Scanning electron microscopy of gametophyte characters and antheridial opening in some Ceylonese species of Thelypteridaceae

Gametophytes of the fern family Thelypteridaceae were cultivated aseptically under controlled conditions and investigated with the scanning electron microscope. This report concerns six species, viz. Sphaerostephanos arbuscula S. subtruncatus, S. unitus, Macrothelypteris torresiana, Amauropelta hakgalensis and Pneumatopteris truncata . The gametophytes have some features in common. They are more or less heart-shaped and have glandular trichomes on surfaces and margins. In the middle is an elongated cushion bearing gametangia and rhizoids on the lower surface. Antheridia are of the type common to leptosporangiates, consisting of a basal cell, a ring cell and a cap cell. Archegonia consist externally of four rows of cells meeting at the top with triangular cells. The following features are distinguishing. The form of the margin of the thallus, type of hairiness, and the abundance of glandular hairs. Acicular hairs occur in Sphaerostephanos unitus and Pneumatopteris truncata . In Amauropelta hakgalensis the archegonium deviates from the common type in having a basal layer that consists of eight cells instead of four. In Macrothelypteris torresiana the four or three top cells are markedly irregular. In Sphaerostephanos arbuscula and Amauropelta hakgalensis the antheridial cap cell is sometimes divided. The manner of opening of antheridia and release of spermatozoids varies in each of the species investigated. This investigation reveals that it is possible to identify the species from gametophyte characters only.     

Ultrastructural features of spermatocytes and spermatozoids in the fern Phyllitis scolopendrium (L.) Newm. subsp. scolopendrium

Phyllitis scolopendrium Newm. subsp. scolo-pendrium spermatozoids are cells 10 μm long in the form of spirals with about four turns. Their chromatin is partly honeycomb-shaped and partly highly condensed. The nuclear envelope over the latter has a regular, thin intermembrane space crossed by fibers that are probably involved in connecting the chromatin with elements of the microtubular ribbon. The cytoplasm is traversed by long cistern-shaped folds of the plasma membrane, believed to be involved in a late process of cell simplification through segregation and detachment of parts of the cytoplasm. The spermatozoids are embedded in 1–1.5 μm thick amorphous electron-transparent material containing cellulose fibrils. These fibrils are considered a network connected to the original spermatocyte wall and elements of elastic support for the amorphous material. The different polysaccharide composition of the inner and outer parts of the walls causes changes in the size and shape of the ring cells, so that the spermatozoids are pushed against and past the cap cell. The gametes are released through limited laceration of the cap cell. The laceration is due to the generally weak substructure of the cell wall. A light microscope sequence of spermatozoid release and scanning electron microscope features of newly released spermatozoids are shown. Received: 24 November 1999 / Revision accepted: 29 December 1999     

Antheridial dehiscence in ferns

We investigated the mechanism of antheridial dehiscence in ferns for the first time using fluorescence microscopy as well as scanning and transmission electron microscopy. The mechanism leading to antheridial dehiscence in Polystichum setiferum, Asplenium trichomanes and A. onopteris was found to depend on the different cellulose contents of the inner and outer walls of the ring cells detected with calcofluor white stain and the Thiéry test. The extremely low cellulose content of the ring cell walls facing spermatozoids made them less mechanically resilient than external wall cells. When the ring cells absorbed water they expanded only into the antheridial cavity, pushing the gametes against the cap cell, which detached from the ring cell below and enabled spermatozoid release. The newly released spermatozoids were spherical bodies covered in cellulose fibrils. The significance of cellulose fibrils could be to isolate the gametes from each other, to reinforce the electron transparent material and to protect the gamete from pressure created by the ring cells during release.     

