence of the fruits to the ground or to animals (for dispersal). The slime could play important role in the distribution and colonisation of new habitats in many Artemisia taxa.     

The gonadotropic cells in the adenohypophysis of the blind mexican cave fish,Anoptichthys jordani

Summary The development and activity of the basophils in the meso-adenohypophysis of Anopthichthys jordani were studied in relation to the maturation of the gonads. In addition, pituitaries and ovaries of post-spawning females were studied during a period 0–11 days subsequent to spawning. The large and mainly PAS-positive basophilic cells in the meso-adenohypophysis were the only cell type that showed a correlation with the development and maturation of the ovaries and testes. These cells were subjected to a partial or complete degranulation in females following oviposition, when yolk formation in the ovary was at a maximum. It is concluded that the large PAS-positive basophils in the mesoadenohypophysis have a gonadotropic function and that only one gonadotropic cell type is present in the adenohypophysis of Anoptichthys jordani.This study was partly supported by a grant from the Netherlands Organization for the Advancement of Pure Research (Z.W.O.).I wish to express my gratitude to Prof. Dr. P. G. W. J. van Oordt for his active interest and constructive suggestions. Mr. R. van den Hurk and Miss Tjitske van Soelen provided valuable assistence in the course of the experiments. Mr. H. van Kooten made the photographs. Special thanks are due also to Mr. M. J. van Oosterum and Mr. J. Rowaan; without their capable and constant help it would have been hardly possible to obtain such satisfactory spawning results.     

On the presence and localization of glycogen accumulations inside coronet cells of the saccus vasculosus of the dogfish (Scylliorhinus caniculus)

Summary In several coronet cells of the saccus vasculosus of Scylliorhinus large quantities of glycogen occur, as shown by light and electron microscopy. The significance of glycogen as an energy storage necessary for a transcellular ion transport process taking place in the coronet cells is discussed.The authors thank Dr. F.C.G. van de Veerdonk, W. F. Jansen and W. F. G. Flight for reading the manuscipt and for their critical remarks. They are also indebted to Mr. H. van Kooten and his staff for their valuable photographic assistance.     

Somato-dendritic synapses in the paraventricular organ of two anuran species

Summary The ultrastructure of the paraventricular organ ofXenopus laevis andRana esculenta has been investigated. Special attention has been paid to contact regions between nerve cells of the paraventricular organ and other nerve cells.According to the results of the glutaraldehyde-osmium tetroxide fixation as well as the zinc iodide-osmium method, it appears that the perikarya of several nerve cells of the paraventricular organ make synaptic contacts with dendrites of other nerve cells. It is suggested that the presence of the somato-dendritic synapses is a morphological indication for the sensory function of the nerve cells.Thanks are due to Prof. Dr. P. G. W. J. van Oordt for his interest and the many helpful discussions, and to Mr. H. van Kooten and his co-workers for their skilful photographic assistance.     

The rostral pars distalis of the pituitary gland of the freshwater and marine alewife (Alosa pseudoharengus)

Summary In the alewife the orohypophyseal duct, a remnant of Rathke's pouch, persists in adults as a tube passing from the rostral pars distalis to the pharyngeal region. Its lumen is not open to the buccal cavity. The prolactin cells are situated around the bifurcations of this duct in the rostral pars distalis. Contents from prolactin cells, such as granules, nuclei, mitochondria and Golgi structures were found in these bifurcations. These contents were indistinguishable from those of intact prolactin cells. Evidence of actual release into the duct was often noted. At the presumptive point of release, the cells lining the lumen separate and the contents, probably of an entire prolactin cell, are extruded. The cilia usually found at the point of extrusion arise from prolactin cells. The prolactin cells of freshwater fish were more heavily granulated than those from a marine environment. Prolactin cells of fish entering freshwater streams were not heavily granulated but showed evidence of increased activity. Granule size was not affected by salinity. The ACTH cells are arranged in bands along branches of the neurohypophysis in the rostral pars distalis. No differences in ACTH cells from fish of different salinities were noted.We would like to thank Mr. D. D. Zumwalt of the John G. Shedd Aquarium in Chicago, Dr. E. D. Warner, Mr. R. L. Flayter, Dr. J. G. Stanley of the University of Wisconsin, Milwaukee, Mr. L. Wells of the U. S. Fish and Wildlife Service, Great Lakes Fisheries Laboratory, Ann Arbor, and Mr. L. N. Flagg of the Department of Sea and Shore Fisheries, Augusta, Maine, for their assistance in obtaining the fish used in this study. Dr. T. N. Tahmisian and Mr. G. T. Chubb of Argonne National Laboratories, and Dr. L. M. Srivastava and Dr. V. Bourne of Simon Fraser University, Canada, kindly made electron microscope facilities available. Finally, we wish to thank Mr. W. Goossens and Mr. D. J. DeJong for valuable assistance. This project was supported by a grant from the National Marine Fisheries Service.     

