A new interpretation of plasmodesmatal ultrastructure

Summary It is shown that simple, unbranched, plasmodesmata between young xylem ray cells of willow have no direct intercellular continuity apart from the plasmalemma which limits the cytoplasm and lines the plasmodesmatal canal. Each plasmodesma is traversed by a 200 Å diameter tubule (the desmotubule) which has a wall with probably 11 subunits arranged around a central cavity through which runs a 40 Å diameter rod. This rod is connected to the inside of the tubule wall, by fine filaments. At the ends of each plasmodesma the plasmalemma and cell wall are closely appressed to the tubule, thus precluding direct continuity between the cytoplasm of adjacent cells. Through the central part of the plasmodesmata the tubule is separated from the plasmalemma by a 90–100 Å wide gap. Cytoplasmic microtubules in the same tissue have a diameter of approximately 250 Å and a wall probably composed of 13 subunits: both desmotubules and cytoplasmic microtubules therefore have a centre-to-centre subunit spacing of about 47 Å. It is suggested that the desmotubules are not microtubules but may be nuclear spindle fibres which become trapped in the wall during cell plate formation. The endoplasmic reticulum, while closely approaching the plasmodesmata, is not continuous across them. It is thought most unlikely that the endoplasmic reticulum traverses plasmodesmata, as the dimensions of the central tubule — found here as well as by other workers — are smaller than those which would be expected to allow a stable molecular configuration in a unit membrane. The plasmalemma, where it lines the plasmodesmatal canal, appears to have particulate subunits in the outer opaque layers and the presence of these subunits may be attributable to the need for stability in membranes arranged about so small a radius.     

Freeze fracture studies on the annelid septate junction

Summary Freeze-fractured preparations of septate junctions between epidermal cells of annelids (Lumbricus terrestris and Tubifex spec.) have been investigated. In Lumbricus the protoplasmic face (PF) of the plasma membrane is characterized by variously arranged rows of particles. Apically the rows take an undulating course and often are separated by wide distances. In the basal part of the junction the rows run closely together and more or less in parallel. The diameter of the particles measures 80–120 Å, the distance between two particles (centre to centre) is 150–250 Å. Additionally striking rows of large particles (long diameter 150–200 Å). Are to be observed mainly near the basal part of the junction. In Tubifex both faces of the plasma membrane could be studied in detail. The protoplasmic face (PF) contains rows of distinct individual particles (mean diameter 100–150 Å, centre to centre distance approx. 250 Å) whereas the particles of the extracellular face (EF, mean diameter 200–250 Å) usually form continuous strands in which the individual particles seem to fuse. The density of arrangement of the strands varies considerably. Additionally ladder-shaped membrane structures have been observed in plasma membranes of this species.     

Zur Feinstruktur der Plasmodesmen und Plasmakanäle bei Pollenmutterzellen

Zusammenfassung Bei Tomate (Lycopersicum esculentum) und Kürbis (Cucurbita maxima) wurde der Feinbau der zwischen den Pollenmutterzellen bestehenden Plasmaverbindungen elektronenmikroskopisch untersucht.Neben feinen, den Verhältnissen in meristematischen somatischen Zellen entsprechenden Plasmaverbindungen (Plasmodesmen im engeren Sinne, Durchmesser im geometrischen Mittel 253,3 Å) wurden relativ breite, fast durchweg gröbere Cytoplasmaeinschlüsse (Mitochondrien, Vesikel, Potocytose-Bläschen, Dictyosomen usw.) aufweisende Verbin-dungen (Plasmakanäle, Durchmesser im geometrischen Mittel 0,175 ) festgestellt. Elemente des Endoplasmatischen Reticulums finden sich regelmäßig in den Plasmakanälen. Sie lassen sich jedoch häufig auch in größeren Plasmodesmen nachweisen.Weder über den Zeitpunkt der Entstehung, noch über die Entstehungsweise der Plasmakanäle lassen sich bei unserem Pflanzenmaterial konkrete Angaben machen. Gleiches gilt hinsichtlich des Zeitpunktes und der Art, wie die Plasmakanäle schließlich schwinden.Unbekannt ist auch die Art und Weise, wie die Plasmodesmen in Verbindung mit der Bildung der die Pollenmutterzellen bzw. auch die einzelnen Tetradenzellen umhüllenden dicken Callosemembranen schwinden.Bei der Tomate sind die Plasmakanäle bereits vor Aufgabe der Plasmodesmen vorhanden. Andererseits lassen sie sich in späteren Phasen der Tetradenentwicklung nicht mehr nachweisen.Die Beobachtungen werden in Verbindung mit bereits vorliegenden Angaben in der Literatur, insbesondere im Hinblick auf die Bedeutung der Plasmakanäle und ihre Ähnlichkeit mit Siebporen, diskutiert.