SCANNING ELECTRON MICROSCOPY OF ANTHERIDIA AND ARCHEGONIA OF ANEMIA MEXICANA KLOTZSCH

Antheridia and archegonia of the fern Anemia mexicana were viewed with scanning electron microscopy (SEM). The mature antheridium is composed of a cap, ring, and basal cell with spermatozoids inside. The archegonium neck is composed of a neck canal cell surrounded by four rows of neck cells. The ventral canal cell and egg were not observed. The neck bends toward the notched meristem. The neck cells usually are uniform in shape and arrangement, but in some archegonia, shape and arrangement of neck cells was irregular. The apex of these archegonia often appeared swollen because of the random cell arrangement. In the presence of water, the antheridium cap is partially detached and the spermatozoids emerge. At this time, the neck cells open at the end of the archegonium in preparation for fertilization. The basic morphology of the antheridia and archegonia is similar to previous reports, although SEM provides more structural detail and a better three-dimensional visualization of these reproductive structures.     

Structure and Operation of the Feeding Apparatus in a Colorless Euglenoid,Entosiphon sulcatum1

Entosiphon sulcatum is a phagotrophic euglenoid. The tubular ingestion apparatus, called a siphon, is composed of three microtubular rods extending the length of the cell. Within the tube are four large striated vanes arranged much like the blades in a pinwheel. The vanes arise from the microtubular rods and curve towards the center of the feeding apparatus. Sheets of endoplasmic reticulum are positioned adjacent to each of the vanes and surround the perimeter of the apparatus. A cap, supported by a scaffold and anchored into the cytoplasm, covers the opening of the siphon. An elongate invagination of the plasma membrane is positioned adjacent to the edge of the cap and extends downward into the siphon forming the opening. The vanes converge at the anterior end of the siphon and surround the invagination. During feeding, the siphon protrudes from the cell. As the apparatus protrudes the cap is withdrawn to the side, opening the siphon. The vanes spread apart expanding the invagination of the plasma membrane into a large cavity into which ingested food particles are taken.     

ON THE CYTOLOGY OF ANTHERIDIUM FORMATION IN THE FERN SPECIES ONOCLEA SENSIBILIS. I. CYTOLOGY OF CELL PLATE AND CELL WALL FORMATION

In the four-celled antheridium of the fern species Onoclea sensibilis a central spermatogenous cell is enveloped by a jacket of three cells. Starting from the base, the jacket comprises the cup-shaped basal cell, the ring cell—both of which encircle the spermatogenous cell—and the cap cell. The lower wall of the spermatogenous cell has the configuration of a funnel; its upper wall is dome shaped. The choice of whole antheridia for study instead of sectioned ones has, for the first time, made it possible to study the formation of the uniquely shaped antheridial cell plates step by step. The cell plate antecedent of the funnel wall has the configuration of a funnel. This conclusion conflicts with Davie's contention that this cell wall is oriented transversely at first and acquires funnel-shape secondarily. The present studies further show that the funnel cell plate forms from base to rim. This finding contrasts with a report that in another fern species this cell plate begins to form on one side of the initial and then proceeds circularly around it. The base of the funnel cell plate attaches to the basal wall of the antheridium initial in a separate event. The genesis of the dome-shaped upper wall of the spermatogenous cell is described for the first time.     

SPERMATOGENESIS IN A HOMOSPOROUS FERN,ONOCLEA SENSIBILIS

A detailed study of spermatogenesis in a homosporous fern, Onoclea sensibilis L., is presented from the formation of the first spermatogenous cell to the release of the sperm. Two different walls are deposited around the developing spermatids at specific developmental stages as opposed to one wall reported for other species. Most ultrastructural changes that occur in Onoclea during spermatid differentiation resemble those described in previous studies on other fern species, with the following exceptions: 1) A previously undescribed structure appears during midspermatid stage. This dense layer of amorphous material with a row of evenly spaced light areas occurs between the anterior portion of the mitochondrion associated with the multilayered structure and the anterior plasmalemma of the spermatid. 2) An early stage in blepharoplast formation resembles that which occurs in the heterosporous fern Marsilea, in contrast to that which has been reported in Platyzoma, the only other homosporous fern studied at this stage. 3) The osmiophilic crest does not form as early as reported in other ferns. 4) The cap cell of Onoclea is removed intact, rather than collapsing or forming a pore during sperm release. Observations are reported on the number of sperm per antheridium, the time course of spermatogenous cell mitosis, and of differentiation of spermatids into sperm. In Onoclea, an antheridium may contain either 32 or 64 sperm. Regardless of the final number of sperm, each has approximately the same volume.     