The Inhibitory Effect of Staphylococcus epidermidis Slime on the Phagocytosis of Murine Peritoneal Macrophages Is Interferon-Independent

The extracellular slime produced by Staphylococcus epidermidis has been shown to interfere with several human neutrophil functions in vitro, such as chemotaxis, degranulation and phagocytosis. Slime production has been suggested as a useful marker for clinically significant infections with coagulase-negative Staphylococcus. Since the main role of macrophages in defense mechanisms is phagocytosis, the effect of slime on the phagocytic activity of macrophages was investigated. The phagocytic activity of murine peritoneal macrophages treated with slime in vitro decreased in a dose-dependent fashion. A similar decrease was also observed in macrophages isolated from mice that had previously received intraperitoneal injection of slime. To investigate whether interferon also plays a role in this process, mice were treated with interferon or an interferon inducer, polyinosinic-polycytidylic acid (poly I:C), together with slime before macrophage isolation. The slime-suppressed phagocytic activity of macrophages was partially relieved by both agents, and the recovery effect of poly I:C in slime-suppressed phagocytosis of macrophages in vivo might be attributed to the increased interferon level in peritoneal fluid and sera. However, when slime was given to poly I:C-pretreated mice, the phagocytic activity remained suppressed. Thus, it appears that slime is able to suppress the phagocytic activity of macrophages regardless of the state of macrophage activation by poly I:C. The results suggest that the inhibition of phagocytosis by S. epidermidis slime may be independent from the activation of interferon.     

Fine structure of the Paraventricular organ of Xenopus laevis tadpoles

Summary The ultrastructure of the Paraventricular organ in the hypothalamus of Xenopus laevis tadpoles is described. It appeares that the Paraventricular organ of this anuran species is homologous with the Organon vasculosum hypothalami or the Paraventricular organ of other vertebrates.The Paraventricular organ of Xenopus laevis is characterized by an ependymal lining with only few cilia and by two types of nerve cells. Both types of nerve cells have ventricular processes, protruding into the lumen of the third ventricle and forming a network. The protrusions bear cilia of the 8+1 pattern. It has been possible to distinguish both types of nerve cells on account of their dense-core vesicles. A secretory function of both cell types is suggested.In a region close to the Paraventricular organ, another granulated type of nerve cell has been observed. A relationship between these cells and the preoptic nucleus is discussed.The author thanks Prof. Dr. P. G. W. J. van Oordt for his helpful comments and criticism, Mr. H. van Kooten for photographic assistance and Mr. F. Dijk for technical assistance.     

