Polarized endoplasmic reticulum aggregations in the establishing division plane of protodermal cells of the fern Asplenium nidus (original) (raw)

Organization of the endoplasmic reticulum in dividing cells of the gymnosperms Pinus brutia and Pinus nigra, and of the pterophyte Asplenium nidus

Cell Biology International, 2003

Endoplasmic reticulum (ER) organization in the dividing cells of the pterophyte Asplenium nidus and of the gymnosperms Pinus brutia and Pinus nigra has been studied by immunolocalization techniques using the monoclonal antibody 2E7, which recognizes luminar ER resident proteins containing C-terminal HDEL sequences. In the pterophyte, the ER reorganization during cell cycle is similar to that in angiosperms. Among others, prominent ER gatherings were found at the mitotic spindle poles and in the phragmoplast during cytokinesis. However, in the gymnosperms examined, the ER displays a unique pattern of reorganization not described so far. In both the Pinus species, well-defined ER patterns are successively formed during cell cycle. They are the preprophase ER-band, the prophase-metaphase-and anaphase ER-spindle, the interzonal ER-system, the ER-phragmoplast and an ER-system lining the daughter cell wall. The ER patterns are closely similar to that of the correspondent microtubule (MT) arrangements with which they are co-organized.

Nucleus-associated microtubules help determine the division plane of plant epidermal cells: avoidance of four-way junctions and the role of cell geometry

The Journal of cell …, 1990

To investigate the spatial relationship between the nucleus and the cortical division site, epidermal cells were selected in which the separation between these two areas is large. Avoiding enzyme treatment and air drying, Datura stramonium cells were labeled with antitubulin antibodies and the threedimensional aspect of the cytoskeletons was reconstructed using computer-aided optical sectioning. In vacuolated cells preparing for division, the nucleus migrates into the center of the cell, suspended by transvacuolar strands. These strands are now shown to contain continuous bundles of microtubules which bridge the nucleus to the cortex. These nucleus-radiating microtubules adopt different configurations in cells of different shape. In elongated cells with more or less parallel side walls, oblique strands radiating from the nucleus to the long side walls are presumably unstable, for they are progressively realigned into a transverse disc (the phragmosome) as broad, cortical, preprophase bands (PPBs) become tighter. The phragmosome and the PPB are both known predictors of the division plane and our observations indicate that they align simultaneously in elongated epidermal cells. These observations suggest another hypothesis: that the PPB may contain microtubules polymerized from the nuclear surface. In elongated cells, the majority of the radiating microtubules, therefore, come to anchor the nucleus in the transverse plane, consistent

Laser microsurgery demonstrates that cytoplasmic strands anchoring the nucleus across the vacuole of premitotic plant cells are under tension. Implications for division plane alignment

1991

In epidermal cells of the plant Nautilocalyx lynchii, induced to divide by explantation, the nucleus undergoes a series of movements, on cytoplasmic leading to construction of a division plane across the vacuole. In the stage, the nucleus separates from the cortex, occupying an eccentric the cell, suspended across the vacuole by few thin strands. In the central the nucleus occupies a central position anchored to the cortex by more thicker strands. Finally, the phragmosome forms as a coalescence of strands across the cell, constituting the division plane within which cytokinesis take place. The behaviour and alignment of these strands is important since some are precursors of the division plane. In a previous (Flanders et al (1990) J. Cell Biol. 110, 1111–1122), it was pointed out alignment of cytoplasmic strands showed features common to a variety of under tension. That is, provided they are free to move relative to the strands radiating from the nucleus should tend to seek short ra...