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On the fine structure of plasmodesmata and plasma-channels in pollen mother cells (PMC)

Summary The fine structure of plasmatic connections between PMC has been examined by electron microscopy in tomato (Lycopersicum esculentum) and squash (Cucurbita maxima).In addition to plasmodesmata, of geometrical mean diameter 253.3 Å, which correspond to the plasmodesmata in meristematic somatic cells, there are also to be distinguished plasma-channels of geometrical mean diameter 0.175 , which frequently contain cytoplasmic inclusions, such as mitochondria, vesicles, potocytosevesicles, dictyosomata etc. Generally we found elements of the endoplasmic reticulum in the plasma-channels. These elements are also to be found in larger plasmodesmata.We do not know the time nor the manner in which the plasma-channels of our plants originate and disappear. Also it is unknown how the plasmodesmata disappear when the thick callose-membrane is formed around the PMCs and the tetrad-cells.In the tomato the plasma-channels are present before the plasmodesmata disappear. On the other hand they are absent in later stages of tetrad development.The observations are discussed with regard to the possible function of the plasma-channels and their similarity to sievepores.

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Mit 17 Textabbildungen     

Parenchyma cells of secondary phloem in Pinus strobus

Summary Parenchyma cells of the secondary phloem in Pinus strobus have all the cellular organelles common in other plant cells. They have mitochondria, endoplasmic reticulum, ribosomes, dictyosomes, and plastids. Parenchyma cells are very conspicuous because of their organic inclusions, starch and lipids. Plasmodesmata in transverse and tangential walls of axial parenchyma cells and in end walls of ray parenchyma cells are regularly distributed and of uniform size, about 500 Å in diameter. In radial walls of axial parenchyma cells and horizontal walls of ray parenchyma cells plasmodesmata are located in primary pit-fields; there they are of variable size and often divided into several branches. The branches are confluent into a median nodule. Perforation of the transverse wall between two axial parenchyma cells and the resultant union of the cellular material of the two connected cells is reported.This research has been supported by NSF Grant GB 3193.     

Spermatozoen und Spermiohistogenese vonGraphidostreptus spec. (Myriapoda,Diplopoda)

Zusammenfassung Die reifen Spermatozoen des afrikanischen TausendfüßlersGraphidostreptus spec. (Diplopoda) wurden licht- und elektronenmikroskopisch untersucht.Die hutförmigen Spermatozoen sind paarweise in Spermatophoren vereinigt. Sie bestehen aus einer den scheibenförmigen Kern enthaltenden Platte und einem Zylinder, in dem sich der Akrosomkomplex befindet. — Der freie Rand des Hutes und eine basale Schicht unter dem Karyoplasma werden von sehr elektronendichtem Zytoplasma gebildet, das basal halbkugelige Vorwölbungen besitzt. Das basale Zytoplasma enthält helle Röhrchen von ca. 100 Å Durchmesser. — Dem Karyoplasma fehlt eine Kernmembran. Es besteht aus einer elektronendichten Substanz und ist vollständig von langen, 400 Å dicken hellen Röhrchen durchsetzt. Die Röhrchen enthalten einen elektronendichten Tubulus von 200 Å Durchmesser, in dessen Achse ein ca. 40 Å dickes Filament liegt. — In den Rand des Kernes ist dorsal ein Ring von Mitochondrien eingelassen. — Der den Zylinder bildende Akrosomkomplex besteht aus einem Mantel streifigen Materials unter der Zellmembran, aus der nageiförmigen Akrosomvakuole, einem im Schnitt M-förmigen Körper, einer halbkugeligen Kalotte und einem zentral gelegenen Kristalloid.