Ultrastructure of the adenohypophysis in the teleost Poecilia latipinna

Summary In the sailfin molly, Poecilia latipinna, seven morphological endocrine celltypes could be distinguished with the electron microscope. Each of these was identified with one of the seven cell-types distinguished with the light microscope, to most of which endocrine functions have previously been allocated. Corticotrophs and prolactin cells form the rostral pars distalis, and the proximal pars distalis consists of an outer layer of gonadotrophs and an inner zone containing growth hormone cells and thyrotrophs. The pars intermedia contains two cell-types, of uncertain function. Stellate cells (interstitial cells) occur throughout the adenohypophysis, but are most numerous and prominent in the rostral pars distalis. The inner proximal pars distalis contains a cell-type not previously distinguished in this species with the light microscope, the Z-cell, which could be aminergic.The ultrastructural features of each cell-type are described in detail, and discussed in comparisons with the homologous cells described in other teleosts. There is good agreement for different teleosts in the ultrastructural details of each cell type.We thank Mr. L. Ethridge, Mr. M. P. Hancock, Mr. D. Hollingworth and Mr. W. Thomson for technical assistance, and Mr. D. Taylor of the Nuffield Institute of the Zoological Society of London for permission to use the Nuffield Institute electron microscope. We are grateful to Dr. Harry Grier, who collected and embedded glands from P. latipinna in its natural fresh-water habitat in Florida, U.S.A. T. Batten is in receipt of an S.R.C. Research Studentship.     

Functional characterization of alcohol oxidases from Aspergillus terreus MTCC 6324

Short chain alcohol oxidase (SCAO), long chain alcohol oxidase (LCAO), secondary alcohol oxidase (SAO), and aryl alcohol oxidase (AAO) activities were localized in the microsome of Aspergillus terreus during growth of the fungi on n-hexadecane. Zymogram analysis of the microsomes of n-hexadecane-grown cells in polyacrylamide gel electrophoresis showed distinct bands, H4, H3, H2, and H1, in a sequence of their molecular weight (Mr) from high to low. The Mr of the isozymes corresponding to the bands H4, H3, and H2 were close to each other and were higher than 272 kDa. While, the Mr of the isozyme H1 was found to be approximately 48 kDa. H1 gave activity only as SCAO. Although the substrates for other bands were varied, strong (S), medium (M), and weak (W) activity for the bands were as follows: H2: SAO (S), AAO (S), LCAO (M), SCAO (S); H3: LCAO (S), SCAO (S); H4: SCAO (S), LCAO (W), SAO (W). The pH and temperature optima of these isozymes were found to be 8.5±0.5 and 30±1°C, respectively. The stability of the isozymes was drastically decreased beyond 30°C. The SAO showed 33% enantiomeric excess for the R(−)2-octanol over S(+)2-octanol, which may be correlated with the lower Michaelis–Menten constant (K _M) values of the enzyme for the R(−)2-octanol than the S(+)2-octanol. The fluorescence emission spectra of the chromatographically purified SCAO at 443 nm excitation were similar to that obtained with authentic flavin adenine dinucleotide.     

Toxothrix trichogenes (Chol.) Beger et Bringmann: The organism and its biology

Toxothrix trichogenes (Chol.) Beger et Bringmann was found in iron-containing spring water, in tap water, and in a small forest pond of lower Michigan.The use of a partially submerged microscope for continuous observation of undisturbed underwater Aufwuchs on glass slides resulted in the rediscovery of the actualToxothrix organisms: long, often U-shaped and highly flexible bacterial filaments. Direct observation of their growth and movements on immersed glass slides revealed the production byToxothrix trichomes of several slime strands which were typically twisted. Fan-shaped slime structures and parallel tracks were directly seen to be formed by U-shaped organisms as a result of the forward gliding and rolling of their center portion. Chemical iron deposition onto the individual slime strands of such tracks rendered these rigid and brittle; the iron deposition also proceeded in the absence of living trichomes.The trichomes disintegrated rapidly and completely during laboratory observations, althoughToxothrix trichomes were kept viable for several months in refrigerated state. Disintegration under the normal light microscope explains their absence from most stranded sheaths studied by previous investigators.Agricultural Experiment Station Article No. 4935.The investigations were supported by an NSF Institutional Grant for Science to J. T. Staley and by the Michigan State University, Agricultural Experiment Station. J. M. Krul acknowledges gratefully a travel grant from the Ministerie van Landbouw en Visserij. We are thankful for the interest in and help with this work by Dr. G. Lauff, Kellogg Biological Station (Hickory Corners, Mich.) and Mr. W. A. Lemmien, MSU Experimental Forest, Augusta, Mich. Dr. G. A. Zavarzin, Moscow, contributedToxothrix samples and helped with his interest and discussions.MSU Kellogg Biological Station Contribution No. 189     