Relationship of Endo-[beta]-D-Mannanase Activity and Cell Wall Hydrolysis in Tomato Endosperm to Germination Rates

The endosperm tissue enclosing the radicle tip (endosperm cap) governs radicle emergence in tomato (Lycopersicon esculentum Mill.) seeds. Weakening of the endosperm cap has been attributed to hydrolysis of its mannan-rich cell walls by endo-[beta]-D-mannanase. To test this hypothesis, we measured mannanase activity in tomato endosperm caps from seeds allowed to imbibe under conditions of varying germination rates. Over a range of suboptimal temperatures, mannanase activity prior to radicle emergence increased in accordance with accumulated thermal time. Reduced water potential delayed or prevented radicle emergence but enhanced mannanase activity in the endosperm caps. Abscisic acid did not prevent the initial increase in mannanase activity, although radicle emergence was markedly delayed. Sugar composition and percent mannose (Man) content of endosperm cap cell walls did not change prior to radicle emergence under any condition. Man, glucose, and other sugars were released into the incubation solution by endosperm caps isolated from intact seeds during imbibition. Pregerminative release of Man was suppressed and the release of glucose was enhanced when seeds were incubated in osmoticum or abscisic acid; the opposite occurred in the presence of gibberellin. Thus, whereas sugar release patterns were sensitive to environmental and hormonal factors affecting germination, neither assayable endo-[beta]-D-mannanase activity nor changes in cell wall sugar composition of endosperm caps correlated well with tomato seed germination rates under all conditions.     

THE ULTRASTRUCTURE OF MEIOSPORES OF COLEOCHAETE PULVINATA (CHAROPHYCEAE)1

In view of the relative importance of reproductive cell ultrastructure in phylogenetic and systematic studies of green algae, we investigated the fine structure of germinating zygotes and meiospores of Coleochaete pulvinata Braun. Meiospores have a flagellar apparatus very similar to that of zoospores and spermatozoids of the same species. Meiospores differ from zoospores and spermatozoids of C. pulvinata in having pyramidal body scales similar to those present on zoospores of C. scutata. Meiospores of C. pulvinata had as many as twice the number of spline microtubules as zoospores, and four times the number present in splines of spermatozoids of the same species. Developing meiospores of C.pulvinata, like those of other Coleochaete species, are individually surrounded by chamber walls. These differed from vegetative cell walls in lacking plasmodesmata. Moreover, the chamber walls in germinating zygotes of C.pulvinata stained a cobalt blue color with resorcinal blue, and fluoresced yellow in the presence of aniline blue, thus exhibiting the staining characteristics of callose. In location, morphology and presence of callose, chamberwalls resemble “special walls” of land plants, they may represent a charophycean spore development preadaptation useful in the evolution of walled spores characteristic of land     

Structural aspects and ecophysiology of anther opening in Allium triquetrum

BACKGROUND AND AIMS: Tissue desiccation is considered to be involved in anther opening, and it is agreed that environmental humidity affects its timing. Different sources of evidence suggest that the later steps of the process (i.e. stomium opening and outward wall bending) are regulated in different ways. Anther opening was studied in Allium triquetrum under four regimes of relative humidity (RH) to analyse the effect of this parameter and to speculate about its possible regulation. METHODS: Anther histology was studied in cross-sections under a microscope. The times of visible anther opening and complete outward wall bending were recorded separately for each level of RH. Frequency distributions were plotted to express anther behaviour. KEY RESULTS: When a longitudinal stomium breaks the anther remains closed due to adherence of walls on each side of the stomium. Anther opening occurs when the adhering walls subsequently separate. Later, the walls shrink laterally and bend outward. The anthers of the inner whorl opened during the morning of the first day of anthesis, while those of the outer whorl opened during the afternoon. Low RH (20 %) did not cause any evident acceleration of anther opening, but it did cause delay and inhibition of the opening of some anthers in the outer whorl. High RH (55 and 98 %) caused different degrees of delay and also inhibition of anther opening, but most anthers opened within the expected range of time. The time taken for outward wall bending was shortened at 20 % RH. Anther wall outward bending was inhibited at 55 % and 98 % RH. CONCLUSIONS: Anther opening occurred at a specific moment of anther development, separated in time from stomium breakage, and seemed related to dehydration caused by reabsorption of water by contiguous tissues. Outward bending of the wall was facilitated by evaporation. Anther opening and anther wall outward bending seemed to be regulated differently in relation to water control.     