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Spermatozoa and spermiohistogenesis in Graphidostreptus spec. (Myriapoda, Diplopoda)I. The mature spermatozoa

Summary The mature spermatozoa of the African millipedeGraphidostreptus spec. (Diplopoda) were studied by light and electron microscopy. The hat-like spermatozoa are combined two by two in spermatophores. They consist of a plate containing a disk-like nucleus, and a cylinder containing the acrosomal complex. — The free border of the hat and a basal layer below the caryoplasma are formed by a very electron-dense cytoplasma with hemispheric protrusions on the basal side. The basal cytoplasma contains light canaliculi with a diameter of about 100 Å. — There is no membrane around the caryoplasma which is composed of an electrondense substance. It is completely filled up with long and light canaliculi with a diameter of 400 Å. These canaliculi contain an electron-dense tubulus of about 200 Å diameter, in the axis of which a filament of about 40 Å diameter is to be found. — In the border of the nucleus on its dorsal side there is a circle of mitochondria. — The acrosomal complex building up the cylinder is composed of an envelope of striated material below the cell membrane, of a nail-like acrosomal vacuole, of a body appearing in section like a M, of a hemispheric calotte, and of a cristalloid lying in the center.

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Wir danken der Deutschen Forschungsgemeinschaft und der Joachim Jungius-Gesellschaft der Wissenschaften in Hamburg für Sachbeihilfen.     

Electron-microscope studies of Drosophila salivary-gland chromosomes

Summary The submicroscopic structure of the chromosomes of the larval salivary gland cells inDrosophila melanogaster has been studied by means of electron microscopy of thin sections.The three fixatives used were buffered 1% osmium tetroxide, unbuffered Zenker's solution, and buffered formaldehyde in concentrations of 0·1% and 1·0%. It was found that formalin preserves the fine structure of the chromosomes better than the other fixatives.Nucleoprotein is present in the chromosome in the form of granules 200 Å to 300 Å in diameter. The granules are connected together by strands of protein approximately 100 Å in diameter. The length of the strands between successive granules in the banded areas is 100 Å to 300 Å and in the interband regions it is 700 Å to 900 Å.Heterochromatin differs from euchromatin in the absence or reduction in the amount of strand material.The nucleolus is composed of an aggregate of granules 300 Å to 600 Å in diameter contained in an amorphous matrix. Within the nucleolus are a series of canals containing material similar in appearance to that of the euchromatic band material.Submicroscopic granules are also present in the karyoplasm and in the cytoplasm surrounding the nuclear membrane. The cytoplasmic granules are more densely distributed near the nuclear membrane.A model for chromosome structure is proposed.The Applied Fisheries Laboratory is operated by the University of Washington under Contract No. AT(45-1)540 with the United States Atomic Energy Commission.     

Substructure of freeze-substituted plasmodesmata

Summary The substructure of plasmodesmata in freeze-substituted tissues of developing leaves of the tobacco plant (Nicotiana tabacum L. var. Maryland Mammoth) was studied by high resolution electron microscopy and computer image enhancement techniques. Both the desmotubule wall and the inner leaflet of the plasmodesmatal plasma membrane are composed of regularly spaced electron-dense particles approximately 3 nm in diameter, presumably proteinaceous and embedded in lipid. The central rod of the desmotubule is also particulate. In plasmodesmata with central cavities, spoke-like extensions are present between the desmotubule and the plasma membrane in the central cavity region. The space between the desmotubule and the plasma membrane appears to be the major pathway for intercellular transport through plasmodesmata. This pathway may be tortuous and its dimensions could be regulated by interactions between desmotubule and plasma membrane particles.Abbreviations ER endoplasmic reticulum - PJF propane jet freezing - HPF high pressure freezing - CRT cathode ray tube - IP₃ inositoltrisphosphate     