THE YELLOW-PIGMENTED DICTYOSTELIA

The cellular slime molds described herein are of a clear golden yellow color and belong to two naturally occurring groups. One we call Dictyostelium mexicanum sp. n. because it is found in soils from various parts of tropical and subtropical Mexico. The well-tapered stalk and disklike base are somewhat reminiscent of D. discoideum. The other is regarded as D. aureum E. W. Olive (1901) with which we feel it is closely identified if not identical. In the latter group the form of both the aggregation and sorocarp is suggestive of D. mucoroides. Some less pigmented isolates are separated as D. aureum var. luteolum var. n.     

ONTOGENY AND STRUCTURE OF THE SECONDARY PHLOEM IN EPHEDRA

The secondary phloem in Ephedra is atypical of the gymnosperms in general and exhibits several angiosperm-like characteristics. The ray system of the conducting phloem consists of parenchymatous, multiseriate rays. The axial system contains parenchyma cells, sieve cells, and unusual albuminous cells reminiscent of the specialized parenchyma cells found in some angiosperms. These cell types may intergrade with each other. P-protein in the developing sieve element appears early in the form of a single, ovoid slime body. Later, smaller slime bodies appear and quickly disperse. In the mature sieve element the single, ovoid slime body is lost, and P-protein is then evident in the form of a parietal cylinder, thread-like strands, amorphose globules, or a slime plug. Necrotic-appearing nuclei are commonly found in mature sieve cells.     

Transmembrane myosin chitin synthase involved in mollusc shell formation produced in Dictyostelium is active

Several mollusc shells contain chitin, which is formed by a transmembrane myosin motor enzyme. This protein could be involved in sensing mechanical and structural changes of the forming, mineralizing extracellular matrix. Here we report the heterologous expression of the transmembrane myosin chitin synthase Ar-CS1 of the bivalve mollusc Atrina rigida (2286 amino acid residues, M.W. 264 kDa/monomer) in Dictyostelium discoideum, a model organism for myosin motor proteins. Confocal laser scanning immunofluorescence microscopy (CLSM), chitin binding GFP detection of chitin on cells and released to the cell culture medium, and a radiochemical activity assay of membrane extracts revealed expression and enzymatic activity of the mollusc chitin synthase in transgenic slime mold cells. First high-resolution atomic force microscopy (AFM) images of Ar-CS1 transformed cellulose synthase deficient D. discoideumdcsA⁻ cell lines are shown.     

Immunological examination of the glycocalyces ofStaphylococcus aureus strains Wiley and Smith

The immunological examination of the glycocalyces ofStaphylococcus aureus has been concerned with capsular elements while essentially neglecting slime layers. We have found bacterial slime layers to be prevalent in many natural bacterial environments and, in particular, in recently isolatedS. aureus strains Wiley and Smith [1]. Growth in modified staphylococcus 110 medium induces slime layer production in these strains, and investigation of this material has revealed the two slime layers to be immunogenically and antigenically identical. The slime layer of the Smith strain is immunologically distinct from the tight, integral capsule that also comprises the glycocalyx of this strain. The Wiley strain glycocalyx is composed of only a slime layer.     

OBSERVATIONS ON SIEVE ELEMENTS IN THREE PERENNIAL MONOCOTYLEDONS

Seasonal collections were made of rhizomes of Polygonatum canaliculatum and Typha latifolia and of aerial stems of Smilax hispida. Many metaphloem sieve elements in all three species remain functional for 2 or more years, or for the life of the plant parts in which they occur. Although the protoplasts of mature sieve elements remain similar in appearance from one time of year to the next, the amount of callose associated with the sieve plates and lateral sieve areas of such cells apparently varies with the seasons, being heavier in late fall and winter and lighter in late spring and summer. At maturity the metaphloem sieve elements contain strands derived from the slime bodies of immature cells. It is suggested that in mature sieve elements the slime strands normally occur as a network along the wall. Many mature sieve elements of S. hispida contained normal-appearing nuclei.     

