Cell proliferation, cell shape, and microtubule and cellulose microfibril organization of tobacco BY-2 cells are not altered by exposure to near weightlessness in space

The microtubule cytoskeleton and the cell wall both play key roles in plant cell growth and division, determining the plant’s final stature. At near weightlessness, tubulin polymerizes into microtubules in vitro, but these microtubules do not self-organize in the ordered patterns observed at 1g. Likewise, at near weightlessness cortical microtubules in protoplasts have difficulty organizing into parallel arrays, which are required for proper plant cell elongation. However, intact plants do grow in space and therefore should have a normally functioning microtubule cytoskeleton. Since the main difference between protoplasts and plant cells in a tissue is the presence of a cell wall, we studied single, but walled, tobacco BY-2 suspension-cultured cells during an 8-day space-flight experiment on board of the Soyuz capsule and the International Space Station during the 12S mission (March–April 2006). We show that the cortical microtubule density, ordering and orientation in isolated walled plant cells are unaffected by near weightlessness, as are the orientation of the cellulose microfibrils, cell proliferation, and cell shape. Likely, tissue organization is not essential for the organization of these structures in space. When combined with the fact that many recovering protoplasts have an aberrant cortical microtubule cytoskeleton, the results suggest a role for the cell wall, or its production machinery, in structuring the microtubule cytoskeleto

Cortical microtubule arrays are initiated from a nonrandom prepattern driven by atypical microtubule initiation

The ordered arrangement of cortical microtubules in growing plant cells is essential for anisotropic cell expansion and, hence, for plant morphogenesis. These arrays are dismantled when the microtubule cytoskeleton is rearranged during mitosis and reassembled following completion of cytokinesis. The reassembly of the cortical array has often been considered as initiating from a state of randomness, from which order arises at least partly through self-organizing mechanisms. However, some studies have shown evidence for ordering at early stages of array assembly. To investigate how cortical arrays are initiated in higher plant cells, we performed live-cell imaging studies of cortical array assembly in tobacco (Nicotiana tabacum) Bright Yellow-2 cells after cytokinesis and drug-induced disassembly. We found that cortical arrays in both cases did not initiate randomly but with a significant overrepresentation of microtubules at diagonal angles with respect to the cell axis, which coincides with the predominant orientation of the microtubules before their disappearance from the cell cortex in preprophase. In Arabidopsis (Arabidopsis thaliana) root cells, recovery from drug-induced disassembly was also nonrandom and correlated with the organization of the previous array, although no diagonal bias was observed in these cells. Surprisingly, during initiation, only about one-half of the new microtubules were nucleated from locations marked by green fluorescent protein-¿-tubulin complex protein2-tagged ¿-nucleation complexes (¿-tubulin ring complex), therefore indicating that a large proportion of early polymers was initiated by a noncanonical mechanism not involving ¿-tubulin ring complex. Simulation studies indicate that the high rate of noncanonical initiation of new microtubules has the potential to accelerate the rate of array repopulation

Effects of water stress during growth of xylem anatomy, xylem functioning and vase life in three Zinnia elegans cultivars

In cut flowers, hydraulic properties and dimensions of xylem vessels in the stem directly influence vase-life and thus post-harvest quality. Xylem hydraulic conductance as well as recovery from air embolisms at the start of vase life strongly depends on number, diameter and length of xylem vessels in the base of the cut flower stems. In this research we employed different water availability levels (high and low water content) in the growing medium of Zinnia elegans plants of three cultivars ('Envy', 'Purple Prince' and 'Scarlet Flame') to modify xylem anatomy and post-harvest xylem functioning and vase life of cut flowers from these plants. Vase-life was longer among fresh-cut Zinnia flowers in all three cultivars grown under low water content in the root medium. Zinnia flowers of all cultivars grown at high water content were not able to sufficiently restore water uptake at the start of their vase life. Shoot hydraulic conductivity was lower in water-stressed plants but it was not different among the three Zinnia cultivars within the same treatment. Anatomical analysis showed smaller xylem vessel diameters but no differences in xylem number and length, with the exception that in cultivar Purple Prince vessels were longer in well-watered plants. We conclude from these results that within these three Zinnia elegans cultivars water stress conditions in the root environment significantly affected xylem anatomy and functioning which correlates well with a longer vase life. Differences in xylem properties between the three cultivars due to pre-harvest watering treatments were limite

Intrusive growth of flax phloem fibers is of intercalary type

Flax (Linum usitatissimum L.) phloem fibers elongate considerably during their development and intrude between existing cells. We questioned whether fiber elongation is caused by cell tip growth or intercalary growth. Cells with tip growth are characterized by having two specific zones of cytoplasm in the cell tip, one with vesicles and no large organelles at the very tip and one with various organelles amongst others longitudinally arranged cortical microtubules in the subapex. Such zones were not observed in elongating flax fibers. Instead, organelles moved into the very tip region, and cortical microtubules showed transversal and helical configurations as known for cells growing in intercalary way. In addition, pulse-chase experiments with Calcofluor White resulted in a spotted fluorescence in the cell wall all over the length of the fiber. Therefore, it is concluded that fiber elongation is not achieved by tip growth but by intercalary growth. The intrusively growing fiber is a coenocytic cell that has no plasmodesmata, making the fibers a symplastically isolated domain within the stem

Cell wall formation in root hairs: role of plasma membrane and cytoskeleton in microfibril deposition

Contains fulltext : mmubn000001_006584101.pdf (publisher's version ) (Open Access)Promotor : M. Sassen215 p