Ultrastructure of the median eminence of the rat

Summary The ependymal cells bordering the median eminence to the third ventricle are characterised by many microvillus-like projections and bulbous cell processes of the luminal plasma membrane. The latter contain many vesicles 500–1,000 Å in diameter. Cilia with 9+2 fibrillar pattern are seen occasionally. Adhesive devices in the from of zonula adhaerens and zonula occludens are found in the apical part of the intercellular junction. Unmyelinated nerve fibres with a mean diameter of 1 and containing many electron dense granules of 830–1,330 Å are often seen between the ependymal cells.Two types of glial cells are found in the median eminence. One is characterised by a nucleus with dense blods of chromatin and dense cytoplasm, and it is associated chiefly with the nerve fibres in the region of the hypothalamo-hypophysial tract. The other type of glial cell is characterised by fine, uniformly distributed chromatin in the nucleus and a relatively pale cytoplasm and branched processes which terminate perivascularly in the base of the median eminence.Myelinated nerve fibres are seen only in the region of the hypothalamo-hypophysial tract. Only a part of them contain electron dense granules 1,330–2,330 Å in diameter.Three types of unmyelinated nerve fibres can be distinguished in the median eminence according to the size of the electron dense granules they contain: 1. Nerve fibres containing granules 1,330–2,330 Å in diameter. They are seen primarily in the hypothalamo-hypophysial tract, but also in the zona externa; 2. those containing granules with a mean diameter of 1,330 Å; and 3. those containing granules with a mean diameter of 1,000 Å. The last two types are both encountered in the hypothalamo-hypophysial tract, the zona externa and the perivascular region of the base of the median eminence. Under high magnification, the membrane of the granules show evidence of a trilaminar structure and the content of the granules with a low electron density appeares to consist of small microvesicles or globular components. Besides granules, these nerve fibres contain vesicles mostly 420 Å in diameter whose relative number increases towards the perivascular nerve endings. 53 per cent of the inclusions in the hypothalamo-hypophysial tract are granules and 47 per cent vesicles, while the corresponding percentages for the zona externa are 40 and 60 and for the perivascular nerve endings 20 and 80.The mean width of the pericapillary space is 1 , but it varies greatly. It containes many collagen fibrils and fibroblasts. The capillary endothelium is frequently fenestrated and contains many vesicles of various sizes.Two types of granules-containing cells are found in the pars tuberalis depending on the size of the electron dense granules: 1. cells containing granules with a mean diameter of 1,330 Å: and 2. cells containing granules with a mean diameter of 2,000 Å. In addition, there are occasional follicular cavities filled with amorphous material, microvilli and cilia of 9+2 fibrillar pattern.Aided by a grant from the Sigrid Jusélius Stifteise.     

The fine structure of the hypothalamic secretory neurons of the White-crowned Sparrow,Zonotrichia leucophrys gambelii (Passeriformes: Fringillidae)

Summary The fine structures of the neurons and neuropils of the magnocellular supraoptic nucleus and the parvocellular nuclei of the rostral hypothalamus, including the suprachiasmatic and medial, lateral and periventricular preoptic nuclei, and the neuronal apparatus of the organum vasculosum laminae terminalis, have been examined in the male White-crowned Sparrow, Zonotrichia leucophrys gambelii, by correlated light and electron microscopy.The magnocellular supraoptic nucleus is characterized by large neurosecretory perikarya which contain a well developed Golgi complex and densecored granules 1,500–2,200 Å in diameter. The neuropil displays axons, dendrites and glial fibers. Some axonal profiles contain dense-cored vesicles 800–1,000 Å in diameter and clear vesicles 500 Å in diameter. Axo-somatic and axo-dendritic synapses are conspicuous in this nuclear region.The suprachiasmatic nucleus is characterized by an accumulation of small neurons with moderately developed cellular organelles and some dense-cored granules, approximately 1,000 Å in diameter. The profiles of axons within the neuropil contain dense-cored granules 800–1,000 Å in diameter and clear vesicles 500 Å in diameter.The neurons of the medial preoptic nucleus are relatively large and exhibit well developed cellular organelles and dense-cored granules 1,300 to 1,500 Å in diameter. Granular materials are formed within the Golgi complex. The medial preoptic nucleus is rich in secretory perikarya.Occasionally, neurons with granules 1,500–2,200 Å in diameter are encountered in the lateral preoptic and periventricular preoptic nuclei. They may be considered as scattered elements of the magnocellular (supraoptic and paraventricular) system.The organum vasculosum laminae terminalis consists of three layers, i.e., ependymal, internal and external zones, and exhibits a vascular arrangement similar to that of the median eminence. The perikarya of the parvocellular neurons and their axons in the internal zone contain numerous secretory granules ranging from 1,300 to 1,500 Å in diameter.This investigation was supported by Grant No. 5R040 Japan-U.S. Cooperative Science Program of the Japan Society for the Promotion of Science to Professor H. Kobayashi and Professor S.-I. Mikami, by a Scientific Research Grant No. 56019 from the Ministry of Education of Japan to S.-I. Mikami, by support from the Deutsche Forschungsgemeinschaft (Schwerpunktprogramm Biologie der Zeitmessung) to Prof. A. Oksche and by Grant No. GF 33334, U.S.-Japan Cooperative Science Program of the National Science Foundation to Prof. D.S. Farner.Herrn Professor Dr. Dres h.c. Wolfgang Bargmann zu seinem 70. Geburtstag am 27. Januar 1976 gewidmet.     

The ultrastructure of organelles appearing in spermatids and nutritive cells of Cipangopaludina malleata

Summary The ultrastructure of organelles appearing in the early typical and atypical spermatids, and the nutritive cells of Cipangopaludina malleata has been examined by a Siemens' electron microscope Elmiskop I.Mitochondria appearing in the early typical spermatid have doughnut-like profiles in which the internal ridges appear as triple-layered membranes arranged radially and extending into the interior of the organelle without reaching the other side. Each membrane 40–60 Å in width, separated by a clear interspace 60–90 Å wide, is characterized by a porous structure 20–30 Å in diameter which suggests a filtration apparatus for enzymes.Walls of the flattened saccules consisting the Golgi apparatus are calculated 35–60 Å thick, in which an electron-lucent, porous structure about 30 Å wide has been revealed.The smooth-surfaced endoplasmic reticulum is bordered by a triple-layered membrane consisting of two opaque layers with a less opaque interspace 20–30 Å wide. The outer membrane ca. 15 Å wide presents a more linear appearance than the dotted arrangement of the inner membrane 20–25 Å thick.The plasma membrane is composed of a triple-layered structure where two dense lines 15 Å wide are separated by a layer 20–30 Å thick of less density.The electron micrographs for the present studies were taken with the Siemens electron microscope, model Elmiskop I, at the Anatomical Institute of Kiel University, Germany. The one of the authors, G. Yasuzumi is deeply grateful to Prof. Dr. W. Bargmann and Dr. A. Knoop for the privilege of using this instrument and other equipments in the Laboratory.     

Plasmodesmal widening accompanies the short-term increase in symplasmic phloem unloading in pea root tips under osmotic stress

Summary Root tips ofPisum sativum seedlings were exposed to 350 mM mannitol, which was shown to effect a transient but dramatic increase in phloem unloading, and investigated by electron microscopy. After chemical fixation and embedding, extremely thin sections of the root extension zone were examined. Outer, inner, and desmotubule diameters of 830 primary plasmodesmata in transverse walls of cortical cells were measured. Statistical analysis indicated that the majority of plasmodesmata had no neck constriction during osmoregulation. Compared to controls, a highly significant increase in mean plasmodesmata diameter was found, but the desmotubule diameter remained unchanged. Both loss of neck constriction and widening of the cytoplasmic sleeve indicate an increase in effective passage area of plasmodesmata. Spokes between plasma membrane and desmotubule were preserved. Continued exposure of the root tips to mannitol led to a return to control values for plasmodesmal diameters. In contrast to these responses, plasmolysis of cortical cells by 1,000 mM sucrose, diminishing phloem unloading, was accompanied by a reduction in those plasmodesmata classified as open. This is the first report showing a correlation between the ultrastructure of plasmodesmata and the rate of symplasmic transport. The role of the different plasmodesmal components in controlling the passage area of symplasmic transport is discussed.     

THE NATURE OF PLASMODESMATA IN NORMAL (LIVING) PLANT TISSUE

Techniques have been devised for the demonstration and study of plasmodesmata in an unaltered state in plant tissues. Text figures and data are presented for plasmodesmata in the cambium and certain other tissues of Pinus strobus, parenchyma tissues of Lycopersicum esculentum, and ray and wood parenchyma tissue of Sequoia sempervirens. In all cases, the plasmodesmata were of similar morphology, with a diameter of approximately 0.2μ. Comparative studies are presented showing the effects of various swelling agents which were used in past studies, and of dehydration which is a normal concomitant of most histological procedures. The present paper provides an important base line for the comparison of the appearance of plasmodesmata in living tissue to the findings of recent studies with the electron microscope.     

Ultrastructural analysis of leaf trichome plasmodesmata reveals major differences from mesophyll plasmodesmata

Functional studies on molecular transport through plasmodesmata in leaf mesophyll and trichome cells revealed significant differences in their basal size-exclusion limits and their response to microinjected tobacco mosaic virus movement protein (E. Waigmann et al., 1994, Proc. Natl. Acad. Sci. USA 91: 1433–1437; E. Waigmann and P. Zambryski, 1995, Plant Cell 7: 2069–2079). To address the basis for these functional differences, Nicotiana clevelandii trichome and mesophyll plasmodesmata were compared ultrastructurally. Trichome plasmodesmata increase in ultrastructural complexity from the tip to the base cell. Their neck regions, thought to control molecular traffic through plasmodesmata, are clearly distinct from necks of mesophyll plasmodesmata. In contrast to the electron-dense desmotubular area in mesophyll plasmodesmata, trichome plasmodesmata contain an electron-translucent circle in their center, surrounded by an electron-dense ring. This latter ring is connected to the inner leaflet of the plasma membrane by multiple spokes or filaments. Two monoclonal antibodies raised against a maize plasmodesmal protein preparation (A. Turner et al., 1994, J Cell Sci. 107: 3351–3361) interact with both trichome and mesophyll N. clevelandii plasmodesmata. Based on the localization pattern and the high degree of cross-reactivity, both antibodies likely recognize a conserved structural component of plasmodesmata, and may be useful to mark plasmodesma in a variety of plants and tissues. Received: 24 January 1997 / Accepted: 3 March 1997     

Crystal structure of a conserved hypothetical protein from Escherichia coli

The crystal structure of a conserved hypothetical protein from Escherichia coli has been determined using X-ray crystallography. The protein belongs to the Cluster of Orthologous Group COG1553 (National Center for Biotechnology Information database, NLM, NIH), for which there was no structural information available until now. Structural homology search with DALI algorism indicated that this protein has a new fold with no obvious similarity to those of other proteins with known three-dimensional structures. The protein quaternary structure consists of a dimer of trimers, which makes a characteristic cylinder shape. There is a large closed cavity with approximate dimensions of 16 Å × 16 Å × 20 Å in the center of the hexameric structure. Six putative active sites are positioned along the equatorial surface of the hexamer. There are several highly conserved residues including two possible functional cysteines in the putative active site. The possible molecular function of the protein is discussed.     

The fine structure of the pellicle ofEuglena gracilis as revealed by freeze-etching

Summary The ultrastructure of the pellicle ofEuglena gracilis (Klebs) Z strain was studied using the freeze-etching technique and the results were correlated with data obtained from thin sections of fixed material.Examination of freeze-etched pellicles reveals an outer particulate layer and an inner striated layer. The particles of the outer layer measure approximately 150 Å in diameter. The striations of the inner layer are about 50 Å wide and are separated from each other by about 35 Å. A broad repeating pattern is also visible with a periodicity of about 450 Å. When deep etching is employed, a smooth outer layer is seen covering the particulate layer. This is probably the outer surface of the plasma membrane. Mucilage is present on the outer surface of the cell and is seen as a substructure of threads superposed on the smooth layer of plasma membrane.Thin sectioning also shows a striated layer interior to the plasma membrane. This appears to be identical to the striated layer seen after freeze-etching.     

Electron microscopical observations on the brush border of proximal tubule cells of mammalian kidney

Summary The ultrastructure of the plasma membrane and the core of microvilli of proximal tubule cells has been investigated by electron microscopy using sectioned and negatively stained material. By the technique of negative staining, a particulated coat is disclosed on the outside of the plasma membrane of microvilli of brush borders isolated from rat, rabbit and ox. This coat is composed of 30 to 60 Å particles and is 150 to 300 Å thick and appears to be a distinguishing feature for the luminal plasma membrane (brush border) of proximal tubule cells. The plasma membrane of the basal part of tubule cells is found to be smooth. By thin sectioning, an axial bundle of 50 to 70 Å diameter filaments regularly arranged in an 1+6 configuration, one axially located filament being surrounded by a ring of six, is disclosed. The distance from the ring of filaments to the inner surface of the plasma membrane is 250–300 Å, the diameter of the ring 300 Å and the center-to-center distance between filaments 120 Å. Negative staining also discloses 60 Å filaments in microvilli of isolated brush borders. Broken off, single microvilli (fingerstalls) are observed with thin filaments projecting from their broken ends. Filaments up to 1 in length are seen. At high magnification, the filaments appear beaded and show strong resemblance with actin filaments isolated from skeletal muscle. Based on present evidence, it is postulated that microvilli constituting renal brush borders possess contractile properties, which may play a role in the absorption process operating at the luminal part of the cells.The authors are indebted to Miss Kirsten Sjöberg for skilled technical assistance, and to the Danish State Research Foundation and the Tuborg Foundation for financial support.     

Filament Disruption in Funaria Protonemata: Occlusion of Plasmodesmata

Plasmodesmata are occluded when Funaria chloronemata are fragmented by the development of tmema cells (TCs). The TC deposits a new wall layer along the cross wall toward the neighbouring non-sister cell (NC). This wall layer cuts off the plasmodesmata and its connection with the cross wall is soon lost. The plasmodesmata become isolated when the NC forms a new wall layer along the former cross wall. At the end of TC development, before its disintegration, the sister cell (SC) also deposits a new wall layer along the cross wall toward the TC, cutting off the plasmodesmata. For some time the plasmalemma of the plasmodesmata remains connected to the NC or the TC, whereas the desmotubule soon disappears. Relicts of the plasmalemma remain even after the isolation of the plasmodesmata and the disintegration of the TC. During the decay of the plasmodesmata, a cylinder of electron-dense material is frequently formed along the border of the plasmodesmatal channel. This may extend over the surface of the cell wall. Eventually, the plasmodesmatal channel is filled with wall material. Callose is only observed around functional plasmodesmata and does not seem to play a role in their occlusion.     

Tubuläre intranukleäre Einschlußkörper beiLinaria vulgaris,L. alpina (Scrophulariaceae) undIncarvillea variabilis (Bignoniaceae)

The epidermal nuclei of the ovary inLinaria vulgaris andL. alpina, and the nuclei in leaves ofIncarvillea variabilis often contain crystalloid, tubular inclusions. The tubuli in bothLinaria species have an average diameter of 200 Å with a width of 70 Å in the clear and are arranged in a higly organized manner: Parallel tubuli form layers which build up a crystal lattice. There are three directions of tubuli in each inclusion: In each layer they are aligned in an angle of 60° to those of the next, so that the tubuli of the fourth layer are in the same direction as those of the first one. InIncarvillea the tubuli (each with an average diameter of 220 Å, and 70 Å width in the clear) also exhibit compact packing, but their arrangement is not so highly ordered as inLinaria.

     

Chromosome fibers studied by a spreading technique

Chromosomes and interphase nuclei can be spread on the surface of water in a simplified Langmuir trough. Interphase nuclei of Triturus erythrocytes display fibers with a diameter of about 250–300 Å. Very similar fibers are seen in metaphase chromosomes of cultured human cells. Fibers from grasshopper spermatocyte chromosomes (prophase) are more variable in diameter, and many fibers thinner than 200 Å extend laterally from the chromosome. In the grasshopper spermatocyte, fibers align in parallel to form plates. It is suggested that the 250–300 Å fibers may represent an inactive state of the chromosome material, and that only the thinner fibers are involved in RNA synthesis. The 250–300 Å fibers may result from the folding or coiling of a thinner fiber having the approximate dimensions of the nucleohistone molecule.     

Ultrastructure of the neurohaemal region of the toad median eminence

Summary According to the internal structure and size of the granules, six types of nerve endings can be distinguished in the toad median eminence: 1. Endings containing mostly dense granules of 600 Å in diameter; 2. Endings containing dense granules of about 800 Å in diameter; 3. Endings which contain dense granules 1,000–2,000 Å in diameter, with the peak at 1,200–1,400 Å; 4. Endings containing granules with a characteristic structure, which differentiate them from the other three types; 5. Scarce endings containing granules 2,000 to 3,800 Å in diameter; and 6. Endings containing only vesicles 400–500 Å in diameter. Types 3 and 4 endings are mainly found in the outer pericapillary zone, and are probably responsible for the strong Gomori-positive reaction observed in this zone. The other four types of endings occur mainly in the inner pericapillary zone, and appear to be Gomori-negative.The probable origins of the different types of endings, and their possible relations with the different releasing factors is discussed.The subendothelial basement membrane has numerous long processes which form a complicated network in contact with all the nerve endings, some nerve fibres and glial cells.Two types of glial cells are described. Pinocytotic vesicles are frequently seen at the points where these cells contact the basement membrane. All the ultrastructural features suggest that these cells are carrying out transport functions.Fellow of the Consejo Nacional de Investigaciones Científicas y Técnicas de la República Argentina.The author is very grateful to Professor H. Heller for his continued encouragement and criticism and to Mr. J. Lane and Mr. P. Heap for their valuable help.