Light and electron microscope studies on the fruiting bodies of Chondromyces crocatus

Summary The fruiting bodies of Chondromyces crocatus have been examined by both light and electron microscopy. The cysts are bounded by a discrete layer of dense slime enclosing a material of lesser density in which the closely packed resting cells are embedded. The latter, in contrast to the microcysts of other myxobacters, are not enclosed in individual slime capsules. Young resting cells commonly contain numerous mesosomes while older resting cells are characterized by what appear to be large lipid granules.The slime stalk consists largely of a system of vertical, parallel empty tubules through which the cells have migrated during fruiting body development.Supported by grant number A 1022 from the National Research Council of Canada.     

Ca2+-dependent phosphorylation by endogenous kinases of Mr 95 K and 50 K-55 K proteins in PC12 pheochromocytoma cells

Endogenous protein phosphorylation of PC12 cells was investigated with the homogenate as well as intact cells. In the case of the homogenate, the major proteins that were phosphorylated in the presence of Ca²⁺ were found to be of Mr 95 K and Mr 50 K-55 K. Ca²⁺/calmodulin-dependent protein kinase appeared to be responsible for phosphorylation of Mr 50 K-55 K proteins and partly of Mr 95 K protein. The apparentK _m's for Ca²⁺ of Mr 95 K and 50 K-55 K protein phosphorylation were 2.2×10^–7 M and around 1.5×10^–6 M, respectively. Since several cell lines of neuroblastoma exhibited Mr 95 K protein phosphorylation of similar type, the protein phosphorylation may be a common process shared by neuronal cells. Depolarization of intact PC12 cells by high K⁺ concentrations induced Mr 95 K protein phosphorylation. The results suggest that a physiological increase by excitation in the intracellular Ca²⁺ concentration triggers phosphorylation of Mr 95 K protein in neuronal cells and this phosphorylation may play a role in the regulation of transmitter release.     

Slime Production by Pseudomonas aeruginosa

Adequate experimental conditions for slime production by Pseudomonas aeruginosa were investigated using a cellophane plate method. Definite slime production was observed on heart infusion agar, brain heart infusion agar, yeast extract agar and synthetic agar, but not on nutrient agar. The addition of phosphate to the nutrient agar above 0.05% caused visible slime formation. Incubation at 37 C resulted in a higher yield of slime than at 25 C. Longer incubation seemed more favorable for slime production, while the pH reaction of the test media did not effect the slime yield. All the test cultures of P. aeruginosa produced large amounts of slime by this procedure. Cultures of Pseudomonas fluorescens, other Pseudomonas spp. and certain vibrios also produced slime under these experimental conditions.     

Fluorescent <Emphasis Type="Italic">in situ</Emphasis> hybridization and flow cytometry as tools to evaluate the treatments for the control of slime-forming enterobacteria in paper mills

Slime formation is a serious problem nowadays in the paper industry. Some enterobacteria are associated with the formation of slime deposits in paper and board mills. Detection and characterization of slime forming bacteria, belonging to the genus Enterobacter, Raoultella, and Klebsiella have been achieved by fluorescence in situ hybridization (FISH), using one probe based on the enterobacterial repetitive intergenic consensus sequence and other two rRNA targeted oligonucleotide probes. The effects of three kinds of antimicrobiological products (biocides, dispersants, and enzymes) on these enterobacterial cells were analyzed by flow cytometry (FC). Biocides Butrol 1009 and 1072 were the most effective microbiocides against all enterobacterial cells analyzed, reaching 90% of dead bacteria after 24 h. However, the enzymatic treatment (Buzyme) was not equally efficient on enterobacteria and its microbiocide capacity varied depending on the type of microorganism. FISH and FC were effective tools to detect important slime forming enterobacteria and to select specific treatments to control microbial problems in the paper industry.