Eosin Y-sensitive ATPase activity in men's spermatozoids as a biochemical test for oligozoospermia

The experiments performed on preparations of spermatozoids of men of reproductive age (27-44-year old) studied the ATPase activity (sensitive to inhibited effects of eosine Y) in both normal and oligozoospermia conditions when treating cell suspension with detergents. The methodical approaches for testing the so-called "common" and eosin Y-sensitive ATP-hydrolase activities in spermatozoids were developed. Saponin, the optimal detergent for permeabilisation of their plasma membrane was chosen using laser-correlational spectroscopia method. Saponin perforates effectively the membranes of spermatozoids, decreasing the average hydrodynamical diameter of cells from 10-15 microm (the spermatozoids themselves) to 3-8 microm (treating cell suspension with 0.05% solution of saponin) and even to 2-3 microm (treating spermatozoids suspension with 0.5% solution of detergent). A non-specific inhibitor of ATP-hydrolase's systems, eosin Y, decreases effectively the ATP-hydrolase activity of intact spermatozoids up to 40%. The exact effect of eosin depends on composition of incubation medium. In the model of extracellular conditions (the optimal concentration of detergent is 0.05%), eosin Y-sensitive ATP-hydrolase's activity of spermatozoids in both normal and oligozoospermia cases is increased by 220-240% (at an average). If enzymatic reaction was performed during intracellular conditions modeling (the optimal concentration of saponin is 0.5%), the increase of eosin Y-sensitive ATPase activity (up to 350-400% in normal conditions, and only to 130-150% in oligozoospermia conditions) was detected. This specificity can be used as easy-to-use clinical test for such pathology of men's reproductive system. Eosin Y inhibited doze-dependently the common ATPase activity in spermatozoids in both normal and with studied pathology. In both cases, after linearization of curves of catalytic titration of ATPase activity with eosin Y in Hill's plot the two-phase dependency, of high and low affinities, was found (the average values of imaginary inhibition constant I(0,5) are 0.1 and 0.3-0.4 mM correspondingly). In both normal and oligozoospermia conditions, the high-affinity component has a positive cooperativity, while the low-affinity component is characterized by a negative cooperativity. The obtained results may be of both theoretical and practical value for further investigation of membrane mechanisms used in the support of ion homeostasis in men's spermatozoids and its violation in conditions under different pathological states. Besides, the results can be used as a theoretical basis for improvement of simple and accessible clinical biochemical methods used for testing such a pathology as oligozoospermia.     

Effect of arabinogalactan proteins from the root caps of pea and Brassica napus on Aphanomyces euteiches zoospore chemotaxis and germination

Root tips of many plant species release a number of border, or border-like, cells that are thought to play a major role in the protection of root meristem. However, little is currently known on the structure and function of the cell wall components of such root cells. Here, we investigate the sugar composition of the cell wall of the root cap in two species: pea (Pisum sativum), which makes border cells, and Brassica napus, which makes border-like cells. We find that the cell walls are highly enriched in arabinose and galactose, two major residues of arabinogalactan proteins. We confirm the presence of arabinogalactan protein epitopes on root cap cell walls using immunofluorescence microscopy. We then focused on these proteoglycans by analyzing their carbohydrate moieties, linkages, and electrophoretic characteristics. The data reveal (1) significant structural differences between B. napus and pea root cap arabinogalactan proteins and (2) a cross-link between these proteoglycans and pectic polysaccharides. Finally, we assessed the impact of root cap arabinogalactan proteins on the behavior of zoospores of Aphanomyces euteiches, an oomycetous pathogen of pea roots. We find that although the arabinogalactan proteins of both species induce encystment and prevent germination, the effects of both species are similar. However, the arabinogalactan protein fraction from pea attracts zoospores far more effectively than that from B. napus. This suggests that root arabinogalactan proteins are involved in the control of early infection of roots and highlights a novel role for these proteoglycans in root-microbe interactions.     