Organisation of the endosperm and endosperm–placenta syncytia in bladderworts (Utricularia, Lentibulariaceae) with emphasis on the microtubule arrangement

Protoplasma, 2012

Multinucleate cells play an important role in higher plants, especially during reproduction; however, the configurations of their cytoskeletons, which are formed as a result of mitosis without cytokinesis, have mainly been studied in coenocytes. Previous authors have proposed that in spite of their developmental origin (cell fusion or mitosis without cytokinesis), in multinucleate plant cells, radiating microtubules determine the regular spacing of individual nuclei. However, with the exception of specific syncytia induced by parasitic nematodes, there is no information about the microtubular cytoskeleton in plant heterokaryotic syncytia, i.e. when the nuclei of fused cells come from different cell pools. In this paper, we describe the arrangement of microtubules in the endosperm and special endosperm-placenta syncytia in two Utricularia species. These syncytia arise from different progenitor cells, i.e. cells of the maternal sporophytic nutritive tissue and the micropylar endosperm haustorium (both maternal and paternal genetic material). The development of the endosperm in the two species studied was very similar. We describe microtubule configurations in the three functional endosperm domains: the micropylar syncytium, the endosperm proper and the chalazal haustorium. In contrast to plant syncytia that are induced by parasitic nematodes, the syncytia of Utricularia had an extensive microtubular network. Within each syncytium, two giant nuclei, coming from endosperm cells, were surrounded by a three-dimensional cage of microtubules, which formed a huge cytoplasmic domain. At the periphery of the syncytium, where new protoplasts of the nutritive cells join the syncytium, the microtubules formed a network which surrounded small nuclei from nutritive tissue cells and were also distributed through the cytoplasm. Thus, in the Utricularia syncytium, there were different sized cytoplasmic domains, whose architecture depended on the source and size of the nuclei. The endosperm proper was isolated from maternal (ovule) tissues by a cuticle layer, so the syncytium and chalazal haustorium were the only way for nutrients to be transported from the maternal tissue towards the developing embryo.

Endoplasmic reticulum preprophase band in dividing root-tip cells of Pinus brutia

Planta, 2001

In dividing root-tip cells of Pinus brutia Ten., immunolocalization of the luminal endoplasmic reticulum (ER) proteins, which have the C-terminal HDEL sequence, reveals that the ER is reorganized during the preprophase/prophase stage. Portions of ER were arrayed into a ring-like structure at the site of the microtubule preprophase band (Mt-PPB). This preprophase ER band (ER-PPB) resembles that of the Mt-PPB. The former undergoes a maturation process closely similar to that of the latter. Our data show that the PPB region has a more complex organization than is currently believed. The probable function (s) of the ER-PPB is discussed.

Microtubule and actin filament organization during stomatal morphogenesis in the fernAsplenium nidus

Protoplasma, 1997

The newly-formed guard cell mother cells (GMCs) of Asplenium nidus are small, lens-shaped and are formed by one or two asymmetrical divisions. Their growth axis is parallel to the plane of their future division, a process during which the internal periclinal wall (1PW) is detached from the partner wall of the underlying cell(s). This oriented GMC expansion occurs transversely to a microfibril bundle, which is deposited externally to a U-like microtubule (Mt) bundle and a co-localized actin filament (At) bundle. They line the IPW and the major part of the anticlinal walls. The deposition of the microfibril bundle is followed by the slight constriction of the internal part of the GMCs and the broadening of the substomatal cavity. The IPW forms a distinct bulging distal to the neighbouring leaf margin, as well as a less defined proximal one. During the IPW bulging, the Mts and Afs under the external perielinal wall (EPW) attain a radial organization. This is followed by thinning of the central EPW region, which becomes impregnated with a callose-like glucan. The rest of the EPW becomes unequally thickened. The disintegration of the U-like Mt bundle is succeeded by the organization of radial Mt and Af arrays under the IPW. The radial Mt systems, controlling the alignment of the newly-deposited microfibrils, allow the GMC to assume a round paradermal profile. The GMCs form a preprophase Mt band (PPB) perpendicular to the interphase U-like Mt bundle. The anticlinal PPB portions appear first and those lining the periclinal walls later. The cytoplasm adjacent to the latter walls retain the radial Mt systems during early preprophase, simultaneously with the anticlinal PPB portions. The observations suggest that the GMCs of the fern A. nidus obtain a unique form, as a result of a particular polarity established in the cortical cytoplasm of the periclinal walls, in which Mts and Afs appear involved. This polarity persists in cell division and is "inherited" to guard cells (GCs). It provides primary morphogenetic information not only to GMCs but also to GCs.