The peripheral-type benzodiazepine receptor is involved in control of Ca2+-induced permeability transition pore opening in rat brain mitochondria

The peripheral-type benzodiazepine receptor (PBR) is an 18 kDa mitochondrial membrane protein with still elusive function in cell death. Here, we studied whether PBR is involved in Ca2+-induced permeability transition pore (PTP) opening in isolated rat brain mitochondria (RBM). PTP opening is important in mitochondrial events leading to programmed cell death. Immunoblots revealed a single 18 kDa anti-PBR antibody-immunoreactive band in purified RBM. Adenine nucleotide transporter, a key PTP component, was found in the PBR-immunoprecipitate. In isolated intact RBM, addition of a specific anti-PBR antibody [H. Li, Z. Yao, B. Degenhardt, G. Teper, V. Papadopoulos, Cholesterol binding at the cholesterol recognition/interaction amino acid consensus (CRAC) of the peripheral-type benzodiazepine receptor and inhibition of steroidogenesis by an HIV TAT-CRAC peptide, Proc. Natl. Acad. Sci. U.S.A. 98 (2001) 1267-1272] delayed Ca2+-induced dissipation of membrane potential (psi(m)) and diminished cyclosporine A-sensitive Ca2+ efflux, which are both indicative for the suppression of PTP opening. Moreover, anti-PBR antibody caused partial retention of Ca2+ in the mitochondrial matrix in spite of psi(m) dissipation, and reduced activation of respiratory rate at Ca2+-induced PTP opening. A release of pro-apoptotic factors, AIF and cytochrome c, from RBM was shown at threshold Ca2+ load. Anti-PBR antibody blocked the release of AIF but did not affect the cytochrome c release. Addition of ATP was able to initiate PTP closing, associated with psi(m) restoration and Ca2+ re-accumulation. At the same time mitochondrial protein phosphorylation (incorporation of 32P from [gamma-32P]ATP) occurred and anti-PBR antibody was able to inhibit phosphorylation of these proteins. The endogenous PBR ligand, protoporphyrin IX, facilitated PTP opening and phosphorylation of the mitochondrial proteins, thus, inducing effects opposite to anti-PBR antibody. This study provides evidence for PBR involvement in PTP opening, controlling the Ca2+-induced Ca2+ efflux, and AIF release from mitochondria, important stages of initiation of programmed cell death.     

Modulation of the calcium release channel of sarcoplasmic reticulum by adriamycin and other drugs

The calcium release channel of sarcoplasmic reticulum mediates Ca2+ release which triggers muscle contraction in excitation-contraction coupling. The channels have been identified morphologically with the feet structures, which are involved in junctional association of terminal cisternae of sarcoplasmic reticulum with the transverse tubules to form the triad junction. In this study, we further characterize the action of drugs on the calcium release channel from sarcoplasmic reticulum fused into planar bilayers. Adriamycin is an effective cancer chemotherapeutic drug, which is limited by its cardiotoxicity. The drug, when added to the myoplasmic side (cis side), activates channel opening at microM concentrations in a dose dependent manner. Adriamycin together with ATP (mM) gives optimal activation, with an open probability (Po) of approximately 1.0. Ruthenium red added to the cis side, equivalent to the cytoplasmic (myoplasmic) domain, completely blocks channel opening. Qualitatively similar results are obtained with adriamycinol, the major metabolite of adriamycin. The inhibition by adriamycin is not reversed by reperfusion to wash out the drug. Silver ions are also found to activate the channel. The conductance of the channel activated by adriamycin, adriamycinol or Ag+ is approximately 100 ps, similar to that previously reported for activation of the channel with Ca2+ and ATP. Ruthenium red has previously been observed to block channel activation from the cytoplasmic side.(ABSTRACT TRUNCATED AT 250 WORDS)     

Structure and function of the neck cell during fertilization in Ginkgo biloba L.

Key message

Neck cells in Ginkgo biloba contribute to archegonial opening through morphological changes and might be involved in the production of fertilization liquid to attract spermatozoids toward archegonia.

Abstract

Neck cells are an essential part of the archegonium in archegoniate gymnosperms, but their function in the sexual reproductive process remains unclear, particularly in zoidogamous gymnosperms. To clarify the structural characteristics of neck cells and their role in fertilization, we examined the neck cells of Ginkgo biloba L. by means of scanning electron microscopy and transmission electron microscopy. The two curved inner neck cells, which are covered imbricately by the two turgid outer neck cells, were pushed to two sides during fertilization, which indicated that morphological changes in these cells contribute to archegonial opening. The neck cells contained many secretory organelles with some material accumulated outside the cell wall, thus the neck cells might be involved in the production of fertilization liquid to attract spermatozoids toward the archegonium. In addition, the surrounding surface cells of the female gametophyte also cooperate to produce the liquid. Taken together, these results indicate that the neck cells provide an effective mechanism by which zoidogamous gymnosperms achieve reproductive success through altering the morphology and cellular physiology of the neck cells.     

F-actin-dependent endocytosis of cell wall pectins in meristematic root cells. Insights from brefeldin A-induced compartments

Brefeldin A (BFA) inhibits exocytosis but allows endocytosis, making it a valuable agent to identify molecules that recycle at cell peripheries. In plants, formation of large intracellular compartments in response to BFA treatment is a unique feature of some, but not all, cells. Here, we have analyzed assembly and distribution of BFA compartments in development- and tissue-specific contexts of growing maize (Zea mays) root apices. Surprisingly, these unique compartments formed only in meristematic cells of the root body. On the other hand, BFA compartments were absent from secretory cells of root cap periphery, metaxylem cells, and most elongating cells, all of which are active in exocytosis. We report that cell wall pectin epitopes counting rhamnogalacturonan II dimers cross-linked by borate diol diester, partially esterified (up to 40%) homogalacturonan pectins, and (1-->4)-beta-D-galactan side chains of rhamnogalacturonan I were internalized into BFA compartments. In contrast, Golgi-derived secretory (esterified up to 80%) homogalacturonan pectins localized to the cytoplasm in control cells and did not accumulate within characteristic BFA compartments. Latrunculin B-mediated depolymerization of F-actin inhibited internalization and accumulation of cell wall pectins within intracellular BFA compartments. Importantly, cold treatment and protoplasting prevented internalization of wall pectins into root cells upon BFA treatment. These observations suggest that cell wall pectins of meristematic maize root cells undergo rapid endocytosis in an F-actin-dependent manner.     

Unterschiedliche Zusammensetzung von Stiel- und Hutzellwand bei Acetabularia mediterranea

Summary The main constituents of the cell wall of the unicellular green alge Acetabularia mediterranea are mannose, glucose, galactose and rhamnose. There are, however, striking differences in the composition of the cell wall of the stalk and the cap. The glucose and galactose content of the cap wall is much higher than that of the stalk wall. Rhamnose is found in the cap wall only. The different composition of stalk and cap wall is also manifest in cells which were enucleated prior to cap formation. Therefore, regulation of the enzymatic processes which are responsible for the different composition of stalk and cap wall take place in enucleated cells also.     

Red Blood Cell Membrane Dynamics during Malaria Parasite Egress

Precisely how malaria parasites exit from infected red blood cells to further spread the disease remains poorly understood. It has been shown recently, however, that these parasites exploit the elasticity of the cell membrane to enable their egress. Based on this work, showing that parasites modify the membrane’s spontaneous curvature, initiating pore opening and outward membrane curling, we develop a model of the dynamics of the red blood cell membrane leading to complete parasite egress. As a result of the three-dimensional, axisymmetric nature of the problem, we find that the membrane dynamics involve two modes of elastic-energy release: 1), at short times after pore opening, the free edge of the membrane curls into a toroidal rim attached to a membrane cap of roughly fixed radius; and 2), at longer times, the rim radius is fixed, and lipids in the cap flow into the rim. We compare our model with the experimental data of Abkarian and co-workers and obtain an estimate of the induced spontaneous curvature and the membrane viscosity, which control the timescale of parasite release. Finally, eversion of the membrane cap, which liberates the remaining parasites, is driven by the spontaneous curvature and is found to be associated with a breaking of the axisymmetry of the